- Research article
- Open Access
Variation in secondary metabolite production potential in the Fusarium incarnatum-equiseti species complex revealed by comparative analysis of 13 genomes
BMC Genomics volume 20, Article number: 314 (2019)
The Fusarium incarnatum-equiseti species complex (FIESC) comprises 33 phylogenetically distinct species that have been recovered from diverse biological sources, but have been most often isolated from agricultural plants and soils. Collectively, members of FIESC can produce diverse mycotoxins. However, because the species diversity of FIESC has been recognized only recently, the potential of species to cause mycotoxin contamination of crop plants is unclear. In this study, therefore, we used comparative genomics to investigate the distribution of and variation in genes and gene clusters responsible for the synthesis of mycotoxins and other secondary metabolites (SMs) in FIESC.
We examined genomes of 13 members of FIESC that were selected based primarily on their phylogenetic diversity and/or occurrence on crops. The presence and absence of SM biosynthetic gene clusters varied markedly among the genomes. For example, the trichothecene mycotoxin as well as the carotenoid and fusarubin pigment clusters were present in all genomes examined, whereas the enniatin, fusarin, and zearalenone mycotoxin clusters were present in only some genomes. Some clusters exhibited discontinuous patterns of distribution in that their presence and absence was not correlated with the phylogenetic relationships of species. We also found evidence that cluster loss and horizontal gene transfer have contributed to such distribution patterns. For example, a combination of multiple phylogenetic analyses suggest that five NRPS and seven PKS genes were introduced into FIESC from other Fusarium lineages.
Our results suggest that although the portion of the genome devoted to SM biosynthesis has remained similar during the evolutionary diversification of FIESC, the ability to produce SMs could be affected by the different distribution of related functional and complete gene clusters.
The genus Fusarium includes some of the most destructive plant pathogens of food and feed crops and produces some of the mycotoxins of greatest concern to food and feed safety. Collectively, Fusarium species (fusaria) are pathogenic on most economically important crops and produce structurally diverse secondary metabolites (SMs), including mycotoxins that have adverse health effects, including immune suppression and cancer [1, 2]. Phylogenetic analysis has resolved the genus into 22 species complexes and seven monotypic lineages that together include over 300 phylogenetically distinct species [3,4,5].
Advances in Next Generation Sequencing technologies and bioinformatics software have provided powerful tools to expand understanding of variation in genomes within and among lineages of Fusarium [6,7,8,9]. Two recent studies focused on variation within single lineages. The first study compared 10 isolates of the Fusarium graminearum species complex and highlighted the extent of genetic diversity and similarity among the genomes . For example, of the 15,297 genes present in the pan-genome of these fungi, 12% were absent in at least one species. Furthermore, the analyses identified 163 pan-genes that exhibited high variability among genomes that was consistent with allelism and could reflect a role in niche adaptation and disease. The second study compared five members of the F. fujikuroi species complex and revealed that although a large percentage of SM biosynthetic genes were conserved among the fungi examined, there were species and isolate-specific differences in gene content and expression . The authors concluded that the differences had potential to affect host specificity as well as the pathogenic versus endophytic lifestyles of the fungi.
Members of the Fusarium incarnatum-equiseti species complex (FIESC) are cosmopolitan soil inhabitants, but can also occur on aerial plant parts, and are often recovered along with plant pathogens in field surveys of cereals, fruits, and vegetables . FIESC members are regarded as moderately aggressive plant pathogens and are associated with human and insect infections as well [11,12,13,14,15]. Collectively, FIESC species can produce multiple mycotoxins, including apicidin , beauvericin , butenolide , enniatins , equisetin , trichothecenes [21, 22], fusarochromanone  and zearalenone .
FIESC has been resolved into 33 phylogenetically distinct species that group into two major clades, designated Equiseti and Incarnatum, using DNA-based Genealogical Concordance Phylogenetic Species Recognition (GCPSR) [14, 22, 25, 26]. Most species within the complex have not been formally described and are referred to with the designations FIESC 1 – FIESC 33 rather than with Latin binomials. However, three of the species have Latin binomials: F. equiseti (FIESC 14), F. lacertarum (FIESC 4) and F. scirpi (FIESC 9) . Furthermore, analyses indicate that F. camptoceras likely represents a third lineage of FIESC [22, 27].
Although chemical analyses indicate that various members of FIESC produce the SMs noted above, production of all eight SMs has not been reported in all FIESC members. Overall, little is known about the variation in SM biosynthetic gene clusters within the complex. At present, only one FIESC genome (strain CS3069, a member of phylogenetic species FIESC 5) is publically available . The presence of 11 polyketide synthase (PKS) genes and 13 non-ribosomal peptide synthetase (NRPS) genes in the CS3069 genome sequence suggest that the SM production potential of FIESC is much greater than what has been observed by chemical analyses [8, 29, 30].
A number of studies suggest that SM gene content varies among FIESC members and between FIESC and other lineages of Fusarium. One study revealed marked differences in the trichothecene biosynthetic gene (TRI) cluster and other TRI loci in FIESC versus other trichothecene-producing fusaria, such as F. graminearum and F. sporotrichioides . The differences include: translocation of three genes (TRI3, TRI7, and TRI8) within the TRI cluster; translocation of two genes, TRI1 and TRI101, into the FIESC TRI cluster from other genomic locations; absence of the trichothecene transporter gene TRI12 in FIESC; and the presence of a novel Zn2Cys6 transcription factor gene in the FIESC TRI cluster that is absent in other trichothecene-producing fusaria . Other studies provide evidence that production of trichothecenes and other mycotoxins differs among phylogenetic species and haplotypes within FIESC [21, 22, 31]. However, the genetic bases of such variation have not yet been investigated. In addition, the extent of variation among FIESC members irrespective of SM biosynthetic genes remains largely unknown. In the current study, therefore, we employed a comparative genomic approach to examine the distribution and variability of SM biosynthetic genes among 13 members of FIESC. The results indicate that the percent of the genome likely involved in SM synthesis in FIESC is similar to other fusaria, and that there is considerable variation in potential for production of SMs among FIESC members. Our results also revealed genetic variation within FIESC that is consistent with previously observed phenotypic variability.
Although multiple studies have examined the diversity of secondary metabolite biosynthetic genes and gene clusters within lineages of fungi within a genus [8, 9], these studies have not systematically explored possible evolutionary processes that have contributed to the diversity. Therefore, in the current study, we generated genome sequences for a subset of members of FIESC, examined diversity and distribution of secondary metabolite biosynthetic genes in FIESC genomes, and then investigated evolutionary processes that have likely contributed to the observed distribution using a combination of data from FIESC and other fusaria.
The twelve FIESC strains selected for genomic sequence analysis in this study represent a wide range of the phylogenetic diversity that exists within FIESC and were isolated from a broad range of host plants . Analysis of the genome-sequence data indicated that the genomes were similar in size, ranging from 36.7 Mb in F. camptoceras to 39.9 Mb in F. equiseti. This range of sizes is comparable to the 38-Mb genome previously described for FIESC 5 strain CS3069  as well as to other previously described genomes for species in other lineages of Fusarium: e.g., 41.5–43.1 Mb for F. avenaceum, 43.9 Mb for F. fujikuroi , 36 Mb for F. graminearum , and 41.8 Mb for F. verticillioides  (Table 1). The FIESC genome sizes are substantially less than those of F. oxysporum, F. poae and F. solani f. sp. pisi (46–60 Mb), which have large accessory genomes: that is genomic regions not shared by related species and in some cases by different strains of the same species, or duplicated genes, transposons and repetitive sequences [6, 33, 34].
To assess phylogenetic relationships of FIESC members to one another and to other fusaria, we inferred a species tree that included the 13 FIESC members and 24 species from nine other Fusarium species complexes (Fig. 1). For brevity here, we will refer to species complexes, except FIESC, using the specific epithets upon which the complex names are based (e.g., Sambucinum complex instead of the F. sambucinum species complexes). The species tree was generated by the extended majority rule (MRE) consensus approach using Maximum Likelihood (ML) trees inferred separately for each of 30 housekeeping (HK) genes (Additional file 1). For evaluation of branch support, we used internode certainty and bootstrap analyses. The latter were obtained by ML analysis of concatenated sequences of the 30 HK genes. Internode certainty values varied from 0.00 to 0.79, while bootstrap values for almost all branches were 100. Even though the internode certainty and bootstrap analyses indicated marked differences in levels of support for some branches, the topologies of the MRE consensus tree and the ML tree inferred from concatenated sequences were largely the same (Fig. 1; Additional file 2).
In the species tree, FIESC members were resolved as an exclusive clade, as were members of the previously described Incarnatum and Equiseti clades within FIESC (Fig. 1). F. camptoceras was sister to the Equiseti clade in the species tree, but support for this relationship was low (internode certainty value = 0.04). In the concatenated-sequence tree, F. camptoceras was basal to all other members of FIESC, but with low support (bootstrap value = 72; Additional file 2). The two most basal branches of the Incarnatum clade, FIESC 29 and FIESC 28, were more highly supported than other branches in this clade, according to the internode certainty values. Within the Equiseti clade, the internode certainty values for all branches were relatively low, except for the branches leading to the two FIESC 5 and two FIESC 33 strains. The Sambucinum, Tricinctum, Fujikuroi, Nisikadoi and Oxysporum complexes were each represented by two or more members, and were also resolved as exclusive clades in the species tree. The Solani and Torreyae complexes were each represented by one member, and formed the most basal branches in the tree (Fig. 1). The tree topology indicated that FIESC was most closely related to the Chlamydosporum (represented by F. aywerte) and Sambucinum complexes. Support for the FIESC-Chlamydosporum-Sambucinum branch was relatively high (internode certainty = 0.61). This close relationship of FIESC to the Chlamydosporum and Sambucinum complexes relative to other lineages of Fusarium is consistent with previously reported phylogenetic analyses [3, 15, 29, 35].
Secondary metabolite biosynthetic genes
BLAST analysis indicated that there were 9–13 PKS genes and 11–15 NRPS genes per FIESC genome (Fig. 2, Additional file 3). According to antiSMASH analysis, there were 33–42 SM biosynthetic gene clusters per FIESC genome (Table 2). This range is comparable to the numbers of clusters in other Fusarium genomes [6,7,8, 30]. Overall, 3–4% of the genes in each FIESC genome were predicted by antiSMASH to be SM biosynthetic genes (Table 2). The exception to this was FIESC 5 CS3069, in which SM biosynthetic genes were estimated to constitute only 1.6% of the genes. Homologs from approximately 50% of the PKS and NRPS ortholog groups were present in all FIESC genomes examined (Fig. 2). The fusarubin (PKS3), malonichrome (NRPS1), ferricrocin (NRPS2), and fusarinine (NRPS6) biosynthetic gene clusters were among the clusters that were present in all the FIESC genomes examined, as were four terpene biosynthetic genes clusters that included the TS gene required for synthesis of α-acorenol (STC6), koraiol (STC4), carotenoids (TeTC1), or trichothecenes (TRI5) (Fig. 2, Additional file 3). PKS and NRPS genes that were not present in all FIESC genomes often exhibited discontinuous patterns of distribution in that their presence and absence was not correlated with the phylogenetic relationships of the species in which they occurred. Some of these latter PKS and NRPS genes were present in both the Equiseti and Incarnatum clades (Fig. 2). For example, PKS28 was present in five members of the Equiseti clade and two members of the Incarnatum clade, as well as F. camptoceras. Other PKS and NRPS genes were present in only one FIESC strain examined: i.e., PKS65 was only in FIESC 15; NRPS15 was only in FIESC 29; and NRPS17 was only in F. camptoceras. Although PKS65 was found in only FIESC 15, homologs of this gene have been reported previously in F. redolens and F. babinda . Similarly, NRPS15 and NRPS17 were found in other Fusarium species (Fig. 2). In contrast, PKS62, NRPS33, and two novel PKS, hereafter named PKS73 and PKS74, have not been reported in other fusaria so far, and therefore could be unique to FIESC.
The fusaridione (PKS69) cluster and clusters with PKS23, PKS48 or PKS58 gene occurred only in the Incarnatum clade, while a cluster that included PKS42 and NRPS34 occurred only in the Equiseti clade (Fig. 2). The apicidin cluster  was present in one member of the Incarnatum clade and two members of the Equiseti clade (Additional file 3). A butenolide cluster has not been functionally characterized and most likely does not include a PKS, NRPS or TS gene, however, a monooxygenase gene required for butenolide synthesis and a putative biosynthetic cluster have been identified in F. graminearum . Homologs of the monooxygenase gene required for butenolide synthesis were present in two members of the Incarnatum clade (FIESC 15 and 25) and one member of the Equiseti clade (FIESC 33). Thus, some members of FIESC may be able to produce butenolide. Furthermore, the entire fusarin biosynthetic gene cluster was present in three FIESC members, indicating that these fungi have the potential to produce fusarins (Additional file 3).
An intact zearalenone biosynthetic gene (ZEA) cluster  was present in three members of the Equiseti clade and one member of the Incarnatum clade, while degenerated ZEA cluster homologs (i.e., partial cluster consisting of one or two pseudogenized ZEA genes) were present in one member of the Equiseti clade and two members of the Incarnatum clade (Fig. 3). Likewise, part of the equisetin biosynthetic gene cluster appears to have been deleted in some members of FIESC. In F. graminearum, the equisetin cluster consists of PKS18 and ten other genes . Intact homologs of the cluster occur in most of the FIESC strains examined here. However, in FIESC 23, 28, and 29, six of the cluster genes, including PKS18, are absent.
Genes and gene clusters responsible for synthesis of multiple mycotoxins and other SMs produced by other fusaria were not present in any of the FIESC genomes examined. These included genes or clusters responsible for synthesis of the polyketide-derived metabolites aurofusarin, bikaverin, depudecin, fujikurin, fumonisins, and W493 B, and the terpenoid metabolites eremophilene, guaia-6,10(14)-diene, and gibberellins. Synthesis of the terpenoid mycotoxin culmorin requires a TS and a cytochrome P450 monooxygenase encoded by CLM1 and CLM2, respectively . None of the FIESC strains examined had both of these genes, however, FIESC 23 had a CLM1 homolog (Additional file 3).
Homolog of endocrocin cluster in FIESC
As noted above, PKS73 in FIESC 33 and PKS74 in FIESC 28 represent novel PKS clades in Fusarium. To determine whether closely related homologs of these PKS genes occur in other fungi, we did BLASTx analyses using PKS73 and PKS74 sequences as queries against the NCBI fungal protein database. No homologs closely related to PKS73 were identified by this approach, but homologs closely related to PKS74 were identified in multiple fungi. The PKS74 homologs included encA (AFUA_4G00210) from Aspergillus fumigatus, mdpG (AN0150) from A. nidulans, and ptaA (AG059040) from Pestalotiopsis fici, three PKS genes that are required for the synthesis of endocrocin anthrone [41,42,43]. In these fungi, endocrocin anthrone serves as a biosynthetic precursor to more structurally complex SMs. The other enzymes in the endocrocin biosynthetic pathway are encoded by two to four genes located immediately up or downstream of the PKS genes (Fig. 4). In FIESC 28, homologs of three of these genes are adjacent to PKS74 (Fig. 4).
The endocrocin anthrone PKS belongs to PKS group V, a clade of NR-PKSs that lack a thioesterase domain and, thus, require a second protein, a metallo-β-lactamase type thioesterase (MβL-TE), for release of the nascent polyketide from the PKS . In FIESC 28, the gene adjacent to PKS74 is predicted to encode a MβL-TE (Fig. 4a) which could catalyze release of an endocrocin-like polyketide from PKS74. In a previous study, group V PKSs were observed in 39 genera of Ascomycetes, but not in Fusarium . The presence of PKS74 in FIESC 28, therefore, constitutes the first report of a group V PKS in Fusarium.
Phylogenetic relationships of FIESC PKSs
Our analyses identified 146 PKS genes in the 13 FIESC genomes examined in this study. Phylogenetic analysis of these PKSs plus 216 PKSs from other fusaria resolved the 146 FIESC PKSs into four large clades that corresponded to the non-reducing PKS (NR-PKS) and three reducing PKS (R-PKS I, II and III) groups (Fig. 5; Additional files 4 and 5) [29, 45]. The four clades further resolved into 22 well-supported smaller clades. Twenty of these smaller clades corresponded to clades recently described in an analysis of Fusarium PKSs  while clade 74 and clade 73, appear to be novel. Clade 74 consists of a single ortholog from FIESC 28 and is embedded within the NR-PKS group, while clade 73 consists of two orthologs from the FIESC 33 strains and is embedded within the R-PKS III group. PKS clade 62 was previously described based on a single PKS homolog from F. scirpi . Here, we identified four additional clade 62 homologs: one in F. equiseti (FIESC 14), one in each of the two FIESC 33 strains, and one in F. camptoceras. PKS homologs present in six clades (clades 3, 5, 7, 8, 11 and 66) were present in all 13 FIESC genomes examined.
Phylogenetic analysis of FIESC NRPSs
The NRPS analysis included A domains from 269 NRPS genes recovered from the 12 FIESC genome sequences generated in this study and 95 NRPSs from other fusaria. In the resulting tree, the FIESC A domains were resolved into 20 well-supported clades, 15 of which corresponded to NRPS ortholog groups described by Hansen et a1.  (Fig. 6). The 20 A-domain clades could also be grouped into larger assemblages corresponding to the nine NRPS subfamilies described by Bushley and Turgeon . Seven of the FIESC NRPS clades also corresponded to an even larger grouping consisting of mono/bimodular NRPSs described by Bushley and Turgeon . This grouping consisted of the ChNPS10, ChNPS12, PKS:NRPS, and Cyclosporin synthetases (CYCLO) subfamilies. Eight other NRPS clades corresponded to the two subfamilies of multimodular enzymes: the siderophore synthetase (SID) and Euascomycete synthetase (EAS) subfamilies. Within the mono/bimodular enzyme group, clade NRPS10 corresponded to the ChNPS10 subfamily; two clades consisting of the fusarin and equisetin PKS-NRPSs subfamily; clades NRPS11, NRPS12 and NRPS13 corresponded to the ChNPS12 subfamily; and clade NRPS22 corresponded to the CYCLO subfamily. For the multimodular NRPSs, clades NRPS1 and NRPS2 corresponded to the SID subfamily, and clades NRPS3, NRPS4, NRPS6, NRPS14, NRPS15, and NRPS17 corresponded to the EAS subfamily.
Most of the basal branches in the FIESC A-domain tree did not have significant bootstrap support, and because of this it was not possible to assign the NPRS16, NRPS31 or NRPS33 clades to subfamilies. There were some inconsistencies in the phylogenetic relationships inferred in our FIESC A-domain tree compared to those inferred by Bushley and Turgeon . In the FIESC A-domain tree (Fig. 6), the multimodular subfamily SID formed a monophyletic lineage along with the mono/bimodular subfamilies ChNPS10, hybrid PKS-NRPS, and ChNPS12/ETPmodule2 (bootstrap value = 100). This contrasts with the results of Bushley and Turgeon , where the multimoldular subfamilies SID and EAS formed a monophyletic lineage (bootstrap value = 97). Also in the Bushley and Turgeon study, EAS was a monophyletic lineage, whereas in the current study EAS was not monophyletic. The results of the current study are, however, consistent with those of Gallo et al.  in that neither the mono/bimodular nor the multimodular NRPSs formed well supported monophyletic lineages. Thus, results of the Bushley and Turgeon study suggest that all multimodular NRPSs have a common evolutionary history distinct from mono/bimodular NRPSs, whereas results from the current study and Gallo et al.  suggest that this is not the case.
Evolutionary forces acting upon distribution of SM gene clusters within FIESC
A combination of processes, including gene loss, gene duplication and horizontal gene transfer (HGT), likely contributed to the discontinuous distribution patterns and tree topologies observed for other NRPS/PKS genes. Thus, subsequent analyses were aimed at investigating which of these processes have contributed to the distribution of which NRPS/PKS genes in FIESC.
To assess the contribution of gene loss to the distribution of NRPS/PKS genes in FIESC, we re-examined distribution patterns to determine which NRPS/PKS genes were present in one or more FIESC members but absent in closely related member. We found that six NRPS genes and 10 PKS genes exhibited such distribution patterns (Fig. 2). For example, PKS18 was present in all members of the Equiseti clade, and only two members (FIESC 15 and FIESC 25) of the Incarnatum clade. This suggests the gene was present in the common ancestor of the two clades and was subsequently lost during divergence of the Incarnatum clade such that it is currently present only in FIESC 15 and FIESC 25.
We also used NOTUNG analysis to assess loss of NRPS/PKS genes in FIESC. In this analysis, ML trees inferred for each NRPS/PKS gene were reconciled with the species tree shown in Fig. 1. NOTUNG inferred 127–129 loss events of NRPS/PKS genes within FIESC to account for the differences between individual gene trees and the species tree (Additional file 6).
The presence of pseudogenized NRPS/PKS genes (i.e., genes with mutations that result in frameshifts, truncations and/or internal stop codons) in some FIESC members is also consistent with gene loss events. Within FIESC, we detected pseudogenized versions of NRPS14, NRPS16, NRPS19, NRPS31 and PKS13 in FIESC (Fig. 2). PKS13 along with PKS4, ZEB1 and ZEB2 comprise the zearalenone biosynthetic gene cluster (Fig. 3). Intact homologs of this cluster were detected in four members of the Sambucinum complex and five members of FIESC, including one species in the Incarnatum clade and three species in the Equiseti clade. Among the other eight members of FIESC examined, three had a degenerate zearalenone cluster, which always included a pseudogenized PKS13, and five FIESC members did not have detectable full-length or pseudogenized zearalenone biosynthetic genes (Fig. 3).
HGT- manual tree comparisons and reconciliation analysis
We also examined the results of the phylogenetic analyses for evidence that HGT contributed to the introduction of NRPS/PKS genes in FIESC. Manual comparison of the NRPS/PKS gene trees to the species tree revealed 10 branch conflicts that were consistent with HGT of NRPS/PKS genes between FIESC and other Fusarium lineages (Table 3, Additional file 5). In eight of these putative HGT events, FIESC was the recipient of a gene. Figure 7 shows an example of a tree suggestive of HGT of NRPS22. In the species tree (Fig. 1), FIESC and the Fujikuroi complex were relatively distantly related lineages, but in the NRPS22 tree FIESC 23 and FIESC 28 were nested within the Fujikuroi complex in the NRPS22 tree (Fig. 7a). This branch conflict between the species and NRPS22 trees is consistent with HGT of NRPS22 from the Fujikuroi complex to FIESC.
Reconciliation analysis using NOTUNG inferred 17 HGT events of NRPS/PKS genes between FIESC and other Fusarium lineages (Additional file 6). These NOTUNG-inferred events included all the HGT events inferred by the manual tree comparisons noted above, including the putative transfer of NRPS22 from the Fujikuroi complex to FIESC (Fig. 7b). FIESC was the recipient in 10 of the NOTUNG-inferred HGT events. Thus, together NOTUNG reconciliation and manual comparison of species and gene trees revealed 10 putative HGT events in which NRPS/PKS genes were transferred to FIESC from other Fusarium lineages (Table 3).
HGT – Constraint analysis
Constraint analysis has been used previously to assess support for putative HGT events [48, 49]. Therefore, we used it to further assess the 17 putative HGT events of NRPS/PKS genes noted in Table 3. For this analysis, we manually altered the topology of NRPS/PKS gene trees so that individual branches that conflicted with the species tree in the unconstrained trees conformed to the species tree in the constrained trees (Additional files 5 and 7). We then used SH-AU tests to determine whether the constrained trees were less well supported than the corresponding unconstrained trees [48, 49]. For example, we generated two constrained trees from the unconstrained NRPS22 tree (Fig. 7a). In the first tree, taxa from the Fujikuroi, Oxysporum and Nisikadoi complexes, and F. beomiforme were constrained to a clade that excluded FIESC 23 and FIESC 28; and in the other tree, FIESC 23, FIESC 25, F. aywerte, and Sambucinum-complex taxa were constrained to a clade that excluded Fujikuroi-complex taxa. The results of the SH-AU tests indicated that constrained trees were significantly worse (p < 0.05) than the corresponding unconstrained trees for 11 of the 17 putative HGT events, including the putative HGT of NRPS22 from the Fujikuroi complex to FIESC (Table 3). Thus, the SH-AU tests provided additional support for 11 putative HGT events between FIESC and other Fusarium lineages.
HGT – Analysis of synonymous site divergence
Estimates of the number of synonymous changes per synonymous site (dS) in coding regions of HK genes tend to be positively correlated with divergence of Fusarium species [50, 51]. Given this, recent HGT of a gene should result in low dS values for the transferred gene relative to HK genes in the donor and recipient species, because dS values for the transferred gene should reflect divergence levels since the transfer, whereas dS values of HK genes should reflect divergence levels since the speciation event(s) that led to the donor and recipient. Based on this rationale, we used PAML to generate dS values for each NRPS/PKS gene and for concatenated sequences of 30 HK genes (Additional file 1) for all possible pairwise combinations of taxa included in the species tree (Fig. 1). We then compared the dS values for the NRPS/PKS genes and HK genes. For most comparisons, dS values for NRPS/PKS genes were significantly higher than dS values for HK genes (Fig. 7c, Additional file 8). This difference in dS values occurred for almost all comparisons involving NRPS/PKS genes that were continuously or nearly continuously distributed and that yielded phylogenetic trees that were largely concordant with the species tree (Additional files 5 and 8). Thus, NRPS/PKS genes whose distribution and phylogenetic tree were consistent with vertical inheritance tended to have larger dS values than HK genes. This suggests that in Fusarium vertically inherited NRPS/PKS genes tend to diverge more rapidly than HK genes.
Because of the tendency for larger dS values for NRPS/PKS genes than HK genes, the ratio of the NRPS/PKS dS value to HK dS value (dS ratio) for a given pairwise comparison of taxa was most often 1.5–4, and even higher for some comparisons (Fig. 7d, Additional file 8). Examination of dS values for all pairwise combinations of taxa that had homologs of NRPS/PKS genes involved in the 17 putative HGT events revealed dS ratios of less than 1 for taxa involved in 13 of the events (Table 3). For example, for comparisons involving NRPS22, most dS ratios were 2–5, but dS ratios were less than 1 for comparisons of FIESC 23 or FIESC 28 with members of the Fujikuroi, Nisikadoi and Oxysporum complexes (Additional file 8). The dS ratios for comparisons of FIESC 23 or FIESC 28 to F. nygamai (Fujikuroi complex) were particularly low (0.27 and 0.30). This suggested that NRPS22 homologs in FIESC23 and FIESC28 began diverging from homologs in the Fujikuroi, Nisikadoi and Oxysporum complexes after FIESC began diverging from these other complexes. Together, results of dS analysis, manual tree comparisons, NOTUNG analysis, and SH-AU tests are consistent with HGT of NRPS22 from the Fujikuroi complex (a close relative of F. nygamai) to a recent ancestor of FIESC 23 and FIESC 25. Putative HGT events for NRPS4, PKS10 and PKS23 were also consistent with results from all the phylogenetic analyses used in this study, whereas other putative HGT events were consistent with results from only one or a subset of analyses (Table 3).
Evidence for hybrid polyketide-nonribosomal peptide biosynthetic gene cluster
We detected the genes PKS42 and NRPS34 in all Equiseti-clade genomes, except for the genome of FIESC 5, ITEM 11348. In addition, we did not detect the genes in any of the Incarnatum-clade genomes. Further examination of the Equiseti-clade genomes indicated that PKS42 and NRPS34 were located near one another in a region that spanned 62,536–64,747 bp and that included seven other genes (Additional file 9 A). The seven genes were predicted to encode proteins with functions consistent with SM biosynthesis; i.e., ABC transporter, cytochrome P450 monooxygenase, dioxygenase, reductase, and C2H2 Zn finger transcription factor. We also found PKS42, NRPS34 and the other seven genes arranged in the same order in the genome sequences of F. avenaceum strain LH27  and F. aywerte (Additional file 9A). The genes were also present, albeit in a different arrangement, in the genome sequence of Colletotrichum simmondsii (NCBI Accession JFBX00000000.1). The predicted functions of PKS42, NRPS34, and the other seven genes combined with their proximity to one another in multiple taxa suggests that they constitute a SM biosynthetic gene cluster that confers the ability to synthesize a hybrid polyketide-nonribosomal peptide. Examination of the cluster flanking region among members of the Equiseti clade revealed that some of the flanking genes are shared by all members of the clade, suggesting that cluster homologs are in similar genomic contexts (Additional file 9 B). A similar arrangement of the flanking genes also exists in other members of FIESC that lack the cluster, including FIESC 5 ITEM 11348.
Trichothecene cluster organizations
The trichothecene biosynthetic gene (TRI) cluster was detected in all FIESC genomes examined in the current study. In seven of the FIESC genome sequences, TRI cluster orthologs were identical to the cluster ortholog previously reported in FIESC 12 (NRRL 13405)  with respect to gene content, gene order, direction of transcription, and genomic context (Fig. 8). Within the Equiseti clade all genomes examined have an intact and apparently functional TRI1 gene except for FIESC 33 (ITEM 10395). The TRI1 coding region in 10,395 has a single nucleotide deletion near the 5′ end of the coding region that introduces a frameshift and subsequently internal stop codons.
These stop codons should prevent translation of a full length Tri1 protein. Within the Incarnatum clade, FIESC 15 strain has an intact and apparently functional TRI1, while TRI1 is absent in the FIESC 23 and FIESC 25 strains and it is pseudogenized in FIESC 28 and FIESC 29. In FIESC 28 there is only a 127 base fragment of TRI1, corresponding to bases 6–132 of the TRI1 coding region, while FIESC 29 has a 122 base deletion near the 5′ end of the TRI1 coding region.
In all fusaria that have been examined, TRI16 is not located in the TRI cluster, and it is pseudogenized or absent in some species [27, 53, 54]. Analysis of FIESC genomes in the current study indicated that TRI16 was present and in the same genomic context in FIESC 15 and in all members of the Equiseti clade examined, but that it was absent in F. camptoceras and all other members of the Incarnatum clade.
The results of this study revealed that collectively members of FIESC have the potential to produce diverse SMs. This was evident by the presence of 22 PKS and 18 NRPS genes in the FIESC genome sequences analyzed. Homologs from approximately 50% of the PKS and NRPS ortholog groups were present in all FIESC genomes examined (Fig. 2), which suggests that about half of the potential polyketide and non-ribosomal peptide-derived metabolites produced by FIESC species could be produced by most or even all members of FIESC. Some PKS and NRPS genes, as well as the associated gene clusters, were distributed discontinuously in a few species of the Equiseti or Incarnatum clade, or a few species in both clades. The fusarin biosynthetic gene cluster was among those with discontinuous distributions. As far as we are aware, fusarin production has never been reported in members of FIESC. Therefore, finding the fusarin cluster in three FIESC genomes attests to the value of whole genome sequence analysis to determine the genetic potential of fungi to produce metabolites.
Gene deletion and pseudogenization, here identified by alignment against orthologous SM reference sequences and altering the gene coding sequence, have likely contributed to the discontinuous distribution of some SM genes and gene clusters. For example, the distribution of the intact and degenerated ZEA cluster homologs in FIESC is consistent with the presence of the intact cluster in the common ancestor of FIESC followed by pseudogenization and deletion events in some FIESC species that resulted in the absence of the cluster, or presence of only a degenerated cluster, in multiple members of FIESC.
Our analysis showed the presence of a putative cluster, including the PKS42 and NRPS34 genes and seven other genes, distributed in all Equiseti clade species, except for the genome of FIESC 5 ITEM 11348, as well as in the genome of F. avenaceum (LH27), F. aywerte, and C. simmondsii (Additional file 9). The presence of the PKS42-NRPS34 cluster in FIESC 5 (CS3069), and its absence in FIESC 5 ITEM 11348, indicates two possible evolutionary scenarios for the cluster in FIESC 5: 1) the cluster was present in the common ancestor of CS3069 and ITEM 11348, and was subsequently lost during divergence of ITEM 11348; or 2) the genomic region that includes the PKS42-NRPS34 cluster exists as two alternative alleles, one allele with the cluster and another without it. There is evidence for the existence of similar scenarios with the fumonisin and ochratoxin biosynthetic gene clusters in species of Aspergillus [55, 56]. However, unlike the situation in Aspergillus, our efforts to find evidence for or against the two scenarios for the PKS42-NRPS34 cluster in FIESC 5 yielded equivocal results. For example, we searched for remnants of PKS42-NRPS34 cluster genes in the ITEM 11348 genome sequence as evidence for recent deletion of the cluster, but without any success. Analysis of the PKS42-NRPS34 cluster region in the five haplotypes of FIESC 5 already described  could provide further insight into the evolutionary history of the cluster.
In this study, we used antiSMASH to estimate the percentage of genes in a genome that are involved in SM biosynthesis (Table 2). While such antiSMASH-based estimates are likely imperfect, overestimation or underestimation of SM genes are likely to be systematic due to criteria that antiSMASH uses to identify clusters. As a result, overestimates and underestimates are likely similar for genome sequence assemblies with similar properties. Thus, we attributed the low percentage of SM genes in the FIESC 5 CS3069 genome sequence to the high number of contigs in the genome sequence assembly for this strain compared to other FIESC members examined, including FIESC 5 ITEM 11348 (Table 2). The CS3069 genome sequence was assembled into 5111 contigs, that is 3.4–12.1 times as many contigs as the other FIESC strains examined in this study. If we exclude CS3069, estimates of SM genes percentage per genome is similar to other FIESC members, ranging from 3.3–4.3%. This similarity contrasts the finding that only about 50% of the observed PKS and NRPS genes were shared by all the genomes examined. Thus, the estimates of homologs of some clusters were present in all the FIESC strains examined, others clusters were present in subsets of species, sometimes only in members of either the Equiseti or Incarnatum clade, while other clusters were unique to one strain, such as NRPS15 and NRPS17. The antiSMASH prediction of SM clusters is mainly based on PKS, NRPS and terpene synthase (TS) genes, therefore it was not surprising that the predicted gene clusters exhibited the same distribution patterns as PKS and NRPS genes.
Additionally, FIESC appears to have few unique SM gene clusters. The large majority of clusters that occur in FIESC genomes have been already reported in other fusaria. What is unique about FIESC, and most likely other Fusarium species complexes, is the combinations of clusters that are present within each lineage. For example, all members of the FSAMSC that have been examined have the aurofusarin, fusarubin and trichohecene clusters, but not the bikaverin cluster; all members of FFSC that have been examined have the bikaverin and fusarubin clusters but not the aurofusarin or trichothecene cluster; and all members of FIESC examined in the current study have the fusarubin and trichothecene clusters but not the aurofusarin or bikaverin cluster [8, 9, 30, 34, 57]. The trichothecene cluster was the only biosynthetic gene cluster for a major Fusarium mycotoxin (i.e., enniatins/beauvericin, fumonisins, trichothecenes and zearalenone) that occurred in all members of FIESC. In contrast, the enniatin/beauvericin and zearalenone clusters exhibited discontinuous distributions among the genomes (Fig. 2), as well as the fumonisin cluster was absent from all the genomes.
The evidence that all members of FIESC have trichothecene biosynthetic cluster is significant, given previous reports of variation in trichothecene production among members of FIESC [22, 24, 58] and because trichothecenes are among the mycotoxins of greatest concern to agricultural production and food/feed safety. Despite of the presence of the trichothecene cluster in all FIESC strains examined, a variation in gene content of the TRI-cluster homologs was observed. For example, TRI1 was absent or pseudogenized in some members of the Incarnatum clade, while TRI13 was absent and TRI7 was pseudogenized in F. camptoceras. Such differences in gene content determine which trichothecene analogs are produced.
During trichothecene biosynthesis, the TRI13- and TRI7-encoded enzymes catalyze hydroxylation and O-acetylation of carbon atom 4 (C4), respectively . Although trichothecene production has not been reported in F. camptoceras, the absence of TRI13 and pseudogenization of TRI7 suggests that this species would produce trichothecene analogs that lack hydroxyl or acetyl substituent at C4. Within the F. sambucinum species complex (FSAMSC), there is a lineage of closely related species in which TRI13 and TRI7 are pseudogenized. As a result, these fusaria produce only trichothecene analogs that lack modifications at C4, including deoxynivalenol (DON), 3-acetyl DON (3ADON) and 15-acetyl DON (15ADON) [60, 61]. For example, in most strains of F. graminearum, TRI7 and TRI13 are present as pseudogenes and as a result these strains produce either 3ADON or 15ADON. However, most species within FSAMSC have functional TRI13 and TRI7 orthologs. The results of the current study indicate that a similar situation occurs also in FIESC. That is, with the exception of F. camptoceras, FIESC members have functional copies of TRI7 and TRI13 and, therefore, the genetic potential to produce trichothecenes with C4 modifications. Because most members of FIESC and FSAMSC have functional copies of TRI7 and TRI13, we propose that the loss/pseudogenization of TRI7 and TRI13 in F. camptoceras occurred independently of the pseudogenization in FSAMSC. If this hypothesis is correct, it would constitute convergent evolution of the trichothecene biosynthetic pathway in FSAMSC and FIESC. Furthermore, the loss/pseudogenization of TRI7 and TRI13 in two lineages of Fusarium suggests that a lack of selection for production of trichothecenes with a C4 modification has occurred twice during the evolutionary history of trichothecene-producing fusaria.
In FIESC, as well as in all examined fusaria, TRI16 is not located within the TRI core cluster, and it is pseudogenized or absent in some species [27, 53, 54]. The TRI16-encoded acyltransferase catalyzes esterification of a five-carbon metabolite (3-methylbutanoate) to a hydroxyl at C8, resulting in the formation of T-2 toxin and structurally related trichothecenes [52, 53]. Despite the presence of TRI16 in some members of FIESC, multiple survey studies showed that members of FIESC do not produce T-2 toxin or other trichothecenes with a 3-methylbutanoate ester at C8 [22, 24, 58]. This raises the possibility that TRI16 homologs in FIESC species are not expressed, not functional due to changes in its amino acid sequence, or that they have taken on a function in a different metabolic pathway. There is evidence that, during the evolutionary divergence of FIESC from other trichothecenes-producing lineages of Fusarium, TRI1 was translocated into the TRI cluster from elsewhere in the genome . The absence of TRI1 in TRI cluster orthologs of some members of FIESC suggests that following this translocation, TRI1 was lost in some FIESC lineages (Fig. 8).
In the last decade, genome sequence analyses have revealed the existence of frequent variation in the content of secondary metabolite biosynthetic gene clusters among filamentous fungi. Multiple studies suggest that vertical inheritance, gene loss, and HGT are major contributors to this variation [50, 62, 63]. However, the frequency with which each process has contributed to the variation remains unclear. To assess how often vertical inheritance, gene loss, and HGT have contributed to the presence and absence of clusters among FIESC members, we did a series of phylogenetic analyses. In this assessment, we focused on NRPS and PKS (NRPS/PKS) genes, because they are present in a large proportion of SM clusters, and they can contain substantial phylogenetic signal as a result of their large size. To begin the assessment, we used BLAST analysis with NCBI’s GenBank database and a local database to examine the occurrence of homologs of each FIESC NRPS/PKS gene in the fusaria included in the species tree (Fig. 1). This analysis revealed that some of the NRPS/PKS genes were present in all or almost all fusaria examined, others were discontinuously distributed across a wide range of species, and still others were more narrowly distributed, occurring exclusively or almost exclusively in FIESC (Fig. 2).
We presumed that vertical inheritance was the process that most frequently introduced NRPS/PKS genes into and subsequently distributed them within FIESC. This assumption was supported by continuous or wide distribution of NRPS1-NRPS4, NRPS6, NRPS10-NRPS14, NRPS16, NRPS19, PKS3, PKS5, PKS7, and PKS8 in FIESC and fusaria most closely related to FIESC (i.e., the Sambucinum complex and F. aywerte) (Fig. 2, Additional file 5). The results of our study suggest that gene loss and HGT have contributed to the diversity of SM clusters in FIESC. In particular, gene loss has contributed to distribution of 21 clusters. This is likely an overestimation of the true number of losses, because in the absence of polytomy in the species tree, which was the case for the species tree used in this study, NOTUNG does not take into account that topological differences between a gene tree and the species tree can result from sorting of ancestral alleles. Also, NOTUNG suggested that multiple distribution patters were affected by gene duplication, although the hypothesis is not consistent with other analyses.
dS values for NRPS16, NRPS19, NRPS34, PKS42, PKS43 and PKS69 reveal a likely limitation in the use of dS values for assessing putative HGT events, because almost all dS ratios for comparisons involving these genes were less than 1. The cause of these low dS ratios is not clear. One possibility is rampant HGT of the genes. However, in ML trees inferred from these genes, most internal branches were short, and most terminal branches were long (Additional file 5). Furthermore, most branches in these trees had poor bootstrap support (< 70). The cause(s) of these branching characteristics is unclear. Assessment of homoplasy using consistency and retention indices  suggested that the level of homoplasy in NRPS16, NRPS19, NRPS34, PKS42, PKS43, and PKS69 sequences was within the range for sequences of other NRPS/PKS genes. Thus the cause(s) of the low dS ratios for NRPS16, NRPS19, NRPS34, PKS42, PKS43, and PKS69 is not clear.
Low dS ratios also resulted from some pairwise comparisons that involved two strains of the same species (e.g., F. oxysporum strains Fol4287 and FOSC3a) or closely related species (e.g., F. langsethiae and F. sporotrichioides; species within the Incarnatum or Equiseti clades of FIESC). However, in some other comparisons involving strains of the same species or closely related species, dS ratios were high. dS values for both HK and NRPS/PKS genes in comparisons within species or between closely related species tended to be low (i.e., less than 0.1), and as a result small differences in dS values for HK and NRPS genes could lead to very low or very high dS ratios.
Overall, all evolutionary approaches hereby considered, showed that HGT has contributed to distribution of four clusters, such as the known fusarin and enniatin/beauvericin biosynthetic gene clusters and the unknown clusters with PKS23 and NRPS4 genes, respectively. These data provide evidence that a complex interplay of evolutionary processes contributes to variation in secondary metabolite cluster content in fungi and, therefore, to variation in their ability to produce the corresponding metabolites.
The results of this study suggest that: 1) collectively, the FIESC strains examined in this study have the genetic potential to produce 22 structurally distinct PKSs and 18 NRPSs; 2) vertical inheritance has contributed to the distribution of almost all FIESC clusters; 3) HGT has contributed to distribution of four clusters and likely to other nine additional clusters, although the results from all analyses were not consistent.
Environmental factors that affect the maintenance of SM clusters in a recipient of HGT are poorly understood, but they could include soil conditions, competitors, hosts, and/or climate. However, which ones among these factors affected maintenance of SM clusters horizontally transferred to members of FIESC remains to be determined.
In conclusion, all those data can led to understanding which members of FIESC can produce which mycotoxins, concretely impacting growers response to fungal surveys in their fields, and supporting regulators to develop accurate assessments of the risks that members of FIESC pose to the food and feed supply.
The FIESC strains examined in this study are listed in Table 1. Nine strains were obtained from the Agri-Food Toxigenic Fungi Culture Collection (ITEM; http://server.ispa.cnr.it/ITEM/Collection) at the Institute of Science of Food production (ISPA; Bari Italy); two strains were obtained from the U.S. Department of Agriculture (USDA), Agricultural Research Service (ARS) Culture Collection (NRRL; Peoria IL, USA, https://nrrl.ncaur.usda.gov/), and one strain was obtained from the Fusarium Research Center (FRC, Pennsylvania State University, State College PA, USA). Recently, Villani et al.  characterized a phylogenetically distinct group of FIESC isolates and designated them FIESC 31. However, prior to this publication, the designation FIESC 31 had already been applied to a different phylogenetic species . In the current study, therefore, we redesignated FIESC 31 sensu Villani et al.  as FIESC 33, and we use the designation FIESC 31 as described by Short et al. . We compared these genomes to the publicly available genome sequence of FIESC 5 strain CS3069 (National Center for Biotechnology Information (NCBI) accession number: QGEC00000000) . In addition to the strains listed in Table 1, partial genomic sequences for other Fusarium species were obtained from GenBank for inferring species phylogeny, as well as PKS and NRPS analyses.
Genome sequencing and assembly
Genome sequences for FIESC strains were generated using an Illumina MiSeq sequencer. The exception to this was the sequence for F. scirpi NRRL 66328, which was generated using a Life Technologies Ion Torrent PGM™ sequencer. Both sequencers were located at the Mycotoxin Prevention and Applied Mycology Research Unit at USDA ARS, Peoria IL. High-quality genomic DNA was prepared from each species grown in GYP (2% glucose, 1% peptone and 0.3% yeast extract) liquid cultures using Zymo DNA Clean & ConcentratorTM-5 kit as described by the manufacture (Zymo Research, Orange, California). One ng of DNA was used to generate paired-end DNA libraries for the MiSeq using the Nextera XT DNA Library Preparation Kit (Nextera XT DNA Library Preparation Experienced User Card 15,031,943 D). DNA (1 μg) from F. scirpi was used to generate the DNA library for the Ion Torrent using the New England Biolabs NEBnext Fast DNA Library prep set. Sequence reads were processed and assembled with CLC Genomics Workbench version 8.0 (CLC bio-Qiagen, Aarhus, Denmark) using default parameters, except that the minimum contig length was set to 500 bp. The resulting unannotated genome sequences were deposited at DDBJ/ENA/GenBank under the accessions shown in Table 1. Gene predictions for each genome were done with the program Augustus  using F. graminearum as the training species. When we identified predicted gene models that appeared to have errors (e.g., incorrect intron splicing), we subjected the corresponding genomic sequence to FGENESH  analysis and/or manual annotation by aligning the corresponding genomic DNA to predicted genes from other fusaria using the program MEGA 7.0 
A species phylogeny was inferred using coding region sequences of 30 HK genes (Additional file 1) from the 13 members of FIESC and 24 other Fusarium species that spanned the phylogenetic breadth of the genus and for which genome sequence data were publicly available (Additional file 1). FIESC HK gene sequences were mined by BLASTn analysis of individual genome sequence databases in CLC Genomic Workbench, while sequences from other fusaria were downloaded from GenBank. Most of the HK genes have been used previously to assess phylogenetic relationships of Fusarium species [3, 15, 29, 35] and are involved in metabolic processes essential for growth and development. However, some of the genes (e.g., CAR1) are not essential, but occur widely as single-copy genes in Fusarium. All DNA sequences of coding regions were inspected, and when necessary were manually annotated to correct large gaps resulting from incorrect prediction of introns and translational start and stop sites.
Housekeeping gene sequences were aligned using Muscle as implemented in MEGA7 , and the resulting alignments were used to infer ML trees for each gene using IQ-Tree (version 1.6.7) with 1000 bootstrap replicates . The species tree was inferred from the 30 HK gene ML trees using the MRE method as implemented in RAxML (v.8.2.10)  Branch support for the MRE consensus tree was obtained by the internode certainty method as implemented in RAxML [70, 71]. For comparison purposes, a species tree was also inferred using the ML method implemented in IQ-Tree (version 1.6.7) from the concatenated coding region sequences of the 30 housekeeping genes. Branch support for the ML tree was determined by bootstrap analysis with 1000 replicates . Trees with support values were displayed using Dendroscope software V3.5.9  and MEGA7 .
Identification of putative secondary metabolite gene clusters
To investigate the genetic potential of members of FIESC to produce mycotoxin and other SMs, we subjected the FIESC genome sequences to BLAST and antiSMASH [73, 74] analyses. We then assessed the results from both analyses to draw conclusions about the presence and absence of SM gene clusters. In the BLAST analysis, we employed both BLASTn and BLASTx methods in CLC Genomics Workbench. BLAST query sequences consisted of representative genes from previously described PKS and NRPS ortholog groups/clades [29, 30]. We also queried the databases with sequences of 166 genes previously reported to be required for biosynthesis of 27 families of Fusarium SMs (Additional file 3). Proteins encoded by these latter genes included terpene synthases, oxidoreductases, acyltrasferases, transporters, and transcription factors in addition to PKSs and NRPSs. The retrieved sequences were then aligned with sequences of genes or gene clusters publically available for other annotated Fusarium species, known to be involved or considered potentially involved in mycotoxins and related SMs production. The prediction of novel putative secondary metabolite genes was done by analysis of 13 FIESC genomes using Augustus  and FGENESH  selecting Fusarium species as references. The antiSMASH analysis was also performed to obtain information about partition involved in SM biosynthesis in each genome. We used this number and the total number of genes per genome predicted by Augustus program to estimate the percentage of SM biosynthetic genes per FIESC genome.
Conservation of synteny of some clusters between FIESC genomes and other fungal species was examined by BlastP analysis in GenBank and confirmed by the alignment of potential homologous clusters and flanking regions using Sequencher (version 5.2.4; Gene Codes Corp.)
Phylogenetic analyses of NRPS and PKS genes
We used full-length, predicted amino acid sequences to assess diversity and phylogenetic relationships of FIESC PKSs. The PKS analysis included sequences of 135 PKS enzymes identified in the 12 FIESC genome sequences generated during the course of this study, 11 PKSs from CS3069, and 216 PKSs from other fusaria previously identified  or identified as top hits (e-value cutoff 1e− 05) in BLAST searches at NCBI. Sequences were aligned using Mafft  and an ML tree was generated using IQ-TREE  with the fatty acid synthase (FAS) from Gallus gallus serving as the outgroup. To gain further insight into diversity of NRPSs in FIESC, we assessed the phylogenetic relationships of A domains of FIESC NRPSs using the same phylogenomic approach that Bushley and Turgeon  used to assess NRPS diversity in a range of fungal genera. In our analysis, we used BLAST to identify NRPS homologs that were collectively encoded by the 13 FIESC genomes included in this study. We then retrieved and aligned using Mafft all the adenylation domain (A domains) from these and other Fusarium NRPSs , and subjected the alignment to ML analysis, using IQ-TREE with the ultrafast bootstrap with 10,000 bootstrap replicates .
Evolutionary forces acting upon distribution of SM gene clusters within FIESC
We did a series of phylogenetic analyses to assess evolutionary processes that have likely contributed to the introduction of SM gene clusters into FIESC and subsequent distribution of the clusters among FIESC members. The phylogenetic analyses consisted of: 1) assessment of the occurrence of the genes in FIESC and other Fusarium lineages; 2) manual comparison of single NRSP/PKS gene trees to the species tree; 3) constraint analyses using the Shimodaira-Hasegawa and Approximately Unbiased (SH-AU) tests to assess statistical support for branches indicative of HGT [48, 49]; 4) reconciliation analysis using NOTUNG v2.9 with default cost [77, 78]; and 5) genetic divergence analysis using estimates of synonymous substitutions per synonymous site (dS), using the ML method in CodeML program as implemented in PAML  (with the options seqtype = 1, runmode = − 2, and CodonFreq = 0 in the codeml.ctl files).
- A domain:
Horizontal Gene Transfer
Majority Rule Extended tree
non-ribosomal peptide synthetase
Desjardins AE. Fusarium mycotoxins: chemistry, genetics, and biology. American Phytopathological Society (APS Press); 2006.
Moretti A, Susca A, Mulé G, Logrieco AF, Proctor RH. Molecular biodiversity of mycotoxigenic fungi that threaten food safety. Int J Food Microbiol. 2013;167(1):57–66. https://doi.org/10.1016/j.ijfoodmicro.2013.06.033.
O’Donnell K, Rooney AP, Proctor RH, Brown DW, McCormick SP, Ward TJ, Frandsen RJ, Lysøe E, Rehner SA, Aoki T, Robert VA. Phylogenetic analyses of RPB1 and RPB2 support a middle cretaceous origin for a clade comprising all agriculturally and medically important fusaria. Fungal Genet Biol. 2013;52:20–31. https://doi.org/10.1016/j.fgb.2012.12.004.
Laurence MH, Walsh JL, Shuttleworth LA, Robinson DM, Johansen RM, Petrovic T, Vu TT, Burgess LW, Summerell BA, Liew EC. Six novel species of Fusarium from natural ecosystems in Australia. Fungal Divers. 2016;77(1):349–66. https://doi.org/10.1007/s13225-015-0337-6.
Zhou X, O’Donnell K, Aoki T, Smith JA, Kasson MT, Cao ZM. Two novel Fusarium species that cause canker disease of prickly ash (Zanthoxylum bungeanum) in northern China form a novel clade with Fusarium torreyae. Mycologia. 108(4):668–81. https://doi.org/10.3852/15-189.
Ma LJ, van der Does HC, Borkovich KA, Coleman JJ, Daboussi MJ, Di Pietro A, Dufresne M, Freitag M, Grabherr M, Henrissat B, Houterman PM, Kang S, Shim WB, Woloshuk C, Xie X, Xu JR, Antoniw J, Baker SE, Bluhm BH, Breakspear A, Brown DW, Butchko RAE, Chapman S, Coulson R, Coutinho PM, Danchin EGJ, Diener A, Gale LR, Gardiner DM, Goff S, Hammond-Kosack KE, Hilburn K, Hua-Van A, Jonkers W, Kazan K, Kodira CD, Koehrsen M, Kumar L, Lee YH, Li L, Manners JM, Miranda-Saavedra D, Mukherjee M, Park G, Park J, Park SY, Proctor RH, Regev A, Ruiz-Roldan MC, Sain D, Sakthikumar S, Sykes S, Schwartz DC, Turgeon BG, Wapinski I, Yoder O, Young S, Zeng Q, Zhou S, Galagan J, Cuomo CA, Kistler HC, Rep M. Comparative genomics reveals mobile pathogenicity chromosomes in Fusarium. Nature. 2010;464(7287):367–73. https://doi.org/10.1038/nature08850.
Wiemann P, Sieber CM, Von Bargen KW, Studt L, Niehaus EM, Espino JJ, Huß K, Michielse CB, Albermann S, Wagner D, Bergner SV. Deciphering the cryptic genome: genome-wide analyses of the rice pathogen Fusarium fujikuroi reveal complex regulation of secondary metabolism and novel metabolites. PLoS Pathog. 2013;9(6):e1003475. https://doi.org/10.1371/journal.ppat.1003475.
Niehaus E-M, Münsterkötter M, Proctor RH, Brown DW, Sharon A, Idan Y, Oren-Young L, Sieber CM, Novák O, Pěnčík A, Tarkowská D. Comparative “omics” of Fusarium fujikuroi species complex highlights differences in genetic potential and metabolite synthesis. Genome Biol Evol. 2016;8(11):3574–99. https://doi.org/10.1093/gbe/evw259.
Walkowiak S, Rowland O, Rodrigue N, Subramaniam R. Whole genome sequencing and comparative genomics of closely related Fusarium head blight fungi: Fusarium graminearum, F. meridionale and F. asiaticum. BMC Genomics. 2016;17:1014. https://doi.org/10.1186/s12864-016-3371-1.
Leslie JF, Summerell BA. The Fusarium laboratory manual. 1st ed. Ames: Blackwell Publishing Ltd; 2006.
Wilson JP. Fungi associated with the stalk rot complex of pearl millet. Plant Dis. 2002;86:833–9. https://doi.org/10.1094/PDIS.2002.86.8.833.
Seta S, Gonzalez M, Lori G. First report of walnut canker caused by Fusarium incarnatum in Argentina. Plant Pathol 2004;53:248–248. https://doi.org/10.1111/j.0032-0862.2004.00968.x.
Maciá-Vicente JG, Rosso LC, Ciancio A, Jansson H-B, Lopez-Llorca LV. Colonisation of barley roots by endophytic Fusarium equiseti and Pochonia chlamydosporia: effects on plant growth and disease. Ann Appl Biol. 2009;155:391–401. https://doi.org/10.1111/j.1744-348.2009.00352.
O’Donnell K, Sutton DA, Rinaldi MG, Gueidan C, Crous PW, Geiser DM. Novel multilocus sequence typing scheme reveals high genetic diversity of human pathogenic members of the Fusarium incarnatum-F. equiseti and F. chlamydosporum species complexes within the United States. J Clin Microbiol. 2009;47:3851–61.
O’Donnell K, Sutton DA, Rinaldi MG, Sarver BAJ, Balajee SA, Schroers H-J, Summerbell RC, Robert VA, Crous PW, Zhang N, Aoki T. Internet-accessible DNA sequence database for identifying fusaria from human and animal infections. J Clin Microbiol. 2010;48:3708–18. https://doi.org/10.1128/JCM.00989-10.
Singh SB, Zink DL, Polishook JD, Dombrowski AW, Darkin-Rattray SJ, Schmatz DM, Goetz MA. Apicidins: novel cyclic tetrapeptides as coccidiostats and antimalarial agents from Fusarium pallidoroseum. Tetrahedron Lett. 1996;37:8077–80.
Logrieco A, Moretti A, Castella G, Kostecki M, Golinski P, Ritieni A, Chelkowski J. Beauvericin production by Fusarium species. Appl Environ Microbiol. 1998;64:3084–8.
Marasas WFO, Nelson PE, Toussoun TA, Others. Toxigenic Fusarium species. Identity and mycotoxicology. Pennsylvania State University; 1984.
Haese A, Schubert M, Herrmann M, Zocher R. Molecular characterization of the enniatin synthetase gene encoding a multifunctional enzyme catalysing N-methyldepsipeptide formation in Fusarium scirpi. Mol Microbiol. 1993;7:905–14. https://doi.org/10.1111/j.1365-2958.1993.tb01181.
Phillips NJ, Goodwin JT, Fraiman A, Cole RJ, Lynn DG. Characterization of the Fusarium toxin equisetin: the use of phenylboronates in structure assignment. J Am Chem Soc. 1989;111:8223–31. https://doi.org/10.1021/ja00203a025.
Kosiak EB, Holst-Jensen A, Rundberget T, Gonzalez Jaen MT, Torp M. Morphological, chemical and molecular differentiation of Fusarium equiseti isolated from Norwegian cereals. Int J Food Microbiol. 2005;99:195–206. https://doi.org/10.1016/j.ijfoodmicro.2004.08.015.
Villani A, Moretti A, De Saeger S, Han Z, Di Mavungu JD, Soares CMG, Proctor RH, Venâncio A, Lima N, Stea G, Paciolla C, Logrieco AF, Susca A. A polyphasic approach for characterization of a collection of cereal isolates of the Fusarium incarnatum-equiseti species complex. Int J Food Microbiol. 2016;234:24–35. https://doi.org/10.1016/j.ijfoodmicro.2016.06.023.
Krogh P, Christensen DH, Hald B. Natural occurrence of the mycotoxin fusarochromanone, a metabolite of Fusarium equiseti, in cereal feed associated with tibial dyschondroplasia. Appl Environ Microbiol. 1989;55(12):3184–8.
Hestbjerg H, Nielsen KF, Thrane U, Elmholt S. Production of trichothecenes and other secondary metabolites by Fusarium culmorum and Fusarium equiseti on common laboratory media and a soil organic matter agar: an ecological interpretation. J Agric Food Chem. 2002;50:7593–9. https://doi.org/10.1021/jf020432o.
O’Donnell K, Humber RA, Geiser DM, Kang S, Park B, Robert VARG, Crous PW, Johnston PR, Aoki T, Rooney AP, Rehner SA. Phylogenetic diversity of insecticolous fusaria inferred from multilocus DNA sequence data and their molecular identification via FUSARIUM-ID and Fusarium MLST. Mycologia. 2012;104:427–45. https://doi.org/10.3852/11-179.
Short DPG, O’Donnell K, Zhang N, Juba JH, Geiser DM. Widespread occurrence of diverse human pathogenic types of the fungus Fusarium detected in plumbing drains. J Clin Microbiol. 2011;49:4264–72. https://doi.org/10.1128/JCM.05468-11.
Proctor RH, McCormick SP, Alexander NJ, Desjardins AE. Evidence that a secondary metabolic biosynthetic gene cluster has grown by gene relocation during evolution of the filamentous fungus Fusarium. Mol Microbiol. 2009;74:1128–42. https://doi.org/10.1111/j.1365-2958.2009.06927.
Moolhuijzen PM, Manners JM, Wilcox SA, Bellgard MI, Gardiner DM. Genome sequences of six wheat-infecting fusarium species isolates. Genome Announc. 2013;1. https://doi.org/10.1128/genomeA.00670-13.
Brown DW, Proctor RH. Insights into natural products biosynthesis from analysis of 490 polyketide synthases from Fusarium. Fungal Genet Biol. 2016;89:37–51. https://doi.org/10.1016/j.fgb.2016.01.008.
Hansen FT, Gardiner DM, Lysøe E, Fuertes PR, Tudzynski B, Wiemann P, Sondergaard TE, Giese H, Brodersen DE, Sørensen JL. An update to polyketide synthase and non-ribosomal synthetase genes and nomenclature in Fusarium. Fungal Genet Biol. 2015;75:20–9. https://doi.org/10.1016/j.fgb.2014.12.004.
Marín P, Moretti A, Ritieni A, Jurado M, Vázquez C, González-Jaén MT. Phylogenetic analyses and toxigenic profiles of Fusarium equiseti and Fusarium acuminatum isolated from cereals from southern Europe. Food Microbiol. 2012;31:229–37. https://doi.org/10.1016/j.fm.2012.03.014.
Cuomo CA, Güldener U, Xu J-R, Trail F, Turgeon BG, Di Pietro A, Walton JD, Ma LJ, Baker SE, Rep M, Adam G. The Fusarium graminearum genome reveals a link between localized polymorphism and pathogen specialization. Science. 2007;317:1400–2. https://doi.org/10.1126/science.1143708.
Coleman JJ, Rounsley SD, Rodriguez-Carres M, Kuo A, Wasmann CC, Grimwood J, Schmutz J, Taga M, White GJ, Zhou S, Schwartz DC. The genome of Nectria haematococca: contribution of supernumerary chromosomes to gene expansion. PLoS Genet. 2009;5:e1000618. https://doi.org/10.1371/journal.pgen.1000618.
Vanheule A, Audenaert K, Warris S, van de Geest H, Schijlen E, Höfte M, De Saeger S, Haesaert G, Waalwijk C, van der Lee T. Living apart together: crosstalk between the core and supernumerary genomes in a fungal plant pathogen. BMC Genomics. 2016;17:670. https://doi.org/10.1186/s12864-016-2941-6.
Watanabe M, Yonezawa T, Lee KI, Kumagai S, Sugita-Konishi Y, Goto K, Hara-Kudo Y. Molecular phylogeny of the higher and lower taxonomy of the Fusarium genus and differences in the evolutionary histories of multiple genes. BMC Evol Biol. 2011;11(1):322 https://doi.org/10.1186/1471-2148-11-322.
Jin JM, Lee S, Lee J, Baek SR, Kim JC, Yun SH, Park SY, Kang S, Lee YW. Functional characterization and manipulation of the apicidin biosynthetic pathway in Fusarium semitectum. Mol Microbiol. 2010;76:456–66. https://doi.org/10.1111/j.1365-2958.2010.07109.
Harris LJ, Alexander NJ, Saparno A, Blackwell B, McCormick SP, Desjardins AE, Robert LS, Tinker N, Hattori J, Piché C, Schernthaner JP. A novel gene cluster in Fusarium graminearum contains a gene that contributes to butenolide synthesis. Fungal Genet Biol. 2007;44:293–306. https://doi.org/10.1016/j.fgb.2006.11.001.
Kim YT, Lee YR, Jin J, Han KH, Kim H, Kim JC, Lee T, Yun SH, Lee YW. Two different polyketide synthase genes are required for synthesis of zearalenone in Gibberella zeae. Mol Microbiol. 2005;58:1102–13. https://doi.org/10.1111/j.1365-2958.2005.04884.
Kakule TB, Sardar D, Lin Z, Schmidt EW. Two related pyrrolidinedione synthetase loci in Fusarium heterosporum ATCC 74349 produce divergent metabolites. ACS Chem Biol. 2013;8:1549–57. https://doi.org/10.1021/cb400159f.
Bahadoor A, Schneiderman D, Gemmill L, Bosnich W, Blackwell B, Melanson JE, McRae G, Harris LJ. Hydroxylation of Longiborneol by a Clm2-encoded CYP450 monooxygenase to produce Culmorin in Fusarium graminearum. J Nat Prod. 2016;79:81–8. https://doi.org/10.1021/acs.jnatprod.5b00676.
Sanchez JF, Entwistle R, Hung J-H, Yaegashi J, Jain S, Chiang Y-M, Wang CC, Oakley BR. Genome-based deletion analysis reveals the prenyl xanthone biosynthesis pathway in Aspergillus nidulans. J Am Chem Soc. 2011;133:4010–7. https://doi.org/10.1021/ja1096682.
Lim FY, Hou Y, Chen Y, Oh J-H, Lee I, Bugni TS, Keller NP. Genome-based cluster deletion reveals an endocrocin biosynthetic pathway in Aspergillus fumigatus. Appl Environ Microbiol. 2012;78:4117–25. https://doi.org/10.1128/AEM.07710-11.
Xu X, Liu L, Zhang F, Wang W, Li J, Guo L, Che Y, Liu G. Identification of the first diphenyl ether gene cluster for pestheic acid biosynthesis in plant endophyte Pestalotiopsis fici. Chembiochem. 2014;15:284–92. https://doi.org/10.1002/cbic.201300626.
Throckmorton K, Wiemann P, Keller NP. Evolution of chemical diversity in a Group of non-Reduced Polyketide Gene Clusters: using Phylogenetics to inform the search for novel fungal natural products. Toxins. 2015;7:3572–607. https://doi.org/10.3390/toxins7093572.
Baker SE, Kroken S, Inderbitzin P, Asvarak T, Li B-Y, Shi L, Yoder OC, Turgeon BG. Two polyketide synthase-encoding genes are required for biosynthesis of the polyketide virulence factor, T-toxin, by Cochliobolus heterostrophus. Mol Plant-Microbe Interact. 2006;19:139–49. https://doi.org/10.1094/MPMI-19-0139.
Bushley KE, Turgeon BG. Phylogenomics reveals subfamilies of fungal nonribosomal peptide synthetases and their evolutionary relationships. BMC Evol Biol. 2010;10:26. https://doi.org/10.1186/1471-2148-10-26.
Gallo A, Ferrara M, Perrone G. Phylogenetic study of polyketide synthases and nonribosomal peptide synthetases involved in the biosynthesis of mycotoxins. Toxins. 2013;5:717–42. https://doi.org/10.3390/toxins5040717.
Shimodaira H, Hasegawa M. Multiple comparisons of log-likelihoods with applications to phylogenetic inference. Mol Biol Evol 1999;16:1114–1114.
Shimodaira H. An approximately unbiased test of phylogenetic tree selection. Syst Biol. 2002;51:492–508. https://doi.org/10.1080/10635150290069913.
Proctor RH, Van Hove F, Susca A, Stea G, Busman M, van der Lee T, Waalwijk C, Moretti A, Ward TJ. Birth, death and horizontal transfer of the fumonisin biosynthetic gene cluster during the evolutionary diversification of Fusarium. Mol Microbiol. 2013;90:290–306. https://doi.org/10.1111/mmi.12362.
Ward TJ, Bielawski JP, Kistler HC, Sullivan E, O’Donnell K. Ancestral polymorphism and adaptive evolution in the trichothecene mycotoxin gene cluster of phytopathogenic Fusarium. Proc Natl Acad Sci. 2002;99:9278–83. https://doi.org/10.1073/pnas.142307199.
Lysøe E, Harris LJ, Walkowiak S, Subramaniam R, Divon HH, Riiser ES, Llorens C, Gabaldón T, Kistler HC, Jonkers W, Kolseth AK. The genome of the generalist plant pathogen Fusarium avenaceum is enriched with genes involved in redox, signaling and secondary metabolism. PLoS One. 2014;9:e112703.
Brown DW, Proctor RH, Dyer RB, Plattner RD. Characterization of a fusarium 2-gene cluster involved in trichothecene C-8 modification. J Agric Food Chem. 2003;51:7936–44. https://doi.org/10.1021/jf030607.
Peplow AW, Meek IB, Wiles MC, Phillips TD, Beremand MN. Tri16 is required for esterification of position C-8 during trichothecene mycotoxin production by Fusarium sporotrichioides. Appl Environ Microbiol. 2003;69:5935–40.
Susca A, Proctor RH, Butchko RAE, Haidukowski M, Stea G, Logrieco A, Moretti A. Variation in the fumonisin biosynthetic gene cluster in fumonisin-producing and nonproducing black aspergilli. Fungal Genet Biol. 2014;73:39–52. https://doi.org/10.1016/j.fgb.2014.09.009.
Susca A, Proctor RH, Morelli M, Haidukowski M, Gallo A, Logrieco AF, Moretti A. Variation in fumonisin and ochratoxin production associated with differences in biosynthetic gene content in Aspergillus niger and A. welwitschiae isolates from multiple crop and geographic origins. Front Microbiol. 2016;7:1412.
Gardiner DM, McDonald MC, Covarelli L, Solomon PS, Rusu AG, Marshall M, Kazan K, Chakraborty S, McDonald BA, Manners JM. Comparative pathogenomics reveals horizontally acquired novel virulence genes in fungi infecting cereal hosts. PLoS Pathog. 2012;8:e1002952. https://doi.org/10.1371/journal.ppat.1002952.
Morrison E, Rundberget T, Kosiak B, Aastveit AH, Bernhoft A. Cytotoxicity of trichothecenes and fusarochromanone produced by Fusarium equiseti strains isolated from Norwegian cereals. Mycopathologia [Internet]. Springer; 2002;153:49–56. Available from: https://doi.org/10.1023/A:1015201709070
Lee T, Han Y-K, Kim K-H, Yun S-H, Lee Y-W. Tri13 and Tri7 determine deoxynivalenol- and nivalenol-producing chemotypes of Gibberella zeae. Appl Environ Microbiol. 2002;68:2148–54.
Brown DW, McCormick SP, Alexander NJ, Proctor RH, Desjardins AE. Inactivation of a cytochrome P-450 is a determinant of trichothecene diversity in Fusarium species. Fungal Genet Biol. 2002;36:224–33.
Kimura M, Tokai T, Takahashi-Ando N, Ohsato S, Fujimura M. Molecular and genetic studies of fusarium trichothecene biosynthesis: pathways, genes, and evolution. Biosci Biotechnol Biochem. 2007;71:2105–23.
Campbell MA, Rokas A, Slot JC. Horizontal transfer and death of a fungal secondary metabolic gene cluster. Genome Biol Evol. 2012;4:289–93. https://doi.org/10.1093/gbe/evs011.
Qiu H, Cai G, Luo J, Bhattacharya D, Zhang N. Extensive horizontal gene transfers between plant pathogenic fungi. BMC Biol. 2016;14(1):41. https://doi.org/10.1186/s12915-016-0264-3.
Speed MP, Arbuckle K. Quantification provides a conceptual basis for convergent evolution. Biol Rev. 2017;92:815–29. https://doi.org/10.1111/brv.12257.
Stanke M, Morgenstern B. AUGUSTUS: a web server for gene prediction in eukaryotes that allows user-defined constraints. Nucleic Acids Res. 2005;33(suppl_2):W465–7.
Solovyev V, Kosarev P, Seledsov I, Vorobyev D. Automatic annotation of eukaryotic genes, pseudogenes and promoters. Genome Biol. 2006;7(Suppl 1):S10.1–12. https://doi.org/10.1186/gb-2006-7-s1-s10.
Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Molec Biol Evol. 2016;33:1870–4. https://doi.org/10.1093/molbev/msw054.
Nguyen L-T, Schmidt HA, von Haeseler A, Minh BQ. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol Biol Evol. 2015;32:268–74. https://doi.org/10.1093/molbev/msu300.
Stamatakis A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics. 2014;30:1312–3. https://doi.org/10.1093/bioinformatics/btu033.
Salichos L, Rokas A. Inferring ancient divergences requires genes with strong phylogenetic signals. Nature. 2013;497(7449):327. https://doi.org/10.1038/nature12130.
Salichos L, Stamatakis A, Rokas A. Novel information theory-based measures for quantifying incongruence among phylogenetic trees. Mol Biol Evol. 2014;31(5):1261–71 https://doi.org/10.1093/molbev/msu061.
Huson DH, Scornavacca C. Dendroscope 3: an interactive tool for rooted phylogenetic trees and networks. Syst Biol. 2012;61(6):1061–7. https://doi.org/10.1093/sysbio/sys062.
Medema MH, Blin K, Cimermancic P, de Jager V, Zakrzewski P, Fischbach MA, Weber T, Takano E, Breitling R. antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences. Nucleic Acids Res. 2011;39:W339–46. https://doi.org/10.1093/nar/gkr466.
Weber T, Blin K, Duddela S, Krug D, Kim HU, Bruccoleri R, Lee SY, Fischbach MA, Müller R, Wohlleben W, Breitling R. antiSMASH 3.0-a comprehensive resource for the genome mining of biosynthetic gene clusters. Nucleic Acids Res. 2015;43(W1):W237–43.
Katoh K, Misawa K, Kuma K-I, Miyata T. MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Res. 2002;30:3059–66.
Minh BQ, Nguyen MAT, von Haeseler A. Ultrafast approximation for phylogenetic bootstrap. Mol Biol Evol. 2013;30:1188–95. https://doi.org/10.1093/molbev/mst024.
Chen K, Durand D, Farach-Colton M. NOTUNG: a program for dating gene duplications and optimizing gene family trees. J Comput Biol. 2000;7:429–47. https://doi.org/10.1089/106652700750050871.
Stolzer M, Lai H, Xu M, Sathaye D, Vernot B, Durand D. 2012. Inferring duplications, losses, transfers and incomplete lineage sorting with nonbinary species trees. Bioinforma. 2012;28:i409–15. https://doi.org/10.1093/bioinformatics/bts386.
Yang Z. PAML 4: phylogenetic analysis by maximum likelihood. Mol Biol Evol. 2007;24(8):1586–91.
Edwards J, Auer D, de Alwis SK, Summerell B, Aoki T, Proctor RH, Busman M, O'Donnell K. Fusarium agapanthi sp. nov., a novel bikaverin and fusarubin-producing leaf and stem spot pathogen of Agapanthus praecox (African lily) from Australia and Italy. Mycologia. 2016;108:981–92.
Laurence MH, Walsh JL, Shuttleworth LA, Robinson DM, Johansen RM, Petrovic T, Vu TTH, Burgess LW, Summerell BA, Liew ECY. Six novel species of Fusarium from natural ecosystems in Australia. Fungal Divers. 2015;77:1–18.
We are grateful for the excellent technical assistance of Amy McGovern, Marcie L. Moore, Crystal Probyn, and Gaetano Stea.
Mention of trade names or commercial products in this article is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the US Department of Agriculture. USDA is an equal opportunity provider and employer.
This work was financially supported by H2020-EU3.2–678781-MycoKey-Integrated and innovative key actions for mycotoxin management in the food and feed chain.
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Data generated in this study are publicly available from the NCBI/GenBank database at Bioproject Accession: PRJNA436969 ID: 436969.
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List of 30 HK genes and strains used to infer species trees in this study. (DOCX 16 kb)
Fusarium species tree inferred by maximum likelihood analysis of concatenated sequences of 30 housekeeping genes (see Additional file 1). Each gene sequence was aligned separately using MUSCLE as implemented in MEGA7. The resulting alignments were then concatenated using SequenceMatrix, and then subjected to maximum likelihood analysis as implemented in IQ-Tree (version 1.6.7). (PPTX 90 kb)
Results of BLASTn analysis to assess presence and absence of genes or gene clusters for which the secondary metabolic products are known. (XLSX 25 kb)
Trees inferred by maximum likelihood analysis of alignment of predicted amino acid sequences of the four major groups of PKS genes retrieved from FIESC genome sequences examined in this study. Supplementary Figs. A. – D. correspond to the major groups of PKS genes previously described in Fusarium and other fungi . The major groups are the non-reducing PKSs (NR-PKS) (A.) and the three subgroups of reducing PKSs: R-PKS I (B.), R-PKS II (C.) and R-PKS III (D.). For each major group, phylogenetically distinct clades (or homolog groups) are labeled with clade numbers (C3, C5, C8, etc.) that were previously described in analysis of other fusaria (Brown and Proctor 2016). Homologs from other fusaria were included in current study and are designated using the same abbreviations used by Brown and Proctor . Numbers near branches are bootstrap values based on 1000 pseudoreplicates. Bootstrap values below 70% are not shown. (PPTX 154 kb)
Trees inferred by ML analysis of individual NRPS and PKS genes retrieved from FIESC genome sequences examined in this study. All the homologous genes retrieved from NCBI and were included in the analysis. Numbers near branches are bootstrap values based on 1000 pseudoreplicates. Bootstrap values below 70% are not shown. (PPTX 671 kb)
Reconciled NRPS and PKS trees with duplication, losses and HGT events as obtained from NOTUNG. Duplications are indicated with red D, transfers are indicated by yellow T’s, and losses in grey. (PPTX 303 kb)
Results of Shimodaira-Hasegawa (SH) and Approximately Unbiassed (AU) tests used to assess branches that suggest horizontal gene transfer of NRPS and PKS genes between FIESC and other lineages of Fusarium. (DOCX 21 kb)
Results of the dS analyses. (XLSX 1391 kb)
A. Analysis of homologs of the putative PKS42-NRPS34 cluster. On the left, tree inferred by maximum likelihood analysis of concatenated sequences of the nine genes in the PKS43-NRPS34 cluster. Numbers near branches are bootstrap values based on 1000 pseudoreplicates. Right, gene organization in PKS42-NRPS34 cluster homologs. The vertical dashed lines between genes in the F. aywerte homolog indicate that the genes are one different contigs. The genes on either side of a vertical lines are at the ends of contigs and, therefore, could be adjacent to one another in the genome. B. Analysis of genes flanking the putative PKS42-NRPS34 cluster and their homologs in selected members of FIESC that lack the cluster. The tree to the left was inferred by maximum likelihood analysis of flanking gene F2. Numbers near branches are bootstrap values based on 1000 pseudoreplicates. Bootstrap values below 70% are not shown. Genes and their direction of transcription are represented by arrows. Gray arrows represent genes in the PKS42-NRPS34 cluster, white arrows represent cluster flanking genes, and the yellow arrow represents a gene that was unique to the region in F. camptoceras. (PPTX 154 kb)
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Villani, A., Proctor, R.H., Kim, HS. et al. Variation in secondary metabolite production potential in the Fusarium incarnatum-equiseti species complex revealed by comparative analysis of 13 genomes. BMC Genomics 20, 314 (2019). https://doi.org/10.1186/s12864-019-5567-7
- Fusarium incarnatum-equiseti species complex
- Comparative genome analyses
- Secondary metabolite genes
- Horizontal gene transfer