Comparative genomics of Beauveria bassiana: uncovering signatures of virulence against mosquitoes
© The Author(s). 2016
Received: 13 July 2016
Accepted: 23 November 2016
Published: 1 December 2016
Entomopathogenic fungi such as Beauveria bassiana are promising biological agents for control of malaria mosquitoes. Indeed, infection with B. bassiana reduces the lifespan of mosquitoes in the laboratory and in the field. Natural isolates of B. bassiana show up to 10-fold differences in virulence between the most and the least virulent isolate. In this study, we sequenced the genomes of five isolates representing the extremes of low/high virulence and three RNA libraries, and applied a genome comparison approach to uncover genetic mechanisms underpinning virulence.
A high-quality, near-complete genome assembly was achieved for the highly virulent isolate Bb8028, which was compared to the assemblies of the four other isolates. Whole genome analysis showed a high level of genetic diversity between the five isolates (2.85–16.8 SNPs/kb), which grouped into two distinct phylogenetic clusters. Mating type gene analysis revealed the presence of either the MAT1–1–1 or the MAT1–2–1 gene. Moreover, a putative new MAT gene (MAT1-2–8) was detected in the MAT1–2 locus. Comparative genome analysis revealed that Bb8028 contains 163 genes exclusive for this isolate. These unique genes have a tendency to cluster in the genome and to be often located near the telomeres. Among the genes unique to Bb8028 are a Non-Ribosomal Peptide Synthetase (NRPS) secondary metabolite gene cluster, a polyketide synthase (PKS) gene, and five genes with homology to bacterial toxins. A survey of candidate virulence genes for B. bassiana is presented.
Our results indicate several genes and molecular processes that may underpin virulence towards mosquitoes. Thus, the genome sequences of five isolates of B. bassiana provide a better understanding of the natural variation in virulence and will offer a major resource for future research on this important biological control agent.
KeywordsBeauveria bassiana Comparative genomics Virulence Genome sequencing
Beauveria bassiana is a cosmopolitan entomopathogenic fungus (EPF) with a broad host range covering most insect orders (e.g., Coleoptera, Diptera, Hemiptera, Lepidoptera) and also arthropods (subclass Acari) [1, 2]. B. bassiana is currently used commercially as a biological control agent for different arthropod pests in China such as the pine caterpillar (Thaumetopoea pityocampa), corn borer (Ostrinia furnacalis), peach aphid (Myzus persicae), and pine sawyer (Bursaphelenchus xylophilus) . B. bassiana is also being developed as a biological control tool for vectors of human diseases, such as Anopheles mosquitoes that transmit malaria [4, 5], Aedes aegypti mosquitoes that are vectors of Dengue, Chikungunya and Zika virus [6, 7], the Triatoma infestans bug, the Chagas disease vector , and Ixodes ricinus ticks that transmit Lyme disease .
Infection by B. bassiana starts when conidia adhere to the host cuticle via hydrophobic interactions and subsequently germinate. A germ tube is formed that is able to penetrate the cuticle through a combination of mechanical pressure and cuticle degrading enzymes. Once the fungal structures reach the haemocoel, the fungus switches to growth as single-celled blastospores, which are capable of evading the insect immune system, exploit the haemolymph for nutrition, and secrete toxins that eventually kill the host. Once the host is dead, the fungus breaches the cuticle from the inside outwards, allowing the formation of conidia that upon dispersal start new infections .
A good understanding of the life history of B. bassiana as well as the genetic mechanisms of virulence is crucial to develop it as an effective and sustainable biological control agent. Substantial progress has been made in the genetic characterization of the mechanisms involved in the infection cycle of B. bassiana inside insects. Many of the recent findings regarding genes involved in virulence were possible due to the development of reliable protocols that allow genetic manipulation  together with the availability of a draft genome sequence . For instance, it has been found that B. bassiana expresses two hydrophobin genes, hyd1 and hyd2, that are believed to be involved in surface hydrophobicity, adhesion, virulence and composition of the rodlet layer. A Δhyd1 knock-out mutant showed decreased virulence and spore hydrophobicity but unchanged surface adhesion, while a Δhyd2 mutant showed reduced hydrophobicity and surface adhesion but unchanged virulence . Similarly, a cytochrome P450 gene, Bbcyp52x1, was shown to function in enzymatic breakdown of lipids in the waxy layer. A ΔBbcyp52x1 knock-out mutant showed reduced virulence on Galleria mellonella upon topical application of conidia, though not upon intra-hemocoel injection .
Despite all efforts made to understand virulence in B. bassiana (for a review, see ), many of the genes that were functionally analysed thus far are involved in general biological processes (e.g., conidiation, stress response) that pleiotropically affect virulence. This indicates that virulence is tightly connected to the biology and life history of Beauveria. In order to increase the efficacy and specificity of Beauveria against arthropods, we need to identify the genes exclusively implicated in entomopathogenic virulence. Therefore, strategies must be employed that allow de novo identification of genes and mechanisms specifically related to virulence. Our previous identification of ample natural genetic variation for virulence in B. bassiana isolates  opens the way for a comparative genomic approach. Such an approach offers a powerful opportunity to collect comprehensive information of genetic variation and identification of variants of virulence and their evolutionary dynamics. Importantly, knock-out mutant approaches are crucial and will play an important role in verifying the action of the candidate genes that emerge from comparative genomics of natural isolates that differ in virulence.
The aim of this study was to improve our knowledge in understanding the key factors involved in virulence of B. bassiana by a comparative genomics study. B. bassiana is well known for having a broad genetic, host, and virulence diversity. As a consequence, genome structure and DNA sequence variation between any two isolates could be related to many factors in the biology of this fungus (including neutral evolution/genetic drift). Therefore, we sequenced five isolates of contrasting virulence, selected from a panel of 29 B. bassiana isolates of which the natural variation in virulence had been previously characterized . We assembled a gapless near-complete genome for the most virulent B. bassiana isolate, Bb8028, which provides the community a highly suitable reference genome to be used for comparison with other isolates.
Fungal isolates and maintenance
Beauveria bassiana isolates ARSEF 1520 (Bb1520), ARSEF 2597 (Bb2597), ARSEF 4305 (Bb4305), ARSEF 5078 (Bb5078) and ARSEF 8028 (Bb8028) were obtained from the USDA-ARS Collection of Entomopathogenic Fungal Cultures (ARSEF). These isolates were selected based on their previously characterized virulence against malaria mosquitoes. Isolates Bb2597 and Bb8028 were previously shown to display high virulence, Bb1520 has intermediate virulence, while Bb4305 and Bb5078 have low virulence . Isolates were grown on Sabouraud Dextrose Agar with 1% yeast extract (SDAY) at 27 °C before DNA extraction and sequencing.
Genome and transcriptome sequencing
DNA was isolated from freeze-dried mycelium using a CTAB-based method . All isolates were sequenced with paired-end libraries of 180 bp insert size, and with a read length of 2x100 bp. Isolates Bb1520, Bb2597, and Bb8028 were further sequenced with a mate-pair library of 10 kb (Bb1520, Bb2597) or 6 kb (Bb8028). Isolate Bb8028 was selected as a reference based on the quality of the assembly, therefore additional sequencing focussed on this isolate and was performed using two PacBio SMRT cells with an insert size of 20 kb. The paired-end and mate-pair sequencing were performed using Illumina HiSeq2000 technology at the Beijing Genome Institute (BGI, Hongkong, China). PacBio sequencing was performed using the RS II instrument at Keygene N.V. (Wageningen, the Netherlands).
To obtain the transcriptome, RNA from Bb8028 was isolated from three different sources: (1) 5-day old mycelia grown on rice medium; (2) proto fruiting bodies (stromata like-structures) obtained from a cross between Bb8028 and Bb5078 co-cultivated for 2 months on rice medium as described ; and (3) infected mosquitoes that had just died. Rice medium was composed of 60 g of brown rice and 10 g of dried silkworm pupae, and 100 ml of distilled water. RNA was isolated using a RNAeasy Plant mini Kit (Qiagen) following manufacturer’s recommendations and sequenced using a paired-end library of 180 bp insert size on an Illumina HiSeq2000 platform at BGI.
Genome assembly and annotation
For isolates Bb4305 and Bb5078, de novo assembly was performed using Celera assembler  with default settings except k-mer size, which was set to 15. Isolates Bb1520, Bb2597, and Bb8028 were assembled using Allpaths-LG  with default settings. Additionally, PacBio data was used to improve the assembly of Bb8028 using PBJelly  and quiver tools , and erroneously merged contigs were manually corrected. RNA-Seq libraries were assembled de novo with Oases  and Trinity . Also, the RNA-Seq reads were mapped to the Bb8028 assembly using Tophat . Completeness of the genome assemblies was assessed by the Benchmarking Universal Single-Copy Orthologs (BUSCO) v1.1b1 software tool . RepeatMasker  was used to search for homologs of known repeats using the library from Repbase , and previously unknown repeats were predicted de novo with RepeatScout . Local Collinear Blocks (LCBs) were identifed using progressiveMauve (build date Feb 25, 2015), with default settings. Parsing and inversion detection was performed using a custom python script. Genome annotation was performed using the MAKER (v.2.31.8) pipeline  with AUGUSTUS , SNAP , and GeneMark-ES  as ab initio gene predictors. The assembled RNA-Seq reads and all fungal proteins available in the Uniprot database were used as evidence for gene prediction. Furthermore, the predicted proteins were manually inspected and curated. The predicted proteins were functionally annotated using BLASTp  against the non-redundant database of the National Center of Biotechnology Information (NCBI) and InterProScan . The BLASTp and InterproScan results were imported into Blast2GO version 3.2  and Gene Ontology (GO) terms were predicted. Overrepresentation of GO terms was analysed using Fisher’s test as embedded in Blast2GO. Secreted proteins were predicted by SignalP 4.1 .
The pan-genomes and core genomes at the gene level were estimated using OrthoMCL  implemented in GET_HOMOLOGUES-EST  with e-value 1e−5 and 75% coverage. Besides the five newly sequenced genomes presented here, the previously reported genome of B. bassiana ARSEF 2860 (Bb2860)  was also included in the analysis.
The phylogenetic relationships were determined with the software REALPHY  between all isolates of B. bassiana, including the previously sequenced isolate Bb2860 , and using C. militaris  as the outgroup of the tree. All genomes were mapped using Bowtie2  on the genome of Bb8028 as a reference. After the alignment, a maximum likelihood phylogenetic tree was inferred with RAxML  using the generalised time reversible (GTR) plus GAMMA nucleotide substitution model and 100 rapid bootstraps.
To identify single-nucleotide polymorphisms (SNPs), Freebayes (v0.9.21), a Bayesian method based program, was used  with a minimum alteration fraction of 0.90. All sequences were mapped with BWA  to the genome of isolate Bb8028. To minimize false positives, SNPs called at positions with low coverage (<10x) were not considered. SNP density and transition/transversion ratios were calculated using VCFtools .
Secondary metabolite analysis
Putative gene clusters that are predicted to be involved in biosynthesis of secondary metabolites were identified using antiSMASH (antibiotics and Secondary Metabolite Analysis SHell) version 3.0.4 .
Mating type gene analysis
The presence of mating type loci in all isolates of B. bassiana (including Bb2860) were identified by homology to characterized MAT genes of other filamentous fungi using BLASTp. The mating type alleles MAT1–1–1 and MAT1–2–1 were also determined by PCR with the primer pairs MAT112.F4/ MAT111.R5 and MAT2.F4/ MAT2.R5 , respectively.
To detect regions under positive selection, protein-coding DNA alignments based on the orthologous genes were generated with ParaAT. Ratios of non-synonymous (Ka) to synonymous (Ks) nucleotide substitution rates per site were estimated for each alignment using KaKs_Calculator 2.0 . A sliding window of 100 bp was used with a gamma distribution (gMYN) model.
A high-quality Beauveria bassiana reference genome
Summary of the genomic features of the different B. bassiana isolates
Total Assembly Size (Mb)
Sequencing libraries used
PEa + MPb
PE + MP
PE + MP + PBc
Scaffold N50 (kb)
Contig N50 (kb)
GC content (%)
Protein coding genes
Predicted secreted proteins
The three highest quality assemblies (Bb8028, Bb1520 and Bb2597) were used to explore structural rearrangements between these three genomes. In total, 695 locally collinear blocks (LCBs) were shared between two or three genomes. We identified 18 cases of clear inversions, where three adjacent LCBs were shared between the three genomes and in one genome the middle block was inverted with respect to the others. Fifteen of these inversions occurred in strain Bb1520 (Bb8028 and Bb2597 remain collinear), while two inversions occurred in Bb8028 and one in Bb2597. The size of inverted regions ranged from ~1 kb to 220 kb. Some LCBs demonstrated significant size differences between the genomes (ranging from 3 to 65 kb), suggesting insertions or deletions. Two inversions in isolate Bb1520 occurred within the coding sequence of a predicted gene (in the Bb8028 reference genome), thereby truncating the coding sequence of that gene in Bb1520. The vast majority of inversions occurred outside coding sequences and were judged to have no impact on gene structure or regulatory regions.
High levels of genetic diversity as revealed by SNPs and phylogenetic analysis
All the read data that were available in this study were mapped to Bb8028 as a reference in order to detect SNPs. Within cluster 1, there were 2.85 and 4.8 SNPs per kb for isolates Bb5078 and Bb2597, respectively. In contrast, the genetic variation in isolates from cluster 2 against Bb8028 was four-fold higher, with an average of 16.6 and 16.8 SNPs per kb, for Bb1520 and Bb4305, respectively. Similarly, the genetic identity to respect to Bb8028 was higher in Bb5078 (90.4%) and Bb2597 (89.7%), and lower in Bb4305 (88.4%) and Bb1520 (87.9%). We searched for SNPs in coding sequences of a set of 54 genes that have been functionally analysed by knock-out mutagenesis (reviewed in ) between the five B. bassiana isolates sequenced in this study. There are two genes that contain a SNP with potentially high impact: in the α-glucoside transporter gene Bbagt1 in a single isolate, and in the thioredoxin gene trx3 in two isolates. The remaining 52 genes do not display any high impact SNPs.
A new mating type gene
The draft genome of B. bassiana isolate Bb2860 was reported to lack the spo11 gene, a meiosis-specific topoisomerase essential for meiotic recombination, and this observation was used as an explanation for the infrequent occurrence of the sexual cycle of B. bassiana . The spo11 gene was however present in the genomes of all five B. bassiana isolates analysed in this study, and the conclusion about its absence in B. bassiana , based on a draft genome assembly, was thus erroneous.
Isolate-specific genes from Bb8028 include candidate virulence genes
Secondary metabolites play a role in fitness and virulence of fungal (entomo)pathogens . A Non-Ribosomal Peptide Synthetase (NRPS) gene cluster is present in the unique gene set of Bb8028 at the start of contig 8. The NRPS gene (BB8028_0008g00080) has homology (52–54%) to several Metarhizium species, with the difference that BB8028_0008g00080 has a single adenylation domain and is 1059 amino acids in length, while its Metarhizium homologs possess two adenylation domains and encode proteins almost double in size. In addition, Bb8028 contains a unique polyketide synthase gene (BB8028_0001g06000.1).
Five genes unique to Bb8028 (thus lacking in the four other B. bassiana genomes) encode proteins possessing bacterial enterotoxin-like domains. Four of these contain a heat-labile enterotoxin domain (IPR001144) while one protein displays 54% similarity to the Vibrio cholera enterotoxin alpha chain domain (IPR008992). Outside the kingdom Eubacteria, these enterotoxin genes have homology almost exclusively to Beauveria, Cordyceps and Metarhizium species, all of which are entomopathogenic fungi (data not shown). Bb8028 also possesses 11 peptidase genes (from various types) that have no orthologs in any of the other four B. bassiana isolates. Furthermore, two genes encoding the enzyme cyanamide hydratase are uniquely present in Bb8028. Cyanamide hydratase converts cyanamide into urea, and has been studied in relation to fungal survival in the soil since cyanamide is used as a fertilizer and is also synthesized by vetch species [55, 56]. Bb8028 also contains 13 unique genes involved in transport processes, of which five belong to the major facilitator (MFS) superfamily, four to the family of ATP-binding cassette (ABC) transporters, and the remaining four are dedicated siderophore and dicarboxylate transporters, as well as a sodium/proton antiporter. ABC transporters can be involved in (multidrug) resistance to fungicides, as well as the secretion of antibiotics and toxins . Recently, five ABC transporters were characterized in B. bassiana and found to be implicated in fungicide resistance, oxidative stress tolerance, and in virulence .
Finally, among the gene set unique to Bb8028 are also genes encoding enzymes putatively involved in the modification of chromatin proteins, which may modulate changes in gene expression . Specifically, these genes encode three arginine deiminases and a putative histone arginine N-methyltransferase.
Although a detailed analysis of differential gene expression could not be done with the RNA data available due to the lack of sample replication, an exploratory examination was done to see whether unique genes of Bb8028 were highly expressed. Specifically, we looked for genes that had at least (1) double the expression (in Fragments Per Kilobase of transcript per Million mapped reads (FPKM)) in the library isolated from infected mosquitoes compared against the library from fruiting bodies or mycelia, and, (2) a value of at least one FPKM. Of the 163 genes, 15 genes fulfilled these criteria. Notably, three of the five genes annotated as a toxin were among these 15 genes (Additional File 4). Also one of the arginine deiminase genes and one of the cyanamide hydratase genes displayed a high expression in the mosquito library as compared to the other two libraries.
No clear pattern of positive selection in genes of Bb8028
Genes with a signature of positive selection may contribute to the adaptation to a changing environment and could be related to virulence. Therefore, we investigated whether genes were under positive selection in Bb8028. Ka/Ks ratios were calculated in pairwise comparisons between orthologs in Bb8028 and each of the four other isolates, separately. We detected 10, 5, 11, 10 genes of Bb8028 with Ka/Ks > 1 when compared to their orthologs in Bb1520, Bb2597, Bb4305, Bb5078, respectively. In total, 18 genes are considered to be under selection in Bb8028, but intriguingly no gene was shared among the four pairwise comparisons (Additional File 5). Among the genes under positive selection are two calmodulin-dependent protein kinase genes and an ABC transporter gene, while most of the other genes were of unknown function.
In this study, we provide and compare the genomes of five isolates of B. bassiana that were previously characterized in a large-scale analysis of virulence against the malaria mosquito (An. coluzzii) . These isolates have different levels of virulence, with Bb8028 being the most virulent isolate, followed by Bb2597, Bb1520, Bb4305, and finally Bb5078. Comparative genomics at the intraspecific level is an approach to determine the genetic basis of phenotypic variations detected between different isolates. The genome of B. bassiana was previously compared to other entomopathogenic fungi , and in order to avoid a duplication of this previous work, we focused on comparison between B. bassiana isolates, with an emphasis on Bb8028. A pan-genome analysis indicated that the core genome of B. bassiana consists of 7,341 orthologous gene clusters, while the pan-genome consists of 13,068 orthologous gene clusters. These numbers suggest that B. bassiana has an open pan-genome, as may be expected for a species that can typically colonize multiple environments .
The isolates analysed have a high level of diversity with 467,292 SNPs between Bb4305 and Bb8028, and 87,119 SNPs between Bb5078 and Bb8028. Previous studies have suggested that B. bassiana is not monophyletic, but rather is composed of several clusters that are morphologically identical [48, 60, 61]. One study  described seven phylogenetic clusters in B. bassiana that consisted of isolates which did not show any geographic distribution but had common climate characteristics, while a different study  described isolates that were distributed in five clusters in a particular hedgerow habitat, however, genetic distances were not determined on a genome-wide scale in these studies. A comparative genomic study of seven isolates of the plant pathogenic fungus Penicillium expansum revealed a genetic diversity between 1.3 and 7.1 SNPs/kb , while between two isolates of Aspergillus niger it was 7.8 SNPs/kb . In both these cases, the genetic diversity was lower than observed in this study (2.9–16.8 SNPs/kb). The finding that B. bassiana possesses a high genetic diversity seems to be in agreement with the earlier suggestions that B. bassiana is not monophyletic [48, 60, 61] and warrants further studies to elucidate the species phylogeny on a whole genome scale.
B. bassiana normally reproduces asexually, and for a long time it was believed to be exclusively clonal. Developmental and phylogenetic studies, however, have linked it to the teleomorph Cordyceps bassiana [64, 65]. In the five isolates studied, the MAT1-1 and MAT1-2 loci were identified based on homology to the typical fungal mating type genes, encoding the alpha domain protein and the high mobility group box domain, respectively. The presence of either of two distinct alleles of the MAT locus in each B. bassiana isolate indicates that the species is putatively heterothallic. A new MAT gene was detected next to the MAT1–2–1 gene which, based on homology to a newly described gene in Villosiclava virens , is referred to as MAT1–2–8 following the nomenclature proposed by Dyer et al. . We attempted to sexually cross different isolates of B. bassiana in several combinations to generate fertile fruiting bodies. Based on the mating type, six combinations were possible (Additional File 6). Unfortunately, none of the crosses generated ascospores, but the cross between Bb8028 and Bb5078 generated fruiting body-like structures without ascospores; these structures were used to generate a transcriptome library. When taking into consideration the phylogenetic clusters found, we realized that only Bb8028 and B5078 belong to the same cluster and had the lowest number of SNPs/kb, compared to the other possible combinations. Since B. bassiana could be polyphyletic, and reports have found a single mating type in several populations , it is not surprising that B. bassiana is limited mainly to asexual reproduction. It is worthwhile to invest in a reproducible protocol for sexual crosses under laboratory conditions. The ability to achieve sexual reproduction will enable genome-wide association studies (GWAS) of quantitative virulence in the offspring of two isolates that markedly differ in virulence, for instance Bb8028 and Bb5078.
In this analysis, we identified a suite of genes that are unique to Bb8028. Among these are a PKS gene and a gene cluster comprising an NRPS gene with homology to a M. anisopliae gene annotated as tyrocidine synthase (KJK81377). Tyrocidine has antibiotic activity, and the peptide synthesized by the NRPS gene product could thus have antibiotic activity. The set of genes unique to Bb8028 also comprised five genes encoding bacterial-like toxins and 13 transporter genes. The B. bassiana genome contains many more bacterial-like toxins than most other fungi . Interestingly, we found preliminary evidence that some of the bacterial-like toxins are highly expressed in fungal infection of mosquitoes. A recent study  analysed gene expression in B. bassiana ARSEF 2860 infecting Plutella xylostella larvae at three different time points after inoculation (24 h, 36 h, 48 h). In the latter study, an enrichment of genes with functions in antioxidant activity, peroxidase activity, and proteolysis was detected among the genes that are highly expressed in B. bassiana during infection of the host insect. In contrast, toxin genes were not reported to be highly expressed during infection of P. xylostella larvae . The mortality rate of P. xylostella larvae infected by B. bassiana at 48 h was 33%, which is much lower than the mortality rate of almost 100% of infected mosquitoes at the time that we sampled RNA for library construction. The infection cycle of B. bassiana is a complex process which includes several developmental transitions that require an intricate genetic regulation . This biological complexity may explain why no overlap is found between these studies. Furthermore, B. bassiana is capable of infecting a wide range of hosts that have different chemical and physical compositions, which most likely requires a tailored response for each host-pathogen interactions.
The availability of a near-complete genome assembly of Bb8028 provided with a manually curated gene set, adds significant value to the previously published draft genome of B. bassiana . As argued by , a high quality assembly including proper assembly of centromeres, telomeres, and other repetitive elements provides the ability to characterize structural rearrangements and facilitates a better identification of secondary metabolite gene clusters. Therefore, a high quality genome is a key step to uncover the biological complexity of an organism, as our analyses showed. The Bb8028 genome assembly represents a significant resource for future research into the biology of this entomopathogenic fungus and its relevance as a biological control agent. Understanding the key factors involved in virulence of B. bassiana will improve our methods to use this fungus as an effective and sustainable biological control agent against, amongst others, vectors of human diseases.
CAVJ thanks Dr. Michael Seidl for advice and assistance with bioinformatics analysis.
This research was funded by the Graduate School Production Ecology & Resource Conservation, grant 12072. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and material
This Whole Genome Shotgun project has been deposited at DDBJ/ENA/GenBank under the accessions: JRHA00000000, JTCW00000000, JTCX00000000, JTCY00000000, and JTCZ00000000. The raw data for this study are deposited in NCBI Sequence Read Archive under BioProject number PRJNA260878. Bb8028: SRR3269141 (DNA reads Illumina, short insert library), SRR3269142 (DNA reads Illumina, long insert library), SRR3269778 (RNA reads mycelium), SRR3269779 (RNA reads “fruiting bodies”), SRR3269780 (RNA reads infected mosquitoes), SRR3269861 (DNA reads PacBio library), and SRR3269862 (DNA reads PacBio library). Bb1520 data: SRR3269145 (DNA reads Illumina, short insert library) and SRR3269146(DNA reads Illumina, long insert library). Bb2597: SRR3269425 (DNA reads Illumina, short insert library) and SRR3269550 (DNA reads Illumina, long insert library). Bb4305: SRR326914 (DNA reads Illumina, short insert library). Bb5078: SRR3269144 (DNA reads Illumina, short insert library). The genome of B. bassiana strain Bb8028 will be accessible from Ensembl Fungi (release October 2016).
CAVJ, SS, BJZ, and JALvK conceived the study and participated in its design and coordination. CAVJ carried out the laboratory work. CAVJ, DSV and LF performed the bioinformatics analysis. CAVJ, BJZ, and JALvK wrote the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
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