- Research article
- Open Access
Chaperone-usher fimbriae in a diverse selection of Gallibacterium genomes
© Kudirkienė et al.; licensee BioMed Central. 2014
- Received: 18 August 2014
- Accepted: 3 December 2014
- Published: 12 December 2014
Fimbriae are bacterial cell surface organelles involved in the pathogenesis of many bacterial species, including Gallibacterium anatis, in which a F17-like fimbriae of the chaperone-usher (CU) family was recently shown to be an important virulence factor and vaccine candidate. To reveal the distribution and variability of CU fimbriae 22 genomes of the avian host-restricted bacteria Gallibacterium spp. were investigated. Fimbrial clusters were classified using phylogeny-based and conserved domain (CD) distribution-based approaches. To characterize the fimbriae in depth evolutionary analysis and in vitro expression of the most prevalent fimbrial clusters was performed.
Overall 48 CU fimbriae were identified in the genomes of the examined Gallibacterium isolates. All fimbriae were assigned to γ4 clade of the CU fimbriae of Gram-negative bacteria and were organized in four-gene clusters encoding a putative major fimbrial subunit, a chaperone, an usher and a fimbrial adhesin. Five fimbrial clusters (Flf-Flf4) and eight conserved domain groups were defined to accommodate the identified fimbriae. Although, the number of different fimbrial clusters in individual Gallibacterium genomes was low, there was substantial amino acid sequence variability in the major fimbrial subunit and the adhesin proteins. The distribution of CDs among fimbrial clusters, analysis of their flanking regions, and evolutionary comparison of the strains revealed that Gallibacterium fimbrial clusters likely underwent evolutionary divergence resulting in highly host adapted and antigenically variable fimbriae. In vitro, only the fimbrial subunit FlfA was expressed in most Gallibacterium strains encoding this protein. The absence or scarce expression of the two other common fimbrial subunits (Flf1A and Flf3A) indicates that their expression may require other in vitro or in vivo conditions.
This is the first approach establishing a systematic fimbria classification system within Gallibacterium spp., which indicates a species-wide distribution of γ4 CU fimbriae among a diverse collection of Gallibacterium isolates. The expression of only one out of up to three fimbriae present in the individual genomes in vitro suggests that fimbriae expression in Gallibacterium is highly regulated. This information is important for future attempts to understand the role of Gallibacterium fimbriae in pathogenesis, and may prove useful for improved control of Gallibacterium infections in chickens.
- Mobile Element
- Conserve Domain
- Fimbrial Subunit
- Fimbrial Protein
- Fimbrial Adhesin
Gallibacterium is among the most important bacteria infecting the reproductive organs of laying hens [1, 2]. The bacterium often constitutes a part of the normal microflora in the upper respiratory and lower reproductive tract of chickens, however under certain conditions it causes lesions such as peritonitis and salpingitis. Following infection, egg production is significantly reduced and infected birds may also be more susceptible to other infections [3–6]. Organisms within the genus Gallibacterium appear to be restricted to avian hosts, including both domesticated and wild bird species [7–9]; however, there are three closely related species including Gallibacterium anatis, Gallibacterium genomospecies 1 and Gallibacterium genomospecies 2 that mainly affect chickens . All three species are strongly haemolytic (except G. anatis bv. anatis) due to the expression of a RTX-toxin GtxA, which is an important and well-described virulence factor of Gallibacterium [10, 11]. Several other virulence-associated factors including a polysaccharide capsule , secreted metalloproteases  and several fimbriae have been identified in Gallibacterium [13, 14]. Among these, the role of one fimbrial type in the pathogenesis of Gallibacterium anatis was recently investigated. A 1 to 2 μm -long F17-like fimbriae on the surface of Gallibacterium anatis bv. haemolytica strain 12656–12 was initially described by Bager et al. . The fimbria is encoded by the four-gene fimbrial cluster flf and assembled via the chaperone-usher (CU) pathway. In vitro studies using chicken epithelial cells as well as animal infection experiments demonstrated that this fimbrium might be involved in G. anatis colonization of the upper respiratory tract  and play an important role in the pathogenesis in chickens . Whole genome sequencing of Gallibacterium strains has revealed the presence of at least two homologous flf fimbrial clusters in several Gallibacterium genomes , however the function and role of these fimbriae in the pathogenesis of Gallibacterium is yet unknown.
Fimbriae are surface organelles expressed by many commensal and pathogenic bacteria. They are often involved in the adhesion of the bacteria to epithelial and/or sub-epithelial surfaces of various tissues [16–27]. Among a wide range of fimbriae expressed by Gram-negative bacteria the CU type fimbriae are the most prevalent  and the presence of up to 17 fimbrial clusters of this type in a single bacterial genome have previously been reported . Most of the CU fimbriae are composed of the four structural genes; a major fimbrial subunit, a chaperone, an usher and a tip adhesin. However some CU fimbrial clusters may contain additional genes encoding structural, assembly or regulatory proteins [28, 29]. Different studies have showed that the tip adhesin encodes various receptors recognizing specific ligands in the host tissues. Consequently the interaction of the CU fimbriae with the host is highly specific, and the expression of different fimbriae may be associated with different stages and sites of the infection [19, 30, 31]. To be able to determine the evolutionary and functional relationship between different CU fimbriae present in Gram-negative bacteria, they were classified into seven phylogenetic clades, each including fimbriae sharing conserved domains in the major fimbrial subunit and the tip adhesin proteins with common characteristics . Fimbriae have been intensively studied, not only because they are important virulence factors of bacteria, but also because they are among the most widely used targets for the development of interventions such as vaccines [25, 31–38]. Recently, the Gallibacterium F17-like fimbrial subunit protein (FlfA) was identified as a promising candidate that may be used to vaccinate laying hens .
This study aimed to analyze the distribution and variation of CU fimbrial clusters in the genomes of a selection of genetically diverse Gallibacterium strains, and to characterize their expression levels during in vitro conditions. Detailed phylogenetic analysis of the genes encoding fimbrial proteins allowed the development of a fimbrial classification system within Gallibacterium based on the evolutionary relationship between different fimbrial types.
Identification of chaperone-usher type fimbrial clusters
Strains used in the study
Strain name_alternative name
G. anatis biovar anatis
G. anatis biovar haemolytica
G. genomospecies 1
G. genomospecies 2
Phylogenetic analysis of GallibacteriumCU fimbrial clusters
To represent possible antigenic variation between Gallibacterium fimbrial clusters, all Gallibacterium CU fimbriae were classified into five types based on fimbrial subunit phylogeny. All fimbrial clusters in which a previously described FlfA  homolog was detected were named as Flf, and those in which major fimbrial subunits were assigned to the different phylogenetic groups than FlfA were named as Flf1, Flf2, Flf3 and Flf4. Out of the five defined CU fimbrial clusters, the most common fimbrial cluster was Flf1 found in 74% Gallibacterium genomes, followed by Flf and Flf3 detected in 65% and 52% of the genomes, respectively.
Pair-wise comparison of CU fimbrial proteins
A pair-wise comparison of the amino acid sequences of all proteins in the CU clusters was performed to determine the similarity between the fimbrial proteins assigned to the different fimbrial types. The protein similarity within the phylogenetic groups was ≥80.3%, ≥70.2% and ≥66.7% for the chaperones, ushers and the major fimbrial subunits, respectively, whereas the adhesins were much more variable with similarities ≥16.2% found between adhesins belonging to the same phylogenetic group. Fimbrial subunits belonging to different phylogenetic groups were 30.5% to 50.8% similar, chaperones 52.9% to 68.5%, ushers 44.0% to 71.4%, and adhesins 9.7% to 24.2% similar, respectively. The analysis revealed that both within and between the phylogenetic groups, the fimbrial adhesins show the most variable amino acid sequences in comparison to the sequences of the major fimbrial subunit, the chaperone and the usher.
Analysis of the regions flanking CU clusters
Analysis of the flanking regions of the fimbrial clusters was employed to identify possible homology between different CU clusters found in Gallibacterium spp. and the grouping based on major fimbrial subunit phylogeny. Most of the CU clusters assigned to the different fimbrial types were flanked by non-homologous genes (see Additional file 5: Table S2). However there were some exceptions to this observation. The flf and flf4 CU fimbrial clusters were surrounded by homologous genes. An additional exception was found for the fimbriae of strain 4895. Although the CU cluster found in this strain was assigned to fimbrial clusters flf3, it was flanked with genes homologous to the genes flanking the fimbrial cluster flf. This may suggest the common ancestry of the flf3 and the flf fimbriae. Interestingly, the genes flanking CU clusters were found in all analyzed Gallibacterium genomes independently from the presence or absence of the CU clusters in the genome. In some cases other genes were found inserted instead of the CU cluster (data not shown). Further flanking region analysis revealed the presence of mobile elements and transposases upstream or downstream of the CU clusters. The mobile elements were found upstream the major fimbrial subunit gene flf3A in 10 out of the 12 strains harboring the flf3 cluster. Such mobile elements were not detected in strain 4895, whereas in strain F000340, a mobile element downstream the gene encoding the fimbrial adhesin was detected. A lower prevalence of mobile elements was found around the fimbrial cluster flf. Only two strains (12158–5 and UMN179) belonging to this fimbrial type had mobile elements present upstream the major fimbrial subunit gene flfA. No mobile elements were detected in the flanking regions of CU clusters belonging to the other fimbrial subunit phylogenetic groups.
The widespread presence of mobile elements and transposases in the regions flanking the CU clusters supports previous suggestions that fimbriae may be horizontally transferred within G. anatis . Additionally, the high similarity of the flanking regions virtually in all Gallibacterium genomes indicates that homologous recombination likely is involved in the exchange of the fimbriae between closely related strains of G. anatis .
Conserved domain identification in CU fimbrial cluster proteins
This analysis showed that different combinations of CDs are present in the proteins encoded by fimbrial clusters of Gallibacterium. CD identification in the CU clusters would enable future insight into the evolutionary and functional relationships of Gallibacterium CU fimbriae with fimbriae from other Gram-negative bacteria and fimbriae in uncharacterized Gallibacterium isolates.
GallibacteriumCU fimbriae similarity to the fimbriae of other bacterium species
To reveal the evolutionary relationship of Gallibacterium fimbriae to the fimbriae of other Gram-negative bacterial species protein sequences of all 48 ushers identified in this study were compared to the usher protein sequences used by Nuccio and Bäumler . Based on this analysis, all Gallibacterium fimbriae were assigned to Nuccio clade γ and more specifically clustered together with fimbrial ushers of γ4 sub-clade [see Additional file 6: Figure S4].
The dominating cluster assemblies of Gallibacterium spp. were compared to the assemblies of fimbriae found in E. coli. The same structural proteins and CDs as in Gallibacterium CD class “a” was found in F17 and same as “b” in Yeh-like fimbriae of E.coli, both belonging to γ4 Nuccio clade .
The BLASTp of amino acid sequences against UniProt/SwissProt database revealed that the major fimbrial subunits of the CU clusters Flf, Flf1, Flf2 and Flf3 were most similar (from 32% to 45%, from p = 1e-11 to p = 6e-34, depending on the strain) to the F17 fimbrial subunit of E. coli [GenBank: P11312.2]. However, fimbrial subunits of the fimbrial cluster Flf4 were most similar (from 30% to 35%, from p = 4e-13 to p = 1e-19, depending on the strain) to FimA fimbrial subunit protein of Salmonella enterica serovar Tyhimurium [GenBank: P37921].
To further examine the relationships between Gallibacterium CU fimbriae and fimbriae of other bacteria, BLASTp analysis against the NCBI non-redundant protein database was performed. This analysis showed that the ushers and chaperones of the CU fimbriae Flf, Flf1, Flf3 and Flf4 were most similar to those found in Gallibacterium strain UMN179 and Avibacterium paragallinarum. The CU fimbriae Flf2 were most similar to the chaperones and ushers present in F17-like fimbriae of uropathogenic E. coli. The major fimbrial subunit proteins and adhesins of the CU fimbriae Flf, Flf3 and Flf4 were most similar to the proteins found in Gallibacterium strain UMN179 and Avibacterium paragallinarum. However, Flf1A and Flf2A homologs were detected in Acinetobacter baumannii, uropathogenic Proteus mirabilis and Esherichia coli, Haemophilus influenza and Haemophilus aegypticus [see Additional file 7: Table S3].
In conclusion, the proteins of the Gallibacterium CU clusters Flf, Flf3 and Flf4 are most similar to each other, suggesting that these clusters may have evolved from a common ancestor or have arisen due to gene duplication. Moreover, the presence of a fimbrial cluster identical to the Gallibacterium FlfA in the genome of A. paragallinarum suggest that this fimbriae may have been recently exchanged between these two species, which could theoretically occur during natural co-colonization of the chicken upper respiratory tract.
Distribution of different CU fimbrial clusters among MLST types of G. anatis and G.genomospecies 1 and 2
In vitroexpression of FlfA, Flf1A and Flf3A
Research on the chaperone – usher (CU) fimbriae of Gallibacterium spp. initially gained interest because they were found to be important virulence factors and possible vaccine candidates [13, 15, 39]. In the present study we aimed to examine the presence, diversity and in vitro expression levels of CU fimbriae in a diverse collection of Gallibacterium strains isolated from different sites in healthy and diseased birds of different geographical origin. We propose an expandable classification system of Gallibacterium CU fimbriae based on the phylogenetic- and CD-based approaches corresponding to the generic Gram-negative bacteria CU fimbriae classification system developed by Nuccio and Bäumler .
The few types of CU fimbrial clusters encoded by Gallibacteriumhave a similar structure
Sequence analysis of the 22 genomes representing three Gallibacterium species commonly associated with the chicken host, enabled an identification of 48 chromosomally located CU fimbriae. All fimbrial clusters resembled the archetype structure of the fimbrial gene cluster , encoding four essential structural fimbrial proteins: the major fimbrial subunit, the chaperone, the usher and an adhesin. The order of the genes was congruent in all of the investigated genomes. The structure of the CU fimbriae in Gallibacterium corresponded to what has been described for the F17 and yeh fimbriae of E. coli [23, 26], as well as in stc and sti fimbriae of S. enterica serovar Typhimurium .
Multiple alignment and phylogenetic comparison of the individual proteins encoded by each of the fimbrial clusters revealed a higher variation among the major fimbrial subunits compared to the other structural proteins (Figure 1) [see Additional file 2: Figure S1, Additional file 3: Figure S2, Additional file 4: Figure S3]. Previous findings indicate that major fimbrial subunits are the primary antigenic determinants of the fimbriae  and the pattern of evolutionary divergence of their amino acid sequences strongly correlates with the antigenic properties of the fimbriae [34, 43]. Therefore fimbrial subunit proteins were used for the primary classification of the fimbrial clusters of Gallibacterium spp. Based on the fimbrial subunit phylogenies, all Gallibacterium fimbriae were classified into five types named Flf, Flf1, Flf2, Flf3 and Flf4. Three of these types (Flf, Flf1 and Flf3) constituted the majority of the fimbrial clusters found in the examined Gallibacterium genomes and were homologous to the previously reported fimbrial clusters of UMN179_809-812, UMN179_750-753 and UMN179_295-292, respectively . In addition, two distinct, previously unreported fimbrial clusters were identified in several Gallibacterium genomes (Flf2 and Flf4). Interestingly, the Flf2 fimbrial type was detected only in two Gallibacterium strains (F149 and Gerl.3348/80), which were isolated from a duck and a goose, respectively. Considering that the Flf2 flanking regions were more widespread among the strains investigated than the Flf2 locus itself could suggest that this fimbrial locus may have been more prevalent and possibly have been lost during adaptation in a chicken host .
Frequently two to three different CU fimbrial clusters were identified in each individual Gallibacterium genome. In contrast, possession of up to 7, 16, 12 and 17 distinct CU fimbrial clusters have been reported from individual strains of E. coli O157:H7 [19, 26], E. coli K-12 , S. enterica serovar Typhimurium [18, 45] and P. mirabilis, respectively. In general, CU fimbriae belonging to evolutionary distinct clades as defined by Nuccio and Bäumler  can be simultaneously detected in the genomes of Gram-negative bacteria (24,26,27), whereas all the identified Gallibacterium fimbriae were assigned to a single γ4 clade. The extensive variability between fimbriae in other bacterial species, such as P. mirabilis, Salmonella and E. coli suggest that there may be an evolutionary pressure for these bacteria to maintain a large fimbrial arsenal. Common to all these species is that they are found in variety of ecological niches including different hosts, animals and humans, as well as in the environment, whereas G. anatis is known as avian restricted pathogen .
High sequence variation in the major fimbrial subunit and in the adhesin proteins may be related to the antigenic variation
In comparison to other bacterial species [27, 30, 46, 47]Gallibacterium generally did not possess a broad range of different fimbrial clusters, yet high sequence diversity of the major fimbrial subunits and adhesins within each fimbrial type was observed. Both the major fimbrial subunit protein and the adhesin protein are exposed on the surface of the bacterial cell and therefore determine the antigenic characteristics of the fimbriae [32, 42]. High sequence diversity in these proteins is thus likely to be maintained to enable specific interaction with different oligosaccharide motifs or receptors in host tissues, as well as to allow escape from recognition of the host immune system [30, 43, 48, 49]. As a result, host immunity exerts a constant pressure shaping new antigenic variants evading acquired host immunity . The antigenic variation of Gallibacterium fimbriae may be a result of homologous recombination as described for many virulence-associated factors including fimbrial proteins of the human restricted pathogen N. meningitidis . All identified Gallibacterium fimbrial clusters were embedded in one of five regions flanked by genes conserved even in distantly related Gallibacterium genomes. Therefore, we suggest that homologous recombination of the fimbrial loci may be the most likely explanation of the observed sequence diversity and a likely cause of antigenic variation in Gallibacterium spp.
Gallibacterium fimbriae may be transferred between Gallibacteriumstrains, species and closely related genera
According to the BLASTp analyses, fimbrial clusters Flf, Flf3 and Flf4 were phylogenetically related and most similar to each other as well as to the fimbriae of A. paragallinarum, whereas Flf1 and Flf2 shared close relatedness with the fimbrial proteins found in A. baumanni, P. mirabilis, E. coli and Haemophilus species [see Additional file 7: Table S3]. Interestingly, the Flf1 and Flf2 fimbrial clusters possessed a highly conserved domain structure, belonging to only one CD group (group ‘a’). The same domain structure was also present in the very well characterized F17 fimbriae of E. coli . Even though similar domain structures were shared with the fimbriae of E. coli suggesting a common ancestry, Gallibacterium fimbriae may be functionally different . Duplication of the fimbrial clusters Flf1 and Flf2 is very likely, as several Gallibacterium clusters of the Flf type also possessed the ‘a’ CD structure. The CD structure of the remaining Flf clusters was highly diverse and represented by seven (b-h) CD groups in total (Figure 2). Some of these CD groups were shared with the fimbrial types Flf3 and Flf4 suggesting that fimbrial cluster duplication in Gallibacterium may occur . If this is the case fimbrial clusters maintaining different CD structure may encode functionally different fimbriae that may interact with different host tissues and the receptors. Furthermore, the change of the domain structure may induce altered pilus attachment properties or even fimbrial structure, which again could help Gallibacterium to evade the host immune response and improve its survival within the host [23, 53].
The comparison of Gallibacterium strains based on the sequence similarity of eight loci conserved in 22 Gallibacterium genomes  confirmed that all examined Gallibacterium strains were genetically diverse. Different MLST lineages shared fimbrial clusters belonging to different fimbrial types identified in Gallibacterium strains. We found no relationship between the presence of a specific fimbrial type or CD group and the health status or isolation site in the host, which may indicate that distinct fimbrial types may be equally present in different Gallibacterium strains, whereas their gene expression levels may be tightly regulated during the colonization process in the host [54–56]. The distribution of different fimbrial types in genetically distinct isolates of Gallibacterium strains indicates that horizontal transfer of the fimbrial clusters occurs between strains. Moreover, similar fimbrial types appear in closely related species G. anatis, G. genomospecies 1 and G. genomospecies 2 [see Additional file 8: Figure S5], which were all isolated from the chicken host suggesting a horizontal gene transfer between less-related strains of different Gallibacterium species. The presence of mobile genetic elements in close proximity of the fimbrial gene clusters further supports this notion. The major fimbrial subunit protein FlfA of Gallibacterium was highly similar (66-100%) to a protein from Avibacterium paragallinarum [see Additional file 9: Figure S6] indicating that lateral gene transfer even may take place between closely related genera [see Additional file 8: Figure S5]. G. anatis and A. paragallinarum share the upper respiratory tract of chickens as their main habitat [1, 57], thus it is very likely that Flf fimbriae has been exchanged between these two genera during co-colonization of this niche. Similar to our findings, the presence of closely related Type 3 fimbriae was also demonstrated in E. coli and K. pneumonia catheter-associated urinary tract infection strains , further supporting that fimbriae may be transferred between different genera sharing niche in the same host.
Only two fimbrial types of Gallibacterium, yet only one at once, are expressed in vitro
Of the five Gallibacterium fimbriae types defined in the present study, evidence for in vitro expression of the fimbrial proteins was only available for Flf . In the present study we examined the expression levels of the three fimbrial subunit proteins (FlfA, Flf1A and Flf3A). Western Blot analysis revealed that each antiserum was highly specific for each individual type supporting previous findings that the phylogenetic grouping of the major fimbrial subunits correlates well with the antigenic properties of the proteins [34, 43].
Results from the in vitro expression study demonstrated expression of the two of the three fimbrial subunit proteins (FlfA and Flf3A) in the Gallibacterium strains investigated. Yet generally, only a single fimbrial subunit protein was expressed at a time in the same strain, suggesting that the expression of Gallibacterium fimbriae may be regulated by one of the many fimbrial regulation mechanisms described in other bacteria . Interestingly, the most commonly found fimbriae Flf1A was not expressed in any of 16 G. anatis strains encoding the fimbrial cluster. There may be several explanations to this finding: i) as many fimbriae are poorly expressed during laboratory conditions it is likely that the expression of Flf1A requires specific factors only provided by the natural host [18, 19]; ii) highly conserved domain structure belonging to only one CD group ‘a’ observed in Flf1 indicates that these fimbriae likely experience low immune pressure from the host and thus may be a silent or non-functional copy fimbriae of Gallibacterium spp.; iii) Flf1 may be important and expressed in the environment outside the host. Based on the whole genome RNA sequencing of G. anatis strain UMN179, the flf1A gene (UMN179_00750) is transcribed under in vitro growth conditions (unpublished results), which suggest that there may be additional processes between the transcription and translation involved in the reduced expression or stability of Flf1A. To reveal the role and expression patterns of the individual fimbrial clusters during in vitro and in vivo conditions, further investigations, including biologically relevant animal trials, are warranted.
In this study, the presence of up to three CU fimbrial clusters per individual Gallibacterium genome was identified. All fimbrial clusters found in the diverse set of Gallibacterium strains shared similar morphology and phylogenetically and were assigned to a single γ4 clade of chaperone-usher fimbriae. The major fimbrial subunit and adhesion proteins encoded in Gallibacterium genomes displayed high amino acid sequence variation, suggesting that the observed diversity may be maintained through homologous recombination between fimbrial clusters of Gallibacterium spp. Fimbriae within a given strain were typically not co-expressed in vitro, indicating that different Gallibacterium fimbrial types may be expressed during different conditions and may have different role at bacteria-host interaction. Importantly, all Gallibacterium fimbriae were systemically classified, and the fimbrial clusters defined in this study allow future research by use of a common framework.
Strains and genome sequences
All genomes used in this study were sequenced and de novo assembled as described by Kudirkiene et al. . The genome of G. anatis strain 12656/12 Liver is available under the BioProject ID: 213810 [GenBank: AVOX00000000]. The remaining 21 Gallibacterium genomes were annotated with the NCBI Prokaryotic Genomes Automatic Annotation Pipeline (http://www.ncbi.nlm.nih.gov/genomes/static/Pipeline.html) and have been deposited at DDBJ/EMBL/GenBank under the BioProject ID: 217951 [GenBank: JPXO00000000, JPXP00000000, JPXQ00000000, JPXR00000000, JPXS00000000, JPXT00000000, JPXU00000000, JPXV00000000, JPXW00000000, JPXX00000000, JPXY00000000, JPHO00000000, JPTU00000000, JPJK00000000, JPJL00000000, JPJM00000000, JPJN00000000, JPJO00000000, JPJP00000000, JPJQ00000000, JPHN00000000]. All annotated genomes were imported into CLC Genomics Workbench v.6.5.1 (CLC, Denmark) for further analysis.
Detection of Chaperone-Usher (CU) fimbrial clusters
Three fimbrial usher nucleotide sequences (UMN179_00811, UMN179_00293 and UMN179_00752) annotated in G. anatis strain UMN179  were used as BLASTn queries against examined Gallibacterium genomes. BLASTn searches were performed using CLC Genomics Workbench with default parameters. Ushers with the reported E-value of 0 were selected for further analysis. To enable detection of more variable ushers all genomes were additionally screened for the presence of an usher protein family domain PF00577. Subsequently, the genomic regions encoding all identified ushers were visualized to enable search for other potential fimbrial proteins flanking the genes. Whole clusters containing all fimbrial assembly proteins (major fimbrial protein, chaperone, usher and fimbrial adhesin) along with flanking sequences extended by approximately 300 bp were extracted from the genomes, reversed and complemented if needed, and added to the CLC database.
Alignments and phylogenetic analysis of CU fimbrial clusters
Nucleotide sequences of the identified CU fimbrial clusters were exported from the database and aligned with the corresponding CU fimbrial clusters UMN179_00809-00812, UMN179_00295-00292 and UMN179_00750-00753  using MAFFT v7.130b . The multiple alignments were viewed using Jalviewv.2.8.0b1  to identify the start and the end positions of the protein encoding sequences for each fimbrial assembly protein in the cluster. Accordingly, the annotations for each gene of the CU fimbrial cluster were corrected to obtain final amino acid sequences for further analyses. After the analysis described below the annotations of the identified chaperone – usher (CU) clusters were edited and resubmitted to GenBank. The locus_tags for the individual fimbrial clusters are listed in Additional file 1: Table S1. Pair-wise comparison of the fimbrial assembly proteins was generated using ClustalOmega .
Phylogenetic relationships between the identified Gallibacterium CU clusters and CU clusters of other Gram-negative bacteria were inferred using usher amino acid sequences as described by Nuccio and Bäumler . Additionally, amino acid sequences of all four fimbrial assembly proteins (major fimbrial subunit, chaperone, usher and fimbrial adhesin) were used to examine the relationship of CU fimbrial clusters within the genus Gallibacterium. The Neighbour-Joining method implemented in the MEGA v.6 software package  was used to generate phylogenetic trees. Three previously described UMN179 CU fimbrial clusters  were included in the phylogenetic and evolutionary analyses described below.
NCBI Conserved Domain Database (CDD) CDSEARCH/cdd v3.11 tool  was used to identify conserved domains in the amino acid sequences of each fimbrial assembly protein of the CU clusters.
To examine the similarity of fimbrial assembly proteins in genus Gallibacterium to the proteins of other bacterial species all amino acid sequences were submitted to BLASTp at NCBI. The sequences were compared to both UniProt/SwissProt and the non-redundant protein databases using default parameters.
Evolutionary analysis of Gallibacteriumstrains
The inferred evolutionary relationship between strains belonging to G. anatis and G. genomospecies 1 and 2 was revealed using MLST scheme developed by Johnson et al. . All sequences were retrieved from the sequenced genome deposited in CLC Genomics Workbench using reference sequences of housekeeping locus fragments (adk, atpD, fumC, gyrB, mdh, recN, infB and thdF) (http://pubmlst.org/gallibacterium/) as BLASTn queries against the genomes. The Maximum Likelihood method based on the Hasegawa-Kishino-Yano model was used to create a phylogenetic tree of the aligned concatenated 8 locus sequences for MLST analysis.
Western blotting was used to investigate cross-reaction of anti-serum raised against recombinant FlfA, Flf1A (previously Gab_0572) and Flf3A (previously Gab_2156), as well as in vitro expression of these proteins. The production of recombinant FlfA, Flf1A and Flf3A is described in Bager et al. . FlfA and Flf1A were purified in a soluble form, while Flf3A was purified in an insoluble form. The production of polyclonal antisera against FlfA is described in Bager et al. . The production of polyclonal antisera against Flf1Aand Flf3A was carried out as described for FlfA. Rabbit antiserum was collected at day 0 (pre-immune) and day 41 (immune). To investigate in vitro expression, whole cell extracts were prepared from in vitro cultured cells. In short, 22 Gallibacterium strains were incubated in liquid BHI to reach the early-stationary growth phase. Cells were harvested by centrifugation, washed and resuspended in PBS, and lysed by four freeze-thaw cycles. The samples were quantified as described in Bager et al. . For the Western blotting, a volume corresponding to an OD260-value of 8 of each whole cell extract, or 0.1 μg recombinant protein, was electrophoresed in a 4-12% NuPAGE Bis-Tris gel (Invitrogen) under reducing conditions. The proteins were transferred to a polyvinylidenedifluoride (PVDF) membrane by use of the iBlot dry blotting system (Invitrogen) and blocked overnight in phosphate-buffered saline (PBS) plus 0.1% Tween-20 plus 5% skim milk. The membranes were incubated with pre-immune or immune rabbit antiserum. FlfA anti-serum was diluted 1:4,000 in diluting buffer (PBS plus 0.1% Tween-20 plus 3% skim milk), while Flf1A and Flf3A rabbit antiserum was diluted 1:2,000. Polyclonal goat anti-rabbit IgG (Fc): HRP (AbDSerotec, diluted 1:10,000 in diluting buffer) was used as the secondary antibody. The blots were developed using the Novex® ECL Chemiluminescent Substrate Reagent Kit (Invitrogen).
This work was supported by grants from the Faculty of Health and Medical Sciences, University of Copenhagen.
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