Background

Beauveria bassiana (B. bassiana), a well-known entomopathogenic fungus, is belonged to the family Clavicipitaceae, order Hypocreales [1]. Owing to the high genetic variability, B. bassiana exhibits high adaptability to various environmental conditions and thus could parasitize a wide range of insect populations [2]. Currently, B. bassiana is actively developed as a biological control tool for various insects in all regions of world [3, 4]. According to Li et al. report, approximately one million hectares are usually treated with B. bassiana to reduce the occurrence of forest insects in China every year [5]. Generally, B. bassiana is thus a generalist with no strict host preference and can be used as an effective and sustainable biological control agent against a myriad of insect pests [6].

Virulence is variable and not universal for a prescribed host and pathogen [7]. Increasing studies have confirmed that the virulence of B. bassiana strains from a specific insect host varies frequently [8]. It has been recognized that the strain of B. bassiana isolated from a given insect showed low virulence against other insects, and showed stronger virulence against these insects after domestication [9], indicating that the virulence of B. bassiana to hosts has a great plasticity. Genome structure and DNA sequence variation in these isolates could be related to many factors in the biology of this fungus. Recently, the re-sequencing of numerous individuals within pathogen species has been as a forceful tool to explore the genetic mechanism in fungal and fungal-host interaction studies [10]. For example, Mburu et al. compared the gene sequences of two B. bassiana isolates with different levels of virulence and repellence to the termite, and then some differences were found in the nucleotide sequences of the two isolates of B. bassiana, suggesting a genetic basis for the observed intra-specific differences in their virulence against the termite [11]. Valero-Jiménez et al. sequenced the genomes of five isolates of B. bassiana with low/high virulence, and finally identified several genes and molecular processes that effect the virulence towards Mosquitoes [12]. These studies provide a better understanding of the natural variation in virulence by genome analysis. Thus, understanding genetic polymorphisms is helpful to understand its potential virulence diversity of B. bassiana isolates isolated from different hosts.

In the present study, we aim to gain our knowledge in understanding genomic diversity involved in virulence and host-pathogen interaction for 17 B. bassiana strains by a comparative genomics analysis. Thus, we sequenced the 17 B. bassiana isolates from different hosts compared to the reference genome B. bassiana strain ARSEF 2860. Based on the analysis, understanding the potential factors of genetic variation on the virulence of B. bassiana will improve our methods to use this fungus as an effective and sustainable biological control agent against.

Results

Sequencing and mapping summary

Quality control results of sequencing data of 17 B. bassiana strains were summarized in Table S1. Finally, a total of 160 Gb containing 459 million raw reads were produced, with an average of 27,048,202 reads for each sample. After filtering low quality reads and duplicate reads, 396 million high quality reads were extracted. Approximately 71.22% of the cleaned reads could be successfully mapped to the B. bassiana strain ARSEF 2860 reference genome, with varying 67.30 to 75.30% among different strains (Table 1). These mapped sequences were used for subsequent analyses.

Table 1 Comparison results of sequenced reads of 17 B. bassiana isolates aligned to the reference genome of B. bassiana strain ARSEF 2860
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SNPs and InDels identification

All clean reads were aligned to the reference genome assembly of B. bassiana strain ARSEF 2860. As a result, a total of 2,779,949 SNPs were identified across 17 B. bassiana isolates genotypes, among which 1,959,716 (70.49%) are synonymous and 820,233(29.51%) are nonsynonymous. In addition, a total of 884,811 Indels were obtained, with 423,409 (47.85%) InDel-Ins and 461,402 (52.15%) InDel-Del (Table 2). The distributions of SNP-types and Indel-types of 17 samples were obtained, it showed that majority of SNP variation were belonged to different types including the upstream gene variants (40.82%), the synonymous variants (37.54%), and the missense variants (15.55%) (Fig. 1a). Most of the InDels variation were located in the upstream region of the genes (79.15%) (Fig. 1b). At last, we detected 7421 missense genes are shared by all strains, accounting for 73.49% of all missense genes (10,098).

Table 2 Number of mutations observed in the seventeen B. bassiana isolates comparing with the reference genome of B. bassiana strain ARSEF 2860
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Fig. 1
figure 1

The stacked-column displays the distribution of SNP-types (a) and Indel-types (b) in each B. bassiana isolate genotype. The horizontal axis represents 17 samples of B. bassiana, and the vertical axis represents the relative content of different SNP/Indel distribution types. The number of genes shared between the 17 isolates presented in each category in Table S5

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Functional annotation

A hierarchical clustering analysis of the top 50 high frequency missense mutation genes in 17 B. bassiana samples was conducted (Fig. 2a). Clearly, there was no significant numerical difference of each gene in different samples sequenced in this study. However, among different genes, more variation was relatively abundant in four genes (gene_8222, gene_358, gene_6727, and gene_5020) but few variations were relatively lacking in other 46 genes in all B. bassiana isolates. Next, we determined the functional categories of these top 50 genes using Gene Ontology database, then their functions were belonged to three general directions. In the biological process category, the top three highly enriched GO terms included binding, catalytic activity, and nucleic acid binding transcription transporter activity. The GO terms of extracellular region, cell part, membrane part, and organelle part were significantly enriched in the cellular component. The molecular function category showed a high percentage of metabolic process, cellular process, and single-organism process (Fig. 2b).

Fig. 2
figure 2

The mutation numbers and annotation information of 50 genes with high frequency of missense mutations. a A hierarchical clustering analysis showing the relative difference in the number of SNPs in these top 50 genes in 17 B. bassiana samples. The red 4 genes exhibit a higher number of SNP mutations in 17 B. bassiana samples, while the blue 46 genes exhibit a low number of SNP mutations in 17 B. bassiana samples. b Gene Ontology (GO) functional annotation of the top 50 genes with missense mutations in the re-sequencing data of 17 B. bassiana isolates. The results are summarized in three main categories: biological process (BP), cellular component (CC) and molecular function (MF)

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Species clustering analysis

To observe the divergence contained in the individual SNPs among the 17 B. bassiana isolates at the genomic level, we constructed a phylogenetic tree based on the full coding sequence of the genes containing the SNPs obtained from the sequence comparisons. As shown in Fig. 3a, three separate clusters were generated including the isolates of S2\S3\S4\S5\S6\S8\S14, the isolates of S9\S10\S13\S15\S18\S19\S20\S21, and the isolates of S7/S11. Besides, we performed a principal component analysis (PCA) to examine the genetic relationships among these 17 samples, a clearer separation of three clusters was constructed (Fig. 3b).

Fig. 3
figure 3

The genetic diversity of the missense SNPs in the re-sequencing data of seventeen B. bassiana isolates. a A phylogenetic tree was constructed. All missense mutated nucleotide sequences of 17 strains of B. bassiana were used to construct an evolutionary tree based on the similarity of SNP missense mutations according to modelfinder and iqtree software. The phylogenetic tree was constructed with 100 bootstrapping replicates. Similar missense mutations were distributed in the same cluster. b Principal component analysis (PCA) analysis of 17 samples based on missense SNPs. Principle component plot constructed by Plink software

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Ka/Ks analysis

To confirm the genes subjected to significant selection in of B. bassiana domestication, we estimated the statistic Ka/Ks with the 10,098 genes contained missense mutation in re-sequencing data of 17 B. bassiana isolates. Finally, a total of 7050 and 720 genes are respectively showed with negative selection or positive section (strong purifying selection) in seventeen samples (Fig. 4a). Subsequently, GO and KEGG pathway analyses were conducted on the positively selected genes. GO enrichment analysis showed highlight a significant enrichment in genes involved in NAD + ADP-ribosyltransferase activity, chromatin, chitin catabolic process, chromatin assembly or disassembly, phosphoenolpyruvate-dependent sugar phosphotransferase system, tRNA-intron endonuclease complex, actin cytoskeleton, tRNA-introendonuclease activity, L-malate dehydrogenase activity, protein geranygeranyltransferase activity, 4-hydroxybenzoate octaprenyltransferase activity, and so on (Fig. 4b). The KEGG pathway analysis revealed that the genes were overrepresented in 5 pathways, of which the highest represented pathway is glycosphingolipid biosynthesis-ganglio series (PATH: ko00604), followed by methane metabolism (PATH: KO00680), proximal tubule bicarbonate reclamation (PATH: KO04964), two component systems (TCSs) (PATH: KO02020), and carbon fixation in photosynthetic organisms (PATH: ko00710) (Fig. 4b). Herein, a total of seven genes (gene_664, gene_2709, gene_3056, gene_3362, gene_7254, gene_7433, gene_8336) with positive selection were abundantly enriched in this pathway, and the proteins encoded by these genes were Oxidoreductase short-chain dehydrogenase/reductase family, Galactoside O-acetyltransferase, Ulp1 protease family protein, UcrQ family protein, Acyl-CoA N-acyltransferase, Ubiquinol-cytochrome c reductase complex subunit, and CAAX amino terminal protease (Table 3). The corresponding mutation information of these seven genes was presented in Table S2.

Fig. 4
figure 4

Ka (non-synonymous)/Ks (synonymous) analysis and functional annotation of the genes with missense mutations in the re-sequencing data of 17 B. bassiana isolates. a The overall Ka/Ks distribution. The red dots represent genes with positive selection in 17 samples, while the green dots represent genes with negative selection in 17 samples. b Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) functional enrichment analysis of 720 positive selection genes. The GO annotation results were summarized in three main categories: biological process (BP), cellular component (CC) and molecular function (MF). The KEGG annotation results were summarized in pathways

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Table 3 The information of the seven positively selected genes that are enriched in the two component systems
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Structural variations detection

The detection of SVs was achieved by making use of BreakDancer programs. A total of 4163 individual SVs were predicted, with an average of 245 SVs in each B. bassiana strain genotype (Table 2). Most of the SVs were unique in each sample, and only 6 structural variation loci were shared among different samples, as shown in Table S3.

Protein domain analysis

Finally, we investigated the effect of the missense mutations of the 720 positively selected genes on protein structure by the comparation of 17 samples. Collectively, 13 putative domains encoded by 13 protein-coding genes were identified, of which the genome regions encoding proteins with MutS_IV domain, Zn_clus domain, Fungal_trans_2 family, Metallophos domain, and Metallophos_2 domain were most richest and shared by seventeen samples (Table 4).

Table 4 Genes and domain prediction information for domain changes in the seventeen B. bassiana isolates
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Discussion

B. bassiana, originated from the different hosts shows distinct virulence and pathogenic. Identification of the genetic variation of B. bassiana strains infecting the different hosts would improve our understanding of the differences towards the hosts, and may help clarify the potential virulence of B. bassiana against the insects. Recently, several researches have been performed to investigate the genetic variation within the pathogen originated from different hosts using re-sequencing technology and bioinformatics [13,14,15]. Based on that, it is of great significance to investigate the genomic alterations of 17 B. bassiana isolates of the fungus with different levels of virulence to other Fungi in the present study.

Firstly, 17 strains of B. bassiana originated from different hosts were sequenced by genome re-sequencing. In general, the alignment rate obtained by comparing the assembled sequences is not comparable, and the mutation frequency cannot be known. For example, if a mutation occurs at a partial site of a sample, i.e. a heterozygote appears, the mutation cannot be counted. Therefore, we chose to match the quality-controlled clean reads to the reference genome of B. bassiana strain ARSEF 2860 [16], which identify the difference loci and calculate their genotype frequency, so as to be more accurate. The results showed approximately 71.22% of the cleaned reads were mapped to the B. bassiana strain ARSEF 2860, and a total of 2,779,949 SNPs, 884,811 Indels, and 4163 SVs, were identified in seventeen genomes when compared to the reference genome. As the most credible genome-wide genetic markers, single-nucleotide polymorphisms (SNPs) have been widely applied to characterize potentially adaptive genetic variation [17]. Herein, the proportion of nonsynonymous SNPs among all the SNPs is 29.51%, which is supported by Valero-Jiménez’s work of 87,119 SNPs between Bb5078 and Bb8028, and 467,292 SNPs between Bb4305 and Bb8028 [18], revealing a high level of genetic diversity among different strains of B. bassiana. Among the Indels, the number of InDel-Ins variants (423,409, 47.85%) is almost equal to the InDel-Del variants (461,402, 52.15%), and most of the variants were located in the upstream region of the genes (79.15%). Furthermore, structural variation is known to be a key component of phenotypic diversity in organisms [19]. In this study, all types of the identified SVs were inter-chromosomal translocations (CTXs), which may be due to the incomplete splicing of genomes caused by the existence of a considerable amount of gaps in the fungus genome [20].

Secondly, a hierarchical clustering analysis was carried out on the top 50 genes with missense SNPs in 17 samples. The results showed that there was no significant difference in the frequency of missense SNP mutations among different hosts, which revealing the population identity of the seventeen sequenced B. bassiana isolates. However, significant nucleotide variations were identified in four genes (gene_8222, gene_358, gene_6727, and gene_5020) in all samples, and two of them encoding the common protein non-ribosomal peptide synthase (NRPS, gene_8222 and gene_6727). NRPS is a key mechanism for the biosynthesis of bioactive metabolites in fungi and plays an important role in the production of fungaltoxin. For example, NRP synthetase Pes3 has been found to contribute to Aspergillus. fumigatus virulence, and disruption of pes3 resulted in an augmented virulence phenotype in invertebrate for invasive aspergillosis. NRP synthetase mgoA has a role in the virulence of Pseudomonas. syringae pv. Syringae, and A Tn5 mutant disrupted in mgoA was defective in mangotoxin production and virulence. NRP synthetase gliP was predicted to be involved in gliotoxin production, and mutants with a disrupted gliP locus failed to produce gliotoxin [21,22,23]. Based on these findings, nonribosomal peptide synthesis (NRPS) is considered to be a documented virulence factor for fungi, its mutations affect the different virulence of the hosts. Importantly, the two genes encoding NRPS in this study showed more missense mutations in 17 B. bassiana trains, which may be closely related to the maintenance of the pathogenesis during the evolution process, but the specific virulence effects of each mutation need to be further explored. Furthermore, GO annotations showed that the functions of mutated genes were mainly related to binding, catalytic activity, extracellular region, metabolic process, and nucleic acid binding transcription transporter activity. Mutated genes involved in binding, transport and other biological processes may be associated with increased interaction between virulence associated proteins and hosts when B. bassiana exerts a toxic infection. Additionally, among these groups, the variation involved in the metabolic process may be related to the production of antibacterial compounds, it is very important for B. bassiana to resist microbial competition in the process of killing insects [24].

Thirdly, the phylogenetic relationships and principal component analysis (PCA) between isolates of B. bassiana were determined using the whole missense SNPs. Three distinct B. bassiana clusters were formed, namely the isolates of S2\S3\S4\S5\S6\S8\S14\S19, the isolates of S2\S9\S10\S13\S15\S18\S19\S20\S21, and the isolates of S7/S11. Previously, the study of Ghikas et al. revealed that seven phylogenetic clusters in B. bassiana that consisted of isolates which had common climate features but did not exhibit any geographic distribution [25]. Our finding is partly in agree with the earlier suggestions that B. bassiana is not monophyletic, but rather is composed of several clusters that are morphologically identical [25,26,27], which jointly confirmed a high genetic diversity of B. bassiana. Additionally, the results showed that similar mutations occurred in B. bassiana strains in each cluster during evolution, which indicated a close relationship among B. bassiana isolates isolated different hosts in each cluster, but the relationship between the virulence of B. bassiana isolates in each cluster is not clear and further studies are needed. Furthermore, in the PCA plot, an obvious separation of three clusters was found, which also revealed a clear genetic differentiation among these 17 samples.

In previous study, genes with a signature of positive selection is possible to result in the adaptation to a dynamic environment and may be associated with fungi virulence [18]. Herein, we calculated the Ka/Ks values to identify the genes subjected to selection in the evolution of B. bassiana. Finally, a total of 7050 genes with Ka/Ks > 1 and 720 genes with Ka/Ks < 1 are confirmed, respectively. Among genes predicted to be under strong purification selection, there is enrichment for GO categories involving NAD + ADP-ribosyltransferase activity, chromatin, chromatin assembly or disassembly, chitin catabolic process, and actin cytoskeleton. In Salmonella, spv genes can establish successful systemic infection in experimental animals, and SpvB virulence-associated protein has recently been shown to contain the ADP-ribosyltransferase domain, suggesting that NAD + ADP-ribosyltransferase activity is associated with the regulation of virulence [28]. Chromatin is densely packed with the nucleosome that contains the genetic information in eukaryotes. Many events involve chromatin alterations that are crucial for virulence and have been considered to be a hopeful antifungal targets. For example, chromatin function affects pathogenicity of the most prevalent human fungal pathogen Candida albicans [29]. Earlier study has confirmed that the important role of drastic actin cytoskeleton reorganization in various different aspects of host-pathogen interaction [30]. Chitin is one of the main components of insect cuticle that acts as the first barrier against fungal pathogens. The entomopathogenic fungi B. bassiana could secrete several chitin-degrading enzymes, such as Endo chitosanase and Chitinase D [31], which are the critical cuticle-degrading enzymes and act synergistically with proteases to digest insect cuticle, and thus cause the enhancement of B. bassiana virulence [32]. Additionally, KEGG pathways analysis suggested the positively selected genes were highly enriched in glycosphingolipid biosynthesis-ganglio series, methane metabolism, proximal tubule bicarbonate reclamation, two component systems, and carbon fixation in photosynthetic organisms with some important physiological functions. Of which, two component systems (TCSs) are widely distributed in various bacteria and play important roles in the organisms in the face of different external stimuli via controlling gene expression [33]. In the present study, seven genes among these 17 B. bassiana strains with positive selection were abundantly enriched in this pathway. Increasing studies have revealed the involvement of this pathway in regulating resistance processes and diverse virulence in a wide range of pathogenic bacteria, such as Mycobacterium tuberculosis [33], Salmonella typhimurium [34], Staphylococcus aureus [35], Pseudomonas aeruginosa [36]. Taken together, GO and KEGG annotation analysis identified some positive selection genes associated with these above functional processes in the present study, which may serve as potential factors for virulence mechanisms, providing new support for studying of the virulence of B. bassiana strains.

Finally, a comprehensive protein domain analysis was performed on 720 positively selected genes with missense mutations. Significant differences in 13 domains encoded by 13 protein-coding genes were identified. Among these, three domain proteins involved in the host-pathogen interaction, such as ankyrin repeat domain protein, Metallophos domain protein and MutS domain V that were encoded by gene-7731, gene-5369, and gene-10,314 may affect host-pathogen interactions. For example, Zahrt et al. found that the alteration in virulence on Salmonella was the direct result of the inactivation of both of the mutS and recD gene products, however, S. typhimurium carrying mutations in either one of these genes behaved similarly to the wild-type strain and without attenuating virulence [37]. Ankyrin repeats are essential to regulate protein-protein interactions involved in a variety of host processes, including cytoskeletal motility, tumor suppression, and transcriptional regulation [38, 39]. Besides, Lamb et al. reported that myxoma virus as an effective vertebrate pest control agent, ANK-R mutant can both activate NF-κB pathway and engender virus-induced apoptosis [40]. The Metallophos domain is located in the conserved region of the Ser/Thr protein phosphatase gene, which is the central mediator of phosphorylation-dependent signals in various pathogenic bacteria and eukaryotes and is responsible for achieving metabolic control [41]. Earlier research has unveiled the important role of Ser/Thr phosphorylation in the virulence of Mycobacterium tuberculosis, which could regulate many intracellular metabolic processes and interfere with signaling pathways of the infected host cell [42]. In summary, based on the correlation between the virulence and these domains from different hosts, the altered protein domain in these 17 B. bassiana strains may be closely related to its plasticity of virulence. Besides, other genes deletion or genes acquisition may also be critical in virulence evolution. Of course, further study is needed in the future.

Conclusion

According to the plasticity and variability of fungal virulence, we sequenced and compared the genome of seventeen B. bassiana isolates obtained from different insect hosts. Subsequently, the relationship between stable genetic variation and virulence function shared by 17 strains of B. bassiana in different hosts, and the correlation between mutated genes and virulence effect of B. bassiana were analyzed. A number of genes with stable mutations in these B. bassiana isolates have been established. Among them, some key factors including NRPS mutations, domain changes of ankyrin repeat domain protein, Metallophos domain protein, and MutS domain occurred in B. bassiana isolates may be crucial for the virulence of B. bassiana. Besides, the 720 positive selection genes and the top 50 genes with missense mutations were significantly enriched in some important biological processes, and pathways may also be related to the virulence of B. bassiana against hosts. The study provided the relevant theoretical basis for targeted changes in the virulence effect of B. bassiana. In this case, we think the virulence of B. bassiana might be influenced by natural variation in the process of evolution, which may benefit future molecular investigations of insect-fungus interactions and promote the development of B. bassiana as cost-effective and sustainable mycoinsecticides. However, do these genetic mutations really play a role in virulence or how do it regulate virulence in biological processes, which is interested and will need to further study.

Methods

Fungal strains and culture conditions

This study employed seventeen isolates of B. bassiana that were obtained from 17 different insects (Table S4). All isolates were preserved on Sabouraud dextrose agar (SDAY: 4% glucose, 1% peptone, 1.5% agar and 1% yeast extract) and maintained at 25 °C.

Genome sequencing and mapping

Genomic DNA of 17 isolates of B. bassiana was extracted using the CTAB method as the previous report [43]. DNA concentration and purity were checked on NanoDrop (Thermo Fisher Scientific Inc. Waltham, MA, USA), and the qualified DNAs were used for library construction. Sequencing libraries for each individual were established using the standard Illumina protocol (Illumina, San Diego, CA, USA) and sequenced using HiSeq 2000 instruments (Illumina inc., San Diego, CA, USA) according to the manufacturer’s protocol by Sangon Biotech (Shanghai) Co., Ltd., Shanghai, China. The generated raw reads were processed using the FASTX-Toolkit version 0.0.13 (http://hannonlab.cshl.edu/fastx_toolkit) to filter the low-quality reads (< 10), reads shorter than 50 nt and duplicated reads [44]. After the filtering, the high quality reads were extracted and mapped to the reference genome of B. bassiana strain ARSEF 2860 [16]. The alignment processing was conducted using BWA (version V0.7.12-r1039) with default parameters [45].

SNP and Indel detection

Picard tools version 1.92 (http://picard.sourceforge.net) was used to discard duplicates, and the obtained BAM files were further processed using SAMtools 1.4.1 (samtools.sourceforge.net) [46]. SNPs and indel calling was performed with the GATK v2.4–9 (software broadinstitute.org/gatk/) UnifiedGenotyper [47]. After that, an initial GATK VariantFiltration step was performed with the filtering conditions: For SNPs: with the filter expression ‘QD < 2.0 || FS > 60.0 || MQ < 40.0 || HaplotypeScore > 13.0 || MappingQualityRankSum < -12.5 || ReadPosRankSum < -8.0’; for Indel: QD < 2.0 || FS > 200.0 || ReadPosRankSum < − 20.0. The annotations for genes with SNPs and Indels were completed using the software SNPEFF (version 4.3 k) variant effect prediction (http://snpeff.sourceforge.net/) [48].

Species clustering analysis

To determine the evolutionary relationship among B. bassiana originates from different hosts. The optimal nucleic acid replacement mode was found by modelfinder. Then a phylogenetic tree was conducted using iqtree with the bootstrapping of 100 replicates [49], and further presented using an R package, ggtree. PCA was carried out using the software Plink1.9 [50] on the missense SNPs that for all genotyped individuals, and presented using ggplot2.

Ka/Ks analysis

The positively selected genes among the genomes of 17 B. bassiana isolates were searched using the bidirectional best hit (BBH) method [51]. The ratio of non-synonymous SNP (Ka) to synonymous SNP (Ks) in each gene was defined, including neutral (Ka/Ks = 1), negative (Ka/Ks > 1) and positive (Ka/Ks < 1) selection. The Ka and Ks in each missense mutant genes were calculated, and the ratio of Ka to Ks was estimated by the Codeml model of the program of phylogenetic analysis by maximum likelihood (PAML). To confirm functionally coherent gene-sets that showed Ka/Ks values significantly < 1, Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were performed.

Functional annotation

A hierarchical clustering analysis of the top 50 genes with missense SNPs was conducted by the clustergram function in the Matlab Bioinformatics toolbox with minor changes. GO analysis was performed with Fisher’s Exact Test and classified under three categories: biological process (BP), cellular component (CC), and molecular function (MF) [52]. Meanwhile, the detected positively selected genes were mapped to the terms of KEGG (http://www.genome.jp/kegg/) database to explore main biological functions [53], and the assignment of differential genes to different gene families was realized using Pfam (protein families) (http://pfam.xfam.org/) annotation [54].

Structure variations (SVs) detection

Structural variants was determined using BreakDancer (v1.1.2) software [55], containing large fragments of SV types, including deletions (DEL), insertions (INS), inversions (INV), inter-chromosomal translocations (CTX), and so on.

Protein domains analysis

To explore the effect of nonsynonymous SNPs in the positively selected genes on protein domains, we first identify the mutant amino acid sequences using Bioperl. Then, the hidden Markov model (HMM) profile for the NBS domain was applied to search the protein sequences in the B. bassiana database using hmmsearch in HMMER (v3.1b) with e-value < 0.00001 [56].