Background

Salmonella is one of the main agents of foodborne bacterial infections in human. In particular, Salmonella enterica subsp. enterica serovars are responsible for around 80 million foodborne cases annually in developed countries [1, 2]. The 2600 known S. enterica subsp. enterica serovars exhibit a broad diversity in phenotypes including infectious patterns, lifestyle, reservoirs, vectors and host spectrum [3]. The genomic determinants of these phenotypes remain however partially characterized [4,5,6,7,8,9,10,11]. The present work tackles the genomic and metabolic signatures highlighting the poorly understood mechanisms of adaptation to animal sources at the pangenome scale of Salmonella enterica subsp. enterica.

From extremely clonal to the freely recombinant, bacterial evolution is mainly governed by stochastic point mutations induced by replication errors or damage of DNA (i.e. single nucleotide polymorphisms SNPs and small insertions/deletions InDels), and Horizontal Gene Transfers (HGT) promoted by homologous and non-homologous recombination events [12]. The homologous recombination events correspond to the replacement or inversion of identical or similar sequences [13], while the non-homologous recombination refers to the incorporation of new genetic material between distinct genomes [12]. The HGT whose large fragments are also named Mobile Genetic Elements (MGEs), can occur in bacterial genomes during transformation (i.e. transfer of pathogenicity islands, transposons or insertion sequences between two bacterial chromosomes), conjugation (i.e. transfer of plasmids between two bacterial genomes) and transduction (i.e. transfer and/or chromosomal incorporation of phages into bacterial genomes) [12].

The molecular mechanisms of host adaptation driven by the evolution were revealed by conventional molecular biology highlighting that S. enterica subsp. enterica extended over a wide range of hosts including birds, fishes, reptiles, amphibians, bovines, pigs and others [14]. Since the divergence from the most recent common ancestor (MRCA) with Escherichia coli approximately 100–160 million years ago [15], the coevolution of Salmonella and animal hosts during millions of years, has led to the acquisition of genes required for intestinal infection (i.e. S. bongori species), colonization of deeper tissues (i.e. other S. enterica subspp.), and expansion toward warm-blooded vertebrates (i.e. S. enterica subsp. enterica) [16]. The adaptation to warm-blooded animals started by generalist host associations related to gastrointestinal infections and transmission induced by the short-term proliferation in the intestine, or independently of the replication in the intestine by dissemination and persistence in systemic niches that are devoid of competing microbiota and can last for the lifetime of the hosts [17].

Without exhaustive data for all known serovars of S. enterica subsp. enterica, some are considered to be more adapted to mono-hosts, like Gallinarum in avian [4, 7, 10] or Dublin in bovine [4, 6]. The evolution of S. enterica subsp. enterica within hosts may have led some serovars to specialize to their host. This adaptation is accompanied by loss of bacterial fitness for inter-host transmission and apparent convergence in pathogenesis [17]. For instance, Typhi and Paratyphi A cause typhoid and paratyphoid in human, Gallinarum is associated with fowl typhoid, Abortusovis induces abortion in sheep, and Dublin and Choleraesuis are involved in bacteraemia of cattle and pigs, respectively [17]. Even if most of studies focusing on transformed seafood products [18, 19] do not provide prevalence of infected fish in natura [20], the serovar Bareilly is also supposed to be adapted to fish. Causing gastroenteritis, other serovars are also considered as adapted to multiple hosts like Typhimurium [9, 21] or Enteritidis [11].

Most of studies based on conventional molecular biology demonstrated that acquisition by HGT of Salmonella Pathogenicity Islands (SPIs) that contain genes coding for invasion, survival, and extraintestinal spread is among the prominent molecular mechanisms explaining the host adaptation of S. enterica subsp. enterica [22]. The 23 known SPIs are mainly involved in adhesion to epithelial cells (i.e. SPI-3, 4 and 5), invasion in their Salmonella containing vacuoles (SCV) (i.e. SPI-1 and 14), resistance to overcoming colonization of the intestinal mucus layer (i.e. SPI-6), induction of inflammation and neutrophil recruitment (i.e. SPI-1), as well as survival (SPI-11, 12 and 16) and outer membrane remodeling (SPI-2, 5 and 13) when they are in macrophages [23,24,25]. More precisely, two type III secretion systems (i.e. T3SS-1 and T3SS-2) encoded on SPI-1 and SPI-2 allow invasion of host epithelium and intracellular survival, respectively [17]. It must also be noted that the prophages Gifsy-2 and Fels-1 are involved in resistance to oxidative stress from neutrophils during infection, while the prophages Gifsy-1 and sopEФ induce downregulation of inflammation in SCV and robust inflammation of the epithelial cells, respectively [25].

Albeit host adaptation of S. enterica subsp. enterica is poorly described at the genomic scale [4,5,6,7,8,9,10,11], the studies focusing on its accessory genome, confirmed that SPIs play a major role in the adaptation of few serovars to avian (e.g. SPI19 in Gallinarum and Pullorum [7, 10]) and bovine (e.g. SPI6 and SPI7 in Dublin [4, 7]) hosts. These studies emphasized that plasmids are also a major determinant explaining adaptation to avian (e.g. resistance-virulence plasmid of Kentucky [5]) and bovine (e.g. plasmid pSDV of Dublin [6]). The unique study focusing on the coregenome demonstrated that the divergence, probably induced by animal diet, between mammalian-host adapted Dublin and multi-host adapted Enteritidis was due to fixed variants targeting regions involved in metabolic pathways of amino acids linked to glutamate [11]. This study also showed that limited ion supply in avian tract and L-arginine used for growth of laying hens, implied modifications of ion transport (i.e. potassium-efflux system in Gallinarum) and L-arginine catabolism (i.e. alanine racemase in Pullorum) of avian-adapted serovars [11].

The Genome Wide Association Study (GWAS) aims to identify the genetic variations associated with particular phenotypic traits within a population [26]. Following the first tool computing GWAS with a correction of Eukaryotic population structure based on SNPs (PLINK) [27], combinations of different methods have been implemented in the recently developed microbial GWAS. Over the last 10 years, microbial GWAS was implemented to explore a diversity of biological problems: genetic backgrounds of microbial origin [28], persistence [29], host preference [30], virulence [31, 32], and antibiotic resistance [33,34,35,36,37,38,39,40,41,42]. In comparison to human GWAS, the confounding factors of the microbial GWAS include genome selection, homologous recombination events, population structure, as well as genome wide significance [43]. Microbial GWAS takes into account these confounding factors and tests for associations between mutations and phenotypes of interest [40, 43,44,45,46,47,48,49,50]. In a context of source tracking for food safety [1, 2], microbial GWAS seems a promising tool to identify mutations associated to animal sources in order to improve models of source attribution [51].

Compared to the 10 years of developments focusing on microbial GWAS, Gene Ontology Enrichment Analysis (GOEA) has been undergoing constant improvements since the beginning of the twenty-first century and recently reached maturity for bacteria. GOEA is indeed rarely applied to bacterial genomes in spite of successful studies applying this approach to decipher host adaptation of S. enterica at the coregenome level [11], compare transcriptome expression profiles of minimally and highly pathogenic S. enterica [52], or cluster orthologous groups among differentially expressed microbial genes [53]. The GOEA proposes to test the hypergeometric distributions of GO-terms from a list of interest (i.e. tested sample) with regards to a broader set of GO-terms (i.e. universe) based on the assumption of dependencies between the GO-terms implemented through a parent-child approach [54]. GOEA was historically proposed by the Gene Ontology Consortium [55] and is today centralized in the universal protein knowledgebase commonly known as UniProt [56]. More precisely, the GO-terms link the genes and/or variants to the metabolic pathways [57] and are synthetized through a directed acyclic graph (DAG) of GO-terms into three independent ontologies called biological process (BP), molecular function (MF) and cellular component (CC) [55].

Taking into account confounding factors (i.e. genome selection, homologous recombination events, population structure and genome wide significance), the present study proposes to decipher Salmonella adaptation to animal sources (i.e. avian, bovine, swine and fish) based on microbial GWAS implementing accessory genes and coregenome variants (i.e. SNPs and InDels), as well as an advanced population structure correction [40]. The mutations (i.e. genes and variants) associated to traits of interest (i.e. avian, bovine, swine and fish sources) were also linked to metabolic pathways by GOEA implementing a parent-child approach [11]. To our knowledge, the present study is the first to apply successively microbial GWAS and GOEA at the pangenome scale.

Results

Distributions of serovars from potential mono-and multi-animal sources

The composition of Salmonella serovars from EnteroBase [58] were investigated in order to build a genome dataset taking into account the confounding factors of microbial GWAS (Additional file 1), namely genome selection [43, 44], recombination [43, 45,46,47], population structure [33, 40, 43, 48] and genome wide significance [43, 50]. Out of 13,635 records from a curated and synthetic subset of Enterobase, Salmonella isolates were mainly distributed in avian, bovine, fish, plant, shellfish and swine sources, enabling the selection of multiple strains for each studied serovar and source when building our dataset (Additional file 2). Because the detailed records from Enterobase were not enough detailed to determine if the strains from plants and shellfishes were isolated inside or outside tissues, the present study focuses on adaption to the following sources: avian, bovine, swine and fish. Among strains isolated from these sources (n = 11,450), most (22 out of 35) serovars (Fig. 1) had single animal sources (p < 4.5 × 10− 1, Chi-square tests of uniformity to find serovars associated with some sources). Respecting high levels of diversity in terms of phylogenomic relationships in agreement with previous studies [59], geographical origins, dates of isolation and BioProject accession numbers, a balanced dataset of serovars from putative mono- and multi-animal sources (Fig. 1) were selected. This dataset was used to detect mutations and metabolic pathways associated with the adaptation of Salmonella serovars to their animal sources. More precisely, isolates of the Salmonella serovars Newport, Typhimurium and Anatum were selected as multi-animal sources, whereas other serovars were selected as mono-animal sources related to avian (i.e. Heidelberg, Kentucky, Hadar), bovine (i.e. Dublin, Cerro, Meleagridis), swine (i.e. Chloraesuis, Rissen, Derby) or fish (i.e. Brunei, Lexington, Bareilly) (Additional file 3).

Fig. 1
figure 1

Relative proportions of serovars of Salmonella enterica subsp. enterica found in each animal source (i.e. avian, bovine, fish and swine) in log-scale and corrected by the baseline proportions in the curated subset of Enterobase (see text for details). The present study focusing on adaptation to animal sources (n = 13,635) does not include isolates from environment, composite foods of the retail market and humans, which are considered as vectors of pathogen expositions and exposed susceptible consumers, respectively. The indexes higher and lower than zero represent sources in which serovars are over- and under-represented, respectively. The total effectives and p-values of Chi-square tests of uniformity applied to indexes are in brackets and square brackets, respectively. The serovars are sorted from the lowest (i.e. potentially mono-animal source) to highest (i.e. potentially multi-animal source) p-values. An asterisk stands for less than 20 samples from fish. A double asterisk stands for less than 20 samples from avian, bovine, swine and fish sources

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Authenticity and completeness of detected mutations

Among the 440 selected isolates, we replaced 25 strains for which paired-end reads presenting signs of exogenous DNA and inconsistencies between in vitro (i.e. sero-agglutination register in Enterobase) [60] and in silico (i.e. SISTR program) identifications of serovars [61]. The absence of exogenous DNA was checked based on the distribution of GC% (i.e. 52.12 ± 0.09) and total sizes of studied draft genomes (i.e. Additional file 4) in comparison with the complete circular genomes selected as references during the scaffolding steps (i.e. 4.73 ± 0.16 × 10− 6; n = 74).

The sizes of these 440 draft genomes (Fig. 2) agreed with the literature and ranged from 3.39 to 5.59 Mbp (i.e. between 3969 and 9898 genes) [62]. In line with studies emphasizing that host adaptation and increased pathogenicity of Salmonella serovars are not necessarily reflected in smaller genome sizes [5], we did not detect significant differences in terms of median values and distributions of total genomes sizes (Fig. 2) between strains from mono- and multi-animal sources (Fig. 1).

Fig. 2
figure 2

Total genome sizes of Salmonella enterica subsp. enterica serovars isolated from potential mono- and multi-animal sources related to avian (n = 120), bovine (n = 120), swine (n = 120) and fish (n = 80). Based on a curated and synthetic dataset of Enterobase, the Salmonella serovars Newport, Typhimurium and Anatum were selected and considered as serovars from potential multi-animal sources. The other selected serovars were considered as serovars from potential mono-animal sources related to avian (i.e. Heidelberg, Kentucky, Hadar), bovine (i.e. Dublin, Cerro, Meleagridis), swine (i.e. Chloraesuis, Rissen, Derby) and fish (i.e. Brunei, Lexington, Bareilly). Normality of the data was checked using Shapiro-Wilk test (p < 1.0 × 10− 2). The statistical differences in terms of median and distribution were assessed by non-parametric Wilcoxon rank sum and Kolmogorov-Smirnov tests, respectively

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NG50 values close to the sizes of the reference circular genomes, low number of long scaffolds (i.e. between 1 and 83 higher than 1000 bp), and almost complete genome fractions (i.e. ≈ 100%) (Additional file 4), were considered as evidences of assembly quality sufficiently high to perform pangenome extraction [63]. The pangenome extraction revealed logarithmic and hyperbolic forms of curves representing the new and conserved genes according to the sizes of genome dataset, respectively (Additional file 4). According to previous studies that estimated strict coregenome sizes of Salmonella between 1500 [64] and 2800 [65] genes, the present open pangenome of Salmonella enterica consists in 2705 core genes and 19,130 accessory genes. Given the high breadth (i.e. ≈ 100%) and depth coverages (i.e. > 30X) (Additional file 4), we performed variant calling analysis based on reference mapping [66]. Overall, 178,351 variants (98% of SNPs and 2% of InDels) were detected in the coregenome, including 139,514 variants from 3030 homologous recombination events. These accessory genes and coregenome variants were considered as genuine mutations, as the analysis followed best practices for genome assembly [63] and variant calling [66].

Congruencies of phylogenomic reconstructions

Visual inspections of the few incongruencies between the phylogenomic trees obtained from 3 different approaches, namely ‘variants including homologous recombination events’ (called A), ‘variants excluding homologous recombination events’ (called B) and ‘concatenated orthologous genes’ (called C) (Additional file 5), are in accordance with the high congruencies of pairwise distances emphasized by the corresponding cophenetic correlation coefficients (Table 1). Even though the trees have some branches in conflicts (see Robinson-Foulds indexes in Table 1), the few incongruencies result from a Subtree Prune Regrafting move and the topologies are globally congruent (see Fowlkes-Mallows indexes in Table 1). Swapped nodes are present comparing the serovars Typhimurim and Heidelberg to Anatum (A versus C), Bareilly (B versus C), or Anatum and Bareilly (A versus B) (Additional file 5). Considering the high level of agreement between the phylogenies, (Table 1 and Additional file 5) and following the recommendations of Hedge and Wilson [67], the present study will discuss the adaptation to animal sources mainly based on the tree retaining most of genetic information (i.e. reconstructed from the approach ‘A’). The phylogenomic reconstruction from the approach ‘A’ (i.e. iVarCall2) was indeed inferred based on coregenome SNPs from intra- and intergenic regions, as well as homologous recombination events, contrary to the approaches ‘B’ (i.e. ‘variants excluding homologous recombination events’ from iVarCall2 and ClonalFrameML) and ‘C’ (i.e. ‘concatenated orthologous genes’ from Roary).

Table 1 Congruency parameters between phylogenomic reconstructions of strains belonging to different serovars of Salmonella enterica subsp. enterica (n = 440) in terms of distance and topology. The phylogenomic reconstructions were performed by maximum likelihood selecting the most appropriate models of evolution and checking ultrafast bootstrap convergences (i.e. IQ-Tree). The compared approaches ‘variants’ and ‘genes’ correspond to phylogenomic trees reconstructed using pseudogenomes from variant calling analysis (i.e. iVARCall2) including (A) or excluding (B) variants from recombination events (i.e. ClonalFrameML), and concatenated orthologous genes (C) from pangenome analysis (i.e. Roary), respectively. The cophenetic function of the ‘dendextend’ R package was used to compute the cophenetic correlations. The dendrogram function of the ‘dendextend’ R package was used to compute the Fowlkes-Mallows indexes. The treedist function of the ‘phangorn’ R package was used to compute the Robinson-Foulds indexes
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Phylogenomic relationships between serovars from potential mono- and multi-animal sources

With the exception of serovars Newport and Cerro, all other serovars were monophyletic (Fig. 3) in all trees (Additional file 5). While the genomes of serovars from multi-animal sources were clustered into three distinct phylogenomic clusters (i.e. first lineage of Newport versus second lineage of Newport and Typhimurium versus Anatum), those from mono-animal sources were grouped by serovar (Fig. 3). The coexistence of purely clonal (i.e. mono-animal sources) and nearly panmictic (i.e. multi-animal sources) serovars (Fig. 3), emphasizes the necessity to correct the population structure when performing a microbial GWAS (Additional file 1) to find mutations associated to animal sources (i.e. avian, bovine, swine and fish).

Fig. 3
figure 3

Maximum likelihood phylogenomic tree of Salmonella enterica subsp. enterica serovars (n = 440) from potential mono- and multi-animal sources. Based on pseudogenomes inferred with the variant calling workflow iVARCall2, the workflow IQ-Tree selected the most appropriate model of evolution (GTR + I + G4) according to Akaike Information Criteria (AIC) and reconstructed the tree with an ultrafast approximation of phylogenomic bootstrap. The present phylogenomic tree was inferred including SNPs from recombination events and was rooted using the most closely related indica subspecies as an outgroup. The potential mono- and multi-animal sources were assigned based on Chi-square tests of uniformity applied on a curated and synthetic subset of Enterobase. Examples of mutations associated with animal sources by microbial GWAS are presented (i.e. Wald tests). These associated mutations refer to polygenicity with regard to Quantile-Quantile (QQ) plots from microbial GWAS (i.e. p < 1 × 10− 2) and present high (i.e. > 5%) and low (i.e. < 5‰) frequencies of presence (i.e. genes and alternative variants) in the studied and compared genomes, respectively. The serovars (i.e. colored squares), potential sources (i.e. black and grew squares), animal sources (i.e. colored squares), as well as annotated (i.e. colored circles) and non-annotated (i.e. colored triangles) mutations associated to animal sources, are represented from the internal to external rings. The colored circles and triangles represent present genes or alternative variants, whereas missing data refers to absente genes or reference variants, respectively. Most of the branches of the tree (i.e. 85%) are supported by bootstrap values higher than 90% (i.e. black circles) and the corresponding newick file is accessible under request

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Consideration of confounding factors during microbial GWAS

With the objective to take into account the confounding factors during microbial GWAS (Additional file 1), we compared different dataset of genomes to assess the correction of population structure and estimated the impact of the homologous recombination events [43]. More precisely, 9 microbial GWAS were performed for each animal sources (i.e. 36 analyses) considering different datasets of genomes from multi- (i.e. panmictic expansion) and/or mono- (i.e. clonal expansion) animal sources in the cluster presenting the phenotype of interest, as well as the cluster without this latter one (Additional file 6). Excluding the variants from homologous recombination events, 9 other microbial GWAS (i.e. 36 analyses) were performed with these different datasets of genomes (Additional file 7). Probably due to the coexistence of purely clonal to nearly panmictic lineages in the dataset of 440 genomes (Additional file 1), the datasets of genomes and variants from homologous recombination events affected the population structure corrections (Additional files 6 and 7). Expected shapes of quantile-quantile (QQ) plots referring to suitable population structure corrections (i.e. inflation for only highly significant observed p-values) were systematically checked including genomes from mono- and multi-animal sources in both studied strains and compared strains for the avian, bovine, swine and fish sources (Additional files 6 and 7). Concerning these expected shapes of QQ plots presenting inflations for only highly significant observed p-values, much more stratification of causal mutations were observed including variants from homologous recombination events (Additional file 6), compared to microbial GWAS excluding them (Additional file 7). All the 440 genomes included, we observed that most of the associated mutations were different comparing microbial GWAS performed with and without variants from recombination events (Table 2). According to this observation and the authors suspecting the homologous recombination events to conceal the detection of causal variants by microbial GWAS [43, 45,46,47], we decided to exclude the coregenome variants from these regions during microbial GWAS (i.e. 139,514 variants from 3030 homologous recombination events). Taking into account all the known confounding factors (Additional file 1), and even if common genome wide significance of human GWAS is around p ≤ 1 × 10− 6, the polygenicity was estimated at p ≤ 1 × 10− 2 according to the QQ plots of the present study focusing on microbial GWAS (Additional file 7). Without consensus concerning the genome wide significance of microbial GWAS [43], and with regards to frequencies of presence and absence of genes and alternative variants (Additional file 8), we estimated and checked visually that associated mutations present p-values of association between p = 8.78 × 10− 3 and p = 2.32 × 10− 15 (Fig. 3 and Additional file 8). These mutations associated by microbial GWAS have been retained to apply downstream GOEA.

Table 2 Mutations of Salmonella enterica subsp. enterica serovars (n = 440) associated with animal sources (i.e. avian bovine, swine and fish) by microbial GWAS including or excluding variants from recombination events. The accessory genes and coregenome variants (i.e. SNPs and InDels) were annotated with Prokka (1.12) and SNPeff (4.1 g), respectively. After potential exclusion of variants from recombination events based on iVARCall2 and ClonalFrameML, the workflow ‘microbial-GWAS’ corrects the population structure based on Linear Mixed Model (LMM), then perform associations with Wald tests implemented in GEMMA. The associated mutations (i.e. Wald tests) refer to polygenicity with regard to Quantile-Quantile (QQ) plots from microbial GWAS (i.e. p < 1 × 10− 3 and p < 1 × 10− 2, with or without recombination events) and present high (i.e. > 5%) and low (i.e. < 5‰) frequencies of presence (i.e. genes and alternative variants) in the studied and compared genomes, respectively
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Mutation associated with animal sources (i.e. microbial GWAS)

No matter the phenotype of interest, only partial associated mutations were detected by microbial GWAS (Fig. 3). While the presence of genes and presence of alternative variants were associated with animal sources, the absence of genes and presence of reference variants were not associated with animal sources. This observation is in accordance with the fact that losses of unessential functions do not necessarily refer to the adaptation to animal sources, as previously reported [12], or unconfirmed [5], concerning the host adaptation and restricted host transmission. As suspected with regard to higher functional impacts of accessory genes compared to coregenome variants, 38 genes were detected as associated with animal sources, whereas only 3 intergenic, 3 synonymous and 8 non-synonymous variants (SNPs and InDels) were associated to these traits of interest (Table 3). Due to the fact that synonymous variants associated to traits of interest (Table 3) may emphasize elements of regulation [68] or phenotypical impacts [69], we decided to retain them in GOEA. To summarize, 38, 34, 26 and 14 associated mutations were detected as signatures of avian, bovine, swine and fish sources, respectively (Additional file 8). Among the latter, annotations are available for only 10, 7, 6 and 2 mutations associated with avian, bovine, swine and fish sources, respectively (Tables 3 and 4).

Table 3 Mutations before and after microbial GWAS aiming to associate animal sources (i.e. avian bovine, swine and fish) with mutations from accessory (i.e. genes) and coregenome (i.e. SNPs and InDels) of Salmonella enterica subsp. enterica serovars (n = 440). The accessory genes and coregenome variants (i.e. SNPs and InDels) were annotated with Prokka (1.12) and SNPeff (4.1 g), respectively. After exclusion of variants from recombination events based on iVARCall2 and ClonalFrameML, the workflow ‘microbial-GWAS’ corrects the population structure based on Linear Mixed Model (LMM), then perform associations with Wald tests implemented in GEMMA. The associated mutations (i.e. Wald tests) refer to polygenicity with regard to Quantile-Quantile (QQ) plots from microbial GWAS (i.e. p < 1 × 10− 2) and present high (i.e. > 5%) and low (i.e. < 5‰) frequencies of presence (i.e. genes and alternative variants) in the studied and compared genomes, respectively
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Table 4 Functionally annotated mutations (i.e. excluding genes coding hypothetical proteins) of Salmonella enterica subsp. enterica serovars (i.e. SNPs, InDels and genes) associated by microbial GWAS with animal sources (i.e. avian bovine, swine and fish). The accessory genes and coregenome variants (i.e. SNPs and InDels) were annotated with Prokka (1.12) and SNPeff (4.1 g), respectively. After exclusion of variants from recombination events based on iVARCall2 and ClonalFrameML, the workflow ‘microbial-GWAS’ corrects the population structure based on Linear Mixed Model (LMM), then perform associations with Wald tests implemented in GEMMA. The associated mutations (i.e. Wald tests) refer to polygenicity with regard to Quantile-Quantile (QQ) plots from microbial GWAS (i.e. p < 1 × 10− 2) and present high (i.e. > 5%) and low (i.e. < 5‰) frequencies of presence (i.e. genes and alternative variants) in the studied and compared genomes, respectively. The genes with undefined names are assigned to STM identifiers with regard to the reference genome of Salmonella Typhimurium LT2 (NCBI NC_003197.1). HGVS stands for Human Genome Variation Society. N/A and ND stand for not applicable and not determined. N/A refers to intergenic regions. The term ‘gene’ refers to the gene presence
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Metabolic pathways mainly impacted by mutations associated with animal sources (i.e. GOEA)

Based on the mutations associated by microbial GWAS (Table 3 and Additional file 8), the GO-terms retrieved by GOEA (Additional file 9) were parsed to retain the most accurate (i.e. GO-levels ≥5) and the most enriched (i.e. Bonferroni corrected p-values < 5.0 × 10− 2), as previously described [11]. This resulted in 6, 1, 0 and 2 GO-terms of interest for the avian, bovine, swine and fish sources, respectively (Table 5). These GO-terms (Table 5) were mainly related to molecular functions (i.e. 66%) and biological processes (i.e. 33%).

Table 5 GO-terms mainly enriched by GOEA applied on accessory genes and coregenome variants of Salmonella enterica subsp. enterica serovars associated by microbial GWAS with animal sources (i.e. avian bovine, swine and fish). The GOEA was performed with the workflow ‘fastGSEA’ based on the parent-child approach integrating hypergeometric tests and Bonferroni corrections. The GOEA input sample is a list of corresponding RefSeq identifiers of accessory genes (i.e. RefSeq from Roary) and coregenome variants (i.e. NP from SNPeff 4.1 g) associated by microbial GWAS. The input universe is a list of RefSeq identifiers of all accessory genes (i.e. RefSeq from Roary) and all core genes (i.e. NP from SNPeff 4.1 g). The highest GO-levels presenting the most accurate GO-terms (i.e. ≥ 5) and the lowest Bonferroni corrected p-values representing highly enriched GO-terms (i.e. < 5.0 × 10−2), are presented. BP, MF and CC stand for biological process, molecular function and cellular component, respectively
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Discussion

Restricted and unrestricted animal sources across Salmonella

Salmonella serovars might be considered as having restricted (mono-) or broad (multi-) animal sources. Here we used the Enterobase resource providing both genomic data and metadata to build a dataset to explore the relationships between genotype and adaptation to the animal sources (Fig. 1). As exemplified with Escherichia (only host-unrestricted lineages), Campylobacter (both host-restricted and -unrestricted lineages) and Staphylococcus (only host-restricted lineages), the lineages resulting of phylogenomic reconstructions reflect the genetic structure (i.e. patterns of mutations) established through either host-adapted lineages, physical barriers to colonization, or local clonal spreading induced by selection or genetic drift [12]. The restricted and unrestricted-host lineages can be the result of a diversity of genetic processes: neutral diversification, acquisition of a host-adaptive trait causing a genome-wide purge within the population, large recombination between strains creating a hybrid lineage or negative frequency-dependent selection induced by decreasing of fitness [12]. Our segmentation distinguishing mono- and multi-animal sources should consequently reflect a representation of clonal and panmictic serovars (Additional file 1) [43] rather than a phenomenon of adaptation to single or multiple niches. This hypothesis is supported by our ability to correct population structure considering both serovars from potential mono- and multi-animal sources as genomes of interest during microbial GWAS (Additional files 6 and 7).

Genetic signatures of Salmonella adaptation to animal sources

Especially in highly recombinant bacterial genomes, phylogeographic signatures can be weakened due to dissemination around the world and genomic changes occurring within the reservoir hosts [70]. Even with a dataset of genomes highly diversified in terms of serovars (i.e. 12 clonal and 3 panmictic serovars including 13 monophyletic and 2 polyphyletic serovars), geographical origin (i.e. 26 countries, 68% from United States) and time of isolation (i.e. 25th and 75th percentiles: 2005–2013) origins (Additional file 3), we were able to identify genetic signatures of animal sources (Table 2, Table 4 and Additional file 8) by microbial GWAS (Fig. . 4 and Additional file 7). Host-associated genetic signatures have been previously detected for Staphylococcus aureus [71] and Campylobacter [72] which expanded into vast open livestock niches from humans [73] or pre-agriculture wild animal [73, 74]. Probably because Salmonella enterica subsps. enterica did not evolve as an obligate intracellular pathogens, we did not observe evidence of accumulation of deleterious mutations and losses of unessential functions (Fig. 2 and Table 2), that have been associated [12], or not [5], with host adaptation and restricted host transmission in other organisms. Salmonella genomes from human source were not included in the dataset of genomes, because it would conceal the mutations associated with the avian, bovine, swine and fish sources, but the mutations identified in the present study as associated with animal sources (Table 2 and Additional file 8) could be used as in silico or in vitro markers to identify them from human isolates in a context of source tracking for food safety [1, 2]. In this framework, we plan to develop in a near future a workflow to attribute animal sources from human samples based on the markers identified in the present study to improve the models of source attribution at the genomic scale [51], as recently proposed to prediction sources of S. Typhimurium by machine learning Random Forest classifier [75]. Even if the annotations of hypothetical proteins associated with animal sources have to be improved in the future (Table 2 and Additional file 8), we will discuss about the annotated mutations which have been associated with animal sources (Fig. . 3).

Fig. 4
figure 4

Manhattan plots from microbial GWAS aiming to detect accessory genes and coregenome variants of Salmonella enterica subsp. enterica serovars (n = 440) associated with avian, bovine, swine and fish sources. Strains from both potential mono- and multi-animal sources were considered as having phenotype 1 and others strains (i.e. mono-source with a different animal) as having phenotype 0. The accessory genes were sorted by frequency and the positions of coregenome variants are in accordance with the reference genome of Salmonella Typhimurium LT2 (NCBI NC_003197.1). The blue and red lines (− log10(observed p-values)) correspond to the genome wide significance from human GWAS and polygenicity with regard to Quantile-Quantile (QQ) plots from microbial GWAS (i.e. p < 1 × 10− 2)

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Signatures of adaptation to the avian source

The studied Salmonella genomes from avian sources (Additional file 3) principally come from samples found in the food chain (i.e. 92% of poultry) and may consequently be impacted by the environment and work practices of this sector. The S. Typhimurium mutations associated with avian source (Fig. . 3) impacted mainly the metabolism processes related to detection of visible light (GO:0009584 and GO:0009883), red and far-red light phototransduction (GO:0009585), DNA dependent activities (GO:0043141 and GO:0008094) and C4-dicarboxylate transport (GO:0015740) (Table 5).

Following the same pattern (i.e. a list of mutations observed in the same genomes), the genes zntR2, cph2_2, merP_1 and merP_2 are associated with avian source (Fig. 3, Table 4 and Additional file 8). The zing dependent helix-turn-helix domain (i.e. gene zntR2) allows binding to DNA cognate sites [76]. Never described in Salmonella, the cyanobacterial phytochrome Cph2 activate mobility capacity (i.e. phototaxis) towards red light (i.e. gene cph2_2) [77] and may be related to conditions of poultry growth were red light his frequently used to improve liveweight [78]. The mercuric transport protein periplasmic components (i.e. genes merP_1 and merP_2) may also be an adaptation related to mercury exposure. DNA damage has been reported in rat and mouse fibroblasts as well as cells from Chinese hamster ovary and human cells [79]. Due to anthropogenic activities, the changes in the human chromatin is indeed known to be induced by mercury exposure of the biosphere during 500 years [80]. As recently observed in a large subantarctic avian community, the diet (i.e. crustacean, fish, squid and carrion-consumers), rather than taxonomy, is an important driver of avian mercury exposure [81]. Even if the mercury is considered as undesirable substance in animal feed by European Food Safety Authority [82], and in a context of prevention and control of contagious poultry diseases [83], the domestic avian community have been exposed to mercury through vaccination [84]. The ethyl mercury is very toxic water-soluble form of mercury developed in the 1920s to preserve vaccines, variously called Thimerosal, Merthiolate and Thiomersa. For instance, the Thimerosal contains 49% of mercury mass [85] and is a preservative used in vaccines preventing human flu (A/H1N1) [86], as well as infections of domestic poultry and other bird species with virulent Newcastle disease virus [84].

Following also the same pattern, the SNPs in genes sinH, ilvY and ilvC are associated with avian source (Fig. 3, Table 4 and Additional file 8). Among other delivery devices encoded in type V protein secretion systems (T5SS), the intimin-like inverse autotransporter protein SinH (i.e. synonymous SNP in sinH), also known as SivH, is a virulence factor involved in internal colonization of Salmonella [87]. Organized as a LysR protein-regulated system, the HTH-type transcriptional activator IlvY (i.e. missense SNP in ilvC) is the transcriptional regulator of the ketol-acid reductoisomerase NADP+ (i.e. missense SNP in ilvC) involved in the parallel pathway for the biosynthesis of L-isoleucine and L-valine [88], and was associated by different mutations to avian (p.Glu206Lys) and swine (p.Leu106Gln) sources (Table 4). As detailed latter concerning the diet of weaned piglets [89], the isoleucine and valine are also controlled in practical broiler formulas because these amino acids are limited in nutrition based on corn and soybean meals [90], and may consequently explain this missense SNP in ilvC (p.Glu206Lys) (Table 4).

Associated to different genomes of avian source, the genes recD2 and dcuA are also mutations explaining this animal source. The ATP-dependent RecD-like DNA helicase (i.e. gene recD2) inhibits stress-induced mutations independently of effects on SOS induction in Escherichia coli [91]. Mediated by an anaerobic C4-dicarboxylate transporter DcuA (i.e. gene dcuA), S. Typhimurium performs a complete tricarboxylic acid cycle during colonization of the intestinal lumen to uptake and use poorly fermentable dicarboxylic acids, such as succinate, conferring a fitness advantage in competition with the native gut microbiota [92].

Signatures of adaptation to the bovine source

All the studied Salmonella genomes from bovine sources are related to livestock, and like their avian counterpart, are exposed to the related environment and work practices in the food industry (Additional file 3). The mutations associated with bovine source in S. Cerro, S. Dublin and/or S. Meleagridis (Fig. . 3) affected the metabolism process related to aspartate ammonia-lyase activity (GO:0008797) (Table 5).

With an identical pattern, the SNP in arnD, as well as, the genes arnD, srmB and aspA, are associated with the bovine source (Fig. 3, Table 4 and Additional file 8). The 4-deoxy-4-formamido-L-arabinose phosphoundecaprenol deformylase ArnD (i.e. synonymous SNP in arnD) is involved in modification of LPS with arabinose and required for resistance to polymyxin and cationic antimicrobial peptides [93]. This adaptation signal may be explained by the bovine exposures to polymyxin treatments. The polymyxin and colistin (i.e. polymyxins E2 and E1) are currently last-line therapeutic options to treat infections caused by multidrug-resistant Gram-negative bacteria [94], whose residues can be detected in bovine milk and tissues [95].

The ATP-dependent RNA helicase SrmB (i.e. gene srmB) is a dead-box family of helicase proteins involved in ribosomal biogenesis, but his function in Salmonella remains to be determined [96]. The aspartate ammonia-lyase encoded by aspA, converts aspartate to fumarate which is reduced by a fumarate reductase into succinate [97]. As observed with enterohemorrhagic Escherichia coli, aspartate deamination and anaerobic fumarate respiration, may be important pathways favoring Salmonella adaptation to bovine gut [98].

Present in different genomes from bovine source, the genes repE, hicB and eptC are also associated with bovine source. The replication initiation proteins (i.e. gene repE) relate to incompatibility of plasmids and compete each other, with potential linked accessory genes, for replication in the bacterial host [99]. As demonstrated with E. coli, the antitoxin HicB (i.e. gene hicB) forms probably a complex with the mRNA interferase HicA which becomes active after dissociation induced by nutrient starvation and produces bacteriostatic conditions for growth of other bacterial cells [100]. The phosphoethanolamine transferase EptC (i.e. gene eptC) adds a phosphoethanolamine to the inner core lipooligosaccharide of C. jejuni, promoting recognition by a human Toll-like receptor and providing resistance to relevant mammalian and avian antimicrobial peptides [101].

Signatures of adaptation to the swine source

The studied Salmonella genomes from swine sources are mainly representative of livestock of this sector (i.e. 88% of livestock) and potentially exposed to the environment and work habits of this food chain (Additional file 3). The mutations associated by microbial GWAS to different genomes of S. Choleraesuis, S. Derby and/or S. Rissen from swine source (Fig. 3 and Additional file 8), are not over-enriched by GOEA (Table 5) and are only constituted of core variants including an InDel in the intergenic region STM4562-yjjU and SNPs, as well as genes pepE, iroN, priA, ybeK and ilvY (Table 4). The dipeptidase E of S. Typhimurium (i.e. missense SNP in pepE) is hypothetically involved in sequestration of peptide aspartate used in synthesis of the aspartate family of amino acids [102], and the aspartate may be added in diets of piglets to improve growth performance and protect them against oxidative stress and mycotoxin infection [103]. Keeping in mind that iron availability increases the pathogenic potential of S. Typhimurium [104], the TonB-dependent siderophore receptor protein (i.e. missense SNP in iroN) is involved in iron acquisition in S. enterica [105]. The primosomal protein N (i.e. missence SNP in priA) allows restarting of stalled replication forks via its helicase activity [106] and the pyrimidine-specific ribonucleoside hydrolase RihA (i.e. synonymous SNP in rihA, also called ybeK) is involved in conversion of cytidine into cytosine [107]. Requiring more elements to consolidate the following hypothesis, this mutation associated to swine (i.e. synonymous SNP in rihA) may be linked to the pig specific pathway including the cytidine-5′-monophospho-N-acetylneuraminic acid hydroxylase (CMAH). This CMAH is implicated in production of carbohydrates on the surface of intestinal epithelial cells, which are considered as the primary elements interacting with microbes and viruses during foreign parasitic infection [108]. As previously emphasized, the HTH-type transcriptional activator IlvY (i.e. missense SNPs in gene ilvY: p.Glu206Lys in avian and p.Leu106Gln in swine) is involved in the parallel pathway for the biosynthesis of L-isoleucine and L-valine [88]. Just as the practical broiler formulas (Corzo et al. 2009), the isoleucine and valine are limited and added in the diet of weaned piglets (i.e. barley, wheat, maize and soya) [89], impacting expression of metabolisms involved in branched-chain amino acid, as well as amino acid composition of tissues [109].

Signatures of adaptation to the fish source

The fish sources of the studied genomes may be related to environment and work habits of this food chain because the corresponding Salmonella samples were isolated from fresh (i.e. 28%), frozen (42%) and processed fresh (27%) fish (Additional file 3). Without annotated mutations associated with S. Bareilly, the mutations associated with fish source in S. Lexington and S. Brunei impacted mainly the metabolic processes involved in kappa-carrageenase (GO:0033918) and tetrahydrodipicolinate N-acetyltransferase activities (GO:0047200), respectively (Table 5). Never studied in Salmonella, the kappa-carrageenase (i.e. gene cgkA) has been described the first time in a marine bacterium Alteromonas carrageenovora [110] and is involved in degradation of k-carrageenan, a linear sulfated polysaccharides extracted from red edible seaweeds [111]. The 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase (i.e. gene dapH) is known as the first step of the L-lysine biosynthesis via diaminopimelate pathway [112] and the fish diets based on plant ingredients are deficient in lysine which is added in fish feed to improve growth [113] and liveweight [114]. These mutations associated with fish may consequently refer to adaptation induced by natural (e.g. gene cgkA) and artificial (e.g. gene dapH) diets.

Conclusions

The strains of different serovars of the recombinant taxa Salmonella enterica subsp. enterica, evolved through clonal and panmictic lineages and adapted their genomic contents to animal sources of food chains at the accessory and coregenome scales. The major genetic and metabolic determinants of Salmonella adaptation to animal sources may have been driven by the natural feeding environment of the animal (e.g. k-carrageenan from red edible seaweeds for fish) and distinct livestock diets modified by human (e.g. isoleucine and valine for poultry and pig, aspartate for piglets, and lysine for fish). Environmental stimuli (e.g. red light exposure of poultry), physiological properties of the animal itself (e.g. aspartate deamination related to bovine gut adaptation), and work habits for health protection of livestock (e.g. exposure of poultry to mercury-based vaccines and exposure of bovine to polymyxin) may have also contributed to Salmonella adaptation underpinned by genetic and metabolic mutations associated with animal sources through the food chain.

Methods

Approach

We propose to decipher the adaptation to animal sources of Salmonella serovars. Our approach aimed at selecting 440 isolates, representative of most animal sources, sequenced using paired-end reads and recorded in a curated and synthetized subset of Enterobase (i). Secondly, accessory genes and coregenome variants (i.e. SNPs and InDels) were detected (ii). Thirdly, accessory genes and coregenome variants (i.e. SNPs and InDels) were associated with the animal sources of interest (i.e. avian, bovine, swine and fish) based on an implementation of microbial GWAS correcting for strong population structure (iii). Finally, GOEA were performed in order to decipher metabolic pathways mainly impacted by the pangenomic mutations associated with the animal sources (i.e. accessory genes and coregenome variants) (iv).

Selection of a genome dataset (i)

With regard to metadata from Enterobase (i.e. December 2016: 83618 records), we selected 440 isolates in order to depict a high level of genomic diversity of Salmonella enterica subsp. enterica serovars, potentially related to mono- or multi-animal sources [58]. The corresponding reads were downloaded from the ENA [115]. With a homemade python script (version 2.7), the metadata from Enterobase was curated retaining complete records (i.e. BioProject, ENA ID, Host, sample Matrix, serovar, source niche, source origin, source details, country and collection years) and standardizing typos. Based on this curated subset of Enterobase (i.e. 37,747 records), the samples from environment, composite foods of the retail market and humans were not retained because they are considered as vectors of pathogen expositions and exposed susceptible consumers in the present study focusing on adaptation to animal sources (i.e. 13,635 records of considered sources). Taking into account the unbalanced distributions of serovars and sources in this curated database, indexes representative of the association levels of animal sources were calculated for each serovar and each source. These indexes (\( i=\mathit{\log}\frac{\%\left(\frac{serovar}{source}\right)}{\%\left(\frac{strains}{source}\right)} \)) represent the common logarithm of the number of strains per source for each specific serovar (\( \%\left(\frac{serovar}{source}\right) \)) divided by the number of strains per source in the full curated database (\( \%\left(\frac{strains}{source}\right) \)). Deviations from 0 correspond to over- or under-representation of the serovar in the source. Chi-square tests of uniformity of these indexes for each serovar allowed sorting of serovars from potential multi-animal sources (p > 0.02 with i ≈ 0) to potential mono-animal sources (p < 0.02 with i > 0 for over-represented serovars or i < 0 for under-represented serovars). Based on the curated and synthetic subset, we built a collection of 440 genomes so that its composition was genetically diversified (i.e. 15 serovars) and roughly balanced considering animal sources (i.e. mono- and multi-animal sources from 4 animal sources). More precisely, 20 genomes from each of 3 serovars from potential mono-animal sources were selected for each of the studied sources: avian, bovine, swine and fish (i.e. 240 genomes). Between 60 and 80 genomes from each of 3 serovars from potential multi-animal sources (i.e. 200 genomes) were added in order to get a roughly balanced dataset of potential mono- and multi-animal sources. The balance between mono- and multi-animal sources was deliberate and used to evaluate the impact on several confounding factors during microbial GWAS. The manual selection of isolates was performed checking the animal sources and respecting high levels of diversity concerning the geographical origins, isolation dates and BioProject accession numbers.

Coregenome variants (ii)

The coregenome SNPs and small InDels were detected based on the variant caller HaplotypeCaller implemented in the iVARCall2 workflow [11], using Salmonella Typhimurium LT2 (NCBI NC_003197.1) as a reference genome, and following the best practices proposed by the Genome Analysis ToolKit [116]. More precisely, secondary alignments around small InDels were performed and duplications were excluded before variant calling analysis via local de novo assembly of haplotypes in active regions. The variants (i.e. SNPs and InDels) were flagged with SnpSift (version 4.1 g) [117] and the functional annotations of these variants were obtained with SNPeff (version 4.1 g without variants from intron, UTR-5′, UTR-3′, upstream regions, and downstream regions) [118]. As previously described, variants from homologous recombination events were detected with ClonalFrameML [13] and excluded to build set of 38,837 variants, or not to build set of 178,351 variants, with the script ‘Clonal_VCFilter’ [11]. The pseudogenomes were produced with the script ‘VCFtoPseudoGenome’ and correspond to the reference genome where the genotypes of detected variants were replaced in each genome [11].

Accessory genome (ii)

With an in-house workflow called ARTwork, the assembly was performed based on coverage control (i.e. > 100X) with Bbmap [119], read normalization (i.e. 100X) with Bbnorm [120], control of read quality with FastQC [121], read trimming (i.e. > 20 of Quality Control) with Trimmomatic [122], de novo assembly with SPAdes [123], selection of the closely related reference genomes with MinHash among 74 reference circular genomes [124], scaffolding with MeDuSa [125], gap filling with GMcloser [126], trimming of small scaffolds (i.e. < 200 bases) with Biopython [127], as well as control of assembly quality with QUAST [128], MultiQC [129] and ggplot2 [130] graphics. Based on these draft genomes, pangenome was constructed with Roary [131] setting 95% of identity for blastp and a strict definition of the coregenome (i.e. 100% of isolates with core genes).

Population structure (iii)

The phylogenomic reconstructions were performed based on the coregenome variants including or excluding variants from homologous recombination events (i.e. pseudogenomes from iVARCall2 [11]), as well as core genes (i.e. concatenated orthologous genes from Roary [131]). IQ-Tree [132] was applied on our datasets made up of millions of aligned sites to perform fast selections of the models of evolution based on Akaike Information Criteria (AIC) [133] and efficient tree reconstructions by maximum likelihood based on the most appropriated model of evolution [132]. More precisely, the consensus trees were produced considering all possible Nearest-Neighbor-Interchanges (NNIs) instead of only surrounded computed NNIs [132]. The search in the tree space started from a BIONJ tree [132] and an improved version [134] of the ultrafast bootstrap [135] was applied with 1000 iterations to compute boostrap support values. UFBoot convergences were checked after the IQ-Tree computation [132]. As stated in the literature, Salmonella enterica subsp. indica is the subspecies closest to subsp. enterica and was consequently used as an outgroup to root the tree of the subspecies enterica [59, 64]. Practically, this subspecies enterica root was identify using three isolates of the subsp. indica (SRR1840570, SRR1060719 and SRR1060512) and three isolates of each studied serovar. The tree distances were compared numerically with the cophenetic function of the ‘dendextend’ R package based on the Pearson, Kendall and Spearman correlations (i.e. between − 1 and + 1, referring to anti-correlated and correlated distances) [136]. The tree topologies were compared visually with the cophylo function of the ‘phytools’ R package [137]. The tree distances were also numerically compared computing the Fowlkes-Mallows index (i.e. between 0 and 1, referring to dissimilar and similar topologies, respectively) with the dendrogram function of the ‘dendextend’ R package [138], and the Robinson-Foulds index (i.e. number of different nodes between both tree) with the treedist function of the ‘phangorm’ R package [139].

Genome wide association study (iii)

Within a range from 51 Listeria monocytogenes [29] to 3701 Streptococcus pneumoniae strains [35] and without consensus on the appropriated size of genome dataset, most of the microbial GWAS includes around 500 samples under clonal and/or panmictic status (Table 6) [43]. Contrary to human GWAS focusing on the effects of individual SNPs, microbial GWAS has also to access phenotype associations based on presence/absence of genes alongside SNPs [43]. In addition, microbial GWAS has to take into account confounding factors such as genome selection, homologous recombination events, population structure related to Linkage Disequilibrium (LD), and genome wide significance, because they can induce false positive identifications of seemingly causal mutations [43, 141]. With regard to the confounding factors (Additional file 1), we applied the developed microbial GWAS (Fig. 5) based on GEMMA [40]. This workflow was applied to 440 genomes, comparing different sizes of genome dataset, taking into account variants from homologous recombination events and checking population structure corrections. The associated mutations (i.e. Wald tests) refer to polygenicity with regard to QQ plots from microbial GWAS (i.e. p < 1 × 10− 2), and present high (i.e. > 5%) and low (i.e. < 5‰) frequencies of presence or absence (i.e. genes and alternative variants) in the studied and compared genomes, respectively.

Table 6 Summary of microbial GWAS. Microbial GWAS developed until now are listed comparing their workflows, mutations of interest, studied phenotypes and genome dataset
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Fig. 5
figure 5

Developed scripts and published programs (i.e. black letters) with their corresponding effects (i.e. green letters) implemented in the driving script ‘microbial-GWAS’ performing microbial GWAS integrating Linear Mixed Model (LMM) for population structure correction. Based on the LMM integrated in GEMMA, the sequential workflow called ‘microbial-GWAS’ is written in R and Python 2.7. It runs successively scripts called ‘binary’, ‘panGWAS’, ‘coreGenVarNb’, ‘overImpacted’ and ‘AllResults’ in order to standardize SNPs, InDels and genes as binary data, compute Kinship matrix, fit a LMM and perform Wald tests, as well as detect coregenome variants presenting high gene densities (i.e. hotspots of variants) and high functional impacts (i.e. non-synonymous variants)

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Gene ontology enrichment analysis (iv)

Based on our recently published workflows called ‘GetGOxML’ and ‘EveryGO’ aiming at retrieving GO-terms online from coregenome variants and perform GOEA at any node of a phylogenomic reconstruction [11], we developed an improved workflow called ‘fastGSEA’ (Fig. 6). This workflow ‘fastGSEA’ produces a fast GOEA dependently of a local Uniprot dataset of GO-terms to decrease the execution duration, and provide a complete automatic workflow applicable to many kinds of gene identifiers (i.e. 15 different gene identifiers) [56]. This workflow can also produce a slower GOEA dependently of the current version of an application programming interface provided by QuickGO (i.e. ‘Annotations’ https://www.ebi.ac.uk/QuickGO/api/index.html). The driver script ‘fastGSEA’ is written in Python (version 2.7) and uses as input a dataset of gene identifiers (i.e. idmapping.selected.table.gz; current release from Uniprot: ftp://ftp.uniprot.org/). It requires also two lists of gene identifiers from the sample of interest and universe, as well as a file representing the DAG of GO-terms (i.e. go-basic.obo including eukaryotic and prokaryotic GO-terms or gosubset_prok.obo including only prokaryotic GO-terms). The first step of the workflow ‘fastGSEA’ aims at selecting from the dataset ‘idmapping’, a subset of gene identifiers linking the gene identifiers provided by the user, corresponding Uniprot identifiers and associated GO-terms from the sample and universe lists locally (i.e. based on GO-terms from the subset) or online (i.e. based on Uniprot identifiers from the subset). Secondly, the workflow uses the DAG of GO-terms to retain prokaryotic GO-terms and avoid obsolete GO-terms. The third step of the workflow tests the hypergeometric distributions of GO-terms (i.e. ‘phyper’ R function) [142] and corrects the produced p-values based on the Bonferroni correction (‘p.ajust’ R function) [143]. In parallel to a file centralizing the results (i.e. GO-terms, number of hits, GO levels, p-values, ontology), the workflow ‘fastGSEA’ produces finally a graphical representation of the GOEA with the plotting system ggplot2 [130].

Fig. 6
figure 6

Developed scripts and published programs (i.e. black letters) with their corresponding effects (i.e. grew letters) implemented in the driving script ‘fastGOEA’ performing GOEA based on the parent-child approach integrating hypergeometric tests and Bonferroni corrections. This workflow examines the Uniprot API (i.e. slow mode) or by default a local dataset of gene identifiers (fast mode) from Uniprot (i.e. idmapping.selected.table.gz) in order to associate GO-terms to gene identifiers provided by the user as two lists referring to the sample and universe of hypergeometric tests. With regard to a directed acyclic graph (DAG) of GO-terms (i.e. go-basic.obo including eukaryotic and prokaryotic GO-terms or gosubset_prok.obo including prokaryotic GO-terms), this workflow retains prokaryotic GO-terms and avoids obsolete GO-terms before to perform GOEA. These scripts were written with Python 2.7 and implement R libraries ‘p.ajust’, ‘phyper’ and ‘ggplot2’. The whole workflow is automated and the scripts ‘trim’ and ‘enrich’ has to be performed for each GO-terms during trimming and enrichment steps, respectively

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