Abstract
Three E. coli O157:H7 outbreaks have been attributed to contaminated pork in Alberta, Canada, recently. This study investigates the phylogenetic relatedness of E. coli O157:H7 from pigs, cattle, and pork-production environments for source attribution. Limited strain diversity was observed using five conventional subtyping methods, with most or all strains being in one subgroup. Whole-genome single nucleotide polymorphism analysis confirmed the recent ancestry of the isolates from all three sources. Most environmental isolates clustered closer with pig isolates than cattle isolates. Also, a direct link was observed between 2018-outbreak environmental isolates and isolates collected from a pig farm in 2018. The majority of pig isolates harbor only one Shiga toxin gene, stx2a, while 70% (35/50) of the cattle isolates have both stx1a and stx2a. The results show some E. coli O157:H7 strains could establish persistence on pig farms and as such, pigs can be a significant source of the organism.
Similar content being viewed by others
Introduction
Shiga toxin-producing Escherichia coli (STEC) can cause human enteric illness ranging from uncomplicated diarrhea to bloody diarrhea, with a fraction (2–22%) of patients developing life-threatening hemolytic uremic syndrome (HUS)1,2,3,4,5,6. The predominant STEC serotype associated with human infections and outbreaks in North America is O157:H7/NM, which also has a higher association with severe patient outcomes, compared to other serotypes1,7.
Beef has been frequently implicated in STEC O157 outbreaks1,7. Ruminants including cattle, are regarded as a natural reservoir of STEC O157:H78. On the contrary, swine is not a recognized reservoir of STEC O157:H7, and their contribution to human STEC O157 infections has been a matter for debate9. Unlike cattle which are asymptomatic carriers, pigs can develop edema when infected with STEC strains harboring stx2e10. Outbreaks attributed to STEC O157:H7 contaminated pork products are scarce worldwide11; however, a higher frequency has been observed in Alberta, Canada, with three outbreaks having occurred in four years (2014, 2016, and 2018)12,13,14. The outbreak in 2014 was the second-largest foodborne outbreak in Canadian history with 119 lab-confirmed cases, while the 2018 outbreak had 42 confirmed cases with one death likely due to the infection with E. coli O157:H712,13.
A large number of studies from various geographical regions have been conducted to investigate the prevalence of STEC O157:H7 in healthy pigs15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33. Most of these studies did not find this pathogen in pigs16,17,18,19,20,22,25,26,27,31,33, except for the studies from Japan32, Ireland23, UK24, Sweden28, Norway30, USA29, and Canada15 where up to 2% prevalence was reported. Among these studies, a recent survey performed at 39 provincially inspected abattoirs in Alberta found 1.4% of pigs and 1.8% of pork carcasses were positive for STEC O157:H7, and 12.8% of abattoirs had at least one positive sample15. In addition, an outbreak-related investigation in Alberta in 2018 recovered STEC O157:H7 from pig fecal samples on the outbreak-associated farms (Keenliside, unpublished data). It is not clear whether pigs are transient carriers of STEC O157, or some strains of the pathogen can circulate on pig farms, with pigs being the primary reservoir.
With the decrease in cost and increase in throughput for WGS, subtyping methods for surveillance and phylogenetic analysis of pathogenic bacteria have been rapidly evolving from analyzing a limited number of sites/genes in a bacterial genome to genome-wide comparisons. Analysis based on single nucleotide polymorphism (SNP) and core genome (cg)/whole genome (wg) multilocus sequence typing (MLST) are the most often used WGS subtyping methods, followed by gene content analysis34,35,36,37. Despite the much improved discriminatory power of WGS-based methods38,39, it is still of value to link findings from WGS-based analysis to conventional subtyping methods, and make use of the large body of information in the literature. Thus, in the present study, we analyzed the population structure and phylogenetic relatedness of 121 STEC O157:H7 isolates from pigs (n = 41), cattle (n = 51), and pork-production environments (n = 30) in Alberta, Canada using both conventional and WGS-based subtyping methods. Also, the genomes of these isolates were characterized with a focus on virulence and antibiotic resistance genes.
Results
Subtyping of E. coli O157:H7 isolates using conventional methods
All 121 E. coli O157:H7 isolates (Table S1) were subtyped for Manning clade40, lineage-specific polymorhpism (LSPA)41, MLST type, and Clermont phylo-group42 via in silico analysis. Most of the isolates (115/121, 95%) were identified to be of Manning clade 2 although cattle isolates showed more diversity (Table 1). The clades 4-7 and 9 strains share the same SNP profile for the target genes and hence cannot be differentiated by the clade typing method. Of the 121 isolates, 115 belonged to LSPA lineage I. Again, cattle isolates showed more diversity, with Cat02-Cat04 and Cat13 belonging to lineage I/II, and Cat46 belonging to lineage II. Cat24 lacked the rbsB gene and as such, could not be subtyped by LSPA41. Using the Pasteur Institute’s eight-gene scheme, Env06 (from a pig carcass) and Cat12 did not match any MLST type in the database as the two isolates had a unique allele for the target genes polB and icdA, respectively. Cat02-Cat04, Cat13 and Cat46 were identified as MLST type 628 and all the other isolates as 822. Neither Achtman’s seven-gene MLST scheme nor the Clermont’s E. coli phylo-typing method42 was able to distinguish the isolates, with all being identified as MLST type 11 or phylo-group E, respectively (Table 1).
Comparison of WGS-based subtyping methods
The phylogenetic relationships among the isolates were further mined using core SNP analysis, cgMLST, wgMLST, and gene content analysis. The core SNPs between the reference strain E. coli O157:H7 EDL 93343 and the 121 isolates included 2565 sites in total. CgMLST and wgMLST included 2513 and 24952 genes, respectively. The distances among isolates were 0–770 SNPs, 0–297 alleles, 0–669 alleles, and 0.012–0.222 (Jaccard distance) for core SNP analysis, cgMLST, wgMLST, and gene content analysis, respectively (Fig. 1; Tables S2–S5).
Distance-based dendrograms constructed using the unweighted pair group method with arithmetic mean (UPGMA) showed significant correlation/similarity (P < 0.01) among the four dendrograms (Fig. 2). The pair-wise Cophenetic correlation coefficient (CPCC)44 among dendrograms from core SNP analysis, cgMLST, and wgMLST was between 0.995 and 0.996 (Fig. 2). The CPCC between any of the three dendrograms and that from gene content analysis was between 0.602 and 0.617, suggesting the gene content dendrogram was only moderately correlated with the former three dendrograms. Consistent with the statistical analyses, visual comparisons showed that the phylogenetic trees from core SNP analysis, cgMLST and wgMLST clustered the isolates in a similar structure/topology while the gene content tree differed from the rest (Fig. 3 & 4 and S1-S2). For example, the core SNP analysis, cgMLST and wgMLST trees clustered pig and pig production environment isolates mainly into seven groups (Fig. 3, S1 and S2). In the gene content tree (Fig. 4), groups 2, 3, 5, 6, and 7 pig and pig environment isolates were in their respective distinct clusters, while groups 1 and 4 isolates were each separated into two subgroups, suggesting differences in gene gain and/or loss among the isolates within each of the two groups.
Phylogenetic relatedness among the E. coli O157 isolates
The core SNP analysis was selected for interpretation of the phylogenetic relationship among the bacterial isolates. As mentioned above, environmental and/or pig isolates mostly clustered together, forming seven phylogenetic groups, 1–7, except for a few isolates (Env18, an isolate from pig feces on farm 11; Env06, from pig carcasses in plant A; Pig03, from pigs from farm 2) which clustered together with one or more cattle isolate(s) individually (Fig. 3; Table S2). Cut-off values of ≤20, >20 and ≤100 and >100 SNPs have been recommended to cluster bacterial isolates in food surveillance studies as closely related, possibly related and not related, respectively45. Based on this definition, most of the isolates within each of groups 1–7 were closely related (Table S2), except for Env01 (2016-outbreak isolate) which had genetic distances of 38–46 SNPs in comparison to all other isolates in group 4. Group 1–5 environmental isolates clustered closer with pig isolates than cattle isolates (Fig. 5a–e). The distance between environmental isolates of group 1–5 and their respective closest pig isolate(s) was 0–7, 7–8, 9–11, 0–46 and 1–17 SNPs, respectively. In contrast, the distance between group 1 and 5 environmental isolates and their respective closest cattle isolate(s) was ≥25, 55, 23, 45, and 45 SNPs. Groups 6–7 environmental isolates had distances of ≥84 SNPs with either pig or cattle isolates included in this study (Fig. 5f, g). All porcine and environmental isolates had genetic distance of ≤100 SNPs with at least one of the cattle isolates (Fig. S3), suggesting a recent divergence in ancestry of these isolates.
The pig and environmental isolates were recovered from pig fecal samples or environmental samples collected from 11 farms (1–11) or four meat processing plants (a–d) (Figs. 3 and 6). Closely related pig isolates were recovered from farms 1 and 4 over a period of two years and frequently from pigs on farm 9 (Figs. 3 and 6). The genetic distances between the 2018-outbreak isolates (Env02-Env05, Fig. 5d) and pig isolates from farm 9 were ≤10 SNPs, indicating a strong association between this outbreak and farm 9 pigs. Both the 2014-outbreak isolates (Env15, Env26-Env30; Fig. 5f) and a 2016-outbreak isolate (Env01, Fig. 5d) had similar genetic distance to their respectively closest pig (≥93 SNPs, 2014; ≥38 SNPs, 2016) and cattle (≥91 SNPs, 2014; ≥49 SNPs, 2016) isolates.
Pan-genome
In total, 8096 genes were found in the pan-genome of the 121 isolates, including 4052 (50.05%) core genes (shared by all 121 isolates) and 4044 (49.95%) accessory genes (present in between 1 and 120 isolates) (Fig. S4). The database for Clusters of Orthologous Groups of proteins (COGs)46 was used to classify the functional categories of each gene in the pan-genome. In total, 745 core and 2871 accessory genes were not classified. Of note, among the classified genes in the accessory genome, category X (mobilome: prophages, transposons) accounted for the largest proportion (38.9%), indicating the large contribution of this category to the plasticity of E. coli O157:H7 genomes.
Virulence genes
Genes encoding Shiga toxin (stx) subtypes 1a, 2a and 2c were found in the 121 STEC O157:H7 genomes, with the patterns of “1a only”, “2a only”, “2c only”, “1a and 2a”, “1a and 2c” (Fig. 6; Table 2). Of the 41 pig isolates, 61% (25) harbored stx2a only and all the other pig isolates (16; 39%) had both stx1a and stx2a, while 33.3% (10) and 66.7% (20) of environmental isolates had stx2a only and stx1a and stx2a, respectively (Table 2). The most abundant pattern among cattle isolates was “1a and 2a” (35, 70%), followed by “1a only” (5, 10%), “2a only” (5, 10%), “1a and 2c” (4, 8%) and “2c only” (1, 2%). The stx profiles correlated with their respective phylogenetic groups (Fig. 6). For example, group 1, 3, 5, and 6 isolates harbored both stx1a and stx2a, while group 2 and group 4 (except isolate Env01 from the 2016-outbreak) had stx2a only.
Besides stx, 319 other virulence genes were found in the genomes (Table S6). The gene eae located on the locus of enterocyte effacement (LEE), encoding intimin, was found in all but Cat48 (Table S6). The gene paa encoding the porcine attaching/effacing-associated protein47 and toxB encoding an adhesion protein48 were absent in only one genome, Cat13. EhaA encoding an autotransporter protein that contributes to adhesion and biofilm formation49 was found in all genomes. The genes saa and lpfA which encode an autoagglutinating adhesion or long polar fimbriae in LEE negative STEC50,51, respectively, were not found in any of the genomes. Three genes encoding potential adhesion proteins c3610, cah, iha52 were absent in all phylogenetic group 2 isolates, but present in most other isolates. α-hemolysin encoding gene ehxA53 was found in all genomes but Cat45. A heat-stable enterotoxin (EAST1) encoding gene astA54 was found in all isolates. Another thermostable enterotoxin gene estIA often found in enteroaggregative E. coli55 or a subtilase cytotoxin encoding gene subA56 was not found in any of the genomes.
Antibiotic resistance
Of the 121 E. coli O157:H7 isolates, 22 (18.2%) were predicted to be resistant to at least one of six classes of antibiotics including aminoglycoside, beta-lactam, phenicol, sulfonamide, tetracycline, and/or trimethoprim (Fig. 6). The 2014-outbreak isolates (group 6) were resistant to aminoglycosides, phenicols, and sulfonamides while the 2016- and 2018-outbreak isolates were predicted not to be resistant to any group of the antibiotics. Group 2 and 7 isolates were resistant to four and three antibiotic classes, respectively. On the contrary, group 1, 3, 4, and 5 isolates, which were associated with farm 1/plant D, farm 7, farm 9, and farm 4/farm 11/plant C, respectively, were predicted not to be resistant to any of the antibiotics examined.
Plasmid sequences
Bacterial plasmids often carry virulence and antibiotic resistance genes57. The program PlasmidFinder58 evaluates a replicon sequence as a signature to identify plasmid sequence-bearing contigs. In total, 11 variants of replicons were found in the genomes, including Col(BS512), Col156, IncFIA, IncFIB(AP001918), IncFII, IncFII(pHN7A8), IncFII(pCoo), IncI2(Delta), IncI1-I(Gamma), IncN, and pEC4115 (Table S7).
All isolates had replicon sequences of IncFIB (AP001918) and IncFII. Isolates Cat02-04 and Cat46 all had IncFIA as well. A Blast screening against the NCBI nucleotide database found that the contigs containing these replicon sequences all had a >99% identity with the megaplasmid, pO157 often present in E. coli O157:H7 genomes59. The pO157 marker gene ehxA and relevant transport protein-encoding genes etpC-O were found in these contigs.
A larger percentage of cattle isolates (26%, 13/50) carried other plasmids/replicons compared to pig isolates (2/41, 4.9%). For pig and environmental isolates, the presence of replicons was related to their phylogenetic group with groups 2, 6, and 7 having Col(BS512) and IncI1-I(Gamma), IncFII(pCoo), IncFII(pCoo) and IncI1-I(Gamma), respectively (Table S7). The IncN replicon in Env18 (recovered from pig feces on farm 11) had resistance genes to four classes of antibiotics including aph(3”)-Ib and aph(6)-Id, blaTEM-1B, sul2, and tet(A) for aminoglycosides, beta-lactams, sulfonamides, and tetracyclines, respectively. The plasmids with IncFII(pCoo) in group 6 isolates harbored genes encoding resistance to aminoglycosides (aadA2b and aadA1), phenicols (cmlA1) and sulfonamides (sul3). For isolates Cat50, Cat31, and Cat24, the plasmids with IncFII(pHN7A8) carried the resistance genes for aminoglycosides (aph(3”)-Ib and aph(6)-Id) and sulfonamides (sul2). However, in the genome of Cat30 the IncFII(pHN7A8)-containing contig only carried aminoglycoside resistance genes (aph(3”)-Ib and aph(6)-Id).
Discussion
This study investigated the phylogenetic relatedness of STEC O157:H7 (n = 121) recovered from pigs, cattle, and pork-production-related environments in Alberta, Canada, using both conventional subtyping schemes and WGS-based methods. To date, a paucity of information on the genetic relationship between cattle and swine STEC strains is available in published accounts. E. coli O157:H7 strains from the two animal species showed distinct randomly amplified polymorphic DNA (RAPD) patterns in a Korean study60, while similar pulsed-field gel electrophoresis (PFGE) patterns were found in a Norwegian study30. The present study observed very limited strain diversity for isolates from both animal species determined by all five conventional subtyping methods: 95%, 95%, 94.2%, 100%, and 100% of the isolates belonging to one Manning clade (2), LPSA lineage (I), MLST type (822; Pasteur Institute’s eight-gene scheme), MLST type (11, Achtman’s seven-gene scheme) or Clermont phylo-group (E). Genetic variation of E. coli O157 can be driven by geographical locations61,62,63,64. Published data reviewed by Pianciola and Rivas63 showed that the most predominant Manning clade of E. coli O157:H7 in the USA, Argentina, and Australia is 2, 8, and 7, respectively. Strachan et al.64 showed the predominant E. coli O157:H7 in Canada between 1995 and 2012 is clade 2, followed by clade 3. LSPA lineage I have been reported to be predominant among cattle E. coli O157:H7 isolates in Canada, followed by lineage II and I/II63, which is consistent with the findings in this study.
The four WGS-based subtyping methods all showed a much higher discriminatory power compared to conventional typing methods, as would be expected. Phylogenetic trees from the former three subtyping methods congruously separated the porcine and environmental isolates mainly into seven phylogenetic groups, with cgMLST having the lowest resolution. However, the gene content analysis further separated group 1 and group 4 into two subgroups, with different positioning for some isolates, and divided clonal isolates, especially in the phylogenetic trees based on SNP and cgMLST analysis into well-defined branches. SNP analysis uses the genome of a closely related bacterial strain as a reference and infers phylogeny among bacterial strains based on the variants in both intragenic and intergenic regions shared by both reference and query genomes34. On the other hand, cgMLST and wgMLST analyze the allelic difference of genes in the core (cgMLST) and pan (wgMLST) genomes, respectively34. For both cgMLST and wgMLST, the missing alleles are ignored in pairwise comparison and one allelic difference is counted for a given gene if two genomes have different alleles no matter how many SNPs are found in this gene. The difference in discriminatory power of SNP and cg/wgMLST was then to be expected. A gene content-based method infers the phylogeny based on the presence or absence of genes in the pan-genome of included bacterial strains and hence reflects difference in the accessory genome rather than the core genome36,37. The differences between the accessory genome tree (gene content analysis) and core genome trees (SNP and cgMLST) are in agreement with the previous observations on the plasticity of E. coli genomes, with horizontal gene transfer being the primary driving force for the evolution of E. coli37,65. The observation that some cattle isolates (e.g. Cat07 and Cat18) intermingled with pig isolates suggest that those pig isolates may have originated from cattle or a common source with cattle isolates, and that a subgroup of cattle isolates may have acquired accessory genomes to adapt to the pig gut environment.
Pightling et al.45 suggested a cutoff value of 21 and 100 SNPs for defining clonal strains and possibly related strains of E. coli for outbreak investigations. All porcine and environmental isolates had genetic distance of <100 SNPs with at least one cattle isolate included in this study, suggesting the recent common ancestry shared between E. coli O157:H7 from both animal species. This is consistent with the low strain diversity observed by conventional subtyping methods. The genetic differences among isolates within each phylogenetic group of pig and environmental isolates are mostly less than 20 SNPs. A large number of clonal STEC O157:H7 strains, as determined by SNP analysis, were frequently recovered from pigs (farm 9, ≤13 SNPs; farm 1, ≤7 SNPs). The prevalence of STEC O157:H7 in pigs is low in most geographical areas globally and whether swine are competent carriers of this pathogen has long been debated9. A study carried out by Wöchtl and co-workers66 reported clinical symptoms including diarrhea, dehydration, and neurological disorders in piglets infected with STEC O157:H7. In contrast, Booher et al.67 found pigs can be persistently colonized by STEC O157:H7 for >2 months. The repeated recovery of the clonal strain of STEC O157 from pigs on individual farms over an extended period of time in the present study supports the latter of the two studies. The 2018-outbreak isolates and pig isolates from farm 9 differed by less than 10 SNPs. To the authors’ best knowledge, a direct link between STEC O157:H7 of pig origin and an outbreak found in this study was not reported before. The 2016-outbreak isolates and farm 9 isolates recovered in 2018 may share a recent common ancestor as they differed only by 38–46 SNPs. In addition, most (66.7%, 20/30) environmental isolates are more closely related to pig isolates than cattle isolates. These findings suggest that pigs can be a significant source of STEC O157 contamination on pork and in pork-production environments.
Shiga toxins, carried by prophages, are the defining feature of STEC. There are two types of Shiga toxins, Stx1 and Stx2, each further divided into several subtypes (Stx1a and Stx1c-1e; Stx2a-2i, Stx2k, and Stx2l) based on the serological reaction and the amino acid sequence1. Stx2e can cause edema disease in pigs68. In general, Stx2 is more associated with the human disease than Stx1, with the subtype Stx2a being often associated with patients with HUS than other subtypes1,69,70,71. A study of Chui et al.72 reported negative interactions between Stx1a and Stx2a, proposing that STEC O157 isolates carrying only Stx2a are more virulent than those with both Stx1 and Stx2a. The cattle and pig/environmental isolates had different stx gene profiles. The cattle isolates mostly carried stx1a and stx2a, and this agrees with previous reports on the stx profile of STEC O157 recovered from Alberta cattle73. On the other hand, most pig isolates carried stx2a only. An Indonesian study reported that STEC O157:H7 from pigs (n = 7) all had stx2a74; however, only stx2a was examined in that study. There are a total of 14 genomes of STEC O157:H7 pig isolates deposited in GenBank (2 from China and 12 from USA), with six, six, and two of the isolates having both stx1a and stx2a, stx2c and stx1a, respectively (Table S8). Studies reporting the recovery of STEC O157:H7 from pigs are very limited. A number of studies on non-O157 STEC from pigs found stx2e to be the predominant stx subtype9,19,75,76. The eae gene was present in all of the isolates included in this study except for Cat48, which is in agreement with the prevalence of this gene in STEC O157 in published accounts73,77,78,79,80,81,82,83. All the isolates have the gene ehxA, located on the megaplasmid pO15759. In addition, most of the STEC O157:H7 isolates also harbor additional genes involved in intestinal adhesion (e.g. paa, toxB, and ehaA), encoding other toxins (e.g. astA), involved in type II/III secretion system, and encoding fimbrial proteins. The distribution of these virulence genes does not seem to be associated with origin of isolation, i.e., pigs, cattle, or environment.
Only one (Pig04) of the 41 pig STEC O157 isolates was predicted to be antibiotic-resistant. On the contrary, a relatively larger proportion of cattle isolates, 8/50, harbored antibiotic resistance genes. Resistance to at least two antibiotic classes have been found for 16% of O157 isolates from Alberta feedlots cattle84. Among non-type specific E. coli recovered from cattle in Alberta feedlots, the resistance to tetracyclines, aminoglycosides (represented by streptomycin), and sulfonamides (represented by sulfisoxazole) have been the most commonly detected85. The pattern of antibiotic resistance in environmental isolates was closely related to the phylogenetic group, with group 2, 6, and 7 isolates and Env18 (from pig feces on farm 11) predicted to be resistant to at least one type of antibiotics. This suggests potential cross-contamination between two animal species as plant B processed both pork and beef and farm 10 had both cattle and swine during the period in which the isolates were recovered.
Unlike the plasmid pO157, other plasmids carried by E. coli O157:H7 are not well studied. Rusconi et al.38 investigated the plasmids in STEC O157:H7 associated with seven outbreaks in the USA and found plasmids of the incompatible groups IncI1, IncI2, IncK, IncFII, and pEC4115. The preliminary analysis in this study found the plasmids with replicon sequences Col (BS512), Col156, IncFII (pHN7A8), IncFII (pCoo), IncI2 (Delta), IncI1-I(Gamma), IncN and pEC4115 in STEC O157:H7 isolates, with IncN, IncFII (pCoo) and IncFII (pHN7A8) plasmids carrying genes resistant to four, three and two/one classes of antibiotics including aminoglycosides, beta-lactams, sulfonamides, tetracyclines, and phenicols. Similar to the present pattern of antibiotic resistance genes, a larger proportion of cattle isolates carried additional plasmid(s).
In conclusion, pig and pork-production environmental STEC O157:H7 isolates were classified mainly into seven distinct yet related phylogenetic groups, with each group primarily associated with the specific farm(s)/plant(s). The results demonstrated that some STEC O157:H7 strains originating from pigs can establish persistence on farms, and that pigs can be a significant source for STEC O157:H7 to contaminate pork, and of the environmental dissemination. Different antibiotic resistance and stx profiles were observed for STEC O157:H7 isolates originating from Alberta cattle and pigs, with strains from the latter having a higher proportion of the more virulent stx2a subtype.
Methods
Bacterial isolates
A total of 121 STEC O157:H7 isolates from pigs (n = 41; Pig01-41), pork-production environments (n = 30; Env01-30), and cattle (n = 50; Cat01-50) in Alberta, Canada, were included in this study15,86,87,88,89,90,91,92,93,94 (Stanford et al., unpublished data; Reuter et al., unpublished data; Keenliside et al., unpublished data) (Table S1). Pig and cattle isolates were recovered from fecal samples of pigs and cattle, respectively. The environmental isolates were recovered from various types of samples collected from the pork production and distribution environments including retailers, pork processing facilities, and pig barns/lagoons. Among the environmental isolates, Env15 and Env26-Env30 (2014 outbreak), Env01 (2016), and Env02-Env05 (2018) were associated with the three E. coli O157:H7 outbreaks attributed to contaminated pork in Alberta. Cattle isolates were recovered from the feces of cattle from various feedlots or at two slaughter plants in Alberta, Canada between 2002 and 2015. The pig and environmental isolates were from 11 farms (1–11) and four meat processing plants (A-D) between 2014 and 2018. We sequenced the genomes of Pig01-41, Cat01-12, Cat14-19, Cat21-23, Cat25-41, and Env01-2595. The genomes of Cat13, Cat20, Cat24, and Cat42-5087,89 were downloaded from the National Center for Biotechnology Information (NCBI) GenBank database. For Env26-3093, the raw sequencing data were downloaded from GenBank and assembled as described by Zhang, et al.95.
Conventional genotyping using WGS data
To determine the Manning clade of the isolates, the SNPs in four target genes including ECs2357, ECs2521, ECs3881, and ECs4130 were analyzed96. The clade for each isolate was then assigned as described previously96. For LSPA lineage, a perl script (https://github.com/egonozer/in_silico_pcr) and the primers designed by Yang et al.41. were used to perform in silico PCR. For MLST, mlst (https://github.com/tseemann/mlst) was used, with both Achtman’s seven-gene scheme and Pasteur Institute’s eight-gene scheme. The Clermont E. coli phylo-typing42, which assigns phylo-group to E. coli based on the presence/absence of the genes arpA, chuA, and yjaA and an anonymous DNA fragment TspE4.C2, was also performed.
Whole-genome SNP analysis and core SNP tree
For SNP analysis, Snippy 4.4.0 (https://github.com/tseemann/snippy) was used with the complete genome of EDL933 (ATCC 43895) as a reference (GenBank Accession no.: chromosome: CP008957.1, plasmid: CP008958.1)43. For all isolates except Cat13, Cat20, Cat24, and Cat42-Cat50, trimmed sequencing reads were used as input for “snippy” with default settings. The isolates Cat13, Cat20, Cat24, and Cat42-Cat50 only had genome sequences available, and as such, –contigs options were used for “snippy”. The contig-option shreds the contigs into synthetic reads and calls SNPs based on the generated reads. The recombination sites in the alignment file were removed using Gubbins97. Pairwise SNP distance matrix was generated using snp-dists (https://github.com/tseemann/snp-dists). A best-scoring maximum likelihood tree based on core SNP alignment was constructed using RAxML version 8 with general time reversible gamma nucleotide model (GTRGAMMA) and 100 times of bootstrap analyses98. iTOL v499 and the ggtree package100 in R were both used to display and annotate the phylogenetic tree.
cgMLST and wgMLST
ChewBBACA101 was used to perform both cgMLST and wgMLST. The published Escherichia schemes were downloaded from Enterobase (http://enterobase.warwick.ac.uk/schemes/). Both schemes were respectively adapted to chewBBACA and loci which did not meet the following criteria were removed: both valid start and stop codons were present in the coding sequence; the sequence length must be a multiple of 3; the sequence does not contain ambiguous character, i.e. containing ATGC only. The final schemes included 2513 and 24952 genes for cgMLST and wgMLST, respectively. The alleles were called with the default settings in chewBBACA. Neighbor joining trees were generated using GrapeTree102 based on the allele profiles of cgMLST and wgMLST, respectively, with the missing alleles ignored for pairwise comparison.
Pan-genome analysis and gene content tree
The 121 genomes were annotated using Prokka v1.13.7103. The pan-genome of the isolates was parsed using Roary104, with the identity threshold to cluster proteins set at 90%. The functional category of the annotated coding sequences was assigned as described by Zhang et al.105. The Jaccard distances based on the presence or absence of genes between genomes were calculated using the dist() function in R with the method option set at “binary”106. A neighbor-joining tree was created using phangorn package107 in R.
Comparison of WGS-based subtyping methods
To compare the four WGS subtyping methods, the distance matrices from four methods were used to generate UPGMA dendrograms via the hclust() function in R. For pairwise visual comparison, tanglegrams were created using the dendextend package in R. Cophenetic correlation coefficient was calculated for each pair of trees. To provide statistical support for the correlation, a permutation test was performed for each combination to produce one-sided P values. If P < 0.05, the similarity between two trees was regarded statistically significant.
Virulence and antibiotic resistance genes
The presence of stx and their subtypes were determined using the webserver of the Center for Genomic Epidemiology (CGE) (https://cge.cbs.dtu.dk/services/VirulenceFinder/) with 90% as the threshold for identity and 80% for the minimum coverage, respectively108. For other virulence genes, the reference database ecoli_vf (June 15, 2020; https://github.com/phac-nml/ecoli_vf) and the virulence gene database (version, 2020-05-29) from CGE were both used. ABRicate v1.0.1 (https://github.com/tseemann/abricate) was used to scan the contig sequences of each genome against the reference databases. A match with >80% coverage and >90% identity was regarded as positive. Antibiotic resistance genes and plasmid sequences were identified using ResFinder109 and PlasmidFinder58 in CGE, respectively.
Data availability
The authors declare that the data supporting the findings of this study are presented within the manuscript and supplementary files. The raw sequencing data and genome sequences can be found at: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA661559.
Change history
19 July 2021
A Correction to this paper has been published: https://doi.org/10.1038/s41538-021-00104-4
References
Gill, A. et al. Review of the state of knowledge on verotoxigenic Escherichia coli and the role of whole genome sequencing as an emerging technology supporting regulatory food safety in Canada. (2020).
Thorpe, C. M. Shiga toxin-producing Escherichia coli infection. Clin. Infect. Dis. 38, 1298–1303 (2004).
Valilis, E., Ramsey, A., Sidiq, S. & DuPont, H. L. Non-O157 Shiga toxin-producing Escherichia coli-A poorly appreciated enteric pathogen: systematic review. Int. J. Infect. Dis. 76, 82–87 (2018).
Karmali, M. A., Steele, B. T., Petric, M. & Lim, C. Sporadic cases of haemolytic-uraemic syndrome associated with faecal cytotoxin and cytotoxin-producing Escherichia coli in stools. Lancet 1, 619–620 (1983).
O’Brien, A. O., Lively, T. A., Chen, M. E., Rothman, S. W. & Formal, S. B. Escherichia coli O157:H7 strains associated with haemorrhagic colitis in the United States produce a Shigella dysenteriae 1 (SHIGA) like cytotoxin. Lancet 1, 702 (1983).
Gill, A. & Gill, C. O. Non-O157 verotoxigenic Escherichia coli and beef: a Canadian perspective. Can. J. Vet. Res 74, 161–169 (2010).
Heiman, K. E., Mody, R. K., Johnson, S. D., Griffin, P. M. & Gould, L. H. Escherichia coli O157 outbreaks in the United States, 2003–2012. Emerg. Infect. Dis. 21, 1293–1301 (2015).
Callaway, T. R., Carr, M. A., Edrington, T. S., Anderson, R. C. & Nisbet, D. J. Diet, Escherichia coli O157:H7, and cattle: a review after 10 years. Curr. Issues Mol. Biol. 11, 67–79 (2009).
Tseng, M., Fratamico, P. M., Manning, S. D. & Funk, J. A. Shiga toxin-producing Escherichia coli in swine: the public health perspective. Anim. Health Res. Rev. 15, 63–75 (2014).
Waddell, T. E., Coomber, B. L. & Gyles, C. L. Localization of potential binding sites for the edema disease verotoxin (VT2e) in pigs. Can. J. Vet. Res. 62, 81–86 (1998).
Omer, M. K. et al. A systematic review of bacterial foodborne outbreaks related to red meat and meat products. Foodborne Pathog. Dis. 15, 598–611 (2018).
Honish, L. et al. Escherichia coli O157:H7 infections associated with contaminated pork products - Alberta, Canada, July–October 2014. Mmwr. Morbidity Mortal. Wkly. Rep. 65, 1477–1481 (2017).
AHS. E. coli outbreak linked to certain pork products in Alberta declared over, https://www.albertahealthservices.ca/news/releases/2018/Page14457.aspx (2018).
News, F. S. Alberta outbreak prompts raw pork and pork organ recall, https://www.foodsafetynews.com/2016/02/alberta-e-coli-outbreak-prompts-raw-pork-and-pork-organ-recall/ (2016).
Essendoubi, S. et al. Prevalence and characterization of Escherichia coli O157:H7 on pork carcasses and in swine colon content from provincially-licensed abattoirs in Alberta, Canada. J Food Prot, (2020).
Colello, R. et al. From farm to table: follow-up of Shiga toxin-producing Escherichia coli throughout the pork production chain in Argentina. Front Microbiol. 7, 93 (2016).
Tseng, M., Fratamico, P. M., Bagi, L., Manzinger, D. & Funk, J. A. Shiga toxin-producing E. coli (STEC) in swine: prevalence over the finishing period and characteristics of the STEC isolates. Epidemiol. Infect. 143, 505–514 (2015).
Rajkhowa, S. & Sarma, D. K. Prevalence and antimicrobial resistance of porcine O157 and non-O157 Shiga toxin-producing Escherichia coli from India. Trop. Anim. Health Prod. 46, 931–937 (2014).
Meng, Q. et al. Characterization of Shiga toxin-producing Escherichia coli isolated from healthy pigs in China. BMC Microbiol 14, 5 (2014).
Ho, W. S., Tan, L. K., Ooi, P. T., Yeo, C. C. & Thong, K. L. Prevalence and characterization of verotoxigenic-Escherichia coli isolates from pigs in Malaysia. BMC Vet. Res. 9, 109 (2013).
Choi, Y. M. et al. Changes in microbial contamination levels of porcine carcasses and fresh pork in slaughterhouses, processing lines, retail outlets, and local markets by commercial distribution. Res. Vet. Sci. 94, 413–418 (2013).
Farzan, A., Friendship, R. M., Cook, A. & Pollari, F. Occurrence of Salmonella, Campylobacter, Yersinia enterocolitica, Escherichia coli O157 and Listeria monocytogenes in swine. Zoonoses Public Health 57, 388–396 (2010).
Lenahan, M. et al. The potential use of chilling to control the growth of Enterobacteriaceae on porcine carcasses and the incidence of E. coli O157:H7 in pigs. J. Appl. Microbiol. 106, 1512–1520 (2009).
Milnes, A. S. et al. Factors related to the carriage of Verocytotoxigenic E. coli, Salmonella, thermophilic Campylobacter and Yersinia enterocolitica in cattle, sheep and pigs at slaughter. Epidemiol. Infect. 137, 1135–1148 (2009).
Kaufmann, M. et al. Escherichia coli O157 and non-O157 Shiga toxin-producing Escherichia coli in fecal samples of finished pigs at slaughter in Switzerland. J. Food Prot. 69, 260–266 (2006).
Fratamico, P. M., Bagi, L. K., Bush, E. J. & Solow, B. T. Prevalence and characterization of Shiga toxin-producing Escherichia coli in swine feces recovered in the National Animal Health Monitoring System’s Swine 2000 study. Appl Environ. Microbiol 70, 7173–7178 (2004).
Bonardi, S. et al. Detection of Salmonella spp., Yersinia enterocolitica and verocytotoxin-producing Escherichia coli O157 in pigs at slaughter in Italy. Int J. Food Microbiol 85, 101–110 (2003).
Eriksson, E., Nerbrink, E., Borch, E., Aspan, A. & Gunnarsson, A. Verocytotoxin-producing Escherichia coli O157:H7 in the Swedish pig population. Vet. Rec. 152, 712–717 (2003).
Feder, I. et al. Isolation of Escherichia coli O157:H7 from intact colon fecal samples of swine. Emerg. Infect. Dis. 9, 380–383 (2003).
Johnsen, G., Wasteson, Y., Heir, E., Berget, O. I. & Herikstad, H. Escherichia coli O157:H7 in faeces from cattle, sheep and pigs in the southwest part of Norway during 1998 and 1999. Int J. Food Microbiol 65, 193–200 (2001).
Leung, P. H., Yam, W. C., Ng, W. W. & Peiris, J. S. The prevalence and characterization of verotoxin-producing Escherichia coli isolated from cattle and pigs in an abattoir in Hong Kong. Epidemiol. Infect. 126, 173–179 (2001).
Nakazawa, M. & Akiba, M. Swine as a potential reservoir of Shiga toxin-producing Escherichia coli O157:H7 in Japan. Emerg. Infect. Dis. 5, 833–834 (1999).
Chapman, P. A., Siddons, C. A., Gerdan Malo, A. T. & Harkin, M. A. A 1-year study of Escherichia coli O157 in cattle, sheep, pigs and poultry. Epidemiol. Infect. 119, 245–250 (1997).
Tang, S. et al. Assessment and comparison of molecular subtyping and characterization methods for Salmonella. Front Microbiol. 10, 1591 (2019).
Schurch, A. C., Arredondo-Alonso, S., Willems, R. J. L. & Goering, R. V. Whole genome sequencing options for bacterial strain typing and epidemiologic analysis based on single nucleotide polymorphism versus gene-by-gene-based approaches. Clin. Microbiol Infect. 24, 350–354 (2018).
McNally, A. et al. Combined analysis of variation in core, accessory and regulatory genome regions provides a super-resolution view into the evolution of bacterial populations. PLoS Genet. 12, e1006280 (2016).
Kaas, R. S., Friis, C., Ussery, D. W. & Aarestrup, F. M. Estimating variation within the genes and inferring the phylogeny of 186 sequenced diverse Escherichia coli genomes. BMC Genomics 13, 577 (2012).
Rusconi, B. et al. Whole genome sequencing for genomics-guided investigations of Escherichia coli O157:H7 outbreaks. Front Microbiol 7, 985 (2016).
Rumore, J. et al. Evaluation of whole-genome sequencing for outbreak detection of Verotoxigenic Escherichia coli O157:H7 from the Canadian perspective. BMC Genomics 19, 870 (2018).
Manning, S. D. et al. Variation in virulence among clades of Escherichia coli O157:H7 associated with disease outbreaks. Proc. Natl Acad. Sci. USA 105, 4868–4873 (2008).
Yang, Z. et al. Identification of common subpopulations of non-sorbitol-fermenting, beta-glucuronidase-negative Escherichia coli O157:H7 from bovine production environments and human clinical samples. Appl Environ. Microbiol. 70, 6846–6854 (2004).
Clermont, O., Christenson, J. K., Denamur, E. & Gordon, D. M. The Clermont Escherichia coli phylo-typing method revisited: improvement of specificity and detection of new phylo-groups. Environ. Microbiol Rep. 5, 58–65 (2013).
Latif, H., Li, H. J., Charusanti, P., Palsson, B. O. & Aziz, R. K. A gapless, unambiguous genome sequence of the enterohemorrhagic Escherichia coli O157:H7 strain EDL933. Genome Announc. 2, e00821-14 (2014).
Sokal, R. R. & Rohlf, F. J. The comparison of dendrograms by objective methods. Taxon 11, 33–40, (1962).
Pightling, A. W. et al. Interpreting whole-genome sequence analyses of foodborne bacteria for regulatory applications and outbreak investigations. Front Microbiol. 9, 1482 (2018).
Galperin, M. Y., Makarova, K. S., Wolf, Y. I. & Koonin, E. V. Expanded microbial genome coverage and improved protein family annotation in the COG database. Nucleic acids Res. 43, D261–269 (2015).
Batisson, I. et al. Characterization of the novel factor paa involved in the early steps of the adhesion mechanism of attaching and effacing Escherichia coli. Infect. Immun. 71, 4516–4525 (2003).
Tatsuno, I. et al. toxB gene on pO157 of enterohemorrhagic Escherichia coli O157:H7 is required for full epithelial cell adherence phenotype. Infect. Immun. 69, 6660–6669 (2001).
Wells, T. J. et al. EhaA is a novel autotransporter protein of enterohemorrhagic Escherichia coli O157:H7 that contributes to adhesion and biofilm formation. Environ. Microbiol. 10, 589–604 (2008).
Paton, A. W., Srimanote, P., Woodrow, M. C. & Paton, J. C. Characterization of Saa, a novel autoagglutinating adhesin produced by locus of enterocyte effacement-negative Shiga-toxigenic Escherichia coli strains that are virulent for humans. Infect. Immun. 69, 6999–7009 (2001).
Galli, L., Torres, A. G. & Rivas, M. Identification of the long polar fimbriae gene variants in the locus of enterocyte effacement-negative Shiga toxin-producing Escherichia coli strains isolated from humans and cattle in Argentina. FEMS Microbiol Lett. 308, 123–129 (2010).
Tarr, P. I. et al. Iha: a novel Escherichia coli O157:H7 adherence-conferring molecule encoded on a recently acquired chromosomal island of conserved structure. Infect. Immun. 68, 1400–1407 (2000).
Stanley, P., Koronakis, V. & Hughes, C. Acylation of Escherichia coli hemolysin: a unique protein lipidation mechanism underlying toxin function. Microbiol Mol. Biol. Rev. 62, 309–333 (1998).
Veilleux, S. & Dubreuil, J. D. Presence of Escherichia coli carrying the EAST1 toxin gene in farm animals. Vet. Res 37, 3–13 (2006).
Savarino, S. J. et al. Enteroaggregative Escherichia coli heat-stable enterotoxin 1 represents another subfamily of E. coli heat-stable toxin. Proc. Natl Acad. Sci. USA 90, 3093–3097 (1993).
Paton, A. W., Srimanote, P., Talbot, U. M., Wang, H. & Paton, J. C. A new family of potent AB(5) cytotoxins produced by Shiga toxigenic Escherichia coli. J. Exp. Med 200, 35–46 (2004).
Thomas, C. M. & Summers, D. Encyclopedia of life sciences. (John Wiley & Sons, Ltd, 2008).
Carattoli, A. et al. In silico detection and typing of plasmids using PlasmidFinder and plasmid multilocus sequence typing. Antimicrob. Agents Chemother. 58, 3895–3903 (2014).
Lim, J. Y., Yoon, J. & Hovde, C. J. A brief overview of Escherichia coli O157:H7 and its plasmid O157. J. Microbiol Biotechnol. 20, 5–14 (2010).
Kim, J. Y. et al. Isolation and identification of Escherichia coli O157:H7 using different detection methods and molecular determination by multiplex PCR and RAPD. J. Vet. Sci. 6, 7–19 (2005).
Jaros, P. et al. Geographic divergence of bovine and human Shiga toxin–producing Escherichia coli O157: H7 genotypes. NZ 20, 1980 (2014).
Mellor, G. E. et al. Geographically distinct Escherichia coli O157 isolates differ by lineage, Shiga toxin genotype, and total shiga toxin production. J. Clin. Micro. 53, 579–586 (2015).
Pianciola, L. & Rivas, M. Genotypic features of clinical and bovine Escherichia coli O157 strains isolated in countries with different associated-disease incidences. Microorganisms 6, 36 (2018).
Strachan, N. J. et al. Whole genome sequencing demonstrates that geographic variation of Escherichia coli O157 genotypes dominates host association. Sci. Rep. 5, 14145 (2015).
Touchon, M. et al. Organised genome dynamics in the Escherichia coli species results in highly diverse adaptive paths. PLoS Genet. 5, e1000344 (2009).
Wochtl, B. et al. Comparison of clinical and immunological findings in gnotobiotic piglets infected with Escherichia coli O104:H4 outbreak strain and EHEC O157:H7. Gut Pathog. 9, 30 (2017).
Booher, S. L., Cornick, N. A. & Moon, H. W. Persistence of Escherichia coli O157:H7 in experimentally infected swine. Vet. Microbiol. 89, 69–81 (2002).
Moxley, R. A. Edema disease. Vet. Clin. North Am. Food Anim. Pr. 16, 175–185 (2000).
Melton-Celsa, A. R. Shiga toxin (Stx) classification, structure, and function. Microbiol Spectr. 2, EHEC-0024-2013 (2014).
Fuller, C. A., Pellino, C. A., Flagler, M. J., Strasser, J. E. & Weiss, A. A. Shiga toxin subtypes display dramatic differences in potency. Infect. Immun. 79, 1329–1337 (2011).
Tesh, V. L. et al. Comparison of the relative toxicities of Shiga-like toxins type I and type II for mice. Infect. Immun. 61, 3392–3402 (1993).
Tarr, G. A. M. et al. Contribution and interaction of Shiga toxin genes to Escherichia coli O157:H7 virulence. Toxins (Basel) 11, 607 (2019).
Chui, L. et al. Molecular profiling of Escherichia coli O157:H7 and non-O157 strains isolated from humans and cattle in Alberta, Canada. J. Clin. Microbiol. 53, 986–990 (2015).
Goma, M. K. E., Indraswari, A., Haryanto, A. & Widiasih, D. A. Detection of Escherichia coli O157:H7 and Shiga toxin 2a gene in pork, pig feces, and clean water at Jagalan slaughterhouse in Surakarta, Central Java Province, Indonesia. Vet. World 12, 1584–1590 (2019).
Baranzoni, G. M. et al. Characterization of Shiga toxin subtypes and virulence genes in porcine Shiga toxin-producing Escherichia coli. Front Microbiol. 7, 574 (2016).
Mohlatlole, R. P. et al. Virulence profiles of enterotoxigenic, Shiga toxin and enteroaggregative Escherichia coli in South African pigs. Trop. Anim. Health Prod. 45, 1399–1405 (2013).
Blanco, M. et al. Serotypes, virulence genes, and intimin types of Shiga toxin (verotoxin)-producing Escherichia coli isolates from cattle in Spain and identification of a new intimin variant gene (eae-xi). J. Clin. Microbiol. 42, 645–651 (2004).
Kobayashi, N. et al. Virulence gene profiles and population genetic analysis for exploration of pathogenic serogroups of Shiga toxin-producing Escherichia coli. J. Clin. Microbiol. 51, 4022–4028 (2013).
Meng, J., Zhao, S. & Doyle, M. P. Virulence genes of Shiga toxin-producing Escherichia coli isolated from food, animals and humans. Int J. Food Microbiol 45, 229–235 (1998).
Mora, A. et al. Phage types, virulence genes and PFGE profiles of Shiga toxin-producing Escherichia coli O157:H7 isolated from raw beef, soft cheese and vegetables in Lima (Peru). Int J. Food Microbiol. 114, 204–210 (2007).
Sallam, K. I., Mohammed, M. A., Ahdy, A. M. & Tamura, T. Prevalence, genetic characterization and virulence genes of sorbitol-fermenting Escherichia coli O157:H- and E. coli O157:H7 isolated from retail beef. Int J. Food Microbiol 165, 295–301 (2013).
Solomakos, N. et al. Occurrence, virulence genes and antibiotic resistance of Escherichia coli O157 isolated from raw bovine, caprine and ovine milk in Greece. Food Microbiol. 26, 865–871 (2009).
Tóth, I. et al. Virulence genes and molecular typing of different groups of Escherichia coli O157 strains in cattle. Appl. Environ. Microbiol. 75, 6282 (2009).
Rao, S. et al. Antimicrobial drug use and antimicrobial resistance in enteric bacteria among cattle from Alberta feedlots. Foodborne Pathog. Dis. 7, 449–457 (2010).
Benedict, K. M. et al. Antimicrobial resistance in Escherichia coli recovered from feedlot fattle and associations with antimicrobial use. PLoS ONE 10, e0143995 (2015).
Stanford, K., Johnson, R. P., Alexander, T. W., McAllister, T. A. & Reuter, T. Influence of season and feedlot location on prevalence and virulence factors of seven serogroups of Escherichia coli in feces of western-Canadian slaughter cattle. PLoS ONE 11, e0159866 (2016).
Mercer, R. G. et al. Genetic determinants of heat resistance in Escherichia coli. Front Microbiol. 6, 932 (2015).
Stanford, K. et al. Monitoring Escherichia coli O157:H7 in inoculated and naturally colonized feedlot cattle and their environment. J. Food Prot. 68, 26–33 (2005).
Munns, K. D. et al. Comparative genomic analysis of Escherichia coli O157:H7 isolated from super-shedder and low-shedder cattle. PLoS ONE 11, e0151673 (2016).
Bach, S. J. et al. Electrolyzed oxidizing anode water as a sanitizer for use in abattoirs. J. Food Prot. 69, 1616–1622 (2006).
Stanford, K., Gibb, D. & McAllister, T. A. Evaluation of a shelf-stable direct-fed microbial for control of Escherichia coli O157 in commercial feedlot cattle. Can. J. Anim. Sci. 93, 535–542 (2013).
Stanford, K., Hannon, S., Booker, C. W. & Jim, G. K. Variable efficacy of a vaccine and direct-fed microbial for controlling Escherichia coli O157:H7 in feces and on hides of feedlot cattle. Foodborne Pathog. Dis. 11, 379–387 (2014).
Berenger, B. M. et al. The utility of multiple molecular methods including whole genome sequencing as tools to differentiate Escherichia coli O157:H7 outbreaks. Euro Surveill. 20, 30073 (2015).
Stephens, T. P., McAllister, T. A. & Stanford, K. Perineal swabs reveal effect of super shedders on the transmission of Escherichia coli O157:H7 in commercial feedlots. J. Anim. Sci. 87, 4151–4160 (2009).
Zhang, P. et al. Genome sequences of 104 Escherichia coli O157:H7 isolates from pigs, cattle, and pork production environments in Alberta, Canada. Microbiol. Resour. Announc. 10, (2021).
Riordan, J. T., Viswanath, S. B., Manning, S. D. & Whittam, T. S. Genetic differentiation of Escherichia coli O157:H7 clades associated with human disease by real-time PCR. J. Clin. Microbiol. 46, 2070–2073 (2008).
Croucher, N. J. et al. Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins. Nucleic Acids Res. 43, e15–e15 (2014).
Stamatakis, A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinforma. (Oxf., Engl.) 30, 1312–1313 (2014).
Letunic, I. & Bork, P. Interactive Tree Of Life (iTOL) v4: recent updates and new developments. Nucleic acids Res. 47, W256–W259 (2019).
Yu, G. Using ggtree to visualize data on tree-like structures. Curr. Protoc. Bioinform. 69, e96 (2020).
Silva, M. et al. chewBBACA: A complete suite for gene-by-gene schema creation and strain identification. Micro. Genom. 4, e000166 (2018).
Zhou, Z. et al. GrapeTree: visualization of core genomic relationships among 100,000 bacterial pathogens. Genome Res. 28, 1395–1404 (2018).
Seemann, T. Prokka: rapid prokaryotic genome annotation. Bioinformatics (Oxf., Engl.) 30, 2068–2069 (2014).
Page, A. J. et al. Roary: rapid large-scale prokaryote pan genome analysis. Bioinformatics (Oxf., Engl.) 31, 3691–3693 (2015).
Zhang, P., Gänzle, M. & Yang, X. Complementary antibacterial effects of bacteriocins and organic acids as revealed by comparative analysis of Carnobacterium spp. from meat. Appl. Environ. Microbiol. 85, e01227-19 (2019).
Zheng, J., Zhao, X., Lin, X. B. & Ganzle, M. Comparative genomics Lactobacillus reuteri from sourdough reveals adaptation of an intestinal symbiont to food fermentations. Sci. Rep. 5, 18234 (2015).
Schliep, K., Potts, A. J., Morrison, D. A. & Grimm, G. W. Intertwining phylogenetic trees and networks. Methods Ecol. Evol. 8, 1212–1220 (2017).
Joensen, K. G. et al. Real-time whole-genome sequencing for routine typing, surveillance, and outbreak detection of verotoxigenic Escherichia coli. J. Clin. Microbiol. 52, 1501–1510 (2014).
Bortolaia, V. et al. ResFinder 4.0 for predictions of phenotypes from genotypes. J. Antimicrob. Chemother. 75, 3491–3500 (2020).
Acknowledgements
Alberta Agriculture and Forestry and Alberta Innovates are acknowledged for funding (2019F108R). Dr. Lisa Tymensen and Dr. Gary Gensler are acknowledged for their assistance on project planning and bacteria shipping. The bioinformatics analysis was performed using the high performance computing servers hosted by Agriculture and Agri-Food Canada through the Biocluster and Compute Canada.
Author information
Authors and Affiliations
Contributions
PZ: formal analysis, methodology and writing the original draft; SE: conceptualization, funding acquisition, and review and editing manuscript; JK: funding acquisition, and review and editing manuscript; TR: funding acquisition, methodology, and review and editing manuscript; KS: funding acquisition, methodology, and review and editing manuscript; RK: methodology and review and editing manuscript; PL: methodology and review and editing manuscript; XY: conceptualization, funding acquisition, supervision, project administration, and review and editing manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Zhang, P., Essendoubi, S., Keenliside, J. et al. Genomic analysis of Shiga toxin-producing Escherichia coli O157:H7 from cattle and pork-production related environments. npj Sci Food 5, 15 (2021). https://doi.org/10.1038/s41538-021-00097-0
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41538-021-00097-0