National Microbiology Laboratory, Public Health Agency of Canada, Lethbridge, Alberta, Canada.
Alberta Agriculture and Forestry, Lethbridge, Alberta, Canada.
Microb Genom. 2020 Jun;6(6). doi: 10.1099/mgen.0.000376. Epub 2020 Jun 3.
Verotoxigenic (VTEC) are food- and water-borne pathogens associated with both sporadic illness and outbreaks of enteric disease. While it is known that cattle are reservoirs of VTEC, little is known about the genomic variation of VTEC in cattle, and whether the variation in genomes reported for human outbreak strains is consistent with individual animal or group/herd sources of infection. A previous study of VTEC prevalence identified serotypes carried persistently by three consecutive cohorts of heifers within a closed herd of cattle. This present study aimed to: (i) determine whether the genomic relatedness of bovine isolates is similar to that reported for human strains associated with single source outbreaks, (ii) estimate the rates of genome change among dominant serotypes over time within a cattle herd, and (iii) identify genomic features of serotypes associated with persistence in cattle. Illumina MiSeq genome sequencing and genotyping based on allelic and single nucleotide variations were completed, while genome change over time was measured using Bayesian evolutionary analysis sampling trees. The accessory genome, including the non-protein-encoding intergenic regions (IGRs), virulence factors, antimicrobial-resistance genes and plasmid gene content of representative persistent and sporadic cattle strains were compared using Fisher's exact test corrected for multiple comparisons. Herd strains from serotypes O6:H34 (=22), O22:H8 (=30), O108:H8 (=39), O139:H19 (=44) and O157:H7 (=106) were readily distinguishable from epidemiologically unrelated strains of the same serotype using a similarity threshold of 10 or fewer allele differences between adjacent nodes. Temporal-cohort clustering within each serotype was supported by date randomization analysis. Substitutions per site per year were consistent with previously reported values for ; however, there was low branch support for these values. Acquisition of the phage-encoded Shiga toxin 2 gene in serotype O22:H8 was observed. Pan-genome analyses identified accessory regions that were more prevalent in persistent serotypes (≤0.05) than in sporadic serotypes. These results suggest that VTEC serotypes from a specific cattle population are highly clonal with a similar level of relatedness as human single-source outbreak-associated strains, but changes in the genome occur gradually over time. Additionally, elements in the accessory genomes may provide a selective advantage for persistence of VTEC within cattle herds.
产肠毒素性(VTEC)是与散发性疾病和肠道疾病暴发相关的食源性和水源性病原体。虽然众所周知牛是 VTEC 的储主,但对牛中 VTEC 的基因组变异知之甚少,也不知道报告的人类暴发菌株基因组的变异是否与感染的个体动物或群体/畜群来源一致。先前对 VTEC 流行率的研究确定了在一个封闭牛群中连续三批小母牛持续携带的血清型。本研究旨在:(i)确定牛分离株的基因组相关性是否与与单一来源暴发相关的人类菌株报告的相似,(ii)估计在牛群内随时间推移主导血清型的基因组变化率,以及(iii)确定与牛群中持久性相关的血清型的基因组特征。完成了基于等位基因和单核苷酸变异的 Illumina MiSeq 基因组测序和基因分型,同时使用贝叶斯进化分析采样树测量随时间的基因组变化。使用 Fisher 精确检验校正多重比较,比较了代表持久性和散发性牛株的辅助基因组,包括非蛋白编码基因间区(IGRs)、毒力因子、抗生素耐药基因和质粒基因含量。使用相似性阈值为 10 或更少的相邻节点之间的等位基因差异,很容易将血清型 O6:H34(=22)、O22:H8(=30)、O108:H8(=39)、O139:H19(=44)和 O157:H7(=106)的牛群菌株与流行病学上无关的相同血清型菌株区分开来。每个血清型内的时间队列聚类得到了日期随机化分析的支持。每个位点每年的替换与先前报道的值一致;然而,这些值的分支支持度很低。在血清型 O22:H8 中观察到噬菌体编码的志贺毒素 2 基因的获得。泛基因组分析确定了在持久性血清型中更为普遍(≤0.05)而在散发性血清型中较少的辅助区域。这些结果表明,来自特定牛群的 VTEC 血清型具有高度克隆性,与人类单源暴发相关菌株的相关性相似,但随时间的推移,基因组发生逐渐变化。此外,辅助基因组中的元素可能为 VTEC 在牛群中的持久性提供选择优势。