Genomic and phenotypic comparison of two Salmonella Typhimurium strains responsible for consecutive salmonellosis outbreaks in New Zealand

IF 4.5 3区 医学 Q1 MICROBIOLOGY International Journal of Medical Microbiology Pub Date : 2021-10-01 DOI:10.1016/j.ijmm.2021.151534
Samuel J. Bloomfield , Jackie Benschop , Anne C. Midwinter , Patrick J. Biggs , Jonathan C. Marshall , David T.S. Hayman , Philip E. Carter , Marian Price-Carter , Leah Toombs-Ruane , Holly Gray , Sara Burgess , Nigel P. French
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引用次数: 1

Abstract

Salmonella enterica serovar Typhimurium DT160 was the predominant cause of notified human salmonellosis cases in New Zealand from 2000 to 2010, before it was superseded by another S. Typhimurium strain, DT56 variant (DT56v). Whole genome sequencing and phenotypic testing were used to compare 109 DT160 isolates with eight DT56v isolates from New Zealand animal and human sources. Phylogenetic analysis provided evidence that DT160 and DT56v strains were distantly related with an estimated date of common ancestor between 1769 and 1821. The strains replicated at different rates but had similar antimicrobial susceptibility profiles. Both strains were resistant to the phage expressed from the chromosome of the other strain, which may have contributed to the emergence of DT56v. DT160 contained the pSLT virulence plasmid, and the sseJ and sseK2 genes that may have contributed to the higher reported prevalence compared to DT56v. A linear pBSSB1-family plasmid was also found in one of the DT56v isolates, but there was no evidence that this plasmid affected bacterial replication or antimicrobial susceptibility. One of the DT56v isolates was also sequenced using long-read technology and found to contain an uncommon chromosome arrangement for a Typhimurium isolate. This study demonstrates how comparative genomics and phenotypic testing can help identify strain-specific elements and factors that may have influenced the emergence and supersession of bacterial strains of public health importance.

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导致新西兰沙门氏菌病连续暴发的两种鼠伤寒沙门氏菌的基因组和表型比较
在被另一种鼠伤寒沙门氏菌菌株DT56变体(DT56v)所取代之前,2000年至2010年新西兰通报的人类沙门氏菌病病例中主要原因是肠沙门氏菌血清型鼠伤寒沙门氏菌DT160。采用全基因组测序和表型检测将109株DT160与8株来自新西兰动物和人源的DT56v进行比较。系统发育分析表明,DT160和DT56v菌株亲缘关系较远,共同祖先估计在1769 ~ 1821年之间。菌株的复制速率不同,但具有相似的抗菌敏感性。两株菌株都对另一株菌株的染色体表达的噬菌体具有抗性,这可能是导致DT56v出现的原因。DT160含有pSLT毒力质粒,以及sseJ和sseK2基因,这可能是与DT56v相比报告的更高患病率的原因。在一株DT56v分离株中也发现了线性pbssb1家族质粒,但没有证据表明该质粒影响细菌复制或抗菌敏感性。利用长读技术对其中一株DT56v分离株进行了测序,发现其含有一种罕见的鼠伤寒菌分离株染色体排列。本研究证明了比较基因组学和表型检测如何能够帮助识别可能影响对公共卫生具有重要意义的细菌菌株出现和消失的菌株特异性元素和因素。
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来源期刊
CiteScore
9.70
自引率
0.00%
发文量
18
审稿时长
45 days
期刊介绍: Pathogen genome sequencing projects have provided a wealth of data that need to be set in context to pathogenicity and the outcome of infections. In addition, the interplay between a pathogen and its host cell has become increasingly important to understand and interfere with diseases caused by microbial pathogens. IJMM meets these needs by focussing on genome and proteome analyses, studies dealing with the molecular mechanisms of pathogenicity and the evolution of pathogenic agents, the interactions between pathogens and host cells ("cellular microbiology"), and molecular epidemiology. To help the reader keeping up with the rapidly evolving new findings in the field of medical microbiology, IJMM publishes original articles, case studies and topical, state-of-the-art mini-reviews in a well balanced fashion. All articles are strictly peer-reviewed. Important topics are reinforced by 2 special issues per year dedicated to a particular theme. Finally, at irregular intervals, current opinions on recent or future developments in medical microbiology are presented in an editorial section.
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