Quadram Institute Bioscience, Norwich Research Park, Norwich, Norfolk, UK.
Massey University's Molecular Epidemiology and Public Health Laboratory, Hopkirk Research Institute, Massey University, Palmerston North, 4410, New Zealand.
Int J Med Microbiol. 2021 Oct;311(7):151534. doi: 10.1016/j.ijmm.2021.151534. Epub 2021 Aug 18.
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DT160 was the predominant cause of notified human salmonellosis cases in New Zealand from 2000 to 2010, before it was superseded by another S. Typhimurium strain, DT56 variant (DT56v).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.
从 2000 年到 2010 年,肠炎沙门氏菌 Typhimurium DT160 是新西兰报告的人类沙门氏菌病病例的主要原因,之后它被另一种沙门氏菌 Typhimurium 菌株 DT56 变体(DT56v)所取代。全基因组测序和表型测试用于比较来自新西兰动物和人类来源的 109 个 DT160 分离株和 8 个 DT56v 分离株。系统发育分析提供了证据,表明 DT160 和 DT56v 菌株是远缘相关的,它们的共同祖先估计在 1769 年至 1821 年之间。这些菌株的复制速度不同,但具有相似的抗菌药物敏感性谱。两种菌株都对来自另一菌株染色体表达的噬菌体具有抗性,这可能导致了 DT56v 的出现。DT160 含有 pSLT 毒力质粒,以及 sseJ 和 sseK2 基因,这可能导致其报告的流行率高于 DT56v。在一个 DT56v 分离株中还发现了一个线性的 pBSSB1 家族质粒,但没有证据表明该质粒影响细菌复制或抗菌药物敏感性。其中一个 DT56v 分离株还使用长读测序技术进行了测序,发现其染色体排列对于鼠伤寒沙门氏菌分离株来说并不常见。本研究表明比较基因组学和表型测试如何有助于确定菌株特异性元素和因素,这些因素可能影响了具有公共卫生重要性的细菌菌株的出现和取代。