Yan Shigan, Zhang Wencheng, Li Chengyu, Liu Xu, Zhu Liping, Chen Leilei, Yang Baowei
Shandong Provincial Key Laboratory of Bioengineering, School of Bioengineering, Qilu University of Technology, Shandong Academy of Sciences, Jinan, China.
Institute of Agro-Food Sciences and Technology, Shandong Academy of Agricultural Sciences, Jinan, China.
Front Microbiol. 2021 Sep 16;12:688614. doi: 10.3389/fmicb.2021.688614. eCollection 2021.
Salmonella enterica () is an important foodborne pathogen, causing food poisoning and human infection, and critically threatening food safety and public health. typing is essential for bacterial identification, tracing, epidemiological investigation, and monitoring. Serotyping and multilocus sequence typing (MLST) analysis are standard bacterial typing methods despite the low resolution. Core genome MLST (cgMLST) is a high-resolution molecular typing method based on whole genomic sequencing for accurate bacterial tracing. We investigated 250 isolates from poultry, livestock, food, and human sources in nine provinces of China from 2004 to 2019 using serotyping, MLST, and cgMLST analysis. All isolates were divided into 36 serovars using slide agglutination. The major serovars in order were Enteritidis (31 isolates), Typhimurium (29 isolates), Mbandaka (23 isolates), and Indiana (22 isolates). All strains were assigned into 43 sequence types (STs) by MLST. Among them, ST11 (31 isolates) was the primary ST. Besides this, a novel ST, ST8016, was identified, and it was different from ST40 by position 317 C → T in . Furthermore, these 250 isolates were grouped into 185 cgMLST sequence types (cgSTs) by cgMLST. The major cgST was cgST235530 (11 isolates), and only three cgSTs contained isolates from human and other sources, indicating a possibility of cross-species infection. Phylogenetic analysis indicated that most of the same serovar strains were putatively homologous except Saintpaul and Derby due to their multilineage characteristics. In addition, serovar I 4,[5],12:i:- and Typhimurium isolates have similar genomic relatedness on the phylogenetic tree. In conclusion, we sorted out the phenotyping and genotyping diversity of isolates in China during 2004-2019 and clarified the temporal and spatial distribution characteristics of from different hosts in China in the recent 16 years. These results greatly supplement strain resources, genetic information, and traceability typing data; facilitate the typing, traceability, identification, and genetic evolution analysis of ; and therefore, improve the level of analysis, monitoring, and controlling of foodborne microorganisms in China.
肠炎沙门氏菌(Salmonella enterica)是一种重要的食源性病原体,可导致食物中毒和人类感染,对食品安全和公众健康构成严重威胁。分型对于细菌鉴定、溯源、流行病学调查和监测至关重要。血清分型和多位点序列分型(MLST)分析是标准的细菌分型方法,尽管分辨率较低。核心基因组MLST(cgMLST)是一种基于全基因组测序的高分辨率分子分型方法,用于准确的细菌溯源。我们使用血清分型、MLST和cgMLST分析,对2004年至2019年期间从中国九个省份的家禽、家畜、食品和人类来源分离的250株菌株进行了调查。所有分离株通过玻片凝集分为36个血清型。按顺序主要的血清型为肠炎型(31株)、鼠伤寒型(29株)、姆班达卡型(23株)和印第安纳型(22株)。所有菌株通过MLST被分为43个序列型(STs)。其中,ST11(31株)是主要的ST。除此之外,还鉴定出一个新的ST,即ST8016,它在[基因名称]中第317位由C→T与ST40不同。此外,这250株分离株通过cgMLST被分为185个cgMLST序列型(cgSTs)。主要的cgST是cgST235530(11株),只有三个cgSTs包含来自人类和其他来源的分离株,表明存在跨物种感染的可能性。系统发育分析表明,除圣保罗型和德比型因其多谱系特征外,大多数相同血清型菌株被推测为同源。此外,血清型I 4,[5],12:i:-和鼠伤寒型分离株在系统发育树上具有相似的基因组相关性。总之,我们梳理了2004 - 2019年期间中国肠炎沙门氏菌分离株的表型和基因型多样性,阐明了近16年来中国不同宿主来源肠炎沙门氏菌的时空分布特征。这些结果极大地补充了肠炎沙门氏菌菌株资源、遗传信息和溯源分型数据;促进了肠炎沙门氏菌的分型、溯源、鉴定和遗传进化分析;从而提高了中国食源微生物的分析、监测和控制水平。