肉类加工生产环境中李斯特菌的遗传多样性检测。

Pub Date : 2023-01-01 Epub Date: 2023-06-11 DOI:10.3103/S0891416823010111
O L Voronina, N N Ryzhova, E I Aksenova, M S Kunda, A V Kutuzova, T I Karpova, Yu K Yushina, I S Tartakovsky
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引用次数: 0

摘要

李斯特菌所关注的食品生产安全是制成品卫生健康的关键。用于分析李斯特菌的分子遗传学方法,包括全基因组测序,在监测持久性污染物和食源性感染病例的流行病调查中是有效的。它们已在欧盟、美国和加拿大获得通过。在俄罗斯,多点和全基因组测序已在分析临床食品分离株和环境中的李斯特菌方面得到证明。本研究的目的是对在肉类加工工业环境中检测到的李斯特菌进行分子遗传学鉴定。为了鉴定李斯特菌分离株,根据GOST(国家标准)32031-2012使用微生物学方法,以及多点测序,包括分析7个持家基因和4个毒力基因,以及全基因组测序。在莫斯科两家肉类加工厂采集的李斯特菌阳性拭子中,单核细胞增多性李斯特菌占81%,韦尔希梅里李斯特菌占19%。单核细胞增多性李斯特菌的优势基因型(序列型,ST)为ST8。该品种补充了ST321、ST121和ST2330(CC9(克隆复合体9))。在第二次生产中占主导地位的L.welshimeri由ST1050和ST2331代表。韦尔希梅里乳杆菌分离株的基因组特征证实,无论是在生产条件(包括对消毒剂的耐药性)还是动物胃肠道的代谢特性方面,它们都具有很高的适应能力。李斯特菌CC9和CC121也与其他国家的食品生产有关。然而,李斯特菌CC8和CC321可引起侵袭性李斯特菌病。来自工业环境的ST8分离株与临床分离株ST8和ST2096(CC8)的内在蛋白谱的一致性令人担忧。该研究表明了分子遗传学方法在确定肉类加工生产环境中检测到的李斯特菌多样性方面的有效性,并为监测持久性污染物奠定了基础。
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Genetic Diversity of Listeria Detected in the Production Environment of Meat Processing.

The safety of food production as concerns Listeria is the key to the sanitary wellbeing of manufactured products. Molecular-genetic methods for the analysis of Listeria, including whole-genome sequencing, are effective in monitoring persistent contaminants and in the epidemic investigation of cases of foodborne infections. They have been adopted in the European Union, United States, and Canada. In Russia, multilocus and whole-genome sequencing has proven itself in the analysis of clinical food isolates and Listeria from the environment. The objective of the study was molecular-genetic characterization of Listeria detected in the industrial environment of meat processing. To characterize the Listeria isolates, microbiological methods were used according to GOST (State Standard) 32031-2012, as well as multilocus sequencing, including the analysis of seven housekeeping genes and four virulence genes, as well as whole-genome sequencing. In swabs that were positive for the presence of Listeria spp. taken at two meat-processing plants in Moscow, Listeria monocytogenes constituted 81% and L. welshimeri 19%. The predominant genotype (Sequence Type, ST) of L. monocytogenes was ST8. The variety was supplemented with ST321, ST121, and ST2330 (CC9 (Clonal Complex 9)). L. welshimeri, which prevailed in the second production, was represented by ST1050 and ST2331. The genomic characteristics of L. welshimeri isolates confirmed that they have high adaptive capabilities both as concerns production conditions (including resistance to disinfectants) and the metabolic peculiarities of the gastrointestinal tract of animals. L. monocytogenes CC9 and CC121 are also correlated with food production in other countries. However, L. monocytogenes CC8 and CC321 can cause invasive listeriosis. The concordance in the internalin profile of the ST8 isolates from the industrial environment with the clinical isolates ST8 and ST2096 (CC8) is a cause for concern. The study showed the effectiveness of molecular-genetic methods in determining the diversity of Listeria detected in the production environment of meat processing, and laid the foundation for monitoring of persistent contaminants.

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