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T6SS-ClpV 介导的定植破坏宿主肠道微生物群并增强鼠伤寒血清型的毒力。

Colonization Mediated by T6SS-ClpV Disrupts Host Gut Microbiota and Enhances Virulence of serovar Typhimurium.

机构信息

College of Animal Science and Technology/Laboratory of Functional Microbiology and Animal Health, Henan University of Science and Technology, Luoyang 471023, China.

Luoyang Key Laboratory of Live Carrier Biomaterial and Animal Disease Prevention and Control, Henan University of Science and Technology, Luoyang 471003, China.

出版信息

J Agric Food Chem. 2024 Aug 28;72(34):19155-19166. doi: 10.1021/acs.jafc.4c03735. Epub 2024 Aug 19.

Abstract

serovar Typhimurium ( Typhimurium) is a common foodborne enteric pathogen that infects humans or mammals and colonizes the intestinal tract primarily by invading the host following ingestion. Meanwhile, ClpV is a core secreted protein of the bacterial type VI secretion system (T6SS). Because elucidating ClpV's role in the pathogenesis of T6SS is pivotal for revealing the virulence mechanism of , in our study, gene deletion mutants were constructed using a λ-red-based recombination system, and the effect of mutation on SL1344's pathogenicity was examined in terms of stress resistance, motility, cytokine secretion, gut microbiota, and a BALB/c mouse model. Among the results, ClpV affected SL1344's motility and was also involved in cell invasion, adhesion, and intracellular survival in the MDBK cell model but did not affect invasion or intracellular survival in the RAW264.7 cell model. Moreover, gene deletion significantly reduced the transcription levels of GBP2b, IFNB1, IL-6, NLRP3, NOS2, and TNF-α proinflammatory factor levels but significantly increased transcription levels of IL-4 and IL-10 anti-inflammatory factors. Last, ClpV appeared to closely relate to the pathogenicity of Typhimurium , which can change the gut environment and cause dysbiosis of gut microbiota. Our findings elucidate the functions of ClpV in . Typhimurium and illustrating interactions between T6SS and gut microbiota help to clarify the mechanisms of the pathogenesis of foodborne diseases.

摘要

鼠伤寒血清型(Typhimurium)是一种常见的食源性肠道病原体,主要通过摄入后入侵宿主而感染人类或哺乳动物并在肠道定殖。同时,ClpV 是细菌型 VI 型分泌系统(T6SS)的核心分泌蛋白。因为阐明 ClpV 在 T6SS 发病机制中的作用对于揭示其毒力机制至关重要,在我们的研究中,使用 λ-red 基于重组系统构建了 ClpV 基因缺失突变体,并从应激抗性、运动性、细胞因子分泌、肠道微生物群和 BALB/c 小鼠模型等方面检查了突变对 SL1344 致病性的影响。结果表明,ClpV 影响 SL1344 的运动性,并参与 MDBK 细胞模型中的细胞侵袭、黏附和细胞内存活,但不影响 RAW264.7 细胞模型中的侵袭或细胞内存活。此外,ClpV 基因缺失显著降低了 GBP2b、IFNB1、IL-6、NLRP3、NOS2 和 TNF-α 促炎因子的转录水平,但显著增加了 IL-4 和 IL-10 抗炎因子的转录水平。最后,ClpV 似乎与 Typhimurium 的致病性密切相关,它可以改变肠道环境并导致肠道微生物群失调。我们的研究结果阐明了 ClpV 在 Typhimurium 中的功能,并说明了 T6SS 和肠道微生物群之间的相互作用有助于阐明食源性疾病发病机制的机制。

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