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引用次数: 0
摘要
副溶血性弧菌有两套 III 型分泌系统,它们是主要的致病因素:T3SS1(细胞毒性)和T3SS2(肠毒性)。副溶血性弧菌经口感染后主要在小肠远端定殖,由于这种环境中缺乏现成的碳水化合物,因此可能面临碳限制应激。众所周知,分解酶激活蛋白(CAP)是一种转录因子,参与许多革兰氏阴性细菌的碳限制代谢,并参与许多毒力因子的表达调控。在本研究中,我们确定了 CAP 对该细菌中 T3SSs 表达的影响。根据基于乳酸脱氢酶的细胞毒性试验,我们发现 CAP 对依赖 T3SS2 的细胞毒性表达的影响大于对依赖 T3SS1 的细胞毒性表达的影响。反转录定量 PCR 发现,与亲本菌株相比,cap 基因缺失突变体中许多 T3SS2 相关基因(包括 vpa1348)的表达量减少。电泳迁移试验和 DNase I 标记表明,CAP 与 vpa1348 启动子区域内的富 T 元素结合。在β-半乳糖苷酶报告实验中,CAP也增强了vpa1348的表达。总之,这些结果表明,CAP 通过调节副溶血弧菌中 vpa1348 的表达参与了 T3SS2 介导的毒力。
Expression regulation of type III secretion system 2 in Vibrio parahaemolyticus by catabolite activator protein.
Vibrio parahaemolyticus has two sets of type III secretion systems that are major pathogenic factors: T3SS1 (cytotoxicity) and T3SS2 (enterotoxicity). V. parahaemolyticus mainly colonizes the distal small intestine after oral infection and may be exposed to carbon-limiting stress due to the lack of readily available carbohydrates in this environment. Catabolite activator protein (CAP), a transcription factor involved in carbon-limiting metabolism in many Gram-negative bacteria, is well known to be involved in the regulation of the expression of many virulence factors. In this study, we determined the effects of CAP on the expression of T3SSs in this bacterium. Based on a lactate dehydrogenase-based cytotoxicity assay, CAP was found to have a greater contribution to the expression of T3SS2-dependent cytotoxicity than to that of T3SS1. Reverse transcription quantitative PCR revealed decreased expression of many T3SS2-related genes, including vpa1348, in the cap gene deletion mutant compared to the parent strain. CAP was demonstrated to bind near the T-rich elements within the vpa1348 promoter region in an electrophoretic mobility shift assay and DNase I footprinting. CAP also enhanced the expression of vpa1348 in a β-galactosidase reporter assay. Collectively, these results suggest that CAP is involved in T3SS2-mediated virulence by regulating the expression of vpa1348 in V. parahaemolyticus.
期刊介绍:
FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered.
2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020)
Ranking: 98/135 (Microbiology)
The journal is divided into eight Sections:
Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies)
Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens)
Biotechnology and Synthetic Biology
Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses)
Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies)
Virology (viruses infecting any organism, including Bacteria and Archaea)
Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature)
Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology)
If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.