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肠炎沙门氏菌 RfbD 通过抑制自噬增强细菌定植和毒力。

Salmonella Enteritidis RfbD enhances bacterial colonization and virulence through inhibiting autophagy.

机构信息

Jiangsu Key Laboratory of Zoonosis, Yangzhou University, Yangzhou 225009, Jiangsu, China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, Jiangsu, China; Key Laboratory of Prevention and Control of Biological Hazard Factors (Animal Origin) for Agrifood Safety and Quality, Ministry of A griculture of China, Yangzhou University, Yangzhou, Jiangsu, China; Joint International Research Laboratory of Agriculture and Agri-product Safety of the Ministry of Education, Yangzhou University, Yangzhou, Jiangsu, China.

Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, Jiangsu, China.

出版信息

Microbiol Res. 2023 May;270:127338. doi: 10.1016/j.micres.2023.127338. Epub 2023 Feb 16.

Abstract

Autophagy is a crucial innate immune response that clears pathogens intracellularly. Salmonella enterica serovar Enteritidis (S.E) has emerged as one of the most important food-borne pathogens. Here, we reported that dTDP-4-dehydro-β-ւ-rhamnose reductase (RfbD) was able to enhance bacterial colonization in vivo and in vitro by regulating autophagy. We screened the transposon mutant library of Salmonella Enteritidis strain Z11 by High-Content Analysis System, found that rfbD gene has an effect on autophagy. The Z11ΔrfbD-infected group showed greater expression of LC3-II than the Z11-infected group in HeLa, RAW264.7, and J774A.1 cells. Overall, the survival of Z11ΔrfbD in RAW264.7 cells was reduced after 8 h of infection compared to that of the Z11 wild-type strain. In addition, we observed that inhibition of autophagic flux significantly increased the survival of Z11ΔrfbD in RAW264.7 cells. Mice infection experiments revealed that Z11ΔrfbD virulence was significantly reduced, and bacterial load was reduced in the liver and cecum in mice model, and LC3-II expression was significantly increased. These findings indicate an important role of Salmonella Enteritidis protein as a strategy to suppress autophagy and provides new ideas for manipulating autophagy as a novel strategy to treat infectious diseases.

摘要

自噬是一种清除细胞内病原体的重要先天免疫反应。肠炎沙门氏菌(S.E)已成为最重要的食源性病原体之一。在这里,我们报道了 dTDP-4-去氢-β-阿拉伯糖还原酶(RfbD)能够通过调节自噬来增强细菌在体内和体外的定植。我们通过高通量分析系统筛选肠炎沙门氏菌 Z11 的转座子突变体文库,发现 rfbD 基因对自噬有影响。在 HeLa、RAW264.7 和 J774A.1 细胞中,Z11ΔrfbD 感染组的 LC3-II 表达水平明显高于 Z11 感染组。总的来说,与 Z11 野生型菌株相比,RAW264.7 细胞中 Z11ΔrfbD 的存活时间在感染 8 小时后减少。此外,我们观察到自噬通量的抑制显著增加了 RAW264.7 细胞中 Z11ΔrfbD 的存活。小鼠感染实验表明,Z11ΔrfbD 的毒力显著降低,在小鼠模型中肝脏和盲肠中的细菌载量降低,LC3-II 表达显著增加。这些发现表明肠炎沙门氏菌蛋白作为一种抑制自噬的策略具有重要作用,并为操纵自噬作为一种治疗感染性疾病的新策略提供了新的思路。

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