鲍曼不动杆菌OmpA通过依赖camkk2的ampk途径阻碍宿主自噬。

IF 5.1 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-04-09 Epub Date: 2025-02-25 DOI:10.1128/mbio.03369-24
Kyungho Woo, Dong Ho Kim, Ho-Sung Park, Man Hwan Oh, Je Chul Lee, Chul Hee Choi
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引用次数: 0

摘要

外膜蛋白A (OmpA)在鲍曼不动杆菌与宿主细胞相互作用中起着至关重要的作用。自噬是一种阻止细菌在细胞内复制的防御机制,从而保护细胞免受微生物感染。虽然已经观察到鲍曼不动杆菌触发细胞自噬,但其毒力蛋白OmpA在这一过程中的确切作用仍不确定。在这项研究中,我们研究了鲍曼不动杆菌OmpA (AbOmpA)对自噬的影响,并探讨了其潜在的分子机制。我们发现,AbOmpA通过抑制CaMKK2磷酸化发挥其自噬抑制作用。与野生型菌株相比,ompa缺失突变株通过AMPK-ULK1途径显示出显著增强的自噬诱导。而鲍曼芽孢杆菌- omp33 (AbOmp33)和大肠杆菌- ompa (EcOmpA)则无此作用。重要的是,我们证实了在鲍曼不动杆菌感染期间,外源性的AbOmpA通过CaMKK2-AMPK-ULK1途径抑制了自噬。这些发现揭示了abompa介导的自噬逃避的新机制,为鲍曼不动杆菌感染的发病机制提供了新的见解。重要性鲍曼不动杆菌是引起医院感染的重要临床病原体。它的外膜蛋白A作为毒力因子,帮助细菌逃避宿主的防御。自噬是一种阻碍细菌胞内复制的防御机制。虽然已经观察到鲍曼不动杆菌触发细胞自噬,但其AbOmpA在这一过程中的确切作用仍不确定。我们的研究表明,鲍曼不动杆菌的AbOmpA通过CaMKK2-AMPK-ULK1信号级联抑制细胞防御过程自噬,从而提高细菌的存活率。对AbOmpA如何绕过自噬的了解揭示了鲍曼不动杆菌感染的新毒力策略,并提出了可能的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acinetobacter baumannii OmpA hinders host autophagy via the CaMKK2-reliant AMPK-pathway.

Outer membrane protein A (OmpA) plays a vital role in the interactions between Acinetobacter baumannii and host cells. Autophagy is a defense mechanism that hinders the intracellular replication of bacteria, thereby safeguarding cells against microbial infections. While it has been observed that A. baumannii triggers cellular autophagy, the precise role of its virulence protein OmpA in this process remains uncertain. In this study, we investigated the effects of A. baumannii OmpA (AbOmpA) on autophagy and explored the underlying molecular mechanisms. We found that AbOmpA exerted its autophagy-suppressive effect through inhibition of CaMKK2 phosphorylation. Compared to the wild-type strain, the ompA-deletion mutant strain displayed considerably enhanced autophagy induction, via the AMPK-ULK1 pathway. AbOmpA hindered starvation-induced autophagy, while A. baumannii-Omp33 (AbOmp33) and Escherichia coli-OmpA (EcOmpA) did not. Importantly, we confirmed that exogenous AbOmpA suppressed autophagy through the CaMKK2-AMPK-ULK1 pathway during A. baumannii infection. These findings reveal a novel mechanism for AbOmpA-mediated autophagy evasion, providing new insights into the pathogenesis of A. baumannii infection.IMPORTANCEAcinetobacter baumannii is a significant clinical pathogen notorious for causing infections in hospitals. Its outer membrane protein A acts as a virulence factor and helps the bacteria evade host defenses. Autophagy is a defense mechanism that hinders the intracellular replication of bacteria. While it has been observed that A. baumannii triggers cellular autophagy, the precise role of its AbOmpA in this process remains uncertain. Our studies demonstrate the AbOmpA of A. baumannii inhibits the cellular defense process, autophagy, through the CaMKK2-AMPK-ULK1 signaling cascade, thereby enhancing bacterial survival. This insight into how AbOmpA bypasses autophagy sheds light on A. baumannii infection's novel virulence strategy and suggests possible treatments.

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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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