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双组分系统 LadS/PA0034 通过菌毛蛋白 cupA1 调节巨噬细胞吞噬作用。

two-component system LadS/PA0034 regulates macrophage phagocytosis via fimbrial protein cupA1.

机构信息

Clinical Medical Research Center, The Xinqiao Hospital, Army Medical University, Chongqing, China.

Department of orthopedics, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

出版信息

mBio. 2024 Jun 12;15(6):e0061624. doi: 10.1128/mbio.00616-24. Epub 2024 May 21.

DOI:10.1128/mbio.00616-24
PMID:38771052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11237798/
Abstract

UNLABELLED

is one of the most common nosocomial pathogens worldwide, known for its virulence, drug resistance, and elaborate sensor-response network. The primary challenge encountered by pathogens during the initial stages of infection is the immune clearance arising from the host. The resident macrophages of barrier organs serve as the frontline defense against these pathogens. Central to our understanding is the mechanism by which bacteria modify their behavior to circumvent macrophage-mediated clearance, ensuring their persistence and colonization. To successfully evade macrophage-mediated phagocytosis, bacteria must possess an adaptive response mechanism. Two-component systems provide bacteria the agility to navigate diverse environmental challenges, translating external stimuli into cellular adaptive responses. Here, we report that the well-documented histidine kinase, LadS, coupled to a cognate two-component response regulator, PA0034, governs the expression of a vital adhesin called chaperone-usher pathway pilus cupA. The LadS/PA0034 system is susceptible to interference from the reactive oxygen species likely to be produced by macrophages and further lead to a poor adhesive phenotype with scantily cupA pilus, impairing the phagocytosis efficiency of macrophages during acute infection. This dynamic underscores the intriguing interplay: as macrophages deploy reactive oxygen species to combat bacterial invasion, the bacteria recalibrate their exterior to elude these defenses.

IMPORTANCE

The notoriety of is underscored by its virulence, drug resistance, and elaborate sensor-response network. Yet, the mechanisms by which maneuvers to escape phagocytosis during acute infections remain elusive. This study pinpoints a two-component response regulator, PA0034, coupled with the histidine kinase LadS, and responds to macrophage-derived reactive oxygen species. The macrophage-derived reactive oxygen species can impair the LadS/PA0034 system, resulting in reduced expression of cupA pilus in the exterior of . Since the cupA pilus is an important adhesin of , its deficiency reduces bacterial adhesion and changes their behavior to adopt a planktonic lifestyle, subsequently inhibiting the phagocytosis of macrophages by interfering with bacterial adhesion. Briefly, reactive oxygen species may act as environmental cues for the LadS/PA0034 system. Upon recognition, may transition to a poorly adhesive state, efficiently avoiding engulfment by macrophages.

摘要

未加标签

是世界上最常见的医院病原体之一,以其毒力、耐药性和精细的传感器反应网络而闻名。病原体在感染初期遇到的主要挑战是来自宿主的免疫清除。屏障器官的常驻巨噬细胞是抵御这些病原体的第一道防线。我们理解的核心是细菌改变行为以规避巨噬细胞介导的清除的机制,确保其持续存在和定植。为了成功逃避巨噬细胞介导的吞噬作用,细菌必须具有适应性反应机制。双组分系统为细菌提供了在不同环境挑战中导航的灵活性,将外部刺激转化为细胞适应性反应。在这里,我们报告了有充分文献记录的组氨酸激酶 LadS 与同源的双组分反应调节剂 PA0034 一起,调节一种重要的粘附素称为伴侣-usher 途径菌毛 cupA 的表达。LadS/PA0034 系统易受巨噬细胞产生的活性氧的干扰,进而导致粘附表型不良,菌毛 cupA 稀少,在急性感染期间削弱巨噬细胞的吞噬效率。这种动态突出了有趣的相互作用:当巨噬细胞利用活性氧来对抗细菌入侵时,细菌会重新调整它们的外部结构以逃避这些防御。

重要性

的恶名昭彰是由其毒力、耐药性和精细的传感器反应网络所决定的。然而,在急性感染期间, 逃避吞噬作用的机制仍然难以捉摸。这项研究确定了一个双组分反应调节剂 PA0034,与组氨酸激酶 LadS 相连,并对巨噬细胞衍生的活性氧作出反应。巨噬细胞衍生的活性氧可以损害 LadS/PA0034 系统,导致 外部的 cupA 菌毛表达减少。由于 cupA 菌毛是 的重要粘附素,其缺乏会降低细菌的粘附性并改变其行为以采用浮游生活方式,从而通过干扰细菌粘附来抑制巨噬细胞的吞噬作用。简而言之,活性氧可以作为 LadS/PA0034 系统的环境线索。一旦被识别, 可能会转变为粘附不良状态,有效地避免被巨噬细胞吞噬。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b7/11237798/c9ec5d8b158e/mbio.00616-24.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b7/11237798/fdde10e7f43b/mbio.00616-24.f001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b7/11237798/96983aa3c7ac/mbio.00616-24.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b7/11237798/c9ec5d8b158e/mbio.00616-24.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b7/11237798/fdde10e7f43b/mbio.00616-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b7/11237798/c792bde4c581/mbio.00616-24.f002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b7/11237798/c9ec5d8b158e/mbio.00616-24.f006.jpg

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