不同的细胞分裂模式驱动嗜吞噬细胞无原体形态发育和感染周期。

IF 4.7 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-10-08 Epub Date: 2025-08-25 DOI:10.1128/mbio.01972-25
Travis J Chiarelli, Savannah E Sanchez, Mary Clark H Lind, Nathaniel S O'Bier, Curtis B Read, Richard T Marconi, Jason A Carlyon
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引用次数: 0

摘要

多形性是一种进化适应,不同的微生物通过在不同的形态之间转换来最大限度地适应当地的微环境。在许多多形性细菌系统中,细胞分裂是形态转变的关键。嗜吞噬细胞无形体引起粒细胞无形体病,是一种多形性专性细胞内细菌,生活在病原体修饰的液泡中,除非它被胞外释放传播到naïve细胞。这种细菌在非传染性、复制性网状细胞(RC)和传染性、非复制性密核细胞(DC)之间循环。在这里,我们确定了嗜吞噬细胞芽胞杆菌细胞分裂的不同模式驱动形态发育,其中RC细菌对称分裂以扩大孔内种群,之后它们转向牺牲不对称分裂以产生dc。嗜吞噬细胞芽胞杆菌MreB对细胞分裂,特别是分裂,从而形成两种形态至关重要。抑制细胞分裂不仅可以阻止DC的形成,还可以阻止嗜吞噬细胞芽胞杆菌液泡成熟和感染性子代的释放,这表明这些致病过程是协调的。本研究促进了对嗜吞噬细胞芽胞杆菌生长和形态发育的认识,从而提高了对其病理生物学的认识。它也提供了第一个证据,将细胞分裂与无形体科的形态发育联系起来。嗜吞噬细胞无形体是一种专性细胞内细菌病原体,生活在宿主细胞衍生的液泡中,引起人类和兽医疾病,具有全球重要性。在病原体占据的液泡中,嗜吞噬芽胞杆菌从复制的、非感染性的形态转变为非复制的、感染性的形态,并释放出来传播感染。我们证实了不同的细菌细胞分裂模式不仅驱动嗜吞噬细胞芽胞杆菌的复制,而且驱动其分化为感染形式并传播到naïve细胞。在大多数液泡适应的细菌病原体中,多形性是如何调节的,人们知之甚少。因此,这项研究推进了液泡适应多形性细菌病理生物学的基础知识,并最终确定了治疗它们引起的疾病的常见新型抗生素靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distinct modes of cell division drive Anaplasma phagocytophilum morphotype development and the infection cycle.

Pleomorphism is an evolutionary adaptation by which diverse microorganisms maximize their fitness by transitioning between morphologically distinct forms that perform disparate functions in response to the local microenvironment. Cell division is critical for morphotype transition in many pleomorphic bacterial systems. Anaplasma phagocytophilum, which causes the emerging disease granulocytic anaplasmosis, is a pleomorphic obligate intracellular bacterium that lives in a pathogen-modified vacuole except for when it is exocytically released for dissemination to naïve cells. This bacterium cycles between non-infectious, replicative reticulate cell (RC) and infectious, non-replicative dense-cored (DC) forms. Here, we establish that differential modes of A. phagocytophilum cell division drive morphotype development where RC bacteria divide symmetrically to expand the intravacuolar population after which they switch to sacrificial asymmetric division to produce DCs. A. phagocytophilum MreB is crucial for cell division, specifically septation, and thereby formation of both morphotypes. Inhibition of cell division prevents not only DC formation but also A. phagocytophilum vacuole maturation and infectious progeny release, which suggests that these pathogenic processes are coordinated. This study advances understanding of A. phagocytophilum growth and morphotype development and, thus, pathobiology. It also provides the first evidence linking cell division to morphotype development in the Anaplasmataceae.IMPORTANCEAnaplasma phagocytophilum, an obligate intracellular bacterial pathogen that lives in a host cell-derived vacuole, causes human and veterinary diseases of global importance. In the pathogen-occupied vacuole, A. phagocytophilum transitions from a replicative, non-infectious morphotype to a non-replicative, infectious morphotype that is released to spread infection. We established that distinct modes of bacterial cell division drive not only A. phagocytophilum replication but also its differentiation to the infectious form and dissemination to naïve cells. How pleomorphism is regulated in most vacuole-adapted bacterial pathogens is poorly understood. Therefore, this study advances fundamental knowledge of vacuole-adapted pleomorphic bacteria pathobiology and could ultimately identify common novel antibiotic targets for treating the diseases they cause.

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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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