Recruitment of both the ESCRT and autophagic machineries to ejecting Mycobacterium marinum.

IF 2.6 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Microbiology Pub Date : 2024-03-01 Epub Date: 2023-05-25 DOI:10.1111/mmi.15075
Lilli Gerstenmaier, Ombretta Colasanti, Hannah Behrens, Margot Kolonko, Christian Hammann, Monica Hagedorn
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Abstract

Cytosolic Mycobacterium marinum are ejected from host cells such as macrophages or the amoeba Dictyostelium discoideum in a non-lytic fashion. As described previously, the autophagic machinery is recruited to ejecting bacteria and supports host cell integrity during egress. Here, we show that the ESCRT machinery is also recruited to ejecting bacteria, partially dependent on an intact autophagic pathway. As such, the AAA-ATPase Vps4 shows a distinct localization at the ejectosome structure in comparison to fluorescently tagged Vps32, Tsg101 and Alix. Along the bacterium engaged in ejection, ESCRT and the autophagic component Atg8 show partial colocalization. We hypothesize that both, the ESCRT and autophagic machinery localize to the bacterium as part of a membrane damage response, as well as part of a "frustrated autophagosome" that is unable to engulf the ejecting bacterium.

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弹出分枝杆菌的ESCRT和自噬机制都被招募。
细胞质分枝杆菌以非溶解方式从巨噬细胞或盘状变形虫等宿主细胞中排出。如前所述,自噬机制被招募到弹出的细菌中,并在弹出过程中支持宿主细胞的完整性。在这里,我们发现 ESCRT 机制也被招募到弹射细菌中,部分依赖于完整的自噬途径。因此,与荧光标记的 Vps32、Tsg101 和 Alix 相比,AAA-ATP 酶 Vps4 在弹出体结构中显示出独特的定位。沿着进行弹射的细菌,ESCRT 和自噬成分 Atg8 显示出部分共定位。我们推测,ESCRT 和自噬机制都定位到了细菌上,这是膜损伤反应的一部分,也是无法吞噬弹射细菌的 "受挫自噬体 "的一部分。
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来源期刊
Molecular Microbiology
Molecular Microbiology 生物-生化与分子生物学
CiteScore
7.20
自引率
5.60%
发文量
132
审稿时长
1.7 months
期刊介绍: Molecular Microbiology, the leading primary journal in the microbial sciences, publishes molecular studies of Bacteria, Archaea, eukaryotic microorganisms, and their viruses. Research papers should lead to a deeper understanding of the molecular principles underlying basic physiological processes or mechanisms. Appropriate topics include gene expression and regulation, pathogenicity and virulence, physiology and metabolism, synthesis of macromolecules (proteins, nucleic acids, lipids, polysaccharides, etc), cell biology and subcellular organization, membrane biogenesis and function, traffic and transport, cell-cell communication and signalling pathways, evolution and gene transfer. Articles focused on host responses (cellular or immunological) to pathogens or on microbial ecology should be directed to our sister journals Cellular Microbiology and Environmental Microbiology, respectively.
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