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来自肠道细菌的核调节蛋白:易位的多种机制以及与宿主核过程的相互作用

Nucleomodulins from gut bacteria: diverse mechanisms of translocation and interaction with host nuclear processes.

作者信息

Korgaonkar Sania, Bose Chandrani, Anand Swadha

机构信息

TCS Research, Tata Consultancy Services Limited, Pune, Maharashtra, India.

出版信息

Appl Environ Microbiol. 2025 Aug 20;91(8):e0021125. doi: 10.1128/aem.00211-25. Epub 2025 Jul 18.

DOI:10.1128/aem.00211-25
PMID:40679283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12366366/
Abstract

Nucleomodulins (NMs) are bacterial nuclear-targeted effector proteins that interfere with a multitude of host cellular processes to shield pathogens from host immune responses. Recent years observed a surge in NM-related research owing to their potential role in both infectious diseases and cancer development. However, considering the complex nature of the interaction between NM and host factors, the field of "NM-disease axis" is still in the nascent phase. Thus, a comprehensive view of the known mechanisms of translocation of NMs to the host cell nucleus and mode of action, thereafter, is crucial toward deeper exploration of the "NM-disease axis." The human gut is the major host niche to harbor bacterial cells (as part of "gut microbiota"). The current review provides an extensive collation of nucleomodulin-mediated mechanisms employed by opportunistic gut pathogens. The insights from the review would help in designing future experiments toward utilizing the NM-associated host-pathogen interaction modules in disease diagnostics and therapy.

摘要

核调节蛋白(NMs)是细菌靶向细胞核的效应蛋白,可干扰多种宿主细胞过程,使病原体免受宿主免疫反应的影响。近年来,由于核调节蛋白在传染病和癌症发展中的潜在作用,相关研究激增。然而,鉴于核调节蛋白与宿主因子之间相互作用的复杂性,“核调节蛋白-疾病轴”领域仍处于起步阶段。因此,全面了解核调节蛋白转运至宿主细胞核的已知机制及其作用方式,对于深入探索“核调节蛋白-疾病轴”至关重要。人类肠道是容纳细菌细胞(作为“肠道微生物群”的一部分)的主要宿主生态位。本综述广泛整理了机会性肠道病原体采用的核调节蛋白介导机制。该综述所得出的见解将有助于设计未来的实验,以利用与核调节蛋白相关的宿主-病原体相互作用模块进行疾病诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcb6/12366366/7a7dae4bd2a4/aem.00211-25.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcb6/12366366/0ba133abcb62/aem.00211-25.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcb6/12366366/7a7dae4bd2a4/aem.00211-25.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcb6/12366366/0ba133abcb62/aem.00211-25.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcb6/12366366/7a7dae4bd2a4/aem.00211-25.f002.jpg

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本文引用的文献

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The Mycobacterium tuberculosis methyltransferase Rv2067c manipulates host epigenetic programming to promote its own survival.结核分枝杆菌甲基转移酶 Rv2067c 操纵宿主表观遗传程序以促进自身存活。
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The PPE2 protein of Mycobacterium tuberculosis is secreted during infection and facilitates mycobacterial survival inside the host.结核分枝杆菌的 PPE2 蛋白在感染期间被分泌,并有助于分枝杆菌在宿主内部的存活。
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A bacterial virulence factor interacts with the splicing factor RBM5 and stimulates formation of nuclear RBM5 granules.
一种细菌毒力因子与剪接因子 RBM5 相互作用并刺激核 RBM5 颗粒的形成。
Sci Rep. 2022 Dec 19;12(1):21961. doi: 10.1038/s41598-022-26037-w.
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Enterococcus faecalis alters endo-lysosomal trafficking to replicate and persist within mammalian cells.粪肠球菌通过改变内体-溶酶体运输在哺乳动物细胞内复制和持续存在。
PLoS Pathog. 2022 Apr 7;18(4):e1010434. doi: 10.1371/journal.ppat.1010434. eCollection 2022 Apr.
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Moonlighting by PPE2 Protein: Focus on Mycobacterial Virulence.PPE2 蛋白的兼职行为:关注分枝杆菌毒力。
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Types of nuclear localization signals and mechanisms of protein import into the nucleus.核定位信号的类型和蛋白质入核的机制。
Cell Commun Signal. 2021 May 22;19(1):60. doi: 10.1186/s12964-021-00741-y.
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Oral-Gut Microbiome Axis in Gastrointestinal Disease and Cancer.胃肠道疾病和癌症中的口腔-肠道微生物群轴
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PLoS One. 2021 Mar 18;16(3):e0248975. doi: 10.1371/journal.pone.0248975. eCollection 2021.
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