寄主和共生细菌在单细胞分辨率下协同拮抗机会致病菌。

IF 14.3 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Sheng Zhang, Ziguang Wang, Anqi Liu, Jinshu Li, Jingjing Zhuang, Xiaowen Ji, Paul I Mulama, Maoye Li, Haiqun Cao, Eng-King Tan, Wei Liu
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引用次数: 0

摘要

自然微生物共存于不同的物种种群中,相互竞争空间和营养资源。然而,支持微生物之间及其宿主之间的调节网络的分子机制仍处于起步阶段。在这里,据报道,果蝇和共生的植物乳杆菌形成联盟,利用整合的三种模型系统与致病性粘质沙雷氏菌竞争。在双物种模型中,幼虫减少了l.a plantarum的种群数量,但通过改变其转录重编程可逆地增加了乳酸产量。在三种模型中,幼虫促进了植物乳杆菌的生长,从而赋予了对粘质葡萄球菌的定植抗性。另一方面,S. marcescens启动了复杂的军备竞赛策略,通过感知来自L. plantarum的乳酸来削弱殖民抗性。更重要的是,随着抗性异质性的增加,受到果蝇和植物L.的挑战的粘质S. S. marcescens种群适应性地分化为强毒和弱毒亚群。为了与果蝇形成联盟,植物l.s plantarum亚群中乳酸代的异质性被扩大。总之,这些发现提供了对宿主-共生体-病原体共生的整体和单细胞分辨率的洞察,推进了精确操纵细菌群落的基本概念。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hosts and Commensal Bacteria Synergistically Antagonize Opportunistic Pathogens at the Single-Cell Resolution.

Natural microbes coexist in a diverse species population with competition for space and nutrient resources. However, the molecular mechanisms underpinning the regulatory networks of microbes among themselves and with their host are still in infancy. Here, it is reported that Drosophila and the commensal Lactiplantibacillus plantarum form an alliance to compete with the pathogenic Serratia marcescens using the integrated three-species model system. In the dual-species model, larvae diminish the L. plantarum population, but reversibly increase lactate production through altering its transcriptional reprogramming. In the tripartite-species model, larvae facilitate the growth of L. plantarum that confers colonization resistance against S. marcescens. On the other hand, S. marcescens launches sophisticated arms race strategies to impair colonization resistance by sensing lactate derived from L. plantarum. More importantly, the S. marcescens population challenged with Drosophila and L. plantarum adaptively diverge into virulent and reduced virulence subclusters with an increase in resistance heterogeneity. To form the alliance with Drosophila, heterogeneity in lactate generation is broadened among L. plantarum subpopulations. Altogether, these findings provide an insight into the host-commensal-pathogen symbiosis at both bulk and single-cell resolutions, advancing fundamental concepts of precise manipulation of bacterial communities.

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来源期刊
Advanced Science
Advanced Science CHEMISTRY, MULTIDISCIPLINARYNANOSCIENCE &-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
18.90
自引率
2.60%
发文量
1602
审稿时长
1.9 months
期刊介绍: Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.
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