古细菌六型分泌系统介导依赖接触的拮抗作用

IF 11.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Science Advances Pub Date : 2024-11-15 DOI:10.1126/sciadv.adp7088
Tobias Zachs, Jessie James L. Malit, Jingwei Xu, Alexandra Schürch, Shamphavi Sivabalasarma, Phillip Nußbaum, Sonja-Verena Albers, Martin Pilhofer
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引用次数: 0

摘要

微生物群落是由细胞与细胞之间的相互作用形成的。尽管古细菌经常与其他微生物结合在一起,但人们对这些群落的结构机制却知之甚少。在这里,我们报告了卤代古细菌收缩注射系统(CIS)的结构和功能。通过结合使用功能测试和延时成像技术,我们发现卤虫(Halogeometricum borinquense)通过诱导细胞裂解和抑制增殖,表现出对火山卤虫(Haloferax volcanii)的拮抗作用。这种拮抗作用依赖于接触,需要功能性 CIS,而 CIS 是由一个与毒素-免疫对相关的基因簇编码的。低温聚焦离子束铣削和低温电子断层扫描成像显示,这些 CIS 与细胞质膜结合,类似于细菌的六型分泌系统(T6SS)。我们的研究表明,相关的 T6SS 基因簇在其他表现出拮抗行为的卤虫菌株中是保守和表达的。我们的数据为理解古细菌如何塑造微生物群落并影响其栖息的食物网提供了一个机制框架。
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Archaeal type six secretion system mediates contact-dependent antagonism
Microbial communities are shaped by cell-cell interactions. Although archaea are often found in associations with other microorganisms, the mechanisms structuring these communities are poorly understood. Here, we report on the structure and function of haloarchaeal contractile injection systems (CISs). Using a combination of functional assays and time-lapse imaging, we show that Halogeometricum borinquense exhibits antagonism toward Haloferax volcanii by inducing cell lysis and inhibiting proliferation. This antagonism is contact-dependent and requires a functional CIS, which is encoded by a gene cluster that is associated with toxin-immunity pairs. Cryo–focused ion beam milling and imaging by cryo–electron tomography revealed that these CISs are bound to the cytoplasmic membrane, resembling the bacterial type six secretion systems (T6SSs). We show that related T6SS gene clusters are conserved and expressed in other haloarchaeal strains, which exhibit antagonistic behavior. Our data provide a mechanistic framework for understanding how archaea may shape microbial communities and affect the food webs they inhabit.
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来源期刊
Science Advances
Science Advances 综合性期刊-综合性期刊
CiteScore
21.40
自引率
1.50%
发文量
1937
审稿时长
29 weeks
期刊介绍: Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.
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