细菌c-di-GMP信号基因通过外膜囊泡和脂多糖影响贻贝幼虫的变态过程

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2024-04-04 DOI:10.1038/s41522-024-00508-6
Xiao-Meng Hu, Lihua Peng, Jingxian Wu, Guanju Wu, Xiao Liang, Jin-Long Yang
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引用次数: 0

摘要

生物膜是海洋无脊椎动物定居和变态的关键线索。在细菌系统中,c-di-GMP 是调节生物膜形成和分散的关键信号分子。然而,c-di-GMP 如何调节生物膜诱导的幼虫变态过程的分子机制仍不清楚。我们的研究发现,通过基因敲除技术,在假尾孢单胞菌(Pseudoalteromonas marina)中删除一个与c-di-GMP相关的基因可导致细菌c-di-GMP水平升高,突变株产生更多外膜囊泡和脂多糖(LPS)的能力增强。突变体生物膜对贻贝幼虫变态具有更高的诱导活性,而 OMVs 在诱导活性中发挥了主要作用。我们进一步探讨了 LPS 在 OMVs 中的功能。提取的 LPS 可诱导高的幼体变态率,且 LPS 含量受 c-di-GMP 和 LPS 生物合成基因的影响。因此,我们推测 c-di-GMP 对生物膜诱导的变态反应的影响是通过 OMVs 和 LPS 介导的。
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Bacterial c-di-GMP signaling gene affects mussel larval metamorphosis through outer membrane vesicles and lipopolysaccharides

Biofilms serve as crucial cues for settlement and metamorphosis in marine invertebrates. Within bacterial systems, c-di-GMP functions as a pivotal signaling molecule regulating both biofilm formation and dispersion. However, the molecular mechanism of how c-di-GMP modulates biofilm-induced larval metamorphosis remains elusive. Our study reveals that the deletion of a c-di-GMP related gene in Pseudoalteromonas marina led to an increase in the level of bacterial c-di-GMP by knockout technique, and the mutant strain had an enhanced ability to produce more outer membrane vesicles (OMVs) and lipopolysaccharides (LPS). The mutant biofilms had higher induction activity for larval metamorphosis in mussels Mytilus coruscus, and OMVs play a major role in the induction activity. We further explored the function of LPS in OMVs. Extracted LPS induced high larval metamorphosis rate, and LPS content were subject to c-di-GMP and LPS-biosynthesis gene. Thus, we postulate that the impact of c-di-GMP on biofilm-induced metamorphosis is mediated through OMVs and LPS.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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