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通过宏基因组学和转录组学分析深入了解冷渗 Gigantidas platifrons 中的噬菌体-细菌相互作用。

Insights into phage-bacteria interaction in cold seep Gigantidas platifrons through metagenomics and transcriptome analyses.

机构信息

Center of Deep Sea Research, and CAS Key Laboratory of Marine Ecology and Environmental Sciences, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.

National Deep Sea Center, Qingdao, 266071, China.

出版信息

Sci Rep. 2024 May 8;14(1):10540. doi: 10.1038/s41598-024-61272-3.

Abstract

Viruses are crucial for regulating deep-sea microbial communities and biogeochemical cycles. However, their roles are still less characterized in deep-sea holobionts. Bathymodioline mussels are endemic species inhabiting cold seeps and harboring endosymbionts in gill epithelial cells for nutrition. This study unveiled a diverse array of viruses in the gill tissues of Gigantidas platifrons mussels and analyzed the viral metagenome and transcriptome from the gill tissues of Gigantidas platifrons mussels collected from a cold seep in the South Sea. The mussel gills contained various viruses including Baculoviridae, Rountreeviridae, Myoviridae and Siphovirdae, but the active viromes were Myoviridae, Siphoviridae, and Podoviridae belonging to the order Caudovirales. The overall viral community structure showed significant variation among environments with different methane concentrations. Transcriptome analysis indicated high expression of viral structural genes, integrase, and restriction endonuclease genes in a high methane concentration environment, suggesting frequent virus infection and replication. Furthermore, two viruses (GP-phage-contig14 and GP-phage-contig72) interacted with Gigantidas platifrons methanotrophic gill symbionts (bathymodiolin mussels host intracellular methanotrophic Gammaproteobacteria in their gills), showing high expression levels, and have huge different expression in different methane concentrations. Additionally, single-stranded DNA viruses may play a potential auxiliary role in the virus-host interaction using indirect bioinformatics methods. Moreover, the Cro and DNA methylase genes had phylogenetic similarity between the virus and Gigantidas platifrons methanotrophic gill symbionts. This study also explored a variety of viruses in the gill tissues of Gigantidas platifrons and revealed that bacteria interacted with the viruses during the symbiosis with Gigantidas platifrons. This study provides fundamental insights into the interplay of microorganisms within Gigantidas platifrons mussels in deep sea.

摘要

病毒在调控深海微生物群落和生物地球化学循环方面起着至关重要的作用。然而,它们在深海全动物界生物中的作用仍然知之甚少。贻贝是一种特有的冷渗口物种,其鳃上皮细胞中含有共生菌,以获取营养。本研究揭示了平鳍深海贻贝鳃组织中存在多种病毒,并分析了从南海冷渗口采集的平鳍深海贻贝鳃组织中的病毒宏基因组和转录组。贻贝鳃组织中含有多种病毒,包括杆状病毒科、Rountreeviridae 科、肌病毒科和长尾噬菌体科,但活跃的病毒组是肌病毒科、长尾噬菌体科和短尾噬菌体科,属于长尾噬菌体目。总体而言,病毒群落结构因甲烷浓度不同的环境而异。转录组分析表明,在高甲烷浓度环境中,病毒结构基因、整合酶和限制内切酶基因的表达水平较高,提示频繁的病毒感染和复制。此外,两种病毒(GP-phage-contig14 和 GP-phage-contig72)与平鳍深海贻贝的甲烷营养性鳃共生菌(贻贝宿主的鳃内含有甲烷营养性γ变形菌)相互作用,表现出高表达水平,且在不同甲烷浓度下表达水平差异巨大。此外,通过间接生物信息学方法,单链 DNA 病毒可能在病毒-宿主相互作用中发挥潜在的辅助作用。此外,病毒和平鳍深海贻贝的甲烷营养性鳃共生菌的 Cro 和 DNA 甲基酶基因具有系统发育相似性。本研究还探索了平鳍深海贻贝鳃组织中的多种病毒,并揭示了细菌在与平鳍深海贻贝共生时与病毒相互作用。本研究为深入了解深海平鳍深海贻贝中微生物的相互作用提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a938/11078923/8613ee8bb7bb/41598_2024_61272_Fig1_HTML.jpg

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