Deciphering deep-sea chemosynthetic symbiosis by single-nucleus RNA-sequencing

Bathymodioline mussels dominate deep-sea methane seep and hydrothermal vent habitats and obtain nutrients and energy primarily through chemosynthetic endosymbiotic bacteria in the bacteriocytes of their gill. However, the molecular mechanisms that orchestrate mussel host–symbiont interactions remain unclear. Here, we constructed a comprehensive cell atlas of the gill in the mussel Gigantidas platifrons from the South China Sea methane seeps (1100 m depth) using single-nucleus RNA-sequencing (snRNA-seq) and whole-mount in situ hybridisation. We identified 13 types of cells, including three previously unknown ones, and uncovered unknown tissue heterogeneity. Every cell type has a designated function in supporting the gill’s structure and function, creating an optimal environment for chemosynthesis, and effectively acquiring nutrients from the endosymbiotic bacteria. Analysis of snRNA-seq of in situ transplanted mussels clearly showed the shifts in cell state in response to environmental oscillations. Our findings provide insight into the principles of host–symbiont interaction and the bivalves' environmental adaption mechanisms.

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Publication Details

Journal
eLife
Published
2024-08-05
DOI
https://doi.org/10.7554/elife.88294.4
Citations
9
Primary Topic
Microbial Community Ecology and Physiology
Type
article
Field-Weighted Citation Impact
4.13

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article

Deciphering deep-sea chemosynthetic symbiosis by single-nucleus RNA-sequencing

Chao Lian, Kai He, Minxiao Wang, Pei‐Yuan Qian et al.
9 citations
eLife
Microbial Community Ecology and Physiology
4.13
article

Deciphering deep-sea chemosynthetic symbiosis by single-nucleus RNA-sequencing

Chao Lian, Kai He, Minxiao Wang, Pei‐Yuan Qian, Quanyong Zhang, Chaolun Li, Zhaoshan Zhong, Jing Li, Huan Zhang, Lei Cao, Kai Chen, Zhou Li, Hao Wang, Hao Chen
article en
9 citations

Abstract

Bathymodioline mussels dominate deep-sea methane seep and hydrothermal vent habitats and obtain nutrients and energy primarily through chemosynthetic endosymbiotic bacteria in the bacteriocytes of their gill. However, the molecular mechanisms that orchestrate mussel host–symbiont interactions remain unclear. Here, we constructed a comprehensive cell atlas of the gill in the mussel Gigantidas platifrons from the South China Sea methane seeps (1100 m depth) using single-nucleus RNA-sequencing (snRNA-seq) and whole-mount in situ hybridisation. We identified 13 types of cells, including three previously unknown ones, and uncovered unknown tissue heterogeneity. Every cell type has a designated function in supporting the gill’s structure and function, creating an optimal environment for chemosynthesis, and effectively acquiring nutrients from the endosymbiotic bacteria. Analysis of snRNA-seq of in situ transplanted mussels clearly showed the shifts in cell state in response to environmental oscillations. Our findings provide insight into the principles of host–symbiont interaction and the bivalves' environmental adaption mechanisms.

eLifeVol. 12
Kunming University of Science and Technology (CN), Hong Kong University of Science and Technology (HK), Guangzhou University (CN), Institute of Oceanology (CN), South China Sea Institute Of Oceanology (CN), Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (CN), Qingdao National Laboratory for Marine Science and Technology (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Life below water
Openalex Percentile: Top 6%
Microbial Community Ecology and Physiology
4.13
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