4.7 Article

A glimpse of deep-sea adaptation in chemosynthetic holobionts: Depressurization causes DNA fragmentation and cell death of methanotrophic endosymbionts rather than their deep-sea Bathymodiolinae host

Journal

MOLECULAR ECOLOGY
Volume 30, Issue 10, Pages 2298-2312

Publisher

WILEY
DOI: 10.1111/mec.15904

Keywords

bathymodiolinae mussel; chemosynthetic symbiosis; deep‐ sea adaptation; hydrostatic pressure; methane‐ oxidizing bacteria

Funding

  1. Key Research Program of Frontier Sciences, CAS [ZDBS-LY-DQC032]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA22050303, XDB42020401]
  3. National Key Research and Development Program of China [2018YFC0310800]
  4. National Natural Science Foundation of China [42030407, 42076091, 41906103]
  5. Key Deployment Project of Centre for Ocean Mega-Research of Science, CAS [COMS2020Q02]
  6. Senior User Project of RV KEXUE [KEXUE2020G03]

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This study investigated the potential influence of depressurization on Bathymodiolinae hosts and their methanotrophic symbionts, revealing massive DNA fragmentation in symbionts but certain tolerance in host cells. The study highlights the distinct stress responses of Bathymodiolinae holobionts against depressurization and emphasizes the necessity of using isobaric sampling methods in deep-sea research.
Bathymodiolinae mussels are typical species in deep-sea cold seeps and hydrothermal vents and an ideal model for investigating chemosynthetic symbiosis and the influence of high hydrostatic pressure on deep-sea organisms. Herein, the potential influence of depressurization on DNA fragmentation and cell death in Bathymodiolinae hosts and their methanotrophic symbionts were surveyed using isobaric and unpressurized samples. As a hallmark of cell death, massive DNA fragmentation was observed in methanotrophic symbionts from unpressurized Bathymodiolinae while several endonucleases and restriction enzymes were upregulated. Additionally, genes involved in DNA repair, glucose/methane metabolism as well as two-component regulatory system were also differentially expressed in depressurized symbionts. DNA fragmentation and programmed cell death, however, were rarely detected in the host bacteriocytes owing to the orchestrated upregulation of inhibitor of apoptosis genes and downregulation of caspase genes. Meanwhile, diverse host immune recognition receptors were promoted during depressurization, probably enabling the regain of symbionts. When the holobionts were subjected to a prolonged acclimation at atmospheric pressure, alternations in both the DNA fragmentation and the expression atlas of aforesaid genes were continuously observed in symbionts, demonstrating the persistent influence of depressurization. Contrarily, the host cells demonstrated certain tolerance against depressurization stress as expression level of some immune-related genes returned to the basal level in isobaric samples. Altogether, the present study illustrates the distinct stress responses of Bathymodiolinae hosts and their methanotrophic symbionts against depressurization, which could provide further insight into the deep-sea adaptation of Bathymodiolinae holobionts while highlighting the necessity of using isobaric sampling methods in deep-sea research.

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