transplantation and multiple omics reveal holobiont adaptation in deep-sea mussel .

Fuente: PubMed
Salvato in:
Dettagli Bibliografici
Autori principali: Wei, Tong, Yan, Guoyong, Perez, Maeva, He, Xing, Wong, Wai Chuen, Xu, Ting, Lan, Yi, Sun, Jin, Qian, Pei-Yuan
Natura: Artículo científico
Lingua:en
Pubblicazione: iScience 2026
Accesso online:
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!
_version_ 1868266087582269441
author Wei, Tong
Yan, Guoyong
Perez, Maeva
He, Xing
Wong, Wai Chuen
Xu, Ting
Lan, Yi
Sun, Jin
Qian, Pei-Yuan
author_facet Wei, Tong
Yan, Guoyong
Perez, Maeva
He, Xing
Wong, Wai Chuen
Xu, Ting
Lan, Yi
Sun, Jin
Qian, Pei-Yuan
Wei, Tong
Yan, Guoyong
Perez, Maeva
He, Xing
Wong, Wai Chuen
Xu, Ting
Lan, Yi
Sun, Jin
Qian, Pei-Yuan
collection PubMed - marine biology
contents transplantation and multiple omics reveal holobiont adaptation in deep-sea mussel . Wei, Tong Yan, Guoyong Perez, Maeva He, Xing Wong, Wai Chuen Xu, Ting Lan, Yi Sun, Jin Qian, Pei-Yuan Deep-sea mussels rely on methane-oxidizing bacteria (MOB) endosymbionts for nutrition in methane seeps, yet the molecular mechanisms enabling holobiont resilience to environmental fluctuations remain unclear. Here, we integrate a chromosome-scale genome of . with an transplantation experiment and multi-omics analyses to investigate adaptive responses to methane limitation. Transplanting mussels to a low-methane environment for 6 days reduced MOB abundance by 30.6%. -transcriptomics showed that MOB prioritized methane oxidation via upregulated / genes but downregulated amino acid biosynthesis and non-essential pathways, indicating metabolic resource reallocation. Concurrently, host transcriptomics revealed a shift from symbiont-dependent strategies ("farming" and "milking") to filter-feeding and extracellular matrix remodeling, indicating changes in trophic level. This dynamic interplay demonstrates how the holobiont balances symbiont maintenance with alternative energy acquisition under stress and highlights the vulnerability of chemosynthetic symbioses to methane fluctuations induced by environmental changes.
format Artículo científico
id pubmed_41660251
institution PubMed
language en
publishDate 2026
publisher iScience
record_format pubmed
spellingShingle transplantation and multiple omics reveal holobiont adaptation in deep-sea mussel .
Wei, Tong
Yan, Guoyong
Perez, Maeva
He, Xing
Wong, Wai Chuen
Xu, Ting
Lan, Yi
Sun, Jin
Qian, Pei-Yuan
transplantation and multiple omics reveal holobiont adaptation in deep-sea mussel . Wei, Tong Yan, Guoyong Perez, Maeva He, Xing Wong, Wai Chuen Xu, Ting Lan, Yi Sun, Jin Qian, Pei-Yuan Deep-sea mussels rely on methane-oxidizing bacteria (MOB) endosymbionts for nutrition in methane seeps, yet the molecular mechanisms enabling holobiont resilience to environmental fluctuations remain unclear. Here, we integrate a chromosome-scale genome of . with an transplantation experiment and multi-omics analyses to investigate adaptive responses to methane limitation. Transplanting mussels to a low-methane environment for 6 days reduced MOB abundance by 30.6%. -transcriptomics showed that MOB prioritized methane oxidation via upregulated / genes but downregulated amino acid biosynthesis and non-essential pathways, indicating metabolic resource reallocation. Concurrently, host transcriptomics revealed a shift from symbiont-dependent strategies ("farming" and "milking") to filter-feeding and extracellular matrix remodeling, indicating changes in trophic level. This dynamic interplay demonstrates how the holobiont balances symbiont maintenance with alternative energy acquisition under stress and highlights the vulnerability of chemosynthetic symbioses to methane fluctuations induced by environmental changes.
title transplantation and multiple omics reveal holobiont adaptation in deep-sea mussel .
url https://pubmed.ncbi.nlm.nih.gov/41660251/