Host-Endosymbiont Genome Integration in a Deep-Sea Chemosymbiotic Clam

Research output: Journal Publications and Reviews (RGC: 21, 22, 62)21_Publication in refereed journalpeer-review

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Author(s)

  • Jack Chi-Ho Ip
  • Ting Xu
  • Jin Sun
  • Chong Chen
  • Yi Lan
  • Zhuang Han
  • Haibin Zhang
  • Jiangong Wei
  • Hongbin Wang
  • Jun Tao
  • Zongwei Cai
  • Pei-Yuan Qian
  • Jian-Wen Qiu

Detail(s)

Original languageEnglish
Pages (from-to)502-518
Number of pages17
Journal / PublicationMolecular Biology and Evolution
Volume38
Issue number2
Online published21 Sept 2020
Publication statusPublished - Feb 2021

Link(s)

Abstract

Endosymbiosis with chemosynthetic bacteria has enabled many deep-sea invertebrates to thrive at hydrothermal vents and cold seeps, but most previous studies on this mutualism have focused on the bacteria only. Vesicomyid clams dominate global deep-sea chemosynthesis-based ecosystems. They differ from most deep-sea symbiotic animals in passing their symbionts from parent to offspring, enabling intricate co-evolution between the host and the symbiont. Here, we sequenced the genomes of the clam Archivesica marissinica (Bivalvia: Vesicomyidae) and its bacterial symbiont to understand the genomic/metabolic integration behind this symbiosis. At 1.52 Gb, the clam genome encodes 28 genes horizontally transferred from bacteria, a large number of pseudogenes and transposable elements whose massive expansion corresponded to the timing of the rise and subsequent divergence of symbiont-bearing vesicomyids. The genome exhibits gene family expansion in cellular processes that likely facilitate chemoautotrophy, including gas delivery to support energy and carbon production, metabolite exchange with the symbiont, and regulation of the bacteriocyte population. Contraction in cellulase genes is likely adaptive to the shift from phytoplankton-derived to bacteria-based food. It also shows contraction in bacterial recognition gene families, indicative of suppressed immune response to the endosymbiont. The gammaproteobacterium endosymbiont has a reduced genome of 1.03 Mb but retains complete pathways for sulfur oxidation, carbon fixation, and biosynthesis of 20 common amino acids, indicating the host's high dependence on the symbiont for nutrition. Overall, the host-symbiont genomes show not only tight metabolic complementarity, but also distinct signatures of co-evolution allowing the vesicomyids to thrive in chemosynthesis-based ecosystems.

Research Area(s)

  • cold seep, genome assembly, genome erosion, hydrothermal vent, Mollusca, symbiosis

Bibliographic Note

© The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.

Citation Format(s)

Host-Endosymbiont Genome Integration in a Deep-Sea Chemosymbiotic Clam. / Ip, Jack Chi-Ho; Xu, Ting; Sun, Jin et al.
In: Molecular Biology and Evolution, Vol. 38, No. 2, 02.2021, p. 502-518.

Research output: Journal Publications and Reviews (RGC: 21, 22, 62)21_Publication in refereed journalpeer-review

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