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Evidence for nontraditional mcr-containing archaea contributing to biological methanogenesis in geothermal springs

Recent discoveries of methyl-coenzyme M reductase–encoding genes (mcr) in uncultured archaea beyond traditional euryarchaeotal methanogens have reshaped our view of methanogenesis. However, whether any of these nontraditional archaea perform methanogenesis remains elusive. Here, we report field and...

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Detalles Bibliográficos
Autores principales: Wang, Jiajia, Qu, Yan-Ni, Evans, Paul N., Guo, Qinghai, Zhou, Fengwu, Nie, Ming, Jin, Qusheng, Zhang, Yan, Zhai, Xiangmei, Zhou, Ming, Yu, Zhiguo, Fu, Qing-Long, Xie, Yuan-Guo, Hedlund, Brian P., Li, Wen-Jun, Hua, Zheng-Shuang, Wang, Zimeng, Wang, Yanxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10306296/
https://www.ncbi.nlm.nih.gov/pubmed/37379385
http://dx.doi.org/10.1126/sciadv.adg6004
Descripción
Sumario:Recent discoveries of methyl-coenzyme M reductase–encoding genes (mcr) in uncultured archaea beyond traditional euryarchaeotal methanogens have reshaped our view of methanogenesis. However, whether any of these nontraditional archaea perform methanogenesis remains elusive. Here, we report field and microcosm experiments based on (13)C-tracer labeling and genome-resolved metagenomics and metatranscriptomics, revealing that nontraditional archaea are predominant active methane producers in two geothermal springs. Archaeoglobales performed methanogenesis from methanol and may exhibit adaptability in using methylotrophic and hydrogenotrophic pathways based on temperature/substrate availability. A five-year field survey found Candidatus Nezhaarchaeota to be the predominant mcr-containing archaea inhabiting the springs; genomic inference and mcr expression under methanogenic conditions strongly suggested that this lineage mediated hydrogenotrophic methanogenesis in situ. Methanogenesis was temperature-sensitive , with a preference for methylotrophic over hydrogenotrophic pathways when incubation temperatures increased from 65° to 75°C. This study demonstrates an anoxic ecosystem wherein methanogenesis is primarily driven by archaea beyond known methanogens, highlighting diverse nontraditional mcr-containing archaea as previously unrecognized methane sources.