Active lithoautotrophic and methane-oxidizing microbial community in an anoxic, sub-zero, and hypersaline High Arctic spring

• Published in: The ISME Journal
• Main Authors: Magnuson, Elisse, Altshuler, Ianina, Fernández-Martínez, Miguel Á, Chen, Ya-Jou, Maggiori, Catherine, Goordial, Jacqueline, Whyte, Lyle G
• Other Authors: Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada, Canada Research Chairs, Northern Research Supplement Program, Polar Continental Shelf Project, Fonds de Recherche du Québec - Nature et Technologies, Northern Scientific Training Program
• Format: Article in Journal/Newspaper
• Language: English
• Published: Oxford University Press (OUP) 2022
• Subjects: Nunavut; permafrost
• Online Access: http://dx.doi.org/10.1038/s41396-022-01233-8; https://www.nature.com/articles/s41396-022-01233-8.pdf; https://www.nature.com/articles/s41396-022-01233-8; https://academic.oup.com/ismej/article-pdf/16/7/1798/55013257/41396_2022_article_1233.pdf

Abstract Lost Hammer Spring, located in the High Arctic of Nunavut, Canada, is one of the coldest and saltiest terrestrial springs discovered to date. It perennially discharges anoxic (<1 ppm dissolved oxygen), sub-zero (~−5 °C), and hypersaline (~24% salinity) brines from the subsurface through up to 600 m of permafrost. The sediment is sulfate-rich (1 M) and continually emits gases composed primarily of methane (~50%), making Lost Hammer the coldest known terrestrial methane seep and an analog to extraterrestrial habits on Mars, Europa, and Enceladus. A multi-omics approach utilizing metagenome, metatranscriptome, and single-amplified genome sequencing revealed a rare surface terrestrial habitat supporting a predominantly lithoautotrophic active microbial community driven in part by sulfide-oxidizing Gammaproteobacteria scavenging trace oxygen. Genomes from active anaerobic methane-oxidizing archaea (ANME-1) showed evidence of putative metabolic flexibility and hypersaline and cold adaptations. Evidence of anaerobic heterotrophic and fermentative lifestyles were found in candidate phyla DPANN archaea and CG03 bacteria genomes. Our results demonstrate Mars-relevant metabolisms including sulfide oxidation, sulfate reduction, anaerobic oxidation of methane, and oxidation of trace gases (H2, CO2) detected under anoxic, hypersaline, and sub-zero ambient conditions, providing evidence that similar extant microbial life could potentially survive in similar habitats on Mars.