Deep-Sea Vent Bacterium Sheds Light on Evolutionary Journey

A new bacterial species discovered at the deep-sea hydrothermal vent site 'Crab Spa' provides a deeper understanding of bacterial evolution.

Deep-sea hydrothermal vents are hot springs on the ocean floor. Sea water penetrates into the ocean crust, becomes heated, and rises to the seafloor surface carrying dissolved nutrients. Around these vents, far from any sunlight, vibrant biological communities are found. Here, microbes play the role of primary producers through chemosynthesis-;similar to the role that plants play on land through photosynthesis.

Researchers at Hokkaido University, in collaboration with colleagues at Woods Hole Oceanographic Institution, have been working on understanding microbial diversity at deep-sea hydrothermal environments on the East Pacific Rise based on microbe cultivation studies. They isolated a novel campylobacterial strain from a warm-water vent known as 'Crab Spa' and named it Hydrogenimonas cancrithermarum, after the site. Their findings were published in the journal International Journal of Systematic and Evolutionary Microbiology.

Chemolithoautotrophic species of the class Campylobacteria (aka Epsilonproteobacteria) are recognized as an ecologically important bacterial group at hydrothermal vents, contributing to primary production. On the other hand, some members of this class, e.g., Helicobacter, Arcobacter, and Campylobacter, are also well known pathogens of humans and animals."

Sayaka Mino, Assistant Professor, first author of the paper and research group leader at the Faculty of Fisheries Sciences, Hokkaido University

Hydrogenimonas is known as the thermophilic (adapted to hot temperatures) genus that is most closely related to mesophilic and pathogenic genera in the class Campylobacteria. Yet, only two described species have so far been reported in this genus. The present study revealed that the new strain represents the first mesophilic (adapted to moderate temperatures) and sulfur-oxidizing bacterium in the genus, expanding the physiological and metabolic characteristics of the genus.

"The discovery of a mesophilic Hydrogenimonas species was unexpected. The strain likely provides us with the opportunity to investigate their evolutionary transition from a thermophilic to a mesophilic and from an autotrophic (capable of creating organic compounds) to a heterotrophic (consumes autotrophs to obtain organic compounds) lifestyle," says Mino.

They further conducted a comprehensive comparative study of the genomes of Campylobacteria, and discovered that the genes responsible for the phosphotransacetylase-acetate kinase (Pta-AckA) pathway tend to be conserved between Hydrogenimonas and the mesophilic species that subsequently diverged from Hydrogenimonas, regardless of their metabolism and pathogenicity.

"The Pta-AkaA pathway has been reported in a pathogenic Campylobacter species to play an important role in colonizing hosts. While we don't yet understand its specific role in the genus Hydrogenimonas, the acquisition of the genes might represent a key event that enabled their diversification from deep-sea vents to other environments," says Dr. Stefan Sievert, leader of the research group at the Woods Hole Oceanographic Institution.

"Nowadays, studies of microbial diversity largely rely on cultivation-independent metagenomic sequencing approaches which produce massive amounts of data," concludes Mino, "Yet, it is vital to remember the significance of cultivation, as shown by the isolation of the new strain that differs markedly from other members of the genus Hydrogenimonas." The researchers will continue their efforts to discover new culturable species and thus contribute to the understanding of the diversity of Campylobacteria.

Source:
Journal reference:

Mino, S., et al. (2023). Hydrogenimonas cancrithermarum sp. nov., a hydrogen- and thiosulfate-oxidizing mesophilic chemolithoautotroph isolated from diffuse-flow fluids on the East Pacific Rise, and an emended description of the genus Hydrogenimonas. International Journal of Systematic and Evolutionary Microbiology. doi.org/10.1099/ijsem.0.006132.

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