Replicated life-history patterns and subsurface origins of the bacterial sister phyla Nitrospirota and Nitrospinota

Author:

D’Angelo Timothy1,Goordial Jacqueline2ORCID,Lindsay Melody R1,McGonigle Julia13,Booker Anne1ORCID,Moser Duane4ORCID,Stepanauskus Ramunas1ORCID,Orcutt Beth N1ORCID

Affiliation:

1. Bigelow Laboratory for Ocean Sciences , 60 Bigelow Drive, East Boothbay, ME 04544, USA

2. University of Guelph, School of Environmental Sciences , 50 Stone Road East, Guelph, ON N1G 2W1, Canada

3. Basepaws Pet Genetics , 1820 W. Carson Street, Suite 202-351, Torrance, CA 90501, USA

4. Desert Research Institute , 755 East Flamingo Road, Las Vegas, NV 89119, USA

Abstract

Abstract The phyla Nitrospirota and Nitrospinota have received significant research attention due to their unique nitrogen metabolisms important to biogeochemical and industrial processes. These phyla are common inhabitants of marine and terrestrial subsurface environments and contain members capable of diverse physiologies in addition to nitrite oxidation and complete ammonia oxidation. Here, we use phylogenomics and gene-based analysis with ancestral state reconstruction and gene-tree–species-tree reconciliation methods to investigate the life histories of these two phyla. We find that basal clades of both phyla primarily inhabit marine and terrestrial subsurface environments. The genomes of basal clades in both phyla appear smaller and more densely coded than the later-branching clades. The extant basal clades of both phyla share many traits inferred to be present in their respective common ancestors, including hydrogen, one-carbon, and sulfur-based metabolisms. Later-branching groups, namely the more frequently studied classes Nitrospiria and Nitrospinia, are both characterized by genome expansions driven by either de novo origination or laterally transferred genes that encode functions expanding their metabolic repertoire. These expansions include gene clusters that perform the unique nitrogen metabolisms that both phyla are most well known for. Our analyses support replicated evolutionary histories of these two bacterial phyla, with modern subsurface environments representing a genomic repository for the coding potential of ancestral metabolic traits.

Funder

National Science Foundation

NASA | NASA Astrobiology Institute

Center for Dark Energy Biosphere Investigations

Publisher

Oxford University Press (OUP)

Subject

Ecology, Evolution, Behavior and Systematics,Microbiology

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