Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota

Author:

Seymour Cale O.,Palmer Marike,Becraft Eric D.,Stepanauskas RamunasORCID,Friel Ariel D.,Schulz FrederikORCID,Woyke TanjaORCID,Eloe-Fadrosh EmileyORCID,Lai DengxunORCID,Jiao Jian-Yu,Hua Zheng-ShuangORCID,Liu LanORCID,Lian Zheng-Han,Li Wen-JunORCID,Chuvochina Maria,Finley Brianna K.,Koch Benjamin J.ORCID,Schwartz Egbert,Dijkstra Paul,Moser Duane P.,Hungate Bruce A.ORCID,Hedlund Brian P.ORCID

Abstract

AbstractCandidate bacterial phylum Omnitrophota has not been isolated and is poorly understood. We analysed 72 newly sequenced and 349 existing Omnitrophota genomes representing 6 classes and 276 species, along with Earth Microbiome Project data to evaluate habitat, metabolic traits and lifestyles. We applied fluorescence-activated cell sorting and differential size filtration, and showed that most Omnitrophota are ultra-small (~0.2 μm) cells that are found in water, sediments and soils. Omnitrophota genomes in 6 classes are reduced, but maintain major biosynthetic and energy conservation pathways, including acetogenesis (with or without the Wood-Ljungdahl pathway) and diverse respirations. At least 64% of Omnitrophota genomes encode gene clusters typical of bacterial symbionts, suggesting host-associated lifestyles. We repurposed quantitative stable-isotope probing data from soils dominated by andesite, basalt or granite weathering and identified 3 families with high isotope uptake consistent with obligate bacterial predators. We propose that most Omnitrophota inhabit various ecosystems as predators or parasites.

Funder

National Science Foundation

National Aeronautics and Space Administration

DOE | Office of Science

National Natural Science Foundation of China

Department of Education and Training | Australian Research Council

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Microbiology (medical),Genetics,Applied Microbiology and Biotechnology,Immunology,Microbiology

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