Characterization of sponge‐associated Verrucomicrobia: microcompartment‐based sugar utilization and enhanced toxin–antitoxin modules as features of host‐associated Opitutales. (12th September 2020)

• Record Type: Journal Article
• Authors: Sizikov, Sofia; Burgsdorf, Ilia; Handley, Kim Marie; Lahyani, Matan; Haber, Markus; Steindler, Laura
• Is Part Of: Environmental microbiology. Volume 22:Number 11(2020)
• Page Start: 4669
• Page End: 4688
• Publication Date: 2020-09-12
• Subjects: Microbial ecology -- Periodicals; Environmental Microbiology -- Periodicals; 579.17
• DOI: 10.1111/1462-2920.15210
• Languages: English
• ISSNs: 1462-2912

Abstract

Summary: Bacteria of the phylum Verrucomicrobia are ubiquitous in marine environments and can be found as free‐living organisms or as symbionts of eukaryotic hosts. Little is known about host‐associated Verrucomicrobia in the marine environment. Here we reconstructed two genomes of symbiotic Verrucomicrobia from bacterial metagenomes derived from the Atlanto‐Mediterranean sponge Petrosia ficiformis and three genomes from strains that we isolated from offshore seawater of the Eastern Mediterranean Sea. Phylogenomic analysis of these five strains indicated that they are all members of Verrucomicrobia subdivision 4, order Opitutales . We compared these novel sponge‐associated and seawater‐isolated genomes to closely related Verrucomicrobia . Genomic analysis revealed that Planctomycetes‐Verrucomicrobia microcompartment gene clusters are enriched in the genomes of symbiotic Opitutales including sponge symbionts but not in free‐living ones. We hypothesize that in sponge symbionts these microcompartments are used for degradation of l ‐fucose and l ‐rhamnose, which are components of algal and bacterial cell walls and therefore may be found at high concentrations in the sponge tissue. Furthermore, we observed an enrichment of toxin–antitoxin modules in symbiotic Opitutales . We suggest that, in sponges, verrucomicrobial symbionts utilize these modules as a defence mechanism against antimicrobial activity deriving from the abundant microbial community co‐inhabiting the host.