Genomic diversity of novel strains of mammalian gut microbiome derivedClostridiumXIVa strains is driven by mobile genetic element acquisition

Abstract

AbstractDespite advances in sequencing technologies that enable a greater understanding of mammalian gut microbiome composition, our ability to determine a role for individual strains is hampered by our inability to isolate, culture and study such microbes. Here we describe highly unusualClostridiumXIVa group strains isolated from the murine gut. Genome sequencing indicates that these strains,Clostridium symbiosumLM19B and LM19R andClostridium clostridioformeLM41 and LM42, have significantly larger genomes than most closely related strains. Genomic evidence indicates that the isolated LM41 and LM42 strains diverge from most otherClostridiumXIVa strains and supports reassignment of these groups at genus-level. We attribute increasedC. clostridioformeLM41 and LM42 genome size to acquisition of mobile genetic elements including dozens of prophages, integrative elements, putative group II introns and numerous transposons including 29 identical copies of the IS66 transposase, and a very large 192 Kb plasmid. antiSmash analysis determines a greater number of biosynthetic gene clusters within LM41 and LM42 than in related strains, encoding a diverse array of potential novel antimicrobial compounds. Together these strains highlight the potential untapped microbial diversity that remains to be discovered within the gut microbiome and indicate that, despite our ability to get a top down view of microbial diversity, we remain significantly blinded to microbe capabilities at the strain level.