Metagenomic Analysis of the Sponge Discodermia Reveals the Production of the Cyanobacterial Natural Product Kasumigamide by 'Entotheonella'

PLoS One. 2016 Oct 12;11(10):e0164468. doi: 10.1371/journal.pone.0164468. eCollection 2016.

Abstract

Sponge metagenomes are a useful platform to mine cryptic biosynthetic gene clusters responsible for production of natural products involved in the sponge-microbe association. Since numerous sponge-derived bioactive metabolites are biosynthesized by the symbiotic bacteria, this strategy may concurrently reveal sponge-symbiont produced compounds. Accordingly, a metagenomic analysis of the Japanese marine sponge Discodermia calyx has resulted in the identification of a hybrid type I polyketide synthase-nonribosomal peptide synthetase gene (kas). Bioinformatic analysis of the gene product suggested its involvement in the biosynthesis of kasumigamide, a tetrapeptide originally isolated from freshwater free-living cyanobacterium Microcystis aeruginosa NIES-87. Subsequent investigation of the sponge metabolic profile revealed the presence of kasumigamide in the sponge extract. The kasumigamide producing bacterium was identified as an 'Entotheonella' sp. Moreover, an in silico analysis of kas gene homologs uncovered the presence of kas family genes in two additional bacteria from different phyla. The production of kasumigamide by distantly related multiple bacterial strains implicates horizontal gene transfer and raises the potential for a wider distribution across other bacterial groups.

MeSH terms

  • Animals
  • Cyanobacteria / enzymology
  • Cyanobacteria / genetics*
  • Cyanobacteria / physiology
  • Gene Transfer, Horizontal
  • Metagenome*
  • Metagenomics
  • Multigene Family
  • Oligopeptides / genetics*
  • Oligopeptides / metabolism
  • Phylogeny
  • Polyketide Synthases / genetics
  • Polyketide Synthases / metabolism
  • Porifera / genetics*
  • Porifera / microbiology*
  • Porifera / physiology
  • Symbiosis*

Substances

  • Oligopeptides
  • kasumigamide
  • Polyketide Synthases

Grants and funding

This work was partly supported by the Takeda Science Foundation, the Sumitmo Foundation, the Naito Foundation, the Bilateral Program between Japan and Switzerland from the Japan Society for the Promotion of Science (JSPS), and Grants-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan (JSPS KAKENHI Grant Numbers JP16H06443, JP16H06448, JP16K13084, JP15H01836, JP15H03112, JP15K12740, and JP26303005). Y.N. is a recipient of the JSPS Fellowship for Young Scientist. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.