Characterization of Bacterial Communities Associated with the Tyrian Purple Producing Gland in a Marine Gastropod

PLoS One. 2015 Oct 21;10(10):e0140725. doi: 10.1371/journal.pone.0140725. eCollection 2015.

Abstract

Dicathais orbita is a marine mollusc recognised for the production of anticancer compounds that are precursors to Tyrian purple. This study aimed to assess the diversity and identity of bacteria associated with the Tyrian purple producing hypobranchial gland, in comparison with foot tissue, using a high-throughput sequencing approach. Taxonomic and phylogenetic analysis of variable region V1-V3 of 16S rRNA bacterial gene amplicons in QIIME and MEGAN were carried out. This analysis revealed a highly diverse bacterial assemblage associated with the hypobranchial gland and foot tissues of D. orbita. The dominant bacterial phylum in the 16S rRNA bacterial profiling data set was Proteobacteria followed by Bacteroidetes, Tenericutes and Spirochaetes. In comparison to the foot, the hypobranchial gland had significantly lower bacterial diversity and a different community composition, based on taxonomic assignment at the genus level. A higher abundance of indole producing Vibrio spp. and the presence of bacteria with brominating capabilities in the hypobranchial gland suggest bacteria have a potential role in biosynthesis of Tyrian purple in D. orbita.

MeSH terms

  • Animals
  • Bacterial Typing Techniques
  • Bacteroidetes / genetics
  • Bacteroidetes / isolation & purification
  • Base Sequence
  • Biodiversity
  • Gastropoda / microbiology*
  • High-Throughput Nucleotide Sequencing
  • Indoles / metabolism*
  • Microbiota / genetics*
  • Phylogeny
  • Proteobacteria / genetics
  • Proteobacteria / isolation & purification
  • RNA, Bacterial / genetics*
  • RNA, Ribosomal, 16S / genetics*
  • Sequence Analysis, DNA
  • Spirochaetales / genetics
  • Spirochaetales / isolation & purification
  • Tenericutes / genetics
  • Tenericutes / isolation & purification

Substances

  • 6,6'-dibromoindigo
  • Indoles
  • RNA, Bacterial
  • RNA, Ribosomal, 16S

Grants and funding

The authors received no specific funding for this work.