A factor converting viable but nonculturable Vibrio cholerae to a culturable state in eukaryotic cells is a human catalase

Microbiologyopen. 2015 Aug;4(4):589-96. doi: 10.1002/mbo3.264. Epub 2015 May 13.

Abstract

In our previous work, we demonstrated that viable but nonculturable (VBNC) Vibrio cholerae O1 and O139 were converted to culturable by coculture with eukaryotic cells. Furthermore, we isolated a factor converting VBNC V. cholerae to culturable (FCVC) from a eukaryotic cell line, HT-29. In this study, we purified FCVC by successive column chromatographies comprising UNO Q-6 anion exchange, Bio-Scale CHT2-1 hydroxyapatite, and Superdex 200 10/300 GL. Homogeneity of the purified FCVC was demonstrated by SDS-PAGE. Nano-LC MS/MS analysis showed that the purified FCVC was a human catalase. An experiment of RNAi knockdown of catalase mRNA from HT-29 cells and treatment of the purified FCVC with a catalase inhibitor, 3-amino-1,2,4-triazole confirmed that the FCVC was a catalase. A possible role of the catalase in converting a VBNC V. cholerae to a culturable state in the human intestine is discussed.

Keywords: Catalase; FCVC; VBNC; Vibrio cholerae; factor converting VBNC to culturable.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalase / isolation & purification
  • Catalase / metabolism*
  • Cell Line
  • Chromatography, Liquid
  • Coculture Techniques
  • Electrophoresis, Polyacrylamide Gel
  • Eukaryotic Cells / enzymology*
  • Humans
  • Tandem Mass Spectrometry
  • Vibrio cholerae O1 / growth & development
  • Vibrio cholerae O1 / physiology*

Substances

  • Catalase