Thiol specific oxidative stress response in Mycobacteria

FEMS Microbiol Lett. 2005 Aug 1;249(1):87-94. doi: 10.1016/j.femsle.2005.06.004.

Abstract

The cellular response of mycobacteria to thiol specific oxidative stress was studied in Mycobacterium bovis BCG cultures. Two-dimensional gel electrophoresis revealed that upon diamide treatment at least 60 proteins were upregulated. Fourteen of these proteins were identified by MALDI-MS; four proteins, AhpC, Tpx, GroEL2, and GroEL1 are functionally related to oxidative stress response; eight proteins, LeuC, LeuD, Rv0224c, Rv3029c, AsnB, Rv2971, PheA and HisH are classified as part of the bacterial intermediary metabolism and respiration pathways; protein EchA14 belong to lipid metabolism, and NrdE, belongs to the mycobacterial information pathway category. Reverse transcription followed by quantitative real time PCR in response to diamide stress demonstrated that protein expression is directly proportional to the corresponding gene transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Diamide / pharmacology*
  • Electrophoresis, Gel, Two-Dimensional
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial*
  • Heat-Shock Response*
  • Mycobacterium bovis / drug effects*
  • Mycobacterium bovis / physiology
  • Oxidative Stress
  • Proteome
  • Reverse Transcriptase Polymerase Chain Reaction
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Sulfhydryl Compounds / pharmacology*
  • Transcription, Genetic

Substances

  • Bacterial Proteins
  • Proteome
  • Sulfhydryl Compounds
  • Diamide