3-Ketosteroid 9 alpha-hydroxylase is an essential factor in the pathogenesis of Mycobacterium tuberculosis

Research output: Contribution to journalArticle

Authors

  • Y Hu
  • R van der Geize
  • A Liu
  • M Rohde
  • M Singh
  • A Coates

Colleges, School and Institutes

Abstract

Mycobacterium tuberculosis H37Rv contains the kshA (Rv3526) and kshB (Rv3571) genes, encoding 3-ketosteroid 9a-hydroxylase (KSH). Consistent with their predicted roles, the Delta kshA and Delta kshB deletion mutants of M. tuberculosis H37Rv were unable to use cholesterol and 4-androstene-3,17-dione as primary carbon and energy sources. Interestingly, Delta kshA and Delta kshB mutants were also unable to metabolize the steroid substrate 5 alpha-androstane-3,17-dione, whereas wild-type M. tuberculosis H37Rv could. The deletion of either of these genes lead to rapid death of the microorganism in murine infection models and in macrophages, showing that kshA and kshB are essential factors for M. tuberculosis pathogenesis. Penta-acylated trehalose (PAT) biosynthesis was altered in the Delta kshB mutant, but not the Delta kshA mutant. The Delta kshB mutant synthesizes all other types of lipids. The Delta kshB mutant had a thickened outer layer in its cell wall. KshB thus appears to be involved in multiple processes, probably as a reductase of different oxygenases. We conclude that an impaired 3-ketosteroid 9 alpha-hydroxylase activity is the cause of the highly attenuated phenotype of our M. tuberculosis H37Rv mutants.

Details

Original languageEnglish
Pages (from-to)107-121
Number of pages15
JournalMolecular Microbiology
Volume75
Issue number1
Publication statusPublished - 1 Jan 2010