A metabolomics investigation of the function of the ESX-1 gene cluster in mycobacteria. (November 2016)

• Record Type: Journal Article
• Authors: Loots, Du Toit; Swanepoel, Conrad C.; Newton-Foot, Mae; Gey van Pittius, Nicolaas C.
• Is Part Of: Microbial pathogenesis. Volume 100(2016)
• Page Start: 268
• Page End: 275
• Publication Date: 2016-11
• Subjects: Metabolomics -- Tuberculosis -- ESX-1 -- Virulence -- GCxGC-TOFMS; Pathogenic microorganisms -- Periodicals; Pathology, Molecular -- Periodicals; Communicable Diseases -- microbiology -- Periodicals; Communicable Diseases -- parasitology -- Periodicals; Micro-organismes pathogènes -- Périodiques; Pathologie moléculaire -- Périodiques; Electronic journals; 616.9041
• DOI: 10.1016/j.micpath.2016.10.008
• Languages: English
• ISSNs: 0882-4010

Abstract

Abstract: The ESX-1 gene cluster, encoding the Type-VII secretion (T7S) system and its virulence associated proteins, ESAT-6 and CFP-10, is thought to be responsible for the transport of extracellular proteins across the hydrophobic and highly impermeable, cell envelope of Mycobacterium, and is involved in virulence in Mycobacterium tuberculosis, the causative agent of tuberculosis. Using a GCxGC-TOFMS metabolomics approach, a M. smegmatis ESX-1 knock-out strain (ΔESX-1ms ) was compared to that of the M. smegmatis wild-type parent strain, and the metabolite markers due to the presence or absence of the ESX-1 gene cluster were identified. A general increase in specific metabolites in the ΔESX-1ms, confirmed the roles previously described for ESX-1 in mycolic acid biosynthesis and cell wall integrity. However, a number of other metabolite markers identified indicates ESX-1 has an additional role the in cell envelope structure, altering the levels of antioxidants and energy metabolism. Furthermore, the metabolome profiles correlated with the metabolomic variation observed when comparing a hyper- and hypo-virulent Beijing strain of M. tuberculosis, suggesting that the pathways which modulate virulence in M. tuberculosis are also influenced by ESX-1, reaffirming the previously described association of ESX-1 with virulence and cell envelope biogenesis. Highlights: The metabolite profiles of the ΔESX-1ms relative to wild-type strain of M. smegmatis were compared using metabolomics. Metabolite markers associates ESX-1 with cell wall biosynthesis, redox balance and energy metabolism. Metabolite markers additionally suggests that ESX-1 influences the same pathways which influence virulence in M. tuberculosis .