Tuberculosis is a leading cause of death worldwide and infects thousands of Americans annually. Mycobacterium bovis causes tuberculosis in humans and several animal species. Peracetic acid is an approved tuberculocide in hospital and domestic
environments. This study presents for the first time the transcriptomic changes in M. bovis BCG after treatment with 0.1 mM peracetic acid for 10 and 20 min. This study also presents for the first time a comparison
among the transcriptomic responses of M. bovis BCG to three oxidative disinfectants: peracetic acid, sodium hypochlorite, and hydrogen peroxide after 10 min of treatment.
Results indicate that arginine biosynthesis, virulence, and oxidative stress response genes were upregulated after both peracetic
acid treatment times. Three DNA repair genes were downregulated after 10 and 20 min and cell wall component genes were upregulated
after 20 min. The devR–devS signal transduction system was upregulated after 10 min, suggesting a role in the protection against peracetic acid treatment.
Results also suggest that peracetic acid and sodium hypochlorite both induce the expression of the ctpF gene which is upregulated in hypoxic environments. Further, this study reveals that in M. bovis BCG, hydrogen peroxide and peracetic acid both induce the expression of katG involved in oxidative stress response and the mbtD and mbtI genes involved in iron regulation/virulence.
Keywords Microarrays –
Mycobacterium bovis BCG – Peracetic acid – Sodium hypochlorite – Hydrogen peroxide – Transcriptomics