Global transcriptome analysis of the Mycobacterium bovis BCG response to sodium hypochlorite

被引:16
作者
Jang, Hyeung-Jin [3 ]
Nde, Chantal [2 ]
Toghrol, Freshteh [1 ]
Bentley, William E. [2 ]
机构
[1] US EPA, Microarray Res Lab, Biol & Econ Anal Div, Off Pesticide Programs, Ft George G Meade, MD 20755 USA
[2] Univ Maryland, Inst Biotechnol, Ctr Biosyst Res, College Pk, MD 20742 USA
[3] Kyung Hee Univ, Coll Oriental Med, Dept Biochem, Seoul 130701, South Korea
关键词
Toxicogenomics; Microarray; Mycobacterium bovis BCG; Sodium hypochlorite; Bleach; SINGLET MOLECULAR-OXYGEN; PE-PGRS PROTEINS; STAPHYLOCOCCUS-AUREUS; HYDROGEN-PEROXIDE; ESCHERICHIA-COLI; MYCOLIC ACIDS; PSEUDOMONAS-AERUGINOSA; TOXICOGENOMIC RESPONSE; PERACETIC-ACID; TUBERCULOSIS;
D O I
10.1007/s00253-009-2208-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Tuberculosis is a common and often deadly infectious disease caused by mycobacteria, mainly Mycobacterium tuberculosis and infrequently by other subspecies of the M. tuberculosis complex, such as M. bovis. Sodium hypochlorite (bleach) is routinely used in hospitals and health care facilities for surface sterilization; however, the modes of action of bleach on M. bovis BCG and how this organism develops resistance to sodium hypochlorite have not been elucidated. In this study, we performed a global toxicogenomic analysis of the M. bovis response to 2.5 mM sodium hypochlorite after 10 and 20 min. M. bovis BCG growth was monitored by measuring the quantity of ATP in picomoles produced over a short exposure time (10-60 min) to sodium hypochlorite. This study revealed significant regulation of oxidative stress response genes of M. bovis BCG, such as oxidoreductase, peroxidase, heat shock proteins and lipid transport, and metabolism genes. We interpreted this response as a potentially more lethal interplay between fatty acid metabolism, sulfur metabolism, and oxidative stress. Our results also suggest that sodium hypochlorite repressed transcription of genes involved in cell wall synthesis of M. bovis. This study shows that the treatment of M. bovis BCG with bleach inhibits the biosynthesis of outer cell wall mycolic acids and also induces oxidative damage.
引用
收藏
页码:127 / 140
页数:14
相关论文
共 40 条
[1]  
*AFF INC, 2004, AFF GENECHIP EXPR AN
[2]   OXIDATIVE INACTIVATION OF ESCHERICHIA-COLI BY HYPOCHLOROUS ACID - RATES AND DIFFERENTIATION OF RESPIRATORY FROM OTHER REACTION SITES [J].
ALBRICH, JM ;
HURST, JK .
FEBS LETTERS, 1982, 144 (01) :157-161
[3]   Are the PE-PGRS proteins of Mycobacterium tuberculosis variable surface antigens? [J].
Banu, S ;
Honoré, N ;
Saint-Joanis, B ;
Philpott, D ;
Prévost, MC ;
Cole, ST .
MOLECULAR MICROBIOLOGY, 2002, 44 (01) :9-19
[4]   Mycolic acids: Structure, biosynthesis and physiological functions [J].
Barry, CE ;
Lee, RE ;
Mdluli, K ;
Sampson, AE ;
Schroeder, BG ;
Slayden, RA ;
Yuan, Y .
PROGRESS IN LIPID RESEARCH, 1998, 37 (2-3) :143-179
[5]   Evidence that mycobacterial PE_PGRS proteins are cell surface constituents that influence interactions with other cells [J].
Brennan, MJ ;
Delogu, G ;
Chen, YP ;
Bardarov, S ;
Kriakov, J ;
Alavi, M ;
Jacobs, WR .
INFECTION AND IMMUNITY, 2001, 69 (12) :7326-7333
[6]  
Cahn Pedro, 2003, J Int Assoc Physicians AIDS Care (Chic), V2, P106, DOI 10.1177/154510970300200303
[7]   Tuberculosis among foreign-born persons in the United States [J].
Cain, Kevin P. ;
Benoit, Stephen R. ;
Winston, Carla A. ;
Mac Kenzie, William R. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2008, 300 (04) :405-412
[8]   FREE HYDROXYL RADICALS ARE FORMED ON REACTION BETWEEN THE NEUTROPHIL-DERIVED SPECIES SUPEROXIDE ANION AND HYPOCHLOROUS ACID [J].
CANDEIAS, LP ;
PATEL, KB ;
STRATFORD, MRL ;
WARDMAN, P .
FEBS LETTERS, 1993, 333 (1-2) :151-153
[9]   Toxicogenomic response to chlorination includes induction of major virulence genes in staphylococcus aureus [J].
Chang, Matthew Wook ;
Toghrol, Freshteh ;
Bentley, William E. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2007, 41 (21) :7570-7575
[10]   Microarray analysis of Pseudomonas aeruginosa reveals induction of pyocin genes in response to hydrogen peroxide -: art. no. 115 [J].
Chang, W ;
Small, DA ;
Toghrol, F ;
Bentley, WE .
BMC GENOMICS, 2005, 6 (1) :1-14