Depletion of antibiotic targets has widely varying effects on growth

被引:130
作者
Wei, Jun-Rong [1 ]
Krishnamoorthy, Vidhya [1 ]
Murphy, Kenan [2 ]
Kim, Jee-Hyun [4 ]
Schnappinger, Dirk [4 ]
Alber, Tom [5 ,6 ]
Sassetti, Christopher M. [2 ,3 ]
Rhee, Kyu Y. [4 ,7 ]
Rubin, Eric J. [1 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[2] Univ Massachusetts, Sch Med, Dept Mol Genet & Microbiol, Worcester, MA 01655 USA
[3] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01655 USA
[4] Weill Cornell Med Coll, Dept Microbiol & Immunol, New York, NY 10065 USA
[5] Univ Calif Berkeley, Dept Mol & Biol, Berkeley, CA 94720 USA
[6] Univ Calif Berkeley, Inst QB3, Berkeley, CA 94720 USA
[7] Weill Cornell Med Coll, Dept Med, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
inducible proteolysis; HIV protease; trimethoprim; MYCOBACTERIUM-TUBERCULOSIS; ALANINE RACEMASE; GENE; SYSTEM; DEGRADATION; MECHANISM; DEATH; PURIFICATION; PROTEINS; ENZYME;
D O I
10.1073/pnas.1018301108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is often assumed that antibiotics act on the most vulnerable cellular targets, particularly those that require limited inhibition to block growth. To evaluate this assumption, we developed a genetic method that can inducibly deplete targeted proteins and that mimics their chemical inactivation. We applied this system to current antibiotic targets in mycobacteria. Although depleting some antibiotic targets significantly perturbs bacterial growth, surprisingly, we found that reducing the levels of other targets by more than 97% had little or no effect on growth. For one of these targets, dihydrofolate reductase, metabolic analysis suggested that depletion mimics the use of subinhibitory concentrations of the antibiotic trimethroprim. These observations indicate that some drug targets can exist at levels much higher than are needed to support growth. However, protein depletion can be used to identify promising drug targets that are particularly vulnerable to inhibition.
引用
收藏
页码:4176 / 4181
页数:6
相关论文
共 33 条
[1]   Mycobacterium tuberculosis dihydrofolate reductase is a target for isoniazid [J].
Argyrou, A ;
Vetting, MW ;
Aladegbami, B ;
Blanchard, JS .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (05) :408-413
[2]   Rising standards for tuberculosis drug development [J].
Balganesh, Tanjore S. ;
Alzari, Pedro M. ;
Cole, Stewart T. .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2008, 29 (11) :576-581
[3]   INHA, A GENE ENCODING A TARGET FOR ISONIAZID AND ETHIONAMIDE IN MYCOBACTERIUM-TUBERCULOSIS [J].
BANERJEE, A ;
DUBNAU, E ;
QUEMARD, A ;
BALASUBRAMANIAN, V ;
UM, KS ;
WILSON, T ;
COLLINS, D ;
DELISLE, G ;
JACOBS, WR .
SCIENCE, 1994, 263 (5144) :227-230
[4]   The spectrum of latent tuberculosis: rethinking the biology and intervention strategies [J].
Barry, Clifton E., III ;
Boshoff, Helena I. ;
Dartois, Veronique ;
Dick, Thomas ;
Ehrt, Sabine ;
Flynn, JoAnne ;
Schnappinger, Dirk ;
Wilkinson, Robert J. ;
Young, Douglas .
NATURE REVIEWS MICROBIOLOGY, 2009, 7 (12) :845-855
[5]   Overexpression of the D-alanine racemase gene confers resistance to D-cycloserine in Mycobacterium smegmatis [J].
Caceres, NE ;
Harris, NB ;
Wellehan, JF ;
Feng, ZY ;
Kapur, V ;
Barletta, RG .
JOURNAL OF BACTERIOLOGY, 1997, 179 (16) :5046-5055
[6]   Activity-Based Metabolomic Profiling of Enzymatic Function: Identification of Rv1248c as a Mycobacterial 2-Hydroxy-3-oxoadipate Synthase [J].
de Carvalho, Luiz Pedro S. ;
Zhao, Hong ;
Dickinson, Caitlyn E. ;
Arango, Nancy M. ;
Lima, Christopher D. ;
Fischer, Steven M. ;
Ouerfelli, Ouathek ;
Nathan, Carl ;
Rhee, Kyu Y. .
CHEMISTRY & BIOLOGY, 2010, 17 (04) :323-332
[7]   Mechanism of fluoroquinolone action [J].
Drlica, K .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (05) :504-508
[8]   Gyrase inhibitors induce an oxidative damage cellular death pathway in Escherichia coli [J].
Dwyer, Daniel J. ;
Kohanski, Michael A. ;
Hayete, Boris ;
Collins, James J. .
MOLECULAR SYSTEMS BIOLOGY, 2007, 3 (1)
[9]   Controlling gene expression in mycobacteria with anhydrotetracycline and Tet repressor [J].
Ehrt, S ;
Guo, XZV ;
Hickey, CM ;
Ryou, M ;
Monteleone, M ;
Riley, LW ;
Schnappinger, D .
NUCLEIC ACIDS RESEARCH, 2005, 33 (02) :e21
[10]   BIOSYNTHETIC ALANINE RACEMASE OF THE SALMONELLA-TYPHIMURIUM - PURIFICATION AND CHARACTERIZATION OF THE ENZYME ENCODED BY THE AIR GENE [J].
ESAKI, N ;
WALSH, CT .
BIOCHEMISTRY, 1986, 25 (11) :3261-3267