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Antimicrobial Agents and Chemotherapy, May 2007, p. 1708-1718, Vol. 51, No. 5
0066-4804/07/$08.00+0     doi:10.1128/AAC.01180-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Evaluation of the metS and murB Loci for Antibiotic Discovery Using Targeted Antisense RNA Expression Analysis in Bacillus anthracis{triangledown}

G. C. Kedar, Vickie Brown-Driver, Daniel R. Reyes, Mark T. Hilgers, Mark A. Stidham, Karen Joy Shaw, John Finn, and Robert J. Haselbeck*

Trius Therapeutics, San Diego, California

Received 21 September 2006/ Returned for modification 16 November 2006/ Accepted 16 February 2007

The biowarfare-relevant bacterial pathogen Bacillus anthracis contains two paralogs each of the metS and murB genes, which encode the important antibiotic target functions methionyl-tRNA synthetase and UDP-N-acetylenolpyruvoylglucosamine reductase, respectively. Empirical screens were conducted to detect and characterize gene fragments of each of these four genes that could cause growth reduction of B. anthracis when inducibly expressed from a plasmid-borne promoter. Numerous such gene fragments that were overwhelmingly in the antisense orientation were identified for the metS1 and murB2 alleles, while no such orientation bias was seen for the metS2 and murB1 alleles. Gene replacement mutagenesis was used to confirm the essentiality of the metS1 and murB2 alleles, and the nonessentiality of the metS2 and murB1 alleles, for vegetative growth. Induced transcription of RNA from metS1 and murB2 antisense-oriented gene fragments resulted in specific reduction of mRNA of their cognate genes. Attenuation of MetS1 enzyme expression hypersensitized B. anthracis cells to a MetS-specific antimicrobial compound but not to other antibiotics that affect cell wall assembly, fatty acid biosynthesis, protein translation, or DNA replication. Antisense-dependent reduction of MurB2 enzyme expression caused hypersensitivity to beta-lactam antibiotics, a synergistic response that has also been noted for the MurA-specific antibiotic fosfomycin. These experiments form the basis of mode-of-action detection assays that can be used in the discovery of novel MetS- or MurB-specific antibiotic drugs that are effective against B. anthracis or other gram-positive bacterial pathogens.

* Corresponding author. Mailing address: Trius Therapeutics Inc., 6310 Nancy Ridge Dr., Suite 105, San Diego, CA 92121. Phone: (858) 452-0370, ext. 107. Fax: (858) 452-0412. E-mail: rhaselbeck{at}triusrx.com

{triangledown} Published ahead of print on 5 March 2007.

Antimicrobial Agents and Chemotherapy, May 2007, p. 1708-1718, Vol. 51, No. 5
0066-4804/07/$08.00+0     doi:10.1128/AAC.01180-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Kedar, G. C., Brown-Driver, V., Reyes, D. R., Hilgers, M. T., Stidham, M. A., Shaw, K. J., Finn, J., Haselbeck, R. J. (2008). Comparison of the Essential Cellular Functions of the Two murA Genes of Bacillus anthracis. Antimicrob. Agents Chemother. 52: 2009-2013 [Abstract] [Full Text]  


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