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Antimicrobial Agents and Chemotherapy, February 2007, p. 616-622, Vol. 51, No. 2
0066-4804/07/$08.00+0     doi:10.1128/AAC.01057-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Vancomycin-Intermediate Staphylococcus aureus Strains Have Impaired Acetate Catabolism: Implications for Polysaccharide Intercellular Adhesin Synthesis and Autolysis{triangledown}

Jennifer L. Nelson,1,{dagger} Kelly C. Rice,2 Sean R. Slater,2 Paige M. Fox,3 Gordon L. Archer,3 Kenneth W. Bayles,2 Paul D. Fey,2 Barry N. Kreiswirth,4 and Greg A. Somerville1*

Department of Veterinary and Biomedical Sciences, University of Nebraska, Lincoln, Nebraska 68583,1 Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska 68198,2 Division of Infectious Diseases, Department of Internal Medicine, Virginia Commonwealth University, Richmond, Virginia 23298,3 Public Health Research Institute, 225 Warren Street, Newark, New Jersey 071034

Received 22 August 2006/ Returned for modification 23 October 2006/ Accepted 15 November 2006

The most common mechanism by which Staphylococcus aureus gains resistance to vancomycin is by adapting its physiology and metabolism to permit growth in the presence of vancomycin. Several studies have examined the adaptive changes occurring during the transition to vancomycin-intermediate resistance, leading to a model of vancomycin resistance in which decreased cell wall turnover and autolysis result in increased cell wall thickness and resistance to vancomycin. In the present study, we identified metabolic changes common to vancomycin-intermediate S. aureus (VISA) strains by assessing the metabolic and growth characteristics of two VISA strains (vancomycin MICs of 8 µg/ml) and two isogenic derivative strains with vancomycin MICs of 32 µg/ml. Interestingly, we observed the parental strains had impaired catabolism of nonpreferred carbon sources (i.e., acetate), and this impairment became more pronounced as vancomycin resistance increased. To determine if acetate catabolism impairment is common to VISA strains, we assessed the ability of VISA and vancomycin-sensitive S. aureus (VSSA) clinical isolates to catabolize acetate. As expected, a significantly greater percentage of VISA strains (71%) had impaired acetate catabolism relative to VSSA (8%). This is an important observation because staphylococcal acetate catabolism is implicated in growth yield and antibiotic tolerance and in regulating cell death and polysaccharide intercellular adhesin synthesis.

* Corresponding author. Mailing address: Department of Veterinary and Biomedical Sciences, University of Nebraska, 155 VBS, East Campus Loop, Lincoln, NE 68583-0905. Phone: (402) 472-6063. Fax: (402) 472-9690. E-mail: gsomerville3{at}unl.edu.

{triangledown} Published ahead of print on 27 November 2006.

{dagger} Present address: Biology Department, Morningside College, Sioux City, IA 51106.

Antimicrobial Agents and Chemotherapy, February 2007, p. 616-622, Vol. 51, No. 2
0066-4804/07/$08.00+0     doi:10.1128/AAC.01057-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Somerville, G. A., Proctor, R. A. (2009). At the Crossroads of Bacterial Metabolism and Virulence Factor Synthesis in Staphylococci. Microbiol. Mol. Biol. Rev. 73: 233-248 [Abstract] [Full Text]  
  • Rice, K. C., Bayles, K. W. (2008). Molecular Control of Bacterial Death and Lysis. Microbiol. Mol. Biol. Rev. 72: 85-109 [Abstract] [Full Text]  
  • Meehl, M., Herbert, S., Gotz, F., Cheung, A. (2007). Interaction of the GraRS Two-Component System with the VraFG ABC Transporter To Support Vancomycin-Intermediate Resistance in Staphylococcus aureus. Antimicrob. Agents Chemother. 51: 2679-2689 [Abstract] [Full Text]  


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