Previous Article | Next Article 
Journal of Clinical Microbiology, September 2004, p. 4275-4283, Vol. 42, No. 9
0095-1137/04/$08.00+0 DOI: 10.1128/JCM.42.9.4275-4283.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Uses of Staphylococcus aureus GeneChips in Genotyping and Genetic Composition Analysis
P. M. Dunman,1,
W. Mounts,2 F. McAleese,1 F. Immermann,3 D. Macapagal,1 E. Marsilio,4 L. McDougal,4 F. C. Tenover,4 P. A. Bradford,1 P. J. Petersen,1 S. J. Projan,5 and E. Murphy1*
Wyeth Research,1
Biometrics Research,4
Pearl River, New York,3
Wyeth Genomics,2
Protein Technologies, Cambridge, Massachusetts,6
Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia5
Received 28 January 2004/
Returned for modification 26 March 2004/
Accepted 13 May 2004
Understanding the relatedness of strains within a bacterial species is essential for monitoring reservoirs of antimicrobial resistance and for epidemiological studies. Pulsed-field gel electrophoresis (PFGE), ribotyping, and multilocus sequence typing are commonly used for this purpose. However, these techniques are either nonquantitative or provide only a limited estimation of strain relatedness. Moreover, they cannot extensively define the genes that constitute an organism. In the present study, 21 oxacillin-resistant Staphylococcus aureus (ORSA) isolates, representing eight major ORSA lineages, and each of the seven strains for which the complete genomic sequence is publicly available were genotyped using a novel GeneChip-based approach. Strains were also subjected to PFGE and ribotyping analysis. GeneChip results provided a higher level of discrimination among isolates than either ribotyping or PFGE, although strain clustering was similar among the three techniques. In addition, GeneChip signal intensity cutoff values were empirically determined to provide extensive data on the genetic composition of each isolate analyzed. Using this technology it was shown that strains could be examined for each element represented on the GeneChip, including virulence factors, antimicrobial resistance determinants, and agr type. These results were validated by PCR, growth on selective media, and detailed in silico analysis of each of the sequenced genomes. Collectively, this work demonstrates that GeneChips provide extensive genotyping information for S. aureus strains and may play a major role in epidemiological studies in the future where correlating genes with particular disease phenotypes is critical.
* Corresponding author. Mailing address: Wyeth Vaccines Research, 401 N. Middletown Rd., Pearl River, NY 10965. Phone: (845) 602-4411. Fax: (845) 602-5536. E-mail:
MurphyE3{at}wyeth.com.
Present address: University of Nebraska Medical Center, Omaha, NE 68198.
Journal of Clinical Microbiology, September 2004, p. 4275-4283, Vol. 42, No. 9
0095-1137/04/$08.00+0 DOI: 10.1128/JCM.42.9.4275-4283.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Siboo, I. R., Chaffin, D. O., Rubens, C. E., Sullam, P. M.
(2008). Characterization of the Accessory Sec System of Staphylococcus aureus. J. Bacteriol.
190: 6188-6196
[Abstract]
[Full Text]
-
Cassat, J., Dunman, P. M., Murphy, E., Projan, S. J., Beenken, K. E., Palm, K. J., Yang, S.-J., Rice, K. C., Bayles, K. W., Smeltzer, M. S.
(2006). Transcriptional profiling of a Staphylococcus aureus clinical isolate and its isogenic agr and sarA mutants reveals global differences in comparison to the laboratory strain RN6390.. Microbiology
152: 3075-3090
[Abstract]
[Full Text]
-
Singh, A., Goering, R. V., Simjee, S., Foley, S. L., Zervos, M. J.
(2006). Application of Molecular Techniques to the Study of Hospital Infection. Clin. Microbiol. Rev.
19: 512-530
[Abstract]
[Full Text]
-
Harbottle, H., White, D. G., McDermott, P. F., Walker, R. D., Zhao, S.
(2006). Comparison of Multilocus Sequence Typing, Pulsed-Field Gel Electrophoresis, and Antimicrobial Susceptibility Typing for Characterization of Salmonella enterica Serotype Newport Isolates.. J. Clin. Microbiol.
44: 2449-2457
[Abstract]
[Full Text]
-
Roberts, C., Anderson, K. L., Murphy, E., Projan, S. J., Mounts, W., Hurlburt, B., Smeltzer, M., Overbeek, R., Disz, T., Dunman, P. M.
(2006). Characterizing the Effect of the Staphylococcus aureus Virulence Factor Regulator, SarA, on Log-Phase mRNA Half-Lives.. J. Bacteriol.
188: 2593-2603
[Abstract]
[Full Text]
-
McAleese, F., Wu, S. W., Sieradzki, K., Dunman, P., Murphy, E., Projan, S., Tomasz, A.
(2006). Overexpression of Genes of the Cell Wall Stimulon in Clinical Isolates of Staphylococcus aureus Exhibiting Vancomycin-Intermediate- S. aureus-Type Resistance to Vancomycin. J. Bacteriol.
188: 1120-1133
[Abstract]
[Full Text]
-
Tenover, F. C., McDougal, L. K., Goering, R. V., Killgore, G., Projan, S. J., Patel, J. B., Dunman, P. M.
(2006). Characterization of a Strain of Community-Associated Methicillin-Resistant Staphylococcus aureus Widely Disseminated in the United States. J. Clin. Microbiol.
44: 108-118
[Abstract]
[Full Text]
-
McAleese, F., Murphy, E., Babinchak, T., Singh, G., Said-Salim, B., Kreiswirth, B., Dunman, P., O'Connell, J., Projan, S. J., Bradford, P. A.
(2005). Use of Ribotyping To Retrospectively Identify Methicillin-Resistant Staphylococcus aureus Isolates from Phase 3 Clinical Trials for Tigecycline That Are Genotypically Related to Community-Associated Isolates. Antimicrob. Agents Chemother.
49: 4521-4529
[Abstract]
[Full Text]
-
Witney, A. A., Marsden, G. L., Holden, M. T. G., Stabler, R. A., Husain, S. E., Vass, J. K., Butcher, P. D., Hinds, J., Lindsay, J. A.
(2005). Design, Validation, and Application of a Seven-Strain Staphylococcus aureus PCR Product Microarray for Comparative Genomics. Appl. Environ. Microbiol.
71: 7504-7514
[Abstract]
[Full Text]
-
Wright, J. S. III, Traber, K. E., Corrigan, R., Benson, S. A., Musser, J. M., Novick, R. P.
(2005). The agr Radiation: an Early Event in the Evolution of Staphylococci. J. Bacteriol.
187: 5585-5594
[Abstract]
[Full Text]
-
Kaatz, G. W., McAleese, F., Seo, S. M.
(2005). Multidrug Resistance in Staphylococcus aureus Due to Overexpression of a Novel Multidrug and Toxin Extrusion (MATE) Transport Protein. Antimicrob. Agents Chemother.
49: 1857-1864
[Abstract]
[Full Text]
-
McAleese, F., Petersen, P., Ruzin, A., Dunman, P. M., Murphy, E., Projan, S. J., Bradford, P. A.
(2005). A Novel MATE Family Efflux Pump Contributes to the Reduced Susceptibility of Laboratory-Derived Staphylococcus aureus Mutants to Tigecycline. Antimicrob. Agents Chemother.
49: 1865-1871
[Abstract]
[Full Text]
-
Truong-Bolduc, Q. C., Dunman, P. M., Strahilevitz, J., Projan, S. J., Hooper, D. C.
(2005). MgrA Is a Multiple Regulator of Two New Efflux Pumps in Staphylococcus aureus. J. Bacteriol.
187: 2395-2405
[Abstract]
[Full Text]
-
Cassat, J. E., Dunman, P. M., McAleese, F., Murphy, E., Projan, S. J., Smeltzer, M. S.
(2005). Comparative Genomics of Staphylococcus aureus Musculoskeletal Isolates. J. Bacteriol.
187: 576-592
[Abstract]
[Full Text]
-
Weinrick, B., Dunman, P. M., McAleese, F., Murphy, E., Projan, S. J., Fang, Y., Novick, R. P.
(2004). Effect of Mild Acid on Gene Expression in Staphylococcus aureus. J. Bacteriol.
186: 8407-8423
[Abstract]
[Full Text]