Previous Article | Next Article 
Journal of Clinical Microbiology, June 2002, p. 2119-2125, Vol. 40, No. 6
0095-1137/02/$04.00+0 DOI: 10.1128/JCM.40.6.2119-2125.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Epidemiologic Genotyping of Methicillin-Resistant Staphylococcus aureus by Pulsed-Field Gel Electrophoresis at a University Hospital and Comparison with Antibiotyping and Protein A and Coagulase Gene Polymorphisms
I. Montesinos,1* E. Salido,2 T. Delgado,1 M. Cuervo,1 and A. Sierra1
Microbiology Laboratory,1
Research Unit, Hospital Universitario de Canarias, Tenerife, Canary Islands, Spain2
Received 6 November 2001/
Returned for modification 14 January 2002/
Accepted 3 March 2002
A total of 124 methicillin-resistant Staphylococcus aureus (MRSA) isolates were ascertained at the University Hospital of the Canary Islands between January 1997 and April 2000. Genotyping included pulsed-field gel electrophoresis (PFGE) (SmaI digestion) and PCR-restriction fragment length polymorphism (PCR-RFLP) analysis for the coagulase (coa) and protein A (spa) genes. Antibiotic resistance was the main phenotypic marker correlated with genotyping results. Three main PFGE types were detected: A (with 12 subtypes), B (with 2 subtypes), and C. PFGE type A1 was the most commonly found (61% of isolates) and the one responsible for all the epidemic outbreaks. Other genetics markers used (coa and spa RFLPs) were significantly correlated with the PFGE types detected (P < 0.001). These PCR-RFLP assays were useful as molecular markers for a quick, preliminary study of MRSA outbreaks.
* Corresponding author. Mailing address: Servicio de Microbiología, Hospital Universitario, Canarias, Ofra s/n, La Cuesta, La Laguna, S/C de Tenerife, Islas Canarias, Spain. Phone: 34 922 679065. Fax: 34 922 319378. E-mail:
carlotamontesin{at}terra.es.
Journal of Clinical Microbiology, June 2002, p. 2119-2125, Vol. 40, No. 6
0095-1137/02/$04.00+0 DOI: 10.1128/JCM.40.6.2119-2125.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Ciftci, A., Onuk, E. E., Findik, A., Yildirim, T., Sogut, M. U.
(2009). Molecular typing of Staphylococcus aureus strains from ovine mastitis by pulsed-field gel electrophoresis and polymerase chain reaction based on coagulase and protein A gene polymorphisms. jvdi
21: 849-853
[Abstract]
[Full Text]
-
Strommenger, B., Braulke, C., Heuck, D., Schmidt, C., Pasemann, B., Nubel, U., Witte, W.
(2008). spa Typing of Staphylococcus aureus as a Frontline Tool in Epidemiological Typing. J. Clin. Microbiol.
46: 574-581
[Abstract]
[Full Text]
-
Petersdorf, S., Oberdorfer, K., Wendt, C.
(2006). Longitudinal Study of the Molecular Epidemiology of Methicillin-Resistant Staphylococcus aureus at a University Hospital. J. Clin. Microbiol.
44: 4297-4302
[Abstract]
[Full Text]
-
Francois, P., Huyghe, A., Charbonnier, Y., Bento, M., Herzig, S., Topolski, I., Fleury, B., Lew, D., Vaudaux, P., Harbarth, S., van Leeuwen, W., van Belkum, A., Blanc, D. S., Pittet, D., Schrenzel, J.
(2005). Use of an Automated Multiple-Locus, Variable-Number Tandem Repeat-Based Method for Rapid and High-Throughput Genotyping of Staphylococcus aureus Isolates. J. Clin. Microbiol.
43: 3346-3355
[Abstract]
[Full Text]
-
Shutt, C. K., Pounder, J. I., Page, S. R., Schaecher, B. J., Woods, G. L.
(2005). Clinical Evaluation of the DiversiLab Microbial Typing System Using Repetitive-Sequence-Based PCR for Characterization of Staphylococcus aureus Strains. J. Clin. Microbiol.
43: 1187-1192
[Abstract]
[Full Text]
-
Harmsen, D., Claus, H., Witte, W., Rothganger, J., Claus, H., Turnwald, D., Vogel, U.
(2003). Typing of Methicillin-Resistant Staphylococcus aureus in a University Hospital Setting by Using Novel Software for spa Repeat Determination and Database Management. J. Clin. Microbiol.
41: 5442-5448
[Abstract]
[Full Text]
-
Stranden, A., Frei, R., Widmer, A. F.
(2003). Molecular Typing of Methicillin-Resistant Staphylococcus aureus: Can PCR Replace Pulsed-Field Gel Electrophoresis?. J. Clin. Microbiol.
41: 3181-3186
[Abstract]
[Full Text]