This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yoo, J.-H.
Right arrow Articles by Kang, M.-W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yoo, J.-H.
Right arrow Articles by Kang, M.-W.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, October 1999, p. 3108-3112, Vol. 37, No. 10
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Application of Infrequent-Restriction-Site PCR to Clinical Isolates of Acinetobacter baumannii and Serratia marcescens

Jin-Hong Yoo,1,* Jung-Hyun Choi,1 Wan-Shik Shin,1 Dong-Ho Huh,2 Yoon-Kyung Cho,2 Kyung-Mi Kim,3 Mi-Young Kim,1 and Moon-Won Kang1

Department of Internal Medicine,1 Clinical Research Institute,2 and Hospital Epidemiology & Infection Control Unit,3 College of Medicine, The Catholic University of Korea, Seoul, Korea

Received 15 March 1999/Returned for modification 22 May 1999/Accepted 27 June 1999

We applied infrequent-restriction-site PCR (IRS-PCR) to the investigation of an outbreak caused by 23 isolates of Acinetobacter baumannii in an intensive care unit from November 1996 to May 1997 and a pseudoepidemic caused by 16 isolates of Serratia marcescens in a delivery room from May to September 1996. In the epidemiologic investigation of the outbreak caused by A. baumannii, environmental sampling and screening of all health care workers revealed the same species from the Y piece of a mechanical ventilator and the hands of two health care personnel. IRS-PCR showed that all outbreak-related strains were genotypically identical and that three strains from surveillance cultures were also identical to the outbreak-related strains. In a pseudoepidemic caused by S. marcescens, IRS-PCR identified two different genotypes, and among them one genotype was predominant (15 of 16 [93.8%] isolates). Extensive surveillance failed to find any source of S. marcescens. Validation of the result of IRS-PCR by comparison with that of field inversion gel electrophoresis (FIGE) showed that they were completely concordant. These results suggest that IRS-PCR is comparable to FIGE for molecular epidemiologic studies. In addition, IRS-PCR was less laborious and less time-consuming than FIGE. To our knowledge, this is the first report of the application of IRS-PCR to A. baumannii and S. marcescens.


* Corresponding author. Mailing address: Department of Internal Medicine, St. Mary's Hospital, 62 Yoido-dong, Youngdungpo-Gu, Seoul 150-010, South Korea. Phone: 82-2-3779-1151. Fax: 82-32-340-2669. E-mail: mogul{at}chollian.net.


Journal of Clinical Microbiology, October 1999, p. 3108-3112, Vol. 37, No. 10
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Peleg, A. Y., Seifert, H., Paterson, D. L. (2008). Acinetobacter baumannii: Emergence of a Successful Pathogen. Clin. Microbiol. Rev. 21: 538-582 [Abstract] [Full Text]  
  • Bartual, S. G., Seifert, H., Hippler, C., Luzon, M. A. D., Wisplinghoff, H., Rodriguez-Valera, F. (2005). Development of a Multilocus Sequence Typing Scheme for Characterization of Clinical Isolates of Acinetobacter baumannii. J. Clin. Microbiol. 43: 4382-4390 [Abstract] [Full Text]  
  • Su, L.-H., Ou, J. T., Leu, H.-S., Chiang, P.-C., Chiu, Y.-P., Chia, J.-H., Kuo, A.-J., Chiu, C.-H., Chu, C., Wu, T.-L., Sun, C.-F., Riley, T. V., Chang, B. J. (2003). Extended Epidemic of Nosocomial Urinary Tract Infections Caused by Serratia marcescens. J. Clin. Microbiol. 41: 4726-4732 [Abstract] [Full Text]  
  • Wu, T.-L., Chia, J.-H., Su, L.-H., Kuo, A.-J., Chu, C., Chiu, C.-H. (2003). Dissemination of Extended-Spectrum {beta}-Lactamase-Producing Enterobacteriaceae in Pediatric Intensive Care Units. J. Clin. Microbiol. 41: 4836-4838 [Abstract] [Full Text]  
  • Franciosa, G., Tartaro, S., Wedell-Neergaard, C., Aureli, P. (2001). Characterization of Listeria monocytogenes Strains Involved in Invasive and Noninvasive Listeriosis Outbreaks by PCR-Based Fingerprinting Techniques. Appl. Environ. Microbiol. 67: 1793-1799 [Abstract] [Full Text]  
  • Handley, S. A., Regnery, R. L. (2000). Differentiation of Pathogenic Bartonella Species by Infrequent Restriction Site PCR. J. Clin. Microbiol. 38: 3010-3015 [Abstract] [Full Text]