Efficacy of two DNA fingerprinting methods for typing Acinetobacter baumannii isolates

Citation
Ls. Quelle et M. Catalano, Efficacy of two DNA fingerprinting methods for typing Acinetobacter baumannii isolates, DIAG MICR I, 39(4), 2001, pp. 215-223
Citations number
32
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE
ISSN journal
07328893 → ACNP
Volume
39
Issue
4
Year of publication
2001
Pages
215 - 223
Database
ISI
SICI code
0732-8893(200104)39:4<215:EOTDFM>2.0.ZU;2-M
Abstract
Performance of macrorestriction and repetitive extragenic palindromic DNA s equence-based PCR (REP-PCR) to type Acinetobacter baumannii isolates was qu antitatively estimated using a test population of 54 outbreak-related, 29 e ndemic infection-related and 17 epidemiologically-unrelated isolates. Repro ducibility and stability for macrorestriction were 100%, and REP-PCR showed only slightly lower stability. Macrorestriction resolved 18 fingerprints a nd REP-PCR 10 DNA patterns, forming eight and seven clusters at 75% of simi larity level, respectively. Intercluster band variation was >7 bands for bo th methods. Although, all endemic isolates, except one, were concordantly g rouped by both methods, macrorestriction distinguished a greater number of subtypes over one year study. For outbreaks, the epidemiologic concordance for both methods was 88%. The discriminatory index for macrorestriction and REP-PCR was 0.884 and 0.877, respectively. In conclusion, both methods sho wed similar efficacy as epidemiological markers, and by concordance, this s tudy demonstrated that for REP-PCR typing, a greater than or equal to7 band s difference seemed an appropriate threshold to identify unrelated strains. (C) 2001 Elsevier Science Inc. All rights reserved.