Enterobacterial repetitive intergenic consensus PCR is a useful tool for typing Mycobacterium chelonae and Mycobacterium abscessus isolates

Enterobacterial repetitive intergenic consensus PCR is a useful tool for typing Mycobacterium chelonae and Mycobacterium abscessus isolates

Autor Sampaio, JLM Google Scholar
Viana-Niero, C. Google Scholar
De Freitas, D. Google Scholar
Hofling-Lima, A. L. Google Scholar
Leao, S. C. Google Scholar
Instituição Universidade Federal de São Paulo (UNIFESP)
Inst Fleury Ensino & Pesquisa
Resumo Outbreaks of rapidly growing mycobacterium (RGM) infections are increasingly being reported worldwide. Information about genetic relatedness of isolates obtained during outbreaks can provide Opportunities for prompt intervention. Pulsed-field gel electrophoresis (PFGE) is expensive, time consuming, and labor intensive. Other than that, Mycobacterium abscessus isolates call suffer DNA degradation during electrophoresis. Polymerase chain reaction (PCR)-based methods are cheaper, faster, and easier to perform, but discriminatory power varies depending oil the primer used. Ill this study, we tested the competence of enterobacterial repetitive intergenic consensus (ERIC) PCR in comparison with PFGE to distinguish unrelated isolates (24 Mycobacterium chelonae and 24 M. abscessus) obtained front human and/or environmental samples and to group 56 isolates front 6 outbreaks confirmed epidemiologically, caused by M. chelonae and M abscessus after ophthalmologic refractive surgery and mesotherapy. Enterobacterial repetitive intergenic consensus PCR presented discriminatory power. calculated using Simpson's index of diversity, of 0.989 for M abscessus and 0.975 for M. chelonae and grouped outbreak isolates ill distinct groups showing epidemiologic concordance. Pulsed-field gel electrophoresis also grouped outbreak isolates and presented discriminatory power of 0.972 and 0.993 for M. abscessus and M. chelonae, respectively. DNA from 8 (22%) of 36 M. abscessus isolates analyzed showed degradation during electrophoresis. Compared with PFGE and epidemiologic information as the gold standard, ERIC PCR is a simple, high throughput, affordable, reproducible, and discriminatory molecular typing method for inference of genetic relatedness of RGMs of the M. chelonae-abscessus group. (c) 2006 Elsevier Inc. All rights reserved.
Palavra-chave ERIC
molecular typing
Mycobacterium chelonae
Mycobacterium abscessus
Idioma Inglês
Data de publicação 2006-06-01
Publicado em Diagnostic Microbiology and Infectious Disease. New York: Elsevier B.V., v. 55, n. 2, p. 107-118, 2006.
ISSN 0732-8893 (Sherpa/Romeo, fator de impacto)
Publicador Elsevier B.V.
Extensão 107-118
Fonte http://dx.doi.org/10.1016/j.diagmicrobio.2006.01.006
Direito de acesso Acesso restrito
Tipo Artigo
Web of Science WOS:000238228400004
Endereço permanente http://repositorio.unifesp.br/handle/11600/28948

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