Literature DB >> 9675472

Long-term laboratory contamination by Mycobacterium abscessus resulting in two pseudo-outbreaks: recognition with use of random amplified polymorphic DNA (RAPD) polymerase chain reaction.

K K Lai1, B A Brown, J A Westerling, S A Fontecchio, Y Zhang, R J Wallace.   

Abstract

Beginning in 1993, an increase in clinical isolates of Mycobacterium abscessus was observed in a single hospital microbiology laboratory. This involved a cluster of four patients in June 1993 and five patients and a quality-control culture of distilled water in May 1994. Twenty-three M. abscessus isolates recovered between 1991 and 1996 were compared by random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR). Sixteen of 21 clinical isolates recovered over a 6-year period and the distilled water isolate had identical RAPD-PCR patterns consistent with a single strain or clone. Only six of 15 patients had findings suggestive of clinical disease. Since the use of in-house-prepared distilled water was discontinued, no further laboratory contamination of clinical specimens has been observed. Molecular typing was the key to defining distilled water as the source of this pseudo-outbreak. Recognition of such outbreaks is important for prevention of unnecessary therapeutic and diagnostic interventions.

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Year:  1998        PMID: 9675472     DOI: 10.1086/514635

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  9 in total

1.  Outbreak of infection with Mycobacterium abscessus: is sodium dodecyl sulfate-polyacrylamide gel electrophoresis a useful technique for epidemiological typing?

Authors:  J Esteban; F Cabria
Journal:  J Clin Microbiol       Date:  2003-02       Impact factor: 5.948

2.  Total synthesis of an antigenic heptasaccharide motif found in the cell-wall lipooligosaccharide of Mycobacterium gordonae strain 989.

Authors:  Chinmoy Mukherjee; Anup Kumar Misra
Journal:  Glycoconj J       Date:  2008-02-19       Impact factor: 2.916

3.  Concise synthesis of a heptasaccharide antigen found in the cell-wall lipopolysaccharide of Mycobacterium gordonae strain 990.

Authors:  Rajib Panchadhayee; Anup Kumar Misra
Journal:  Glycoconj J       Date:  2008-06-21       Impact factor: 2.916

4.  Comparison of methods for Identification of Mycobacterium abscessus and M. chelonae isolates.

Authors:  M A Yakrus; S M Hernandez; M M Floyd; D Sikes; W R Butler; B Metchock
Journal:  J Clin Microbiol       Date:  2001-11       Impact factor: 5.948

5.  Survival of environmental mycobacteria in Acanthamoeba polyphaga.

Authors:  Toïdi Adékambi; Skandar Ben Salah; Mohamed Khlif; Didier Raoult; Michel Drancourt
Journal:  Appl Environ Microbiol       Date:  2006-09       Impact factor: 4.792

6.  rpoB-based identification of nonpigmented and late-pigmenting rapidly growing mycobacteria.

Authors:  Toïdi Adékambi; Philippe Colson; Michel Drancourt
Journal:  J Clin Microbiol       Date:  2003-12       Impact factor: 5.948

Review 7.  Clinical and taxonomic status of pathogenic nonpigmented or late-pigmenting rapidly growing mycobacteria.

Authors:  Barbara A Brown-Elliott; Richard J Wallace
Journal:  Clin Microbiol Rev       Date:  2002-10       Impact factor: 26.132

Review 8.  Plumbing of hospital premises is a reservoir for opportunistically pathogenic microorganisms: a review.

Authors:  Margaret M Williams; Catherine R Armbruster; Matthew J Arduino
Journal:  Biofouling       Date:  2013       Impact factor: 3.797

9.  A rapid culture independent methodology to quantitatively detect and identify common human bacterial pathogens associated with contaminated high purity water.

Authors:  Elizabeth Minogue; Nina L Tuite; Cindy J Smith; Kate Reddington; Thomas Barry
Journal:  BMC Biotechnol       Date:  2015-02-18       Impact factor: 2.563

  9 in total

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