Literature DB >> 7578732

Diagnosis of Legionella pneumophila infection by polymerase chain reaction.

M Koide1, A Saito.   

Abstract

We examined the application of the polymerase chain reaction (PCR) for the diagnosis of legionellosis. Eight intratracheal aspirates were collected from a patient with pneumonia caused by Legionella pneumophila serogroup 2, and serial 10-fold dilutions of the samples were obtained. Two samples were positive for L. pneumophila by the direct fluorescent antibody (DFA) method down to a 10(-2) concentration, and one was positive down to a 10(-4) concentration. PCR was positive for all eight samples, and the sensitivity was greater than that of the DFA method. Only one of the eight samples yielded organisms in culture: the L. pneumophila serogroup 2 strain was isolated on buffered charcoal yeast extract alpha agar as an atypical white, papillate colony.

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Year:  1995        PMID: 7578732     DOI: 10.1093/clinids/21.1.199

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


  12 in total

1.  Detection of Legionella pneumophila using a real-time PCR hybridization assay.

Authors:  A L Ballard; N K Fry; L Chan; S B Surman; J V Lee; T G Harrison; K J Towner
Journal:  J Clin Microbiol       Date:  2000-11       Impact factor: 5.948

2.  Comparison of sample preparation methods for detection of Legionella pneumophila in culture-positive bronchoalveolar lavage fluids by PCR.

Authors:  B Jaulhac; M Reyrolle; Y K Sodahlon; S Jarraud; M Kubina; H Monteil; Y Piémont; J Etienne
Journal:  J Clin Microbiol       Date:  1998-07       Impact factor: 5.948

3.  Development of conventional and real-time PCR assays for detection of Legionella DNA in respiratory specimens.

Authors:  K Rantakokko-Jalava; J Jalava
Journal:  J Clin Microbiol       Date:  2001-08       Impact factor: 5.948

4.  Direct detection of Legionella species from bronchoalveolar lavage and open lung biopsy specimens: comparison of LightCycler PCR, in situ hybridization, direct fluorescence antigen detection, and culture.

Authors:  R T Hayden; J R Uhl; X Qian; M K Hopkins; M C Aubry; A H Limper; R V Lloyd; F R Cockerill
Journal:  J Clin Microbiol       Date:  2001-07       Impact factor: 5.948

5.  Detection of Legionella pneumophila by real-time PCR for the mip gene.

Authors:  Deborah A Wilson; Belinda Yen-Lieberman; Udo Reischl; Steve M Gordon; Gary W Procop
Journal:  J Clin Microbiol       Date:  2003-07       Impact factor: 5.948

Review 6.  Legionella and Legionnaires' disease: 25 years of investigation.

Authors:  Barry S Fields; Robert F Benson; Richard E Besser
Journal:  Clin Microbiol Rev       Date:  2002-07       Impact factor: 26.132

7.  Utility of real-time PCR for diagnosis of Legionnaires' disease in routine clinical practice.

Authors:  Bram M W Diederen; Jan A J W Kluytmans; Christina M Vandenbroucke-Grauls; Marcel F Peeters
Journal:  J Clin Microbiol       Date:  2007-12-19       Impact factor: 5.948

8.  Rapid identification of clinically relevant Nocardia species to genus level by 16S rRNA gene PCR.

Authors:  F J Laurent; F Provost; P Boiron
Journal:  J Clin Microbiol       Date:  1999-01       Impact factor: 5.948

9.  Direct detection and differentiation of Legionella spp. and Legionella pneumophila in clinical specimens by dual-color real-time PCR and melting curve analysis.

Authors:  Udo Reischl; Hans-Jörg Linde; Norbert Lehn; Olfert Landt; Kevin Barratt; Nele Wellinghausen
Journal:  J Clin Microbiol       Date:  2002-10       Impact factor: 5.948

10.  Development and clinical evaluation of an internally controlled, single-tube multiplex real-time PCR assay for detection of Legionella pneumophila and other Legionella species.

Authors:  Kate E Templeton; Sitha A Scheltinga; Peter Sillekens; Jantine W Crielaard; Alje P van Dam; Herman Goossens; Eric C J Claas
Journal:  J Clin Microbiol       Date:  2003-09       Impact factor: 5.948

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