Literature DB >> 8354920

Use of polymerase chain reaction in an epidemiologic investigation of Pontiac fever.

L A Miller1, J L Beebe, J C Butler, W Martin, R Benson, R E Hoffman, B S Fields.   

Abstract

In June 1992, 13 (38%) of 34 resort guests experienced illness that met a symptom-based case definition of Pontiac fever. Each ill guest reported using an indoor hot tub compared with 6 (29%) of 21 nonill guests (P < .001). Water samples from the indoor hot tub were culture-negative for legionellae using standard techniques, coculture with amebae, and intraperitoneal inoculation of guinea pigs. However, polymerase chain reaction (PCR) testing of the water samples indicated the presence of Legionella pneumophila. Direct fluorescent antibody testing identified the organism as serogroup 6. Seroconversion to L. pneumophila serogroup 6 occurred in 7 (64%) of 11 ill guests and none of 5 nonill guests (P = .03). These results suggest that in certain circumstances, culture of environmental samples should be supplemented with additional tests such as PCR. These results are also consistent with the concept that Pontiac fever can be caused by nonviable legionellae.

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Year:  1993        PMID: 8354920     DOI: 10.1093/infdis/168.3.769

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  16 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.  Septic shock due to Legionella pneumophila serogroup 2: usefulness of molecular biology for diagnosis, treatment and epidemiological investigation.

Authors:  Florence Grattard; Séverine Allegra; Jerome Morel; Isabelle Court-Fortune; Christian Auboyer; Bruno Pozzetto; Philippe Berthelot
Journal:  Intensive Care Med       Date:  2010-03-23       Impact factor: 17.440

3.  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

Review 4.  Current and emerging Legionella diagnostics for laboratory and outbreak investigations.

Authors:  Jeffrey W Mercante; Jonas M Winchell
Journal:  Clin Microbiol Rev       Date:  2015-01       Impact factor: 26.132

Review 5.  Relevance of nucleic acid amplification techniques for diagnosis of respiratory tract infections in the clinical laboratory.

Authors:  M Ieven; H Goossens
Journal:  Clin Microbiol Rev       Date:  1997-04       Impact factor: 26.132

6.  Rapid method for enumeration of viable Legionella pneumophila and other Legionella spp. in water.

Authors:  Pilar Delgado-Viscogliosi; Tristan Simonart; Virginie Parent; Grégory Marchand; Marie Dobbelaere; Eric Pierlot; Véronique Pierzo; Florence Menard-Szczebara; Elisabeth Gaudard-Ferveur; Karine Delabre; Jean Marie Delattre
Journal:  Appl Environ Microbiol       Date:  2005-07       Impact factor: 4.792

7.  The role of arbitrarily primed PCR in identifying the source of an outbreak of Legionnaires' disease.

Authors:  C G Whitney; J Hofmann; J M Pruckler; R F Benson; B S Fields; U Bandyopadhyay; E F Donnally; C Giorgio-Almonte; L A Mermel; S Boland; B T Matyas; R F Breiman
Journal:  J Clin Microbiol       Date:  1997-07       Impact factor: 5.948

8.  Detection of Legionella species in reclaimed water and air with the EnviroAmp Legionella PCR kit and direct fluorescent antibody staining.

Authors:  C J Palmer; G F Bonilla; B Roll; C Paszko-Kolva; L R Sangermano; R S Fujioka
Journal:  Appl Environ Microbiol       Date:  1995-02       Impact factor: 4.792

9.  Detection of legionellae in hospital water samples by quantitative real-time LightCycler PCR.

Authors:  N Wellinghausen; C Frost; R Marre
Journal:  Appl Environ Microbiol       Date:  2001-09       Impact factor: 4.792

10.  V gamma 9V delta 2 T cells in human legionellosis.

Authors:  M Kroca; A Johansson; A Sjöstedt; A Tärnvik
Journal:  Clin Diagn Lab Immunol       Date:  2001-09
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