Comparative Molecular and Microbiologic Diagnosis of Bacterial Endocarditis

Sequencing of 16S rDNA, and of sodAint and rpoBint in some cases, was applied to DNA from heart valves of 46 patients (36 with definite and 10 with possible endocarditis). Sequence-based identifications were compared with those obtained with conventional methods. Among the 36 definite cases, 30 had...

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Main Authors: Isabelle Podglajen, Fabienne Bellery, Claire Poyart, Philippe Coudol, Annie Buu-Hoï, Patrick Bruneval, Jean-Luc Mainardi
Format: Article
Language:English
Published: Centers for Disease Control and Prevention 2003-12-01
Series:Emerging Infectious Diseases
Subjects:
PCR
Online Access:https://wwwnc.cdc.gov/eid/article/9/12/03-0229_article
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spelling doaj-7024cd8c4afe487d81df3a86f464fff72020-11-24T22:15:53ZengCenters for Disease Control and PreventionEmerging Infectious Diseases1080-60401080-60592003-12-019121543154710.3201/eid0912.030229Comparative Molecular and Microbiologic Diagnosis of Bacterial EndocarditisIsabelle PodglajenFabienne BelleryClaire PoyartPhilippe CoudolAnnie Buu-HoïPatrick BrunevalJean-Luc MainardiSequencing of 16S rDNA, and of sodAint and rpoBint in some cases, was applied to DNA from heart valves of 46 patients (36 with definite and 10 with possible endocarditis). Sequence-based identifications were compared with those obtained with conventional methods. Among the 36 definite cases, 30 had positive blood cultures and 6 had negative cultures. Among the 30 positive cases, sequencing of 16S rDNA permitted identification of species (18), genus (8), or neither (4); sodAint and rpoBint sequencing was necessary for species identification in 8 cases. Species identifications were identical in only 61.5%, when conventional techniques and DNA sequencing were used. In five of the six blood culture–negative endocarditis cases, sequencing identified Bartonella quintana (3), B. henselae (1), and Streptococcus gallolyticus (1). Our results demonstrate a clear benefit of molecular identification, particularly in cases of blood culture–negative endocarditis and of possible endocarditis, to confirm or invalidate the diagnosis. Moreover, in 19.4% of the definite cases, the improvement in species identification by sequencing led to improved patient management.https://wwwnc.cdc.gov/eid/article/9/12/03-0229_articleEndocarditisnegative blood culturemolecular diagnosisPCR16S rDNArpoB and sodA genes
collection DOAJ
language English
format Article
sources DOAJ
author Isabelle Podglajen
Fabienne Bellery
Claire Poyart
Philippe Coudol
Annie Buu-Hoï
Patrick Bruneval
Jean-Luc Mainardi
spellingShingle Isabelle Podglajen
Fabienne Bellery
Claire Poyart
Philippe Coudol
Annie Buu-Hoï
Patrick Bruneval
Jean-Luc Mainardi
Comparative Molecular and Microbiologic Diagnosis of Bacterial Endocarditis
Emerging Infectious Diseases
Endocarditis
negative blood culture
molecular diagnosis
PCR
16S rDNA
rpoB and sodA genes
author_facet Isabelle Podglajen
Fabienne Bellery
Claire Poyart
Philippe Coudol
Annie Buu-Hoï
Patrick Bruneval
Jean-Luc Mainardi
author_sort Isabelle Podglajen
title Comparative Molecular and Microbiologic Diagnosis of Bacterial Endocarditis
title_short Comparative Molecular and Microbiologic Diagnosis of Bacterial Endocarditis
title_full Comparative Molecular and Microbiologic Diagnosis of Bacterial Endocarditis
title_fullStr Comparative Molecular and Microbiologic Diagnosis of Bacterial Endocarditis
title_full_unstemmed Comparative Molecular and Microbiologic Diagnosis of Bacterial Endocarditis
title_sort comparative molecular and microbiologic diagnosis of bacterial endocarditis
publisher Centers for Disease Control and Prevention
series Emerging Infectious Diseases
issn 1080-6040
1080-6059
publishDate 2003-12-01
description Sequencing of 16S rDNA, and of sodAint and rpoBint in some cases, was applied to DNA from heart valves of 46 patients (36 with definite and 10 with possible endocarditis). Sequence-based identifications were compared with those obtained with conventional methods. Among the 36 definite cases, 30 had positive blood cultures and 6 had negative cultures. Among the 30 positive cases, sequencing of 16S rDNA permitted identification of species (18), genus (8), or neither (4); sodAint and rpoBint sequencing was necessary for species identification in 8 cases. Species identifications were identical in only 61.5%, when conventional techniques and DNA sequencing were used. In five of the six blood culture–negative endocarditis cases, sequencing identified Bartonella quintana (3), B. henselae (1), and Streptococcus gallolyticus (1). Our results demonstrate a clear benefit of molecular identification, particularly in cases of blood culture–negative endocarditis and of possible endocarditis, to confirm or invalidate the diagnosis. Moreover, in 19.4% of the definite cases, the improvement in species identification by sequencing led to improved patient management.
topic Endocarditis
negative blood culture
molecular diagnosis
PCR
16S rDNA
rpoB and sodA genes
url https://wwwnc.cdc.gov/eid/article/9/12/03-0229_article
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