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Real-time PCR TaqMan assay for rapid screening of bloodstream infection

BACKGROUND: Sepsis is one of the main causes of mortality and morbidity. The rapid detection of pathogens in blood of septic patients is essential for adequate antimicrobial therapy and better prognosis. This study aimed to accelerate the detection and discrimination of Gram-positive (GP) and Gram-n...

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Autores principales: Wang, Hye-young, Kim, Sunghyun, Kim, Hyunjung, Kim, Jungho, Kim, Yeun, Park, Soon-Deok, Jin, Hyunwoo, Choi, Yeonim, Uh, Young, Lee, Hyeyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898783/
https://www.ncbi.nlm.nih.gov/pubmed/24393579
http://dx.doi.org/10.1186/1476-0711-13-3
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author Wang, Hye-young
Kim, Sunghyun
Kim, Hyunjung
Kim, Jungho
Kim, Yeun
Park, Soon-Deok
Jin, Hyunwoo
Choi, Yeonim
Uh, Young
Lee, Hyeyoung
author_facet Wang, Hye-young
Kim, Sunghyun
Kim, Hyunjung
Kim, Jungho
Kim, Yeun
Park, Soon-Deok
Jin, Hyunwoo
Choi, Yeonim
Uh, Young
Lee, Hyeyoung
author_sort Wang, Hye-young
collection PubMed
description BACKGROUND: Sepsis is one of the main causes of mortality and morbidity. The rapid detection of pathogens in blood of septic patients is essential for adequate antimicrobial therapy and better prognosis. This study aimed to accelerate the detection and discrimination of Gram-positive (GP) and Gram-negative (GN) bacteria and Candida species in blood culture samples by molecular methods. METHODS: The Real-GP®, -GN®, and -CAN® real-time PCR kit (M&D, Wonju, Republic of Korea) assays use the TaqMan probes for detecting pan-GP, pan-GN, and pan-Candida species, respectively. The diagnostic performances of the real-time PCR kits were evaluated with 115 clinical isolates, 256 positive and 200 negative blood culture bottle samples, and the data were compared to results obtained from conventional blood culture. RESULTS: Eighty-seven reference strains and 115 clinical isolates were correctly identified with specific probes corresponding to GP-bacteria, GN-bacteria and Candida, respectively. The overall sensitivity and specificity of the real-time PCR kit with blood culture samples were 99.6% and 89.5%, respectively. CONCLUSIONS: The Real-GP®, -GN®, and -CAN® real-time PCR kits could be useful tools for the rapid and accurate screening of bloodstream infections (BSIs).
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spelling pubmed-38987832014-01-23 Real-time PCR TaqMan assay for rapid screening of bloodstream infection Wang, Hye-young Kim, Sunghyun Kim, Hyunjung Kim, Jungho Kim, Yeun Park, Soon-Deok Jin, Hyunwoo Choi, Yeonim Uh, Young Lee, Hyeyoung Ann Clin Microbiol Antimicrob Research BACKGROUND: Sepsis is one of the main causes of mortality and morbidity. The rapid detection of pathogens in blood of septic patients is essential for adequate antimicrobial therapy and better prognosis. This study aimed to accelerate the detection and discrimination of Gram-positive (GP) and Gram-negative (GN) bacteria and Candida species in blood culture samples by molecular methods. METHODS: The Real-GP®, -GN®, and -CAN® real-time PCR kit (M&D, Wonju, Republic of Korea) assays use the TaqMan probes for detecting pan-GP, pan-GN, and pan-Candida species, respectively. The diagnostic performances of the real-time PCR kits were evaluated with 115 clinical isolates, 256 positive and 200 negative blood culture bottle samples, and the data were compared to results obtained from conventional blood culture. RESULTS: Eighty-seven reference strains and 115 clinical isolates were correctly identified with specific probes corresponding to GP-bacteria, GN-bacteria and Candida, respectively. The overall sensitivity and specificity of the real-time PCR kit with blood culture samples were 99.6% and 89.5%, respectively. CONCLUSIONS: The Real-GP®, -GN®, and -CAN® real-time PCR kits could be useful tools for the rapid and accurate screening of bloodstream infections (BSIs). BioMed Central 2014-01-07 /pmc/articles/PMC3898783/ /pubmed/24393579 http://dx.doi.org/10.1186/1476-0711-13-3 Text en Copyright © 2014 Wang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Hye-young
Kim, Sunghyun
Kim, Hyunjung
Kim, Jungho
Kim, Yeun
Park, Soon-Deok
Jin, Hyunwoo
Choi, Yeonim
Uh, Young
Lee, Hyeyoung
Real-time PCR TaqMan assay for rapid screening of bloodstream infection
title Real-time PCR TaqMan assay for rapid screening of bloodstream infection
title_full Real-time PCR TaqMan assay for rapid screening of bloodstream infection
title_fullStr Real-time PCR TaqMan assay for rapid screening of bloodstream infection
title_full_unstemmed Real-time PCR TaqMan assay for rapid screening of bloodstream infection
title_short Real-time PCR TaqMan assay for rapid screening of bloodstream infection
title_sort real-time pcr taqman assay for rapid screening of bloodstream infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898783/
https://www.ncbi.nlm.nih.gov/pubmed/24393579
http://dx.doi.org/10.1186/1476-0711-13-3
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