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Simultaneous Detection of Nine Key Bacterial Respiratory Pathogens Using Luminex xTAG(®) Technology

Early diagnosis and treatment are crucial to the outcome of lower respiratory tract infections (LRTIs). In this study, we developed an assay combining multiplex PCR and Luminex technology (MPLT) for the detection of nine important respiratory bacterial pathogens, which frequently cause LRTIs. These...

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Detalles Bibliográficos
Autores principales: Jiang, Luxi, Ren, Hongyu, Zhou, Haijian, Qin, Tian, Chen, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5369059/
https://www.ncbi.nlm.nih.gov/pubmed/28241513
http://dx.doi.org/10.3390/ijerph14030223
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author Jiang, Luxi
Ren, Hongyu
Zhou, Haijian
Qin, Tian
Chen, Yu
author_facet Jiang, Luxi
Ren, Hongyu
Zhou, Haijian
Qin, Tian
Chen, Yu
author_sort Jiang, Luxi
collection PubMed
description Early diagnosis and treatment are crucial to the outcome of lower respiratory tract infections (LRTIs). In this study, we developed an assay combining multiplex PCR and Luminex technology (MPLT) for the detection of nine important respiratory bacterial pathogens, which frequently cause LRTIs. These were Streptococcus pneumoniae, Moraxella catarrhalis, Staphylococcus aureus, Streptococcus pyogenes, Haemophilus influenzae, Mycoplasma pneumoniae, Legionella spp., Pseudomonas aeruginosa, and Klebsiella pneumoniae. Through the hybridization reaction between two new synthesized multiplex PCR products and MagPlex-TAG Microspheres, we demonstrate that the detection limits for these nine pathogens were as low as 10(2)–10(3) CFU/mL. Furthermore, 86 clinical bronchoalveolar lavage fluid specimens were used to evaluate this method. Compared with the results of nine simplex real-time PCR reactions targeting these nine pathogens, this MPLT assay demonstrated a high diagnostic accuracy for Streptococcus pneumoniae (sensitivity, 87.5% and specificity, 100%). Furthermore, sensitivity and specificity for the other eight pathogens all attained 100% diagnostic accuracy. In addition, the consistency between MPLT and the nine real-time PCR reactions exceeded 98.8%. In conclusion, MPLT is a high-throughput, labor-saving and reliable method with high sensitivity and specificity for identifying nine respiratory pathogens responsible for LRTIs. Indeed, this assay may be a promising supplement to conventional methods used to diagnose LRTIs.
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spelling pubmed-53690592017-04-05 Simultaneous Detection of Nine Key Bacterial Respiratory Pathogens Using Luminex xTAG(®) Technology Jiang, Luxi Ren, Hongyu Zhou, Haijian Qin, Tian Chen, Yu Int J Environ Res Public Health Article Early diagnosis and treatment are crucial to the outcome of lower respiratory tract infections (LRTIs). In this study, we developed an assay combining multiplex PCR and Luminex technology (MPLT) for the detection of nine important respiratory bacterial pathogens, which frequently cause LRTIs. These were Streptococcus pneumoniae, Moraxella catarrhalis, Staphylococcus aureus, Streptococcus pyogenes, Haemophilus influenzae, Mycoplasma pneumoniae, Legionella spp., Pseudomonas aeruginosa, and Klebsiella pneumoniae. Through the hybridization reaction between two new synthesized multiplex PCR products and MagPlex-TAG Microspheres, we demonstrate that the detection limits for these nine pathogens were as low as 10(2)–10(3) CFU/mL. Furthermore, 86 clinical bronchoalveolar lavage fluid specimens were used to evaluate this method. Compared with the results of nine simplex real-time PCR reactions targeting these nine pathogens, this MPLT assay demonstrated a high diagnostic accuracy for Streptococcus pneumoniae (sensitivity, 87.5% and specificity, 100%). Furthermore, sensitivity and specificity for the other eight pathogens all attained 100% diagnostic accuracy. In addition, the consistency between MPLT and the nine real-time PCR reactions exceeded 98.8%. In conclusion, MPLT is a high-throughput, labor-saving and reliable method with high sensitivity and specificity for identifying nine respiratory pathogens responsible for LRTIs. Indeed, this assay may be a promising supplement to conventional methods used to diagnose LRTIs. MDPI 2017-02-24 2017-03 /pmc/articles/PMC5369059/ /pubmed/28241513 http://dx.doi.org/10.3390/ijerph14030223 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jiang, Luxi
Ren, Hongyu
Zhou, Haijian
Qin, Tian
Chen, Yu
Simultaneous Detection of Nine Key Bacterial Respiratory Pathogens Using Luminex xTAG(®) Technology
title Simultaneous Detection of Nine Key Bacterial Respiratory Pathogens Using Luminex xTAG(®) Technology
title_full Simultaneous Detection of Nine Key Bacterial Respiratory Pathogens Using Luminex xTAG(®) Technology
title_fullStr Simultaneous Detection of Nine Key Bacterial Respiratory Pathogens Using Luminex xTAG(®) Technology
title_full_unstemmed Simultaneous Detection of Nine Key Bacterial Respiratory Pathogens Using Luminex xTAG(®) Technology
title_short Simultaneous Detection of Nine Key Bacterial Respiratory Pathogens Using Luminex xTAG(®) Technology
title_sort simultaneous detection of nine key bacterial respiratory pathogens using luminex xtag(®) technology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5369059/
https://www.ncbi.nlm.nih.gov/pubmed/28241513
http://dx.doi.org/10.3390/ijerph14030223
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