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Separation of Mycobacterium abscessus into subspecies or genotype level by direct application of peptide nucleic acid multi-probe- real-time PCR method into sputa samples

BACKGROUND: Recently, we introduced a novel peptide nucleic acid (PNA) multi-probe real time PCR method targeting the hsp65 gene (hsp65 PNA RT-PCR) to distinguish Mycobacterium abscessus groups. METHODS: Here, we evaluated the usefulness of the hsp65 PNA RT-PCR for the direct identification of the M...

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Autores principales: Kim, Kijeong, Hong, Seok-Hyun, Kim, Byoung-Jun, Kim, Bo-Ram, Lee, So-Young, Kim, Ga-Na, Shim, Tae Sun, Kook, Yoon-Hoh, Kim, Bum-Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531893/
https://www.ncbi.nlm.nih.gov/pubmed/26259717
http://dx.doi.org/10.1186/s12879-015-1076-8
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author Kim, Kijeong
Hong, Seok-Hyun
Kim, Byoung-Jun
Kim, Bo-Ram
Lee, So-Young
Kim, Ga-Na
Shim, Tae Sun
Kook, Yoon-Hoh
Kim, Bum-Joon
author_facet Kim, Kijeong
Hong, Seok-Hyun
Kim, Byoung-Jun
Kim, Bo-Ram
Lee, So-Young
Kim, Ga-Na
Shim, Tae Sun
Kook, Yoon-Hoh
Kim, Bum-Joon
author_sort Kim, Kijeong
collection PubMed
description BACKGROUND: Recently, we introduced a novel peptide nucleic acid (PNA) multi-probe real time PCR method targeting the hsp65 gene (hsp65 PNA RT-PCR) to distinguish Mycobacterium abscessus groups. METHODS: Here, we evaluated the usefulness of the hsp65 PNA RT-PCR for the direct identification of the M. abscessus group at the subspecies and genotype levels from sputa samples. The method was applied to total sputa DNA from 60 different patients who were identified as having mycobacterial infections via rpoB PCR restriction analysis of the same cultures. RESULTS: The hsp65 PNA RT-PCR method had higher sensitivity than the multi-probe real-time PCR assay targeting hsp65 (HMPRT-PCR) for the detection of M. abscessus from sputum [96.7 % (29/30 samples) vs. 70 % (21/30 samples); 100 % specificity]. CONCLUSIONS: These results suggest that the PNA-based method is feasible for the detection of M. abscessus members not only from cultures but also directly from sputa. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-015-1076-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-45318932015-08-12 Separation of Mycobacterium abscessus into subspecies or genotype level by direct application of peptide nucleic acid multi-probe- real-time PCR method into sputa samples Kim, Kijeong Hong, Seok-Hyun Kim, Byoung-Jun Kim, Bo-Ram Lee, So-Young Kim, Ga-Na Shim, Tae Sun Kook, Yoon-Hoh Kim, Bum-Joon BMC Infect Dis Research Article BACKGROUND: Recently, we introduced a novel peptide nucleic acid (PNA) multi-probe real time PCR method targeting the hsp65 gene (hsp65 PNA RT-PCR) to distinguish Mycobacterium abscessus groups. METHODS: Here, we evaluated the usefulness of the hsp65 PNA RT-PCR for the direct identification of the M. abscessus group at the subspecies and genotype levels from sputa samples. The method was applied to total sputa DNA from 60 different patients who were identified as having mycobacterial infections via rpoB PCR restriction analysis of the same cultures. RESULTS: The hsp65 PNA RT-PCR method had higher sensitivity than the multi-probe real-time PCR assay targeting hsp65 (HMPRT-PCR) for the detection of M. abscessus from sputum [96.7 % (29/30 samples) vs. 70 % (21/30 samples); 100 % specificity]. CONCLUSIONS: These results suggest that the PNA-based method is feasible for the detection of M. abscessus members not only from cultures but also directly from sputa. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-015-1076-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-11 /pmc/articles/PMC4531893/ /pubmed/26259717 http://dx.doi.org/10.1186/s12879-015-1076-8 Text en © Kim et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article
Kim, Kijeong
Hong, Seok-Hyun
Kim, Byoung-Jun
Kim, Bo-Ram
Lee, So-Young
Kim, Ga-Na
Shim, Tae Sun
Kook, Yoon-Hoh
Kim, Bum-Joon
Separation of Mycobacterium abscessus into subspecies or genotype level by direct application of peptide nucleic acid multi-probe- real-time PCR method into sputa samples
title Separation of Mycobacterium abscessus into subspecies or genotype level by direct application of peptide nucleic acid multi-probe- real-time PCR method into sputa samples
title_full Separation of Mycobacterium abscessus into subspecies or genotype level by direct application of peptide nucleic acid multi-probe- real-time PCR method into sputa samples
title_fullStr Separation of Mycobacterium abscessus into subspecies or genotype level by direct application of peptide nucleic acid multi-probe- real-time PCR method into sputa samples
title_full_unstemmed Separation of Mycobacterium abscessus into subspecies or genotype level by direct application of peptide nucleic acid multi-probe- real-time PCR method into sputa samples
title_short Separation of Mycobacterium abscessus into subspecies or genotype level by direct application of peptide nucleic acid multi-probe- real-time PCR method into sputa samples
title_sort separation of mycobacterium abscessus into subspecies or genotype level by direct application of peptide nucleic acid multi-probe- real-time pcr method into sputa samples
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531893/
https://www.ncbi.nlm.nih.gov/pubmed/26259717
http://dx.doi.org/10.1186/s12879-015-1076-8
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