Cargando…

Rapid identification of mycobacteria from positive MGIT broths of primary cultures by MALDI-TOF mass spectrometry

BACKGROUND: Rapid identification of mycobacteria is important for timely treatment and the implementation of public health measures. The MGIT system ensures rapid detection of mycobacteria, but identification is usually delayed by days to weeks due to further subculture on solid medium. Matrix-assis...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Tsi-Shu, Lee, Chia-Chien, Tu, Hui-Zin, Lee, Susan Shin-Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796708/
https://www.ncbi.nlm.nih.gov/pubmed/29394275
http://dx.doi.org/10.1371/journal.pone.0192291
_version_ 1783297547033378816
author Huang, Tsi-Shu
Lee, Chia-Chien
Tu, Hui-Zin
Lee, Susan Shin-Jung
author_facet Huang, Tsi-Shu
Lee, Chia-Chien
Tu, Hui-Zin
Lee, Susan Shin-Jung
author_sort Huang, Tsi-Shu
collection PubMed
description BACKGROUND: Rapid identification of mycobacteria is important for timely treatment and the implementation of public health measures. The MGIT system ensures rapid detection of mycobacteria, but identification is usually delayed by days to weeks due to further subculture on solid medium. Matrix-assisted laser desorption time-of-flight mass spectrometry (MALDI-TOF MS) was demonstrated to effectively identify mycobacteria isolates subcultured from solid or liquid media. Reports of identification directly from MGIT broths of both sterile and non-sterile clinical specimens, omitting the subculture step, were limited and not satisfactory before. Our identification method dramatically shortened delay from detection to identification of mycobacteria. METHODOLOGY: We assessed the performance of the Vitek MS IVD version 3.0 for direct identification of NTM and M.tuberculosis from primary MGIT cultures, and assessed two sample preparation methods. RESULTS: Direct identification of NTM from positive MGIT broths, using MALDI-TOF VITEK MS with IVD v.3.0, generated high rates of acceptable results reaching 96.4% (80/83), and up to 100% (83/83) for sample preparations including a 0.1% SDS washing step. The sensitivity of VITEK MS to identify M.tuberculosis from MGIT tubes was 58/72 (80.6%), when using immunochromatography (ICA) test as gold standard. A characteristic colony clumping, wool-like appearance was observed in 48, and all 58 (100%) were correctly identified as M.tuberculosis using MALDI-TOF. The detection rate of M.tuberculosis complex was low (10/24, 41.6%) in the 24 MGIT tubes that was polymicrobial. Our method significantly reduced both the reagent cost and turnaround time. CONCLUSIONS: Based on a simplified protocol, we showed that MALDI-TOF MS can be used for rapid identification of NTM directly from primary MGIT cultures within the routine clinical laboratory workflow. However, we recommend an initial ICA test to screen for M.tuberculosis complex, due to a low identification rate of M. tuberculosis in the presence of polymicrobial cultures using MALDI-TOF.
format Online
Article
Text
id pubmed-5796708
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-57967082018-02-16 Rapid identification of mycobacteria from positive MGIT broths of primary cultures by MALDI-TOF mass spectrometry Huang, Tsi-Shu Lee, Chia-Chien Tu, Hui-Zin Lee, Susan Shin-Jung PLoS One Research Article BACKGROUND: Rapid identification of mycobacteria is important for timely treatment and the implementation of public health measures. The MGIT system ensures rapid detection of mycobacteria, but identification is usually delayed by days to weeks due to further subculture on solid medium. Matrix-assisted laser desorption time-of-flight mass spectrometry (MALDI-TOF MS) was demonstrated to effectively identify mycobacteria isolates subcultured from solid or liquid media. Reports of identification directly from MGIT broths of both sterile and non-sterile clinical specimens, omitting the subculture step, were limited and not satisfactory before. Our identification method dramatically shortened delay from detection to identification of mycobacteria. METHODOLOGY: We assessed the performance of the Vitek MS IVD version 3.0 for direct identification of NTM and M.tuberculosis from primary MGIT cultures, and assessed two sample preparation methods. RESULTS: Direct identification of NTM from positive MGIT broths, using MALDI-TOF VITEK MS with IVD v.3.0, generated high rates of acceptable results reaching 96.4% (80/83), and up to 100% (83/83) for sample preparations including a 0.1% SDS washing step. The sensitivity of VITEK MS to identify M.tuberculosis from MGIT tubes was 58/72 (80.6%), when using immunochromatography (ICA) test as gold standard. A characteristic colony clumping, wool-like appearance was observed in 48, and all 58 (100%) were correctly identified as M.tuberculosis using MALDI-TOF. The detection rate of M.tuberculosis complex was low (10/24, 41.6%) in the 24 MGIT tubes that was polymicrobial. Our method significantly reduced both the reagent cost and turnaround time. CONCLUSIONS: Based on a simplified protocol, we showed that MALDI-TOF MS can be used for rapid identification of NTM directly from primary MGIT cultures within the routine clinical laboratory workflow. However, we recommend an initial ICA test to screen for M.tuberculosis complex, due to a low identification rate of M. tuberculosis in the presence of polymicrobial cultures using MALDI-TOF. Public Library of Science 2018-02-02 /pmc/articles/PMC5796708/ /pubmed/29394275 http://dx.doi.org/10.1371/journal.pone.0192291 Text en © 2018 Huang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Huang, Tsi-Shu
Lee, Chia-Chien
Tu, Hui-Zin
Lee, Susan Shin-Jung
Rapid identification of mycobacteria from positive MGIT broths of primary cultures by MALDI-TOF mass spectrometry
title Rapid identification of mycobacteria from positive MGIT broths of primary cultures by MALDI-TOF mass spectrometry
title_full Rapid identification of mycobacteria from positive MGIT broths of primary cultures by MALDI-TOF mass spectrometry
title_fullStr Rapid identification of mycobacteria from positive MGIT broths of primary cultures by MALDI-TOF mass spectrometry
title_full_unstemmed Rapid identification of mycobacteria from positive MGIT broths of primary cultures by MALDI-TOF mass spectrometry
title_short Rapid identification of mycobacteria from positive MGIT broths of primary cultures by MALDI-TOF mass spectrometry
title_sort rapid identification of mycobacteria from positive mgit broths of primary cultures by maldi-tof mass spectrometry
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796708/
https://www.ncbi.nlm.nih.gov/pubmed/29394275
http://dx.doi.org/10.1371/journal.pone.0192291
work_keys_str_mv AT huangtsishu rapididentificationofmycobacteriafrompositivemgitbrothsofprimaryculturesbymalditofmassspectrometry
AT leechiachien rapididentificationofmycobacteriafrompositivemgitbrothsofprimaryculturesbymalditofmassspectrometry
AT tuhuizin rapididentificationofmycobacteriafrompositivemgitbrothsofprimaryculturesbymalditofmassspectrometry
AT leesusanshinjung rapididentificationofmycobacteriafrompositivemgitbrothsofprimaryculturesbymalditofmassspectrometry