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An evaluation of false-positive rifampicin resistance on the Xpert MTB/RIF

BACKGROUND: Mycobacterium tuberculosis (MTB) is one of the most significant causes of mortality and morbidity. Early diagnose is important especially in multiple drug resistant tuberculosis to avoid transmission. Traditional techniques requires at least one to three weeks for diagnosis of tuberculos...

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Autores principales: Cayci, Yeliz Tanriverdi, Bilgin, Kemal, Coban, Ahmet Yilmaz, Birinci, Asuman, Durupınar, Belma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Oswaldo Cruz, Ministério da Saúde 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661898/
https://www.ncbi.nlm.nih.gov/pubmed/29091135
http://dx.doi.org/10.1590/0074-02760170051
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author Cayci, Yeliz Tanriverdi
Bilgin, Kemal
Coban, Ahmet Yilmaz
Birinci, Asuman
Durupınar, Belma
author_facet Cayci, Yeliz Tanriverdi
Bilgin, Kemal
Coban, Ahmet Yilmaz
Birinci, Asuman
Durupınar, Belma
author_sort Cayci, Yeliz Tanriverdi
collection PubMed
description BACKGROUND: Mycobacterium tuberculosis (MTB) is one of the most significant causes of mortality and morbidity. Early diagnose is important especially in multiple drug resistant tuberculosis to avoid transmission. Traditional techniques requires at least one to three weeks for diagnosis of tuberculosis. Diagnostic delays with multiple drug resistant tuberculosis are associated with worse clinical outcomes and increased transmission The Xpert MTB/RIF assay is one of the new diagnostic device for the diagnosis of tuberculosis and rapid detection of rifampicin resistance. OBJECTIVE: We assessed the performance of Xpert MTB/RIF assay for detecting rifampicin resistance using phenotypic drug susceptibility tests as automated BD MGIT 960. METHODS: Total of 2136 specimens were included in the study. Xpert MTB/RIF testing was performed on samples, using version 4 cartridges, according to the manufacturer's recommendations. The MTBC culture and first-line phenotypic DST were performed in automated BD MGIT 960 (Becton & Dickinson, USA) according to the recommendations of the manufacturer. Agar proportion was used in the case of inconsistency for rifampicin resistance. FINDINGS: Thirty-four samples (19 respiratory and 15 nonrespiratory samples) were determined as positive for M. tuberculosis complex by Xpert MTB/RIF (Cepheid GeneXpert® System, USA). Xpert MTB/RIF assay detected 4/34 (11.7%) specimens as rifampicin resistant. One of the rifampicin resistant isolates was determined susceptible in MGIT 960 automated system. This isolate was also tested with agar proportion method and found susceptible to rifampicin. MAIN CONCLUSION: The Xpert MTB/RIF assay can be used as first-line assay for the detection of M. tuberculosis. However, microbiologists must be aware of the limitations of the assay.
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spelling pubmed-56618982017-11-04 An evaluation of false-positive rifampicin resistance on the Xpert MTB/RIF Cayci, Yeliz Tanriverdi Bilgin, Kemal Coban, Ahmet Yilmaz Birinci, Asuman Durupınar, Belma Mem Inst Oswaldo Cruz Article BACKGROUND: Mycobacterium tuberculosis (MTB) is one of the most significant causes of mortality and morbidity. Early diagnose is important especially in multiple drug resistant tuberculosis to avoid transmission. Traditional techniques requires at least one to three weeks for diagnosis of tuberculosis. Diagnostic delays with multiple drug resistant tuberculosis are associated with worse clinical outcomes and increased transmission The Xpert MTB/RIF assay is one of the new diagnostic device for the diagnosis of tuberculosis and rapid detection of rifampicin resistance. OBJECTIVE: We assessed the performance of Xpert MTB/RIF assay for detecting rifampicin resistance using phenotypic drug susceptibility tests as automated BD MGIT 960. METHODS: Total of 2136 specimens were included in the study. Xpert MTB/RIF testing was performed on samples, using version 4 cartridges, according to the manufacturer's recommendations. The MTBC culture and first-line phenotypic DST were performed in automated BD MGIT 960 (Becton & Dickinson, USA) according to the recommendations of the manufacturer. Agar proportion was used in the case of inconsistency for rifampicin resistance. FINDINGS: Thirty-four samples (19 respiratory and 15 nonrespiratory samples) were determined as positive for M. tuberculosis complex by Xpert MTB/RIF (Cepheid GeneXpert® System, USA). Xpert MTB/RIF assay detected 4/34 (11.7%) specimens as rifampicin resistant. One of the rifampicin resistant isolates was determined susceptible in MGIT 960 automated system. This isolate was also tested with agar proportion method and found susceptible to rifampicin. MAIN CONCLUSION: The Xpert MTB/RIF assay can be used as first-line assay for the detection of M. tuberculosis. However, microbiologists must be aware of the limitations of the assay. Instituto Oswaldo Cruz, Ministério da Saúde 2017-11 /pmc/articles/PMC5661898/ /pubmed/29091135 http://dx.doi.org/10.1590/0074-02760170051 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Cayci, Yeliz Tanriverdi
Bilgin, Kemal
Coban, Ahmet Yilmaz
Birinci, Asuman
Durupınar, Belma
An evaluation of false-positive rifampicin resistance on the Xpert MTB/RIF
title An evaluation of false-positive rifampicin resistance on the Xpert MTB/RIF
title_full An evaluation of false-positive rifampicin resistance on the Xpert MTB/RIF
title_fullStr An evaluation of false-positive rifampicin resistance on the Xpert MTB/RIF
title_full_unstemmed An evaluation of false-positive rifampicin resistance on the Xpert MTB/RIF
title_short An evaluation of false-positive rifampicin resistance on the Xpert MTB/RIF
title_sort evaluation of false-positive rifampicin resistance on the xpert mtb/rif
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661898/
https://www.ncbi.nlm.nih.gov/pubmed/29091135
http://dx.doi.org/10.1590/0074-02760170051
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