A practical approach to render tuberculosis samples safe for application of tuberculosis molecular bacterial load assay in clinical settings without a biosafety level 3 laboratory.


Journal

Tuberculosis (Edinburgh, Scotland)
ISSN: 1873-281X
Titre abrégé: Tuberculosis (Edinb)
Pays: Scotland
ID NLM: 100971555

Informations de publication

Date de publication:
01 2023
Historique:
received: 14 08 2022
revised: 05 11 2022
accepted: 12 11 2022
pubmed: 27 11 2022
medline: 1 2 2023
entrez: 26 11 2022
Statut: ppublish

Résumé

Mycobacterium tuberculosis is a category B infectious pathogen requiring level-3-containment laboratories for handling. We assessed the efficacy of heat and Guanidine thiocyanate (GTC) to inactivate M. tuberculosis prior to performance of tuberculosis Molecular Bacterial Load Assay (TB-MBLA). We performed in vitro experiments using M.tb, H37Rv reference strain and replicated in sputum specimens. A 0.5 MacFarland standard of M. tuberculosis was serially diluted to 1x10 No M. tuberculosis growth was observed in MGIT for GTC or heat treated H37Rv cultures. All untreated H37Rv dilutions were MGIT positive except the most diluted specimens. Heat and GTC treatment of H37Rv reduced TB-MBLA load by 2.1log Heat or GTC renders M. tuberculosis non-viable and eliminates the need for BSL3 laboratory for performing TB-MBLA in routine healthcare settings.

Sections du résumé

BACKGROUND
Mycobacterium tuberculosis is a category B infectious pathogen requiring level-3-containment laboratories for handling. We assessed the efficacy of heat and Guanidine thiocyanate (GTC) to inactivate M. tuberculosis prior to performance of tuberculosis Molecular Bacterial Load Assay (TB-MBLA).
METHOD
We performed in vitro experiments using M.tb, H37Rv reference strain and replicated in sputum specimens. A 0.5 MacFarland standard of M. tuberculosis was serially diluted to 1x10
RESULTS
No M. tuberculosis growth was observed in MGIT for GTC or heat treated H37Rv cultures. All untreated H37Rv dilutions were MGIT positive except the most diluted specimens. Heat and GTC treatment of H37Rv reduced TB-MBLA load by 2.1log
CONCLUSION
Heat or GTC renders M. tuberculosis non-viable and eliminates the need for BSL3 laboratory for performing TB-MBLA in routine healthcare settings.

Identifiants

pubmed: 36434867
pii: S1472-9792(22)00112-3
doi: 10.1016/j.tube.2022.102275
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

102275

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Bariki Mtafya (B)

National Institute for Medical Research-Mbeya Medical Research Centre, Mbeya, Tanzania; University of St Andrews, School of Medicine, St Andrews, UK. Electronic address: bmtafya@nimr-mmrc.org.

Paschal Qwaray (P)

National Institute for Medical Research-Mbeya Medical Research Centre, Mbeya, Tanzania.

Joseph John (J)

National Institute for Medical Research-Mbeya Medical Research Centre, Mbeya, Tanzania.

Emanuel Sichone (E)

National Institute for Medical Research-Mbeya Medical Research Centre, Mbeya, Tanzania.

Alice Shoo (A)

National Institute for Medical Research-Mbeya Medical Research Centre, Mbeya, Tanzania.

Stephen H Gillespie (SH)

University of St Andrews, School of Medicine, St Andrews, UK.

Nyanda Elias Ntinginya (NE)

National Institute for Medical Research-Mbeya Medical Research Centre, Mbeya, Tanzania.

Wilber Sabiiti (W)

University of St Andrews, School of Medicine, St Andrews, UK.

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Classifications MeSH