Sensitivity optimisation of tuberculosis bioaerosol sampling.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 19 04 2020
accepted: 11 08 2020
entrez: 4 9 2020
pubmed: 4 9 2020
medline: 29 10 2020
Statut: epublish

Résumé

Detection of Mycobacterium tuberculosis (Mtb) in patient-derived bioaerosol is a potential tool to measure source case infectiousness. However, current bioaerosol sampling approaches have reported low detection yields in sputum-positive TB cases. To increase the utility of bioaerosol sampling, we present advances in bioaerosol collection and Mtb identification that improve detection yields. A previously described Respiratory Aerosol Sampling Chamber (RASC) protocol, or "RASC-1", was modified to incorporate liquid collection of bioaerosol using a high-flow wet-walled cyclone (RASC-2). Individuals with GeneXpert-positive pulmonary TB were sampled pre-treatment over 60-minutes. Putative Mtb bacilli were detected in collected fluid by fluorescence microscopy utilising DMN-Trehalose. Exhaled air and bioaerosol volumes were estimated using continuous CO2 monitoring and airborne particle counting, respectively. Mtb capture was calculated per exhaled air volume sampled and bioaerosol volume for RASC-1 (n = 35) and for RASC-2 (n = 21). Empty chamber samples were collected between patients as controls. The optimised RASC-2 protocol sampled a median of 258.4L (IQR: 226.9-273.6) of exhaled air per patient compared with 27.5L (IQR: 23.6-30.3) for RASC-1 (p<0.0001). Bioaerosol volume collection was estimated at 2.3nL (IQR: 1.1-3.6) for RASC-2 compared with 0.08nL (IQR: 0.05-0.10) for RASC-1 (p<0.0001). The detection yield of viable Mtb improved from 43% (median 2 CFU, range: 1-14) to 95% (median 20.5 DMN-Trehalose positive bacilli, range: 2-155). These improvements represent a lowering of the limit of detection in the RASC-2 platform to 0.9 Mtb bacilli per 100L of exhaled air from 3.3 Mtb bacilli per 100L (RASC-1). This study demonstrates that technical improvements in particle collection together with sensitive detection enable rapid quantitation of viable Mtb in bioaerosols of sputum positive TB cases. Increased sampling sensitivity may allow future TB transmission studies to be extended to sputum-negative and subclinical individuals, and suggests the potential utility of bioaerosol measurement for rapid intervention in other airborne infectious diseases.

Identifiants

pubmed: 32881875
doi: 10.1371/journal.pone.0238193
pii: PONE-D-20-11317
pmc: PMC7470324
doi:

Substances chimiques

Aerosols 0
Carbon Dioxide 142M471B3J

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0238193

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI147347
Pays : United States
Organisme : NIAID NIH HHS
ID : R37 AI051622
Pays : United States

Déclaration de conflit d'intérêts

WB and CC are employed by Zeteo Tech. AK is employed by Edge Embossing. Belonging to these commercial entities does not alter the authors’ adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Benjamin Patterson (B)

Amsterdam Institute for Global Health and Development, University of Amsterdam, Amsterdam, Netherlands.

Ryan Dinkele (R)

Department of Pathology, Faculty of Health Sciences, SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit & DST/NRF Centre of Excellence for Biomedical TB Research, University of Cape Town, South Africa.
Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Sophia Gessner (S)

Department of Pathology, Faculty of Health Sciences, SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit & DST/NRF Centre of Excellence for Biomedical TB Research, University of Cape Town, South Africa.
Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Carl Morrow (C)

Desmond Tutu HIV Centre, University of Cape Town, Cape Town, South Africa.

Mireille Kamariza (M)

Department of Biology, Stanford University, Stanford, California, United States of America.

Carolyn R Bertozzi (CR)

Department of Chemistry, Stanford University, Stanford, California, United States of America.
Howard Hughes Medical Institute, Stanford University, Stanford, California, United States of America.

Andrew Kamholz (A)

Edge Embossing, Charlestown, Boston, Massachusetts, United States of America.

Wayne Bryden (W)

Zeteo Tech, Sykesville, Maryland, United States of America.

Charles Call (C)

Zeteo Tech, Sykesville, Maryland, United States of America.

Digby F Warner (DF)

Department of Pathology, Faculty of Health Sciences, SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit & DST/NRF Centre of Excellence for Biomedical TB Research, University of Cape Town, South Africa.
Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Wellcome Centre for Infectious Disease Research in Africa, University of Cape Town, Cape Town, South Africa.

Robin Wood (R)

Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Desmond Tutu HIV Centre, University of Cape Town, Cape Town, South Africa.

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Classifications MeSH