Sensitivity optimisation of tuberculosis bioaerosol sampling

• Published in: PloS one Vol. 15; no. 9; p. e0238193
• Main Authors: Patterson, Benjamin, Dinkele, Ryan, Gessner, Sophia, Morrow, Carl, Kamariza, Mireille, Bertozzi, Carolyn R, Kamholz, Andrew, Bryden, Wayne, Call, Charles, Warner, Digby F, Wood, Robin
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 03.09.2020; Public Library of Science (PLoS)
• Subjects: Adult; Aerosol sampling; Aerosols - analysis; Air sampling; Airborne microorganisms; Airborne sensing; Bacilli; Bioaerosols; Biology and Life Sciences; Carbon capture and storage; Carbon dioxide; Carbon Dioxide - chemistry; Collection; Collectors; Cyclones; Disease transmission; Earth Sciences; Exhalation; Experiments; Female; Fluorescence; Fluorescence microscopy; Health sciences; Humans; Identification methods; Infections; Infectious diseases; Male; Medicine; Medicine and Health Sciences; Mycobacterium tuberculosis - isolation & purification; Optimization; Pathology; Patients; Physical Sciences; Pretreatment; Quantitation; Research and Analysis Methods; Sampling; Sensitivity; Specimen Handling - methods; Sputum; Trehalose; Tuberculosis; Tuberculosis - diagnosis; Tuberculosis - microbiology; Tutu, Desmond; Yield; South Africa; California; United States > US; Maryland
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0238193

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.