4.7 Article

Aerosolization of Mycobacterium tuberculosis by Tidal Breathing

出版社

AMER THORACIC SOC
DOI: 10.1164/rccm.202110-2378OC

关键词

TB transmission; bioaerosol; cough; forced vital capacity

资金

  1. South African Medical Research Council (SAMRC)
  2. National Treasury under its Economic Competitiveness and Support Package [MRC-RFA-UFSP-01-2013/CCAMP]
  3. Strategic Health Innovations Partnerships (SHIP) Unit of the SAMRC
  4. Bill and Melinda Gates Foundation [OPP1116641]
  5. Research Council of Norway [261669]
  6. National Institute of Allergy and Infectious Diseases [U19AI162584, R01AI093269]
  7. Eunice Kennedy Shriver National Institute of Child Health and Human Development of the NIH [U01HD085531]
  8. Bill and Melinda Gates Foundation [OPP1116641] Funding Source: Bill and Melinda Gates Foundation

向作者/读者索取更多资源

This study compared the aerosolization of Mtb and total particulate matter from patients with TB during three respiratory maneuvers and found that tidal breathing may be the main contributor to the aerosolization of Mtb among TB patients on a daily basis.
Rationale: Interrupting tuberculosis (TB) transmission requires an improved understanding of how and when the causative organism, Mycobacterium tuberculosis (Mtb), is aerosolized. Although cough is commonly assumed to be the dominant source of Mtb aerosols, recent evidence of cough-independent Mtb release implies the contribution of alternative mechanisms. Objectives: To compare the aerosolization of Mtb bacilli and total particulate matter from patients with TB during three separate respiratory maneuvers: tidal breathing (TiBr), FVC, and cough. Methods: Bioaerosol sampling and Mtb enumeration by live-cell, fluorescence microscopy were combined with real-time measurement of CO2 concentration and total particle counts from 38 patients with GeneXpert-positive TB before treatment initiation. Measurements and Main Results: For all maneuvers, the proportions of particles detected across five size categories were similar, with most particles falling between 0.5-5 Rm. Although total particle counts were 4.8-fold greater in cough samples than either TiBr or FVC, all three maneuvers returned similar rates of positivity for Mtb. No correlation was observed between total particle production and Mtb count. Instead, for total Mtb counts, the variability between individuals was greater than the variability between sampling maneuvers. Finally, when modelled using 24-hour breath and cough frequencies, our data indicate that TiBr might contribute more than 90% of the daily aerosolized Mtb among symptomatic patients with TB. Conclusions: Assuming the number of viable Mtb organisms released offers a reliable proxy of patient infectiousness, our observations imply that TiBr and interindividual variability in Mtb release might be significant contributors to TB transmission among active cases.

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