PneumoniaCheck, a novel aerosol collection device, permits capture of airborne Mycobacterium tuberculosis and characterisation of the cough aeromicrobiome in people with tuberculosis

被引:1
作者
Chiyaka, Tinaye L. [1 ,2 ]
Nyawo, Georgina R. [1 ,2 ]
Naidoo, Charissa C. [1 ,2 ]
Moodley, Suventha [1 ,2 ]
Clemente, Jose C. [3 ]
Malherbe, Stephanus T. [1 ]
Warren, Robin M. [1 ]
Ku, David N. [4 ]
Segal, Leopoldo N. [5 ]
Theron, Grant [1 ,2 ]
机构
[1] Stellenbosch Univ, Fac Med & Hlth Sci, DSI NRF Ctr Excellence Biomed TB Res, SAMRC Ctr TB Res,Div Mol Biol & Human Genet, ZA-7505 Cape Town, South Africa
[2] Stellenbosch Univ, African Microbiome Inst, Fac Med & Hlth Sci, Dept Biomed Sci,Div Mol Biol & Human Genet, ZA-7505 Cape Town, South Africa
[3] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[4] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[5] NYU, NYU Langone Hlth, Div Pulm Crit Care & Sleep Med, Grossman Sch Med, New York, NY 10016 USA
基金
英国医学研究理事会; 新加坡国家研究基金会; 美国国家卫生研究院;
关键词
PneumoniaCheck; Tuberculosis; Microbiota; Aerosols; Xpert MTB/RIF Ultra;
D O I
10.1186/s12941-024-00735-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background Tuberculosis (TB), a major cause of disease and antimicrobial resistance, is spread via aerosols. Aerosols have diagnostic potential and airborne-microbes other than Mycobacterium tuberculosis complex (MTBC) may influence transmission. We evaluated whether PneumoniaCheck (PMC), a commercial aerosol collection device, captures MTBC and the aeromicrobiome of people with TB. Methods PMC was done in sputum culture-positive people (>= 30 forced coughs each, n = 16) pre-treatment and PMC air reservoir (bag, corresponding to upper airways) and filter (lower airways) washes underwent Xpert MTB/RIF Ultra (Ultra) and 16S rRNA gene sequencing (sequencing also done on sputum). In a subset (n = 6), PMC microbiota (bag, filter) was compared to oral washes and bronchoalveolar lavage fluid (BALF). Findings 54% (7/13) bags and 46% (6/14) filters were Ultra-positive. Sequencing read counts and microbial diversity did not differ across bags, filters, and sputum. However, microbial composition in bags (Sphingobium-, Corynebacterium-, Novosphingobium-enriched) and filters (Mycobacterium-, Sphingobium-, Corynebacterium-enriched) each differed vs. sputum. Furthermore, sequencing only detected Mycobacterium in bags and filters but not sputum. In the subset, bag and filter microbial diversity did not differ vs. oral washes or BALF but microbial composition differed. Bags vs. BALF were Sphingobium-enriched and Mycobacterium-, Streptococcus-, and Anaerosinus-depleted (Anaerosinus also depleted in filters vs. BALF). Compared to BALF, none of the aerosol-enriched taxa were enriched in oral washes or sputum. Interpretation PMC captures aerosols with Ultra-detectable MTBC and MTBC is more detectable in aerosols than sputum by sequencing. The aeromicrobiome is distinct from sputum, oral washes and BALF and contains differentially-enriched lower respiratory tract microbes.
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