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Microbial burden and diversity of commercial airline cabin air during short and long durations of travel

Total microbial burden and diversity associated with commercial airliner cabin air was assessed by molecular methods in 125 air samples from the business-class sections of 16 domestic and international flights. Viable microbial burden within these cabin air parcels constituted only 1–10% of the tota...

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Autores principales: Osman, Shariff, La Duc, Myron T, Dekas, Anne, Newcombe, David, Venkateswaran, Kasthuri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099242/
https://www.ncbi.nlm.nih.gov/pubmed/18256704
http://dx.doi.org/10.1038/ismej.2008.11
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author Osman, Shariff
La Duc, Myron T
Dekas, Anne
Newcombe, David
Venkateswaran, Kasthuri
author_facet Osman, Shariff
La Duc, Myron T
Dekas, Anne
Newcombe, David
Venkateswaran, Kasthuri
author_sort Osman, Shariff
collection PubMed
description Total microbial burden and diversity associated with commercial airliner cabin air was assessed by molecular methods in 125 air samples from the business-class sections of 16 domestic and international flights. Viable microbial burden within these cabin air parcels constituted only 1–10% of the total microbial population and ranged from below detection limits to 1.2 × 10(4) cells m(–3) as determined with a validated ATP-based technology. Cultivable bacterial diversity was almost entirely limited to Gram-positive bacteria such as Staphylococcus and Bacillus. In contrast, cloning and sequencing 16S rRNA gene directly from the samples without cultivation indicated a significantly broader diversity, as sequences representing more than 100 species, and encompassing 12 classes of bacteria, were retrieved in varying abundance. Sequences of proteobacterial and Gram-positive lineage were retrieved most frequently (58% and 31% of all clone sequences, respectively), with Gram-positive and α-proteobacterial sequences dominating international flight samples and β- and γ-proteobacterial sequences comprising the largest portion of those retrieved from domestic flights. Significant differences in bacterial load and diversity were noted between samples obtained on domestic and international flights. The disparities observed in microbial abundance and diversity further underscore the immense value of state-of-the art molecular assays in augmenting traditional culture-based techniques. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/ismej.2008.11) contains supplementary material, which is available to authorized users.
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spelling pubmed-70992422020-03-27 Microbial burden and diversity of commercial airline cabin air during short and long durations of travel Osman, Shariff La Duc, Myron T Dekas, Anne Newcombe, David Venkateswaran, Kasthuri ISME J Article Total microbial burden and diversity associated with commercial airliner cabin air was assessed by molecular methods in 125 air samples from the business-class sections of 16 domestic and international flights. Viable microbial burden within these cabin air parcels constituted only 1–10% of the total microbial population and ranged from below detection limits to 1.2 × 10(4) cells m(–3) as determined with a validated ATP-based technology. Cultivable bacterial diversity was almost entirely limited to Gram-positive bacteria such as Staphylococcus and Bacillus. In contrast, cloning and sequencing 16S rRNA gene directly from the samples without cultivation indicated a significantly broader diversity, as sequences representing more than 100 species, and encompassing 12 classes of bacteria, were retrieved in varying abundance. Sequences of proteobacterial and Gram-positive lineage were retrieved most frequently (58% and 31% of all clone sequences, respectively), with Gram-positive and α-proteobacterial sequences dominating international flight samples and β- and γ-proteobacterial sequences comprising the largest portion of those retrieved from domestic flights. Significant differences in bacterial load and diversity were noted between samples obtained on domestic and international flights. The disparities observed in microbial abundance and diversity further underscore the immense value of state-of-the art molecular assays in augmenting traditional culture-based techniques. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/ismej.2008.11) contains supplementary material, which is available to authorized users. Nature Publishing Group UK 2008-02-07 2008-05 /pmc/articles/PMC7099242/ /pubmed/18256704 http://dx.doi.org/10.1038/ismej.2008.11 Text en © International Society for Microbial Ecology 2008 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Osman, Shariff
La Duc, Myron T
Dekas, Anne
Newcombe, David
Venkateswaran, Kasthuri
Microbial burden and diversity of commercial airline cabin air during short and long durations of travel
title Microbial burden and diversity of commercial airline cabin air during short and long durations of travel
title_full Microbial burden and diversity of commercial airline cabin air during short and long durations of travel
title_fullStr Microbial burden and diversity of commercial airline cabin air during short and long durations of travel
title_full_unstemmed Microbial burden and diversity of commercial airline cabin air during short and long durations of travel
title_short Microbial burden and diversity of commercial airline cabin air during short and long durations of travel
title_sort microbial burden and diversity of commercial airline cabin air during short and long durations of travel
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099242/
https://www.ncbi.nlm.nih.gov/pubmed/18256704
http://dx.doi.org/10.1038/ismej.2008.11
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