Cargando…

Characterization of the public transit air microbiome and resistome reveals geographical specificity

BACKGROUND: The public transit is a built environment with high occupant density across the globe, and identifying factors shaping public transit air microbiomes will help design strategies to minimize the transmission of pathogens. However, the majority of microbiome works dedicated to the public t...

Descripción completa

Detalles Bibliográficos
Autores principales: Leung, M. H. Y., Tong, X., Bøifot, K. O., Bezdan, D., Butler, D. J., Danko, D. C., Gohli, J., Green, D. C., Hernandez, M. T., Kelly, F. J., Levy, S., Mason-Buck, G., Nieto-Caballero, M., Syndercombe-Court, D., Udekwu, K., Young, B. G., Mason, C. E., Dybwad, M., Lee, P. K. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157753/
https://www.ncbi.nlm.nih.gov/pubmed/34039416
http://dx.doi.org/10.1186/s40168-021-01044-7
_version_ 1783699751845232640
author Leung, M. H. Y.
Tong, X.
Bøifot, K. O.
Bezdan, D.
Butler, D. J.
Danko, D. C.
Gohli, J.
Green, D. C.
Hernandez, M. T.
Kelly, F. J.
Levy, S.
Mason-Buck, G.
Nieto-Caballero, M.
Syndercombe-Court, D.
Udekwu, K.
Young, B. G.
Mason, C. E.
Dybwad, M.
Lee, P. K. H.
author_facet Leung, M. H. Y.
Tong, X.
Bøifot, K. O.
Bezdan, D.
Butler, D. J.
Danko, D. C.
Gohli, J.
Green, D. C.
Hernandez, M. T.
Kelly, F. J.
Levy, S.
Mason-Buck, G.
Nieto-Caballero, M.
Syndercombe-Court, D.
Udekwu, K.
Young, B. G.
Mason, C. E.
Dybwad, M.
Lee, P. K. H.
author_sort Leung, M. H. Y.
collection PubMed
description BACKGROUND: The public transit is a built environment with high occupant density across the globe, and identifying factors shaping public transit air microbiomes will help design strategies to minimize the transmission of pathogens. However, the majority of microbiome works dedicated to the public transit air are limited to amplicon sequencing, and our knowledge regarding the functional potentials and the repertoire of resistance genes (i.e. resistome) is limited. Furthermore, current air microbiome investigations on public transit systems are focused on single cities, and a multi-city assessment of the public transit air microbiome will allow a greater understanding of whether and how broad environmental, building, and anthropogenic factors shape the public transit air microbiome in an international scale. Therefore, in this study, the public transit air microbiomes and resistomes of six cities across three continents (Denver, Hong Kong, London, New York City, Oslo, Stockholm) were characterized. RESULTS: City was the sole factor associated with public transit air microbiome differences, with diverse taxa identified as drivers for geography-associated functional potentials, concomitant with geographical differences in species- and strain-level inferred growth profiles. Related bacterial strains differed among cities in genes encoding resistance, transposase, and other functions. Sourcetracking estimated that human skin, soil, and wastewater were major presumptive resistome sources of public transit air, and adjacent public transit surfaces may also be considered presumptive sources. Large proportions of detected resistance genes were co-located with mobile genetic elements including plasmids. Biosynthetic gene clusters and city-unique coding sequences were found in the metagenome-assembled genomes. CONCLUSIONS: Overall, geographical specificity transcends multiple aspects of the public transit air microbiome, and future efforts on a global scale are warranted to increase our understanding of factors shaping the microbiome of this unique built environment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01044-7.
format Online
Article
Text
id pubmed-8157753
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-81577532021-06-01 Characterization of the public transit air microbiome and resistome reveals geographical specificity Leung, M. H. Y. Tong, X. Bøifot, K. O. Bezdan, D. Butler, D. J. Danko, D. C. Gohli, J. Green, D. C. Hernandez, M. T. Kelly, F. J. Levy, S. Mason-Buck, G. Nieto-Caballero, M. Syndercombe-Court, D. Udekwu, K. Young, B. G. Mason, C. E. Dybwad, M. Lee, P. K. H. Microbiome Research BACKGROUND: The public transit is a built environment with high occupant density across the globe, and identifying factors shaping public transit air microbiomes will help design strategies to minimize the transmission of pathogens. However, the majority of microbiome works dedicated to the public transit air are limited to amplicon sequencing, and our knowledge regarding the functional potentials and the repertoire of resistance genes (i.e. resistome) is limited. Furthermore, current air microbiome investigations on public transit systems are focused on single cities, and a multi-city assessment of the public transit air microbiome will allow a greater understanding of whether and how broad environmental, building, and anthropogenic factors shape the public transit air microbiome in an international scale. Therefore, in this study, the public transit air microbiomes and resistomes of six cities across three continents (Denver, Hong Kong, London, New York City, Oslo, Stockholm) were characterized. RESULTS: City was the sole factor associated with public transit air microbiome differences, with diverse taxa identified as drivers for geography-associated functional potentials, concomitant with geographical differences in species- and strain-level inferred growth profiles. Related bacterial strains differed among cities in genes encoding resistance, transposase, and other functions. Sourcetracking estimated that human skin, soil, and wastewater were major presumptive resistome sources of public transit air, and adjacent public transit surfaces may also be considered presumptive sources. Large proportions of detected resistance genes were co-located with mobile genetic elements including plasmids. Biosynthetic gene clusters and city-unique coding sequences were found in the metagenome-assembled genomes. CONCLUSIONS: Overall, geographical specificity transcends multiple aspects of the public transit air microbiome, and future efforts on a global scale are warranted to increase our understanding of factors shaping the microbiome of this unique built environment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01044-7. BioMed Central 2021-05-26 /pmc/articles/PMC8157753/ /pubmed/34039416 http://dx.doi.org/10.1186/s40168-021-01044-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Leung, M. H. Y.
Tong, X.
Bøifot, K. O.
Bezdan, D.
Butler, D. J.
Danko, D. C.
Gohli, J.
Green, D. C.
Hernandez, M. T.
Kelly, F. J.
Levy, S.
Mason-Buck, G.
Nieto-Caballero, M.
Syndercombe-Court, D.
Udekwu, K.
Young, B. G.
Mason, C. E.
Dybwad, M.
Lee, P. K. H.
Characterization of the public transit air microbiome and resistome reveals geographical specificity
title Characterization of the public transit air microbiome and resistome reveals geographical specificity
title_full Characterization of the public transit air microbiome and resistome reveals geographical specificity
title_fullStr Characterization of the public transit air microbiome and resistome reveals geographical specificity
title_full_unstemmed Characterization of the public transit air microbiome and resistome reveals geographical specificity
title_short Characterization of the public transit air microbiome and resistome reveals geographical specificity
title_sort characterization of the public transit air microbiome and resistome reveals geographical specificity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157753/
https://www.ncbi.nlm.nih.gov/pubmed/34039416
http://dx.doi.org/10.1186/s40168-021-01044-7
work_keys_str_mv AT leungmhy characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT tongx characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT bøifotko characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT bezdand characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT butlerdj characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT dankodc characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT gohlij characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT greendc characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT hernandezmt characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT kellyfj characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT levys characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT masonbuckg characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT nietocaballerom characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT syndercombecourtd characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT udekwuk characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT youngbg characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT masonce characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT dybwadm characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity
AT leepkh characterizationofthepublictransitairmicrobiomeandresistomerevealsgeographicalspecificity