Daylight exposure modulates bacterial communities associated with household dust
Abstract Background Microbial communities associated with indoor dust abound in the built environment. The transmission of sunlight through windows is a key building design consideration, but the effects of light exposure on dust communities remain unclear. We report results of an experiment and com...
Main Authors: | , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2018-10-01
|
Series: | Microbiome |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s40168-018-0559-4 |
id |
doaj-ab28c1993a9b49c8a4242ad50b33acd1 |
---|---|
record_format |
Article |
spelling |
doaj-ab28c1993a9b49c8a4242ad50b33acd12020-11-25T01:13:45ZengBMCMicrobiome2049-26182018-10-016111310.1186/s40168-018-0559-4Daylight exposure modulates bacterial communities associated with household dustAshkaan K. Fahimipour0Erica M. Hartmann1Andrew Siemens2Jeff Kline3David A. Levin4Hannah Wilson5Clarisse M. Betancourt-Román6GZ Brown7Mark Fretz8Dale Northcutt9Kyla N. Siemens10Curtis Huttenhower11Jessica L. Green12Kevin Van Den Wymelenberg13Biology and the Built Environment Center, University of OregonBiology and the Built Environment Center, University of OregonBiology and the Built Environment Center, University of OregonBiology and the Built Environment Center, University of OregonDepartment of Mathematics, University of OregonBiology and the Built Environment Center, University of OregonBiology and the Built Environment Center, University of OregonBiology and the Built Environment Center, University of OregonBiology and the Built Environment Center, University of OregonBiology and the Built Environment Center, University of OregonBiology and the Built Environment Center, University of OregonDepartment of Biostatistics, Harvard T.H. Chan School of Public HealthBiology and the Built Environment Center, University of OregonBiology and the Built Environment Center, University of OregonAbstract Background Microbial communities associated with indoor dust abound in the built environment. The transmission of sunlight through windows is a key building design consideration, but the effects of light exposure on dust communities remain unclear. We report results of an experiment and computational models designed to assess the effects of light exposure and wavelengths on the structure of the dust microbiome. Specifically, we placed household dust in replicate model “rooms” with windows that transmitted visible, ultraviolet, or no light and measured taxonomic compositions, absolute abundances, and viabilities of the resulting bacterial communities. Results Light exposure per se led to lower abundances of viable bacteria and communities that were compositionally distinct from dark rooms, suggesting preferential inactivation of some microbes over others under daylighting conditions. Differences between communities experiencing visible and ultraviolet light wavelengths were relatively minor, manifesting primarily in abundances of dead human-derived taxa. Daylighting was associated with the loss of a few numerically dominant groups of related microorganisms and apparent increases in the abundances of some rare groups, suggesting that a small number of microorganisms may have exhibited modest population growth under lighting conditions. Although biological processes like population growth on dust could have generated these patterns, we also present an alternate statistical explanation using sampling models from ecology; simulations indicate that artefactual, apparent increases in the abundances of very rare taxa may be a null expectation following the selective inactivation of dominant microorganisms in a community. Conclusions Our experimental and simulation-based results indicate that dust contains living bacterial taxa that can be inactivated following changes in local abiotic conditions and suggest that the bactericidal potential of ordinary window-filtered sunlight may be similar to ultraviolet wavelengths across dosages that are relevant to real buildings.http://link.springer.com/article/10.1186/s40168-018-0559-4DustDaylightMicrobiomeBuilt environment |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ashkaan K. Fahimipour Erica M. Hartmann Andrew Siemens Jeff Kline David A. Levin Hannah Wilson Clarisse M. Betancourt-Román GZ Brown Mark Fretz Dale Northcutt Kyla N. Siemens Curtis Huttenhower Jessica L. Green Kevin Van Den Wymelenberg |
spellingShingle |
Ashkaan K. Fahimipour Erica M. Hartmann Andrew Siemens Jeff Kline David A. Levin Hannah Wilson Clarisse M. Betancourt-Román GZ Brown Mark Fretz Dale Northcutt Kyla N. Siemens Curtis Huttenhower Jessica L. Green Kevin Van Den Wymelenberg Daylight exposure modulates bacterial communities associated with household dust Microbiome Dust Daylight Microbiome Built environment |
author_facet |
Ashkaan K. Fahimipour Erica M. Hartmann Andrew Siemens Jeff Kline David A. Levin Hannah Wilson Clarisse M. Betancourt-Román GZ Brown Mark Fretz Dale Northcutt Kyla N. Siemens Curtis Huttenhower Jessica L. Green Kevin Van Den Wymelenberg |
author_sort |
Ashkaan K. Fahimipour |
title |
Daylight exposure modulates bacterial communities associated with household dust |
title_short |
Daylight exposure modulates bacterial communities associated with household dust |
title_full |
Daylight exposure modulates bacterial communities associated with household dust |
title_fullStr |
Daylight exposure modulates bacterial communities associated with household dust |
title_full_unstemmed |
Daylight exposure modulates bacterial communities associated with household dust |
title_sort |
daylight exposure modulates bacterial communities associated with household dust |
publisher |
BMC |
series |
Microbiome |
issn |
2049-2618 |
publishDate |
2018-10-01 |
description |
Abstract Background Microbial communities associated with indoor dust abound in the built environment. The transmission of sunlight through windows is a key building design consideration, but the effects of light exposure on dust communities remain unclear. We report results of an experiment and computational models designed to assess the effects of light exposure and wavelengths on the structure of the dust microbiome. Specifically, we placed household dust in replicate model “rooms” with windows that transmitted visible, ultraviolet, or no light and measured taxonomic compositions, absolute abundances, and viabilities of the resulting bacterial communities. Results Light exposure per se led to lower abundances of viable bacteria and communities that were compositionally distinct from dark rooms, suggesting preferential inactivation of some microbes over others under daylighting conditions. Differences between communities experiencing visible and ultraviolet light wavelengths were relatively minor, manifesting primarily in abundances of dead human-derived taxa. Daylighting was associated with the loss of a few numerically dominant groups of related microorganisms and apparent increases in the abundances of some rare groups, suggesting that a small number of microorganisms may have exhibited modest population growth under lighting conditions. Although biological processes like population growth on dust could have generated these patterns, we also present an alternate statistical explanation using sampling models from ecology; simulations indicate that artefactual, apparent increases in the abundances of very rare taxa may be a null expectation following the selective inactivation of dominant microorganisms in a community. Conclusions Our experimental and simulation-based results indicate that dust contains living bacterial taxa that can be inactivated following changes in local abiotic conditions and suggest that the bactericidal potential of ordinary window-filtered sunlight may be similar to ultraviolet wavelengths across dosages that are relevant to real buildings. |
topic |
Dust Daylight Microbiome Built environment |
url |
http://link.springer.com/article/10.1186/s40168-018-0559-4 |
work_keys_str_mv |
AT ashkaankfahimipour daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT ericamhartmann daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT andrewsiemens daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT jeffkline daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT davidalevin daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT hannahwilson daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT clarissembetancourtroman daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT gzbrown daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT markfretz daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT dalenorthcutt daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT kylansiemens daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT curtishuttenhower daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT jessicalgreen daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust AT kevinvandenwymelenberg daylightexposuremodulatesbacterialcommunitiesassociatedwithhouseholddust |
_version_ |
1725160211121963008 |