The efficient method for simultaneous monitoring of the culturable as well as nonculturable airborne microorganisms.

Cultivation-based microbiological methods are a gold standard for monitoring of airborne micro-organisms to determine the occupational exposure levels or transmission paths of a particular infectious agent. Some highly contagious microorganisms are not easily culturable but it is becoming evident th...

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Main Authors: Barbara Hubad, Aleš Lapanje
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24376520/?tool=EBI
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spelling doaj-e265ede55811470a91e9620a8868019b2021-03-03T20:17:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8218610.1371/journal.pone.0082186The efficient method for simultaneous monitoring of the culturable as well as nonculturable airborne microorganisms.Barbara HubadAleš LapanjeCultivation-based microbiological methods are a gold standard for monitoring of airborne micro-organisms to determine the occupational exposure levels or transmission paths of a particular infectious agent. Some highly contagious microorganisms are not easily culturable but it is becoming evident that cultivation and molecular methods are complementary and in these cases highly relevant. We report a simple and efficient method for sampling and analyzing airborne bacteria with an impactor-type high-flow-rate portable air sampler, currently used for monitoring culturable bacteria or fungi. A method is reported for extraction of nucleic acids from impacted cells without prior cultivation and using agarose as a sampling matrix. The DNA extraction efficiency was determined in spiked samples and, samples taken from a wastewater treatment plant and an alpine area. The abundance, diversity and quantity of total bacteria were analysed by a quantitative polymerase chain reaction, and by construction and analysis of clone libraries. The method does not interfere with downstream PCR analysis and can cover the gap between traditional culture and molecular techniques of bioaerosol monitoring.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24376520/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Barbara Hubad
Aleš Lapanje
spellingShingle Barbara Hubad
Aleš Lapanje
The efficient method for simultaneous monitoring of the culturable as well as nonculturable airborne microorganisms.
PLoS ONE
author_facet Barbara Hubad
Aleš Lapanje
author_sort Barbara Hubad
title The efficient method for simultaneous monitoring of the culturable as well as nonculturable airborne microorganisms.
title_short The efficient method for simultaneous monitoring of the culturable as well as nonculturable airborne microorganisms.
title_full The efficient method for simultaneous monitoring of the culturable as well as nonculturable airborne microorganisms.
title_fullStr The efficient method for simultaneous monitoring of the culturable as well as nonculturable airborne microorganisms.
title_full_unstemmed The efficient method for simultaneous monitoring of the culturable as well as nonculturable airborne microorganisms.
title_sort efficient method for simultaneous monitoring of the culturable as well as nonculturable airborne microorganisms.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Cultivation-based microbiological methods are a gold standard for monitoring of airborne micro-organisms to determine the occupational exposure levels or transmission paths of a particular infectious agent. Some highly contagious microorganisms are not easily culturable but it is becoming evident that cultivation and molecular methods are complementary and in these cases highly relevant. We report a simple and efficient method for sampling and analyzing airborne bacteria with an impactor-type high-flow-rate portable air sampler, currently used for monitoring culturable bacteria or fungi. A method is reported for extraction of nucleic acids from impacted cells without prior cultivation and using agarose as a sampling matrix. The DNA extraction efficiency was determined in spiked samples and, samples taken from a wastewater treatment plant and an alpine area. The abundance, diversity and quantity of total bacteria were analysed by a quantitative polymerase chain reaction, and by construction and analysis of clone libraries. The method does not interfere with downstream PCR analysis and can cover the gap between traditional culture and molecular techniques of bioaerosol monitoring.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24376520/?tool=EBI
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