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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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 |
work_keys_str_mv |
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