PERSONAL MONITORING OF EXPOSURE TO GENETICALLY-MODIFIED MICROORGANISMS IN BIOAEROSOLS - RAPID AND SENSITIVE DETECTION USING PCR

Citation
Pg. Nugent et al., PERSONAL MONITORING OF EXPOSURE TO GENETICALLY-MODIFIED MICROORGANISMS IN BIOAEROSOLS - RAPID AND SENSITIVE DETECTION USING PCR, Journal of aerosol science, 28(3), 1997, pp. 525-538
Citations number
30
Categorie Soggetti
Environmental Sciences","Engineering, Chemical","Metereology & Atmospheric Sciences","Engineering, Mechanical
Journal title
ISSN journal
00218502
Volume
28
Issue
3
Year of publication
1997
Pages
525 - 538
Database
ISI
SICI code
0021-8502(1997)28:3<525:PMOETG>2.0.ZU;2-0
Abstract
E. coli XL1-B cells, genetically modified to contain the gene for the commerically important food-processing enzyme, bovine chymosin, were a erosolised in growth media to simulate a breach of containment. Aeroso ls were generated in a well-characterised bioaerosol test chamber, and sampled using two commonly employed workplace aerosol samplers-the Cy clone static ''area'' sampler, and the IOM Personal Inspirable Aerosol Sampler. PCR-based detection procedures were developed for the specif ic, sensitive, and rapid, detection and discrimination of both capture d aerosolised genetically modified and unmodified E. coli cells. The I OM personal sampler proved to be more useful than the cyclone sampler for aerosol capture and subsequent analysis using the PCR procedure. I t allowed an apparent lower limit of detection of an aerosol containin g 1.7 x 10(4) cells m(-3), with results being obtained within 4-5 h af ter sample collection. (C) 1997 Elsevier Science Ltd.