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dc.contributor.authorNocker, Andreas
dc.contributor.authorCamper, Anne K.
dc.date.accessioned2017-07-13T22:28:10Z
dc.date.available2017-07-13T22:28:10Z
dc.date.issued2006-03
dc.identifier.citationNocker A, Camper AK, "Selective removal of DNA from dead cells of mixed bacterial communities by use of ethidium monoazide," Appl Environ Microbiol 2006 72(3):1997-2004en_US
dc.identifier.issn0099-2240
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/13297
dc.description.abstractThe distinction between viable and dead bacterial cells poses a major challenge in microbial diagnostics. Due to the persistence of DNA in the environment after cells have lost viability, DNA-based quantification methods overestimate the number of viable cells in mixed populations or even lead to false-positive results in the absence of viable cells. On the other hand, RNA-based diagnostic methods, which circumvent this problem, are technically demanding and suffer from some drawbacks. A promising and easy-to-use alternative utilizing the DNA-intercalating dye ethidium monoazide bromide (EMA) was published recently. This chemical is known to penetrate only into “dead” cells with compromised cell membrane integrity. Subsequent photoinduced crosslinking was reported to inhibit PCR amplification of DNA from dead cells. We provide evidence here that in addition to inhibition of amplification, most of the DNA from dead cells is actually lost during the DNA extraction procedure, probably together with cell debris which goes into the pellet fraction. Exposure of bacteria to increasing stress and higher proportions of dead cells in defined populations led to increasing loss of genomic DNA. Experiments were performed using Escherichia coli O157:H7 and Salmonella enterica serovar Typhimurium as model pathogens and using real-time PCR for their quantification. Results showed that EMA treatment of mixed populations of these two species provides a valuable tool for selective removal of DNA of nonviable cells by using conventional extraction protocols. Furthermore, we provide evidence that prior to denaturing gradient gel electrophoresis, EMA treatment of a mature mixed-population drinking-water biofilm containing a substantial proportion of dead cells can result in community fingerprints dramatically different from those for an untreated biofilm. The interpretation of such fingerprints can have important implications in the field of microbial ecology.en_US
dc.titleSelective removal of DNA from dead cells of mixed bacterial communities by use of ethidium monoazideen_US
dc.typeArticleen_US
mus.citation.extentfirstpage1997en_US
mus.citation.extentlastpage2004en_US
mus.citation.issue3en_US
mus.citation.journaltitleApplied and Environmental Microbiologyen_US
mus.citation.volume72en_US
mus.identifier.categoryEngineering & Computer Scienceen_US
mus.identifier.doi10.1128/aem.72.3.1997-2004.2006en_US
mus.relation.collegeCollege of Engineeringen_US
mus.relation.departmentCenter for Biofilm Engineering.en_US
mus.relation.departmentChemical & Biological Engineering.en_US
mus.relation.departmentChemical Engineering.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.relation.researchgroupCenter for Biofilm Engineering.en_US
mus.data.thumbpage7en_US
mus.contributor.orcidNocker, Andreas|0000-0002-5343-9418en_US


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