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dc.contributor.authorLenz, Ailyn P.
dc.contributor.authorWilliamson, Kerry S.
dc.contributor.authorPitts, Betsey
dc.contributor.authorStewart, Philip S.
dc.contributor.authorFranklin, Michael J.
dc.date.accessioned2017-07-07T17:15:55Z
dc.date.available2017-07-07T17:15:55Z
dc.date.issued2008-05
dc.identifier.citationLenz AP, Williamson K, Pitts B, Stewart PS, Franklin MJ, "Localized gene expression in Pseudomonas aeruginosa biofilms," Appl Environ Microbiol 2008 74(14):4463-4471en_US
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/13201
dc.description.abstractGene expression in biofilms is dependent on bacterial responses to the local environmental conditions. Most techniques for studying bacterial gene expression in biofilms characterize average values over the entire population. Here, we describe the use of laser capture microdissection microscopy (LCMM) combined with multiplex quantitative real time reverse transcriptase polymerase chain reaction (qRT-PCR) to isolate and quantify RNA transcripts from small groups of cells at spatially resolved sites within biofilms. The approach was first tested and analytical parameters determined for Pseudomonas aeruginosa containing an IPTG-inducible gene for the green fluorescent protein (gfp). The results show that amounts of gfp mRNA were greatest in the top zones of the biofilms, and that gfp mRNA levels correlated with the zone of active GFP-fluorescence. The method was then used to quantify transcripts from wild-type P. aeruginosa biofilms for a housekeeping gene, acpP; the 16S rRNA; and two genes regulated by quorum-sensing, phzA1 and aprA. The results demonstrated that the amount of acpP mRNA was greatest in the top 30 microm of the biofilm, with little or no mRNA for this gene at the base of the biofilms. In contrast, 16S rRNA amounts were relatively uniform throughout biofilm strata. Using this strategy, the RNA amounts of individual genes are determined, and therefore results are dependent on both gene expression and the half-life of transcripts. Therefore, the uniform amount of rRNA throughout the biofilms is likely due to the stability of the rRNA within ribosomes. Levels of aprA mRNA showed stratification, with the greatest amounts in the upper 30 microm zone of these biofilms. The results demonstrate that mRNA levels for individual genes are not uniformly distributed throughout biofilms, but may vary by orders of magnitude over small distances. The LCMM/qRT-PCR technique can be used to resolve and quantify this RNA variability at high spatial resolution.en_US
dc.titleLocalized gene expression in Pseudomonas aeruginosa biofilmsen_US
dc.typeArticleen_US
mus.citation.extentfirstpage4463en_US
mus.citation.extentlastpage4471en_US
mus.citation.issue14en_US
mus.citation.journaltitleApplied and Environmental Microbiologyen_US
mus.citation.volume74en_US
mus.identifier.categoryEngineering & Computer Scienceen_US
mus.identifier.doi10.1128/aem.00710-08en_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.departmentMicrobiology & Immunology.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.relation.researchgroupCenter for Biofilm Engineering.en_US
mus.data.thumbpage24en_US


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