Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Shawn Siefring"'
Publikováno v:
Journal of Microbiological Methods. 152:135-142
An obstacle to establishing widely useful data acceptance criteria for U.S. Environmental Protection Agency (EPA) qPCR methods has been the unavailability of standardized reference materials. Earlier versions of EPA Methods 1609 and 1611 for enteroco
Autor:
Richard R. Rediske, Mano Sivaganesan, Tiong Gim Aw, Susan Rosenberg, Tami Sivy, Barbara Weberman, Shawn Siefring, Erin A. Dreelin, Julie L. Kinzelman, Kevin Oshima, Abhilasha Shrestha, Richard A. Haugland, Greg Kleinheinz, Samuel Dorevitch, Natasha M. Isaacs, Brian Scull, Asli Aslan, Ben Southwell, Shannon Briggs, Rachel T. Noble
Publikováno v:
Water Res
There is interest in the application of rapid quantitative polymerase chain reaction (qPCR) methods for recreational freshwater quality monitoring of the fecal indicator bacteria Escherichia coli (E. coli). In this study we determined the performance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d78b93880189ad62bded88d933e0bb02
https://europepmc.org/articles/PMC9994418/
https://europepmc.org/articles/PMC9994418/
Autor:
Asli Aslan, Ben Southwell, Shawn Siefring, Erin A. Dreelin, Tami Sivy, Richard A. Haugland, Julie L. Kinzelman, Abhilasha Shrestha, Natasha M. Isaacs, Rachel T. Noble, Brian Scull, Tiong Gim Aw, Richard R. Rediske, Shannon Briggs, Barbara Weberman, Samuel Dorevitch, Greg Kleinheinz, Kevin Oshima, Susan Rosenberg, Mano Sivaganesan
Publikováno v:
Water Res
There is growing interest in the application of rapid quantitative polymerase chain reaction (qPCR) and other PCR-based methods for recreational water quality monitoring and management programs. This interest has strengthened given the publication of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad16a9990b4ad27fa0c7f73a7ed26415
Autor:
Brian Schnitker, Manju Varma, Shawn Siefring, Richard A. Haugland, Alfred P. Dufour, Sharon P. Nappier, Mano Sivaganesan, Kevin Oshima, Shannon Briggs
Publikováno v:
J Microbiol Methods
Fecal pollution remains a challenge for water quality managers at Great Lakes and inland recreational beaches. The fecal indicator of choice at these beaches is typically Escherichia coli (E. coli), determined by culture-based methods that require ov
Autor:
Kevin Oshima, Stephen B. Weisberg, Mano Sivaganesan, Julie L. Kinzelman, A. Denene Blackwood, Tamara Anan’eva, Katrina V. Gordon, Erin A. Stelzer, V.J. Harwood, John F. Griffith, Yiping Cao, Shawn Siefring, Richard A. Haugland, Christopher D. Sinigalliano, Meredith R. Raith, Rachel T. Noble, Rebecca N. Bushon, Manju Varma
Publikováno v:
Journal of Microbiological Methods. 123:114-125
Quantitative polymerase chain reaction (qPCR) has become a frequently used technique for quantifying enterococci in recreational surface waters, but there are several methodological options. Here we evaluated how three method permutations, type of ma
Publikováno v:
Journal of Microbiological Methods. 87:343-349
DNA extracts from enumerated target organism cells (calibrator samples) have been used for estimating Enterococcus cell equivalent densities in surface waters by a comparative cycle threshold (Ct) qPCR analysis method. To compare surface water Entero
Publikováno v:
Letters in Applied Microbiology. 52:298-306
Aims: Compare specificity and sensitivity of quantitative PCR (qPCR) assays targeting single and multi-copy gene regions of Escherichia coli. Methods and Results: A previously reported assay targeting the uidA gene (uidA405) was used as the basis for
Publikováno v:
Water Research. 39:559-568
Cell densities of the fecal pollution indicator genus, Enterococcus, were determined by a rapid (3 h or less) quantitative polymerase chain reaction (QPCR) analysis method in 100 ml water samples collected from recreational beaches on Lake Michigan a
Publikováno v:
Biotechnology Letters. 25:261-265
A 16S rDNA real-time PCR method was developed to detect Enterococcus faecalis in water samples. The dynamic range for cell detection spanned five logs and the detection limit was determined to be 6 cfu/reaction. The assay was capable of detecting E.
Publikováno v:
Journal of microbiological methods. 112
A method, incorporating recently improved reverse transcriptase-PCR primer/probe assays and including controls for detecting interferences in RNA recovery and analysis, was developed for the direct, culture-independent detection of genetic markers fr