Project Title:
Evaluation of Real-Time Quantitative
Polymerase Chain Reaction (QPCR) to Estimate Escherichia coli
Concentrations at Lake Erie Beaches.
Project chief: Christopher Kephart
Project support: Rebecca Bushon
Cooperators:
Northeast Ohio Regional Sewer District (NEORSD), Cleveland, Ohio
Project duration:
2006-2008
Introduction and problem:
There is a distinct need for a method to rapidly determine
concentrations of fecal-indicator bacteria in recreational waters because
current methods require at least 18-24 hours from sample collection to
availability of results. Bacteria concentrations in the water can change
appreciably within hours, and therefore, recreational users may be at risk
of coming into contact with water that is not considered safe for
recreation. Alternatively, recreational use and revenue may be lost if the
beach is erroneously posted when the risk is low. One rapid method that has
gained some favor amongst researchers is using the real-time quantitative
polymerase chain reaction (qPCR) to quantify specific genetic targets within
fecal-indicator bacteria.
Goals and objectives:
The overall goal of the project is to determine if the qPCR rapid method for
E. coli quantification can be used at two Lake Erie beaches in Cleveland,
Ohio, Edgewater and Villa Angela, to improve the timeliness and accuracy of
beach advisories. The specific objectives of this study are to (1) field
test a protocol for applying the qPCR rapid method for E. coli to lake-water
samples, (2) compare results of the rapid method to the standard
membrane-filtration method, and (3) transfer the technology to a local
agency that routinely monitors for E. coli concentrations and provides a
beach warning system based on their results.
Approach:
During the recreational seasons (May–September) of 2006, 2007, and 2008, the
Northeast Ohio Regional Sewer District (NEORSD) conducted a routine
monitoring program for E. coli concentrations at Edgewater and Villa Angela
beaches. This study augments that monitoring program by analyzing a portion
of those samples by means of the qPCR rapid method. During each recreational
season, 12 consecutive weeks of sampling included analysis by qPCR; one
sample from each of the two beaches was analyzed three days per week.
Initial processing of water samples for qPCR was done by NEORSD and required
filtering 100 mL of water through a polycarbonate filter. The filters were
shipped overnight on ice to the USGS Ohio Water Microbiology Laboratory (OWML)
for subsequent DNA extraction and qPCR. During 2008, the qPCR technology was
transferred from the USGS to the NEORSD and a lab-to-lab comparison was done
on a portion of the samples collected. Training was done on-site at the
NEORSD and continued support was provided by the USGS throughout the
recreational season. Additionally in 2008, the method was optimized by
incorporating new DNA extraction kits and qPCR reagents.
Publications:
A USGS Open-File Report documenting the results of the 2006-2007 study will
be published in 2008. Depending on funding, either a second Open-File Report
or a peer-reviewed journal article will be published in 2009.