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1.
Water Res ; 47(3): 996-1004, 2013 Mar 01.
Article in English | MEDLINE | ID: mdl-23260177

ABSTRACT

Human and ecosystem health can be damaged by fecal contamination of recreational waters. Microbial source tracking (MST) can be used to specifically detect domestic sewage containing human waste, thereby informing both risk assessment and remediation strategies. Previously, an inter-laboratory collaboration developed standardized PCR methods for a bacterial, an archaeal, and a viral indicator of human sewage. Here we present results for two subsequent years of field testing in fresh and salt water by five laboratories across the U.S. Gulf Coast (two in Florida and one each in Mississippi, Louisiana and Texas) using common standard operating procedures (SOPs) developed previously. Culturable enterococci were enumerated by membrane filtration, and PCR was used to detect three MST markers targeting domestic sewage: human-associated Bacteroides (HF183), Methanobrevibacter smithii and human polyomaviruses BK and JC (HPyVs). Detection of sewage markers in surface waters was significantly associated with higher enterococci levels and with exceedance of the recreational water quality standard in four or three regions, respectively. Sewage markers were frequently co-detected in single samples, e.g., M. smithii and HF183 were co-detected in 81% of Louisiana samples, and HPyVs and M. smithii were co-detected in over 40% of southwest Florida and Mississippi samples. This study demonstrates the robustness and inter-laboratory transferability of these three markers for the detection of pollution from domestic sewage in the waters impacting the Gulf of Mexico over a coastal range of over 1000 miles.


Subject(s)
Enterococcus/genetics , Feces/microbiology , Environmental Monitoring , Gulf of Mexico , Humans , Polymerase Chain Reaction , Water Microbiology
2.
Appl Environ Microbiol ; 76(12): 4116-7, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20435774

ABSTRACT

Hollow-fiber ultrafiltration (HFUF) and PCR were combined to detect human-associated microbial source tracking marker genes in large volumes of fresh and estuarine Florida water. HFUF allowed marker detection when membrane filtration did not, demonstrating HFUF's ability to facilitate detection of diluted targets by PCR in a variety of water types.


Subject(s)
Bacteriological Techniques/methods , DNA, Bacterial/isolation & purification , Polymerase Chain Reaction/methods , Ultrafiltration/methods , Water Microbiology , DNA, Bacterial/genetics , Florida , Genetic Markers , Humans
3.
Water Res ; 43(19): 4812-9, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19595426

ABSTRACT

Water quality is frequently impacted by microbial pollution from human and animal feces. Microbial source tracking (MST) can identify dominant pollution sources and improve assessment of health risk compared to indicator bacteria alone. This study aims to standardize and validate MST methods across laboratories in coastal Gulf of Mexico states. Three laboratories evaluated library-independent MST methods for human sewage detection via conventional PCR: (1) human-associated Bacteroidales, (2) human polyomaviruses (HPyVs), and (3) Methanobrevibacter smithii. All methods detected targets in human sewage seeded into buffer, freshwater or marine water (100% sensitivity). The limit of detection (LOD) for human sewage was lowest for the Bacteroidales assay (10(-5)-10(-6) dilution). LODs for HPyVs and M. smithii assays were similar to each other (10(-3)-10(-4)), but were higher than Bacteroidales. The HPyVs assay was 100% specific, showing no cross-reactivity to dog, cow, cat, bird, or wild animal feces among >300 samples from three Gulf Coast regions. The human Bacteroidales assay was 96% specific, but cross-reacted with 10% of dog and some chicken samples. The M. smithii assay was 98% specific with limited cross-reactivity with cow, dog and seagull samples. An experts' workshop concluded that all methods showed sufficient accuracy and reliability to move forward. SOPs will be distributed to collaborating laboratories for further inter-laboratory comparison, and field validation will occur in year 2.


Subject(s)
Environmental Monitoring/methods , Feces/microbiology , Seawater/microbiology , Water Pollutants/isolation & purification , Atlantic Ocean , Bacteroidetes/genetics , Bacteroidetes/isolation & purification , DNA, Bacterial/genetics , Enterococcus faecalis/genetics , Enterococcus faecalis/isolation & purification , Environmental Monitoring/standards , Escherichia coli/genetics , Escherichia coli/isolation & purification , Methanobrevibacter/genetics , Methanobrevibacter/isolation & purification , Polymerase Chain Reaction , Sewage/microbiology
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