Biotic Interactions and Sunlight Affect Persistence of Fecal Indicator Bacteria and Microbial Source Tracking Genetic Markers in the Upper Mississippi River

被引:60
作者
Korajkic, Asja [1 ]
McMinn, Brian R. [1 ]
Shanks, Orin C. [2 ]
Sivaganesan, Mano [2 ]
Fout, G. Shay [1 ]
Ashbolt, Nicholas J. [1 ]
机构
[1] US EPA, Natl Exposure Res Lab, Off Res & Dev, Cincinnati, OH 45268 USA
[2] US EPA, Natl Risk Management Res Lab, Off Res & Dev, Cincinnati, OH 45268 USA
关键词
16S RIBOSOMAL-RNA; REAL-TIME PCR; RAPIDLY MEASURED INDICATORS; RECREATIONAL WATER-QUALITY; COMBINED SEWER OVERFLOWS; FRESH-WATER; ESCHERICHIA-COLI; QUANTITATIVE PCR; DIFFERENTIAL DECAY; SURFACE-WATER;
D O I
10.1128/AEM.00388-14
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The sanitary quality of recreational waters that may be impacted by sewage is assessed by enumerating fecal indicator bacteria (FIB) (Escherichia coli and enterococci); these organisms are found in the gastrointestinal tracts of humans and many other animals, and hence their presence provides no information about the pollution source. Microbial source tracking (MST) methods can discriminate between different pollution sources, providing critical information to water quality managers, but relatively little is known about factors influencing the decay of FIB and MST genetic markers following release into aquatic environments. An in situ mesocosm was deployed at a temperate recreational beach in the Mississippi River to evaluate the effects of ambient sunlight and biotic interactions (predation, competition, and viral lysis) on the decay of culture-based FIB, as well as molecularly based FIB (Entero1a and GenBac3) and human-associated MST genetic markers (HF183 and HumM2) measured by quantitative real-time PCR (qPCR). In general, culturable FIB decayed the fastest, while molecularly based FIB and human-associated genetic markers decayed more slowly. There was a strong correlation between the decay of molecularly based FIB and that of human-associated genetic markers (r(2), 0.96 to 0.98; P< 0.0001) but not between culturable FIB and any qPCR measurement. Overall, exposure to ambient sunlight may be an important factor in the early-stage decay dynamics but generally was not after continued exposure (i. e., after 120 h), when biotic interactions tended to be the only/major influential determinant of persistence.
引用
收藏
页码:3952 / 3961
页数:10
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