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

机译:密西西比河上游生物指标和阳光对粪便指示细菌和微生物源追踪遗传标记的持久性的影响

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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 (r2, 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.
机译:可能会受到污水影响的休闲水的卫生质量通过列举粪便指示细菌(FIB)(大肠杆菌和肠球菌)进行评估;这些生物存在于人类和许多其他动物的胃肠道中,因此它们的存在无法提供有关污染源的信息。微生物源跟踪(MST)方法可以区分不同的污染源,向水质管理者提供关键信息,但是对释放到水生环境后影响FIB和MST遗传标记衰减的因素知之甚少。在密西西比河的温带休闲海滩上部署了原位介观膜,以评估环境阳光和生物相互作用(捕食,竞争和病毒裂解)对基于文化的FIB和基于分子的FIB衰减的影响( Entero1a和GenBac3)以及与人类相关的MST遗传标记(HF183和HumM2),通过实时定量PCR(qPCR)进行测量。通常,可培养的FIB衰减最快,而基于分子的FIB和与人类相关的遗传标记衰减更慢。分子基FIB的衰变与人类相关遗传标记的衰变之间有很强的相关性(r 2 ,0.96至0.98; P <0.0001),而可培养的FIB与任何qPCR测量值之间没有相关性。总体而言,暴露于环境阳光下可能是早期衰减动力学的重要因素,但通常在持续暴露后(即120小时后)并不是如此,因为生物相互作用往往是持久性的唯一/主要影响因素。

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