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Development of Goose- and Duck-Specific DNA Markers To Determine Sources of Escherichia coli in Waterways

机译:鹅和鸭特异性DNA标记的开发以确定水道中大肠杆菌的来源

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摘要

The contamination of waterways with fecal material is a persistent threat to public health. Identification of the sources of fecal contamination is a vital component for abatement strategies and for determination of total maximum daily loads. While phenotypic and genotypic techniques have been used to determine potential sources of fecal bacteria in surface waters, most methods require construction of large known-source libraries, and they often fail to adequately differentiate among environmental isolates originating from different animal sources. In this study, we used pooled genomic tester and driver DNAs in suppression subtractive hybridizations to enrich for host source-specific DNA markers for Escherichia coli originating from locally isolated geese. Seven markers were identified. When used as probes in colony hybridization studies, the combined marker DNAs identified 76% of the goose isolates tested and cross-hybridized, on average, with 5% of the human E. coli strains and with less than 10% of the strains obtained from other animal hosts. In addition, the combined probes identified 73% of the duck isolates examined, suggesting that they may be useful for determining the contribution of waterfowl to fecal contamination. However, the hybridization probes reacted mainly with E. coli isolates obtained from geese in the upper midwestern United States, indicating that there is regional specificity of the markers identified. Coupled with high-throughput, automated macro- and microarray screening, these markers may provide a quantitative, cost-effective, and accurate library-independent method for determining the sources of genetically diverse E. coli strains for use in source-tracking studies. However, future efforts to generate DNA markers specific for E. coli must include isolates obtained from geographically diverse animal hosts.
机译:粪便对水道的污染是对公共卫生的持续威胁。粪便污染源的识别对于减少策略和确定每日总最大负荷至关重要。尽管表型和基因型技术已被用来确定地表水中粪便细菌的潜在来源,但大多数方法都需要构建大型的已知来源的库,并且它们通常无法充分区分源自不同动物来源的环境分离株。在这项研究中,我们在抑制消减杂交中使用了合并的基因组测试仪和驱动程序DNA,以丰富源自本地分离鹅的大肠杆菌的宿主来源特异性DNA标记。确定了七个标记。当在菌落杂交研究中用作探针时,结合的标记DNA鉴定出平均76%的鹅分离物经过测试和交叉杂交,它们与5%的人类大肠杆菌菌株和不到10%的从其他动物宿主。此外,组合探针鉴定出73%的鸭鸭分离株,表明它们可能对确定水禽对粪便污染的贡献有用。然而,杂交探针主要与从美国中西部上部的鹅获得的大肠杆菌分离物反应,表明所鉴定的标记物具有区域特异性。结合高通量,自动化的宏和微阵列筛选,这些标记物可以提供定量,经济高效且准确的独立于文库的方法,用于确定遗传多样性大肠杆菌菌株的来源,以用于来源追踪研究。但是,未来产生大肠杆菌特异DNA标记的努力必须包括从地理上不同的动物宿主获得的分离株。

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