Grothen David C, Zach Sydney J, Davis Paul H
Department of Biology, University of Nebraska at Omaha, Omaha NE 68182-0040.
J Genomics. 2017 Jan 17;5:4-11. doi: 10.7150/jgen.18378. eCollection 2017.
Water quality management is an ongoing struggle for many locations worldwide. Current testing of water supplies can be time-consuming, expensive, and lack sensitivity. This study describes an alternative, easy-to-use, and inexpensive method to water sampling and testing at remote locations. This method was employed to detect a number of intestinal pathogens in various locations of Lima, Peru. A total of 34 PCR primer pairs were tested for specificity and high-yield amplification for 12 different pathogens using known DNA templates. Select primers for each pathogen were then tested for minimum detection limits of DNA. Water samples were collected from 22 locations. PCR was used to detect the presence of a pathogen, virulence factors, or differentiate between pathogenic species. In 22 water samples, cholera toxin gene was detected in 4.5% of samples, DNA was detected in 50% of samples, DNA was detected in 54.5% of samples, DNA was detected in 4.5% of samples, spp. DNA was detected in 29% of samples, and DNA was detected in 31.8% of samples. DNA from three pathogens, , , and , were found in residential samples, which accounted for 10 out of 22 samples.
水质管理是全球许多地方一直面临的难题。目前对供水的检测可能既耗时、成本高又缺乏灵敏度。本研究描述了一种在偏远地区进行水样采集和检测的替代方法,该方法简便易用且成本低廉。此方法用于检测秘鲁利马不同地点的多种肠道病原体。使用已知DNA模板,对34对PCR引物进行了针对12种不同病原体的特异性和高产率扩增测试。然后针对每种病原体选择的引物进行DNA最低检测限测试。从22个地点采集了水样。采用PCR检测病原体的存在、毒力因子或区分致病菌种。在22份水样中,4.5%的样本检测到霍乱毒素基因,50%的样本检测到 DNA,54.5%的样本检测到 DNA,4.5%的样本检测到 DNA,29%的样本检测到 spp. DNA,31.8%的样本检测到 DNA。在22份住宅样本中的10份样本中发现了三种病原体 、 和 的DNA。