Bachoon Dave S, Miller Cortney M, Green Christen P, Otero Ernesto
Department of Biological and Environmental Sciences, Georgia College and State University, Campus Box 81, Milledgeville, GA 31061-0490, USA.
Int J Microbiol. 2010;2010. doi: 10.1155/2010/595692. Epub 2010 Aug 5.
We compared the effectiveness of three PCR protocols for the detection of Bifidobacterium adolescentis and one PCR protocol for detecting Bacteroidales as indicators of human fecal pollution in environmental samples. Quantitative PCR indicated that a higher concentration of B. adolescentis DNA was recovered from sewage samples on the 0.2 mum filters compared to the 0.45 mum filters, and there was no evidence of qPCR inhibitors in the DNA extracts. With the Matsuki method (1999), B. adolescentis was detected only in undiluted sewage samples. The King method (2007) performed well and detected B. adolescentis in all of the sewage dilutions (from undiluted to 10(-4)). In contrast, the Bonjoch approach (2004) was effective at detecting B. adolescentis at lower dilutions (10(-3)) of sewage samples and it gave false positive results with some (3/8) pig fecal samples. Human-specific Bacteroidales (HuBacs) were detected in the lower diluents of sewage samples but was positive in pig (6/8) and cattle fecal samples. PCR detection of B. adolescentis in marine samples from Puerto Rico and freshwater samples from Georgia indicated that the PCR method of King et al. (2007) and the modified Layton method for HuBac were in agreement in detecting human fecal pollution in most sites.
我们比较了三种用于检测青春双歧杆菌的聚合酶链式反应(PCR)方案以及一种用于检测拟杆菌目作为环境样品中人类粪便污染指标的PCR方案的有效性。定量PCR结果表明,与0.45微米滤膜相比,从0.2微米滤膜上的污水样品中回收的青春双歧杆菌DNA浓度更高,并且DNA提取物中没有定量PCR抑制剂的迹象。使用松木方法(1999年),仅在未稀释的污水样品中检测到青春双歧杆菌。金方法(2007年)效果良好,在所有污水稀释度(从未稀释到10^(-4))中都检测到了青春双歧杆菌。相比之下,博尼乔克方法(2004年)在检测污水样品较低稀释度(10^(-3))的青春双歧杆菌时有效,但对一些(3/8)猪粪便样品给出了假阳性结果。在污水样品的较低稀释液中检测到了人类特异性拟杆菌目(HuBacs),但在猪(6/8)和牛粪便样品中呈阳性。对来自波多黎各的海洋样品和来自佐治亚州的淡水样品中的青春双歧杆菌进行PCR检测表明,金等人(200,7年)的PCR方法和改良的莱顿HuBac方法在大多数地点检测人类粪便污染方面结果一致。