King Eric L, Bachoon Dave S, Gates Keith W
Department of Biological and Environmental Sciences, Georgia College and State University, Campus Box 81, Milledgeville, GA 31061-0490, USA.
J Microbiol Methods. 2007 Jan;68(1):76-81. doi: 10.1016/j.mimet.2006.06.008. Epub 2006 Jul 28.
Detection of Bifidobacterium adolescentis was used as an effective genetic marker of human fecal contamination in Georgia estuaries. Enterococci enumerations on mEI media indicated that a tributary to the Little Satilla River with 516 CFU/100 ml was the most polluted of all the rivers tested. Extracted DNA from eight river water samples was subjected to a two-step nested PCR protocol using genus and species specific primers for Bifidobacterium spp. and B. adolescentis. B. adolescentis was detected from extracted DNA in Dunbar River, Black Bank Creek, and in a Little Satilla River tributary which demonstrates the presence of human fecal contamination in these three rivers. In the five other estuaries tested including West Point-Federica River and the Altamaha River, which both had less than 16 CFU/100 ml of enterococci, B. adolescentis was not detected.
青春双歧杆菌的检测被用作佐治亚河口人类粪便污染的有效遗传标记。在mEI培养基上对肠球菌进行计数表明,小萨蒂拉河的一条支流每100毫升中有516个菌落形成单位(CFU),是所有测试河流中污染最严重的。从八个河水样本中提取的DNA使用双歧杆菌属和青春双歧杆菌的属特异性和种特异性引物,进行两步巢式聚合酶链反应(PCR)实验。在邓巴河、黑岸溪以及小萨蒂拉河的一条支流的提取DNA中检测到了青春双歧杆菌,这表明这三条河流中存在人类粪便污染。在其他五个测试河口,包括西点-费代里卡河和阿尔塔马哈河,这两条河的肠球菌含量均低于每100毫升16个CFU,未检测到青春双歧杆菌。