Kilvington S, Beeching J
Public Health Laboratory, Royal United Hospital, Combe Park, Bath, England.
Appl Environ Microbiol. 1995 Oct;61(10):3764-7. doi: 10.1128/aem.61.10.3764-3767.1995.
A species-specific PCR for the identification of Naegleria fowleri was developed. In sensitivity studies, 10 trophozoites or cysts and 1 trophozoite or cyst could be detected after 35 and 45 cycles, respectively. In conjunction with a rapid DNA isolation method, this PCR was used to identify N. fowleri directly from primary cultures of environmental samples.
开发了一种用于鉴定福氏耐格里阿米巴的种特异性聚合酶链反应(PCR)。在敏感性研究中,分别经过35个和45个循环后,可检测到10个滋养体或包囊以及1个滋养体或包囊。结合快速DNA提取方法,该PCR被用于直接从环境样本的原代培养物中鉴定福氏耐格里阿米巴。