Réveiller Fabienne L, Cabanes Pierre-André, Marciano-Cabral Francine
Department of Microbiology and Immunology, Medical College of Virginia, Richmond 23298-0678, USA.
Parasitol Res. 2002 May;88(5):443-50. doi: 10.1007/s00436-002-0591-x.
Naegleria fowleri is the causative agent of primary amoebic meningoencephalitis, a fatal disease of the central nervous system that is acquired while swimming or diving in freshwater. A cDNA clone designated Mp2C15 obtained from N. fowleri was used as a probe to distinguish N. fowleri from other free-living amoebae. The Mp2C15 probe hybridized to genomic DNA from pathogenic N. fowleri and antigenically related non-pathogenic N. lovaniensis. Mp2C15 was digested with the restriction enzyme XbaI, resulting in two fragments, Mp2C15.G and Mp2C15.P. Four species of Naegleria and four species of Acanthamoeba were examined for reactivity with Mp2C15.P. Mp2C15.P was specific for N. fowleri and was used in the development of a nested PCR assay which is capable of detecting as little as 5 pg of N. fowleri DNA or five intact N. fowleri amoebae. In summary, a rapid, sensitive, and specific assay for the detection of N. fowleri was developed.
福氏耐格里阿米巴是原发性阿米巴脑膜脑炎的病原体,这是一种在淡水游泳或潜水时感染的致命性中枢神经系统疾病。从福氏耐格里阿米巴中获得的一个名为Mp2C15的cDNA克隆被用作探针,以区分福氏耐格里阿米巴与其他自由生活的阿米巴。Mp2C15探针与致病性福氏耐格里阿米巴和抗原相关的非致病性洛万尼耐格里阿米巴的基因组DNA杂交。用限制性内切酶XbaI消化Mp2C15,产生两个片段,Mp2C15.G和Mp2C15.P。检测了四种耐格里阿米巴和四种棘阿米巴与Mp2C15.P的反应性。Mp2C15.P对福氏耐格里阿米巴具有特异性,并用于开发一种巢式PCR检测方法,该方法能够检测低至5 pg的福氏耐格里阿米巴DNA或五个完整的福氏耐格里阿米巴变形虫。总之,开发了一种用于检测福氏耐格里阿米巴的快速、灵敏和特异的检测方法。