Dumètre Aurélien, Dardé Marie Laure
UPRES EA 3174, Neuroparasitologie et Neuroépidémiologie Tropicale, Faculté de Médecine, 2 Rue du Dr Marcland, F-87025 Limoges, France.
FEMS Microbiol Rev. 2003 Dec;27(5):651-61. doi: 10.1016/S0168-6445(03)00071-8.
Detection of Toxoplasma gondii oocysts in environmental samples is a great challenge for researchers as this coccidian parasite can be responsible for severe infections in humans and in animals via ingestion of a single oocyst from contaminated water, soil, fruits or vegetables. Despite field investigations, oocysts have been rarely recovered from the environment due to the lack of sensitive methods. Immunomagnetic separation, fluorescence-activated cell sorting, and polymerase chain reaction have recently shown promising use in detection of protozoa from complex matrices. Such procedures could be applied to T. gondii detection, if studies on the antigenic and biochemical composition of the oocyst wall are completed. Using such methods, it will be possible to assess the occurrence, prevalence, viability and virulence of T. gondii oocysts in environmental matrices and specify sources of human and animal contamination.
在环境样本中检测刚地弓形虫卵囊对研究人员来说是一项巨大挑战,因为这种球虫寄生虫可通过摄入来自受污染水、土壤、水果或蔬菜中的单个卵囊,导致人类和动物发生严重感染。尽管进行了实地调查,但由于缺乏灵敏的方法,卵囊很少能从环境中被检出。免疫磁珠分离、荧光激活细胞分选和聚合酶链反应最近在从复杂基质中检测原生动物方面显示出有前景的应用。如果完成关于卵囊壁抗原和生化组成的研究,这些方法可应用于刚地弓形虫的检测。使用这些方法,将有可能评估刚地弓形虫卵囊在环境基质中的存在情况、流行程度、活力和毒力,并确定人类和动物污染的来源。