Visvesvara Govinda S
Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30341-3724, USA.
Clin Microbiol Rev. 2002 Jul;15(3):401-13. doi: 10.1128/CMR.15.3.401-413.2002.
Although attempts to develop methods for the in vitro cultivation of microsporidia began as early as 1937, the interest in the culture of these organisms was confined mostly to microsporidia that infect insects. The successful cultivation in 1969 of Encephalitozoon cuniculi, a microsporidium of mammalian origin, and the subsequent identification of these organisms as agents of human disease heightened interest in the cultivation of microsporidia. I describe the methodology as well as the cell lines, the culture media, and culture conditions used in the in vitro culture of microsporidia such as Brachiola (Nosema) algerae, Encephalitozoon cuniculi, E. hellem, E. intestinalis, Enterocytozoon bieneusi, Trachipleistophora hominis, and Vittaforma corneae that cause human disease.
尽管早在1937年就有人尝试开发微孢子虫的体外培养方法,但对这些生物体培养的兴趣大多局限于感染昆虫的微孢子虫。1969年成功培养了源自哺乳动物的微孢子虫兔脑炎微孢子虫,随后将这些生物体鉴定为人类疾病的病原体,这激发了人们对微孢子虫培养的兴趣。我描述了用于体外培养诸如引起人类疾病的阿尔及利亚短膜虫(蜜蜂微孢子虫)、兔脑炎微孢子虫、海伦脑炎微孢子虫、肠脑炎微孢子虫、比氏肠细胞微孢子虫、人气管微孢子虫和角膜变形虫等微孢子虫的方法,以及所使用的细胞系、培养基和培养条件。