Department of Veterinary Science, The University of Melbourne, Werribee, Victoria 3030, Australia.
Biotechnol Adv. 2010 Jan-Feb;28(1):17-26. doi: 10.1016/j.biotechadv.2009.08.003.
Cryptosporidium species (apicomplexan protists) are a major cause of diarrhoeal disease (= cryptosporidiosis) in humans worldwide. The impact of cryptosporidiosis is also compounded by the spread of HIV/AIDS and a lack of cost-effective anti-cryptosporidial chemotherapeutics or vaccines. Mitigation of the impact of cryptosporidiosis in humans needs to focus on prevention and control strategies, built on a sound understanding of the epidemiology of Cryptosporidium species. Refined epidemiological studies rely on the use of molecular tools employing informative genetic markers. Currently, the 60-kDa glycoprotein gene (gp60) is the most suitable and widely used genetic marker for Cryptosporidium species infecting humans. Here, we undertake an analysis of all publicly-available gp60 sequence data and associated literature for C. hominis and C. parvum, and yield useful insights into the richness, diversity and distribution of genetic variants, and link these variants to human cryptosporidiosis. This global analysis reveals that, despite high genetic richness in Cryptosporidium isolates from humans, there is a surprisingly low diversity. It also highlights limited knowledge about the genetics of cryptosporidiosis in developing nations and in many animals that might act as infection sources. Clearly, there is a major need for more comprehensive studies of Cryptosporidium infecting humans and other animals in Africa and Asia. As molecular technologies improve and become affordable, future studies should utilize "next generation" sequencing and bioinformatic platforms to conduct comparative 'genome sequence surveys' to test the validity of current genetic classifications based on gp60 data. Complemented by in vitro and in vivo investigations, these biotechnological advances will also assist significantly in the search for new intervention strategies against human cryptosporidiosis.
隐孢子虫物种(顶复门原生动物)是全球范围内人类腹泻病(即隐孢子虫病)的主要病因。由于 HIV/AIDS 的传播以及缺乏经济有效的抗隐孢子虫化学疗法或疫苗,隐孢子虫病的影响更加严重。减轻人类隐孢子虫病的影响需要侧重于预防和控制策略,建立在对隐孢子虫物种流行病学的充分理解之上。经过改进的流行病学研究依赖于使用具有信息性遗传标记的分子工具。目前,60kDa 糖蛋白基因(gp60)是最适合且广泛用于感染人类的隐孢子虫物种的遗传标记。在这里,我们对所有公开可用的 gp60 序列数据和相关文献进行了分析,以了解人源隐孢子虫和小隐孢子虫的遗传变异体的丰富度、多样性和分布,并将这些变异体与人类隐孢子虫病联系起来。这项全球性分析表明,尽管人类隐孢子虫分离株的遗传丰富度很高,但多样性却出奇地低。它还突出了发展中国家以及许多可能作为感染源的动物中对隐孢子虫病遗传学的了解有限。显然,迫切需要对非洲和亚洲的人类和其他动物感染的隐孢子虫进行更全面的研究。随着分子技术的提高和普及,未来的研究应该利用“下一代”测序和生物信息学平台进行比较“基因组序列调查”,以检验基于 gp60 数据的当前遗传分类的有效性。与体外和体内研究相辅相成,这些生物技术的进步也将极大地有助于寻找针对人类隐孢子虫病的新干预策略。