Gatei Wangeci, Das Pradeep, Dutta Phalguni, Sen Abhik, Cama Vitaliano, Lal Altaf A, Xiao Lihua
Division of Parasitic Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30341, USA.
Infect Genet Evol. 2007 Mar;7(2):197-205. doi: 10.1016/j.meegid.2006.08.006. Epub 2006 Sep 28.
Endemicity of cryptosporidiosis in India has been documented with little genetic characterization of the parasites. Fifty Cryptosporidium-positive specimens collected between 2001 and 2004 from pediatric patients in Kolkata, India were analyzed for parasite genetic structure using multilocus sequence typing (MLST). Genotype analyses showed the presence of Cryptosporidium hominis, Cryptosporidium meleagridis and Cryptosporidium felis in 49, 2 and 1 patients, respectively (two patients had mixed infections of C. hominis and C. meleagridis). To assess the extent of genetic heterogeneity of C. hominis, minisatellites, microsatellites and polymorphic markers in three different chromosomes were sequenced, including genes encoding the 60kDa glycoprotein (GP60), a 47kDa protein (CP47), a mucin-like protein (Mucin1), a serine repeat antigen (MSC6-7), and a 56kDa trans-membrane protein (CP56) in chromosome 6, the 70kDa heat shock protein (HSP70) in chromosome 2, and a T-rich gene fragment (Chrom3T) in chromosome 3. Population sub-structure of C. hominis based on multilocus gene sequences showed that there were 25 multilocus subtypes defined by combined sequence length and nucleotide polymorphism, which formed four distinct groups in this population. Significant intra- and inter-genic linkage disequilibria were observed with minimum recombination or expansion of limited subtypes, all indicative of a mostly clonal population structure. The results highlight the importance of high resolution MLST in studying Cryptosporidium population sub-structure especially when length polymorphism may be inadequate in identifying unique subtypes. The significance of the diverse MLST within C. hominis in relation to geographical and temporal factors and clinical manifestations of disease warrants further investigations.
印度隐孢子虫病的地方性流行已有记录,但对寄生虫的基因特征描述较少。对2001年至2004年间从印度加尔各答的儿科患者中收集的50份隐孢子虫阳性标本,使用多位点序列分型(MLST)分析寄生虫的基因结构。基因型分析显示,分别在49例、2例和1例患者中检测到人隐孢子虫、火鸡隐孢子虫和猫隐孢子虫(2例患者为人隐孢子虫和火鸡隐孢子虫混合感染)。为评估人隐孢子虫的基因异质性程度,对三个不同染色体上的微卫星、微卫星和多态性标记进行了测序,包括6号染色体上编码60kDa糖蛋白(GP60)、47kDa蛋白(CP47)、粘蛋白样蛋白(Mucin1)、丝氨酸重复抗原(MSC6-7)和56kDa跨膜蛋白(CP56)的基因,2号染色体上的70kDa热休克蛋白(HSP70),以及3号染色体上富含T的基因片段(Chrom3T)。基于多位点基因序列的人隐孢子虫群体亚结构显示,由序列长度和核苷酸多态性组合定义的25个多位点亚型,在该群体中形成了四个不同的组。观察到显著的基因内和基因间连锁不平衡,有限亚型的重组或扩展最小,所有这些都表明主要是克隆群体结构。结果突出了高分辨率MLST在研究隐孢子虫群体亚结构中的重要性,特别是当长度多态性可能不足以识别独特亚型时。人隐孢子虫内不同MLST与地理和时间因素以及疾病临床表现的关系的重要性值得进一步研究。