Multilocus sequence typing and genetic structure of Cryptosporidium hominis from children in Kolkata, India

被引:103
作者
Gatei, Wangeci
Das, Pradeep
Dutta, Phalguni
Sen, Abhik
Cama, Vitaliano
Lal, Altaf A.
Xiao, Lihua [1 ]
机构
[1] Ctr Dis Control & Prevent, Div Parasit Dis, Atlanta, GA 30341 USA
[2] Atlanta Res & Educ Fdn, Atlanta, GA 30341 USA
[3] Natl Inst Cholera & Enter Dis, Kolkata, W Bengal, India
[4] US Embassy, New Delhi, India
关键词
Cryptosporidium; population genetics; population structure; linkage disequilibrium; gene diversity; multilocus sequence typing;
D O I
10.1016/j.meegid.2006.08.006
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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 I 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 60 kDa glycoprotein (GP60), a 47 kDa protein (CP47), a mucin-like protein (Mucinl), a serine repeat antigen (MSC6-7), and a 56 kDa trans-membrane protein (CP56) in chromosome 6, the 70 kDa 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 Cyptosporidium 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. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:197 / 205
页数:9
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