Mercado Ruben, Peña Sebastian, Ozaki Luiz Shozo, Fredes Fernando, Godoy Juan
Facultad de Medicina, Universidad de Chile, Santiago, Chile,
Parasitol Res. 2015 May;114(5):1985-8. doi: 10.1007/s00436-015-4364-8. Epub 2015 Feb 13.
To further understand the composition of population of parasite in a single host, we analyzed the GP60 gene of Cryptosporidium parvum amplified from DNA of a randomly selected isolate found in the feces of a diarrheic calf from a dairy farm in Central Chile. Direct sequencing of the amplicon yield the IIaA17G4R1 C. parvum subtype. The same amplicon was cloned in Escherichia coli (22 clones) and sequenced, yielding three different GP60 subtypes, IIaA17G4R1 (16/22), IIaA16G4R1 (1/22), and IIaA15G4R1 (1/22), and four sequences with nucleotide substitutions in the serine repeats, which subtype would be otherwise IIaA17G4R1. It is thus possible to determine allelic polymorphism using Sanger sequencing with an additional step of bacterial cloning. The results also indicate the necessity to further characterize parasite populations in a single host to better understand the dynamics of Cryptosporidium epidemiology.
为了进一步了解单个宿主体内寄生虫种群的组成,我们分析了从智利中部一家奶牛场腹泻小牛粪便中随机选取的分离株DNA中扩增出的微小隐孢子虫的GP60基因。对扩增子进行直接测序得到了微小隐孢子虫IIaA17G4R1亚型。将相同的扩增子克隆到大肠杆菌中(22个克隆)并测序,得到三种不同的GP60亚型,即IIaA17G4R1(16/22)、IIaA16G4R1(1/22)和IIaA15G4R1(1/22),以及四个在丝氨酸重复序列中有核苷酸替换的序列,否则这些序列将属于IIaA17G4R1亚型。因此,通过桑格测序并增加细菌克隆这一步骤,可以确定等位基因多态性。结果还表明,有必要进一步对单个宿主体内的寄生虫种群进行特征分析,以更好地了解隐孢子虫流行病学的动态变化。