Wu Zhiliang, Nagano Isao, Boonmars Thidarut, Nakada Takumi, Takahashi Yuzo
Department of Parasitology, Gifu University School of Medicine, Tsukasa 40, Gifu 500-8705, Japan.
Appl Environ Microbiol. 2003 Aug;69(8):4720-6. doi: 10.1128/AEM.69.8.4720-4726.2003.
A glycoprotein (Cpgp40/15)-encoding gene of Cryptosporidium parvum was analyzed to reveal intraspecies polymorphism within C. parvum isolates. Forty-one isolates were collected from different geographical origins (Japan, Italy, and Nepal) and hosts (humans, calves, and a goat). These isolates were characterized by means of DNA sequencing, PCR-restriction fragment length polymorphism (PCR-RFLP), and RFLP-single-strand conformational polymorphism (RFLP-SSCP) analyses of the gene for Cpgp40/15. The sequence analysis indicated that there was DNA polymorphism between genotype I and II, as well as within genotype I, isolates. The DNA and amino acid sequence identities between genotypes I and II differed, depending on the isolates, ranging from 73.3 to 82.9% and 62.4 to 80.1%, respectively. Those among genotype I isolates differed, depending on the isolates, ranging from 69.0 to 85.4% and 54.8 to 79.2%, respectively. Because of the high resolution generated by PCR-RFLP and RFLP-SSCP, the isolates of genotype I could be subtyped as genotypes Ia1, Ia2, Ib, and Ie. The isolates of genotype II could be subtyped as genotypes IIa, IIb, and IIc. The isolates from calves, a goat, and one Japanese human were identified as genotype II. Within genotype II, the isolates from Japan were identified as genotype IIa, those from calves in Italy were identified as genotype IIb, and the goat isolate was identified as genotype IIc. All of the genotype I isolates were from humans. The Japanese isolate (code no. HJ3) and all of the Nepalese isolates were identified as genotypes Ia1 and Ia2, respectively. The Italian isolates were identified as genotype Ib, and the Japanese isolate (code no. HJ2) was identified as genotype Ie. Thus, the PCR-RFLP-SSCP analysis of this glycoprotein Cpgp40/15 gene generated a high resolution that has not been achieved by previous methods of genotypic differentiation of C. parvum.
对微小隐孢子虫的一种糖蛋白(Cpgp40/15)编码基因进行分析,以揭示微小隐孢子虫分离株的种内多态性。从不同地理来源(日本、意大利和尼泊尔)和宿主(人类、小牛和一只山羊)收集了41株分离株。通过对Cpgp40/15基因进行DNA测序、PCR-限制性片段长度多态性(PCR-RFLP)和RFLP-单链构象多态性(RFLP-SSCP)分析来对这些分离株进行特征鉴定。序列分析表明,基因型I和II之间以及基因型I的分离株内部存在DNA多态性。基因型I和II之间的DNA和氨基酸序列同一性因分离株而异,分别为73.3%至82.9%和62.4%至80.1%。基因型I分离株之间的同一性也因分离株而异,分别为69.0%至85.4%和54.8%至79.2%。由于PCR-RFLP和RFLP-SSCP产生的高分辨率,基因型I的分离株可进一步细分为基因型Ia1、Ia2、Ib和Ie。基因型II的分离株可细分为基因型IIa、IIb和IIc。从小牛、一只山羊和一名日本人体内分离得到的菌株被鉴定为基因型II。在基因型II中,来自日本的分离株被鉴定为基因型IIa,来自意大利小牛的分离株被鉴定为基因型IIb,山羊分离株被鉴定为基因型IIc。所有基因型I的分离株均来自人类。日本分离株(编号HJ3)和所有尼泊尔分离株分别被鉴定为基因型Ia1和Ia2。意大利分离株被鉴定为基因型Ib,日本分离株(编号HJ2)被鉴定为基因型Ie。因此,对这种糖蛋白Cpgp40/15基因进行的PCR-RFLP-SSCP分析产生了高分辨率,这是以前微小隐孢子虫基因型分化方法所未达到的。