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MHC-DRB1/DQB1 Gene Polymorphismand Its Association with Resistance/Susceptibility toCystic Echinococcosis in Chinese Merino Sheep

机译:MHC-DRB1 / DQB1基因多态性与中国美利奴绵羊对囊性棘球chin病的抗药性/敏感性相关

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The aim of this study was to analyze the relationship between polymorphism of the MHC-DRB1/DQB1 gene and its resistance to Cystic Echinococcosis (C.E), as well as to screen out the molecular genetic marker of antiechinococcosis in Chinese Merino sheep. The MHCII-DRB1/DQB1 exon 2 was amplified by polymerase chain reaction (PCR) from DNA samples of healthy and hydatidosis sheep. PCR products were characterized by restriction fragment length polymorphism (RFLP) technique. Five restriction enzymes (Mval,Haelll, SacI, SacII, and Hinll) were employed to cut DRB1, while seven restriction enzymes (Mroxl, Seal, SacII, Neil, TaqI, Mval, and Haelll) were employed to cut DQBl.Results showed that frequencies of patterns Mvalbb (P < 0.01), Saclab in DRB1 exon 2(P < 0.05), and Taqlaa, Haelllnn (P < 0.01) in DQB1 exon 2 were significantly higher in the healthy group compared with the C.E individuals, which implied that there was a strong association between these genotypes and hydatidosis resistance or susceptibility. Chi-square test showed that individuals with the genie haplotype DRBl-SacIab/DRBl-Mvalbb/DQBl-Taqlaa/DQBl-Haelllnn (P < 0.01) were relatively resistant to C.E, while individuals with the genie haplotypes DRBl-Mvalbc/DQBl-Mvalyy/DQBl-Taqlab/DQBl-Haelllmn (P < 0.01) and DRBl-Mvalbb/DQBl-Mvalcc/DQBl-Taqlab/DQBl-Haelllmn (P < 0.01) were more susceptible to C.E. In addition, to confirm these results, a fielding experiment was performed with Chinese Merino sheep which were artificially infected with E.g. The result was in accordance with the results of the first study. In conclusion, MHC-DRB1/DQB1 exon 2 plays an important role as resistant to C.E in Chinese Merino sheep. In addition, the molecular genetic marker of antiechinococcosis (DRBl-SacIab/DRBl-Mvalbb/DQBl-Taqlaa/DQBl-Haelllnn) was screened out in Chinese Merino sheep.
机译:本研究的目的是分析MHC-DRB1 / DQB1基因多态性与其对囊性棘球co病(C.E)的抗性之间的关系,并筛选出中国美利奴绵羊抗棘球co病的分子遗传标记。 MHCII-DRB1 / DQB1外显子2是通过聚合酶链反应(PCR)从健康的羊茅和葡萄虫的DNA样本中扩增得到的。 PCR产物通过限制性片段长度多态性(RFLP)技术进行表征。使用5种限制酶(Mval,Haelll,SacI,SacII和Hinll)切割DRB1,同时使用7种限制酶(Mroxl,Seal,SacII,Neil,TaqI,Mval和Haelll)切割DQB1。与CE个体相比,健康组中DRB1外显子2的Mvalbb(P <0.01),Saclab模式频率(P <0.05),DQB1外显子2的Taqlaa,Haelllnn(P <0.01)频率显着高于CE个体,这表明这些基因型与抗hy虫病或易感性之间有很强的联系。卡方检验表明,具有单倍型DRB1-SacIab / DRB1-Mvalbb / DQB1-Taqlaa / DQB1-Haelllnn(P <0.01)的个体对CE具有相对抗性,而具有单倍型DRB1-Mvalbc / DQB1-Mvalyy的个体/ DQB1-Taqlab / DQB1-Haelllmn(P <0.01)和DRB1-Mvalbb / DQB1-Mvalcc / DQB1-Taqlab / DQB1-Haelllmn(P <0.01)对CE更敏感。此外,为了证实这些结果,我们进行了实地实验用中国人工感染的美利奴绵羊进行结果与第一项研究的结果一致。总之,MHC-DRB1 / DQB1外显子2在中国美利奴绵羊对C.E的抗性中起重要作用。另外,在中国美利奴绵羊中筛选出抗链球菌病的分子遗传标记(DRB1-SacIab / DRB1-Mvalbb / DQB1-Taqlaa / DQB1-Haelllnn)。

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