伊朗无乳支原体p40基因表达的比较研究

F. Yavari, S. A. Pourbakhsh, H. Goudarzi, R. Khavarinejad
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摘要

无乳支原体病原体是导致小反刍动物无乳的主要原因,因此在伊朗造成了一些经济损失。传染性无乳病是一种由多种支原体感染多个脏器引起的综合征。本研究从伊朗11个省的绵羊和山羊的乳腺、关节和眼睛中分离到30份疑似标本,采用PCR技术对2个基因进行属和种检测。这些支原体菌株和三个伊朗无乳支原体疫苗株被提交进行表面脂蛋白p40蛋白的序列分析。对伊朗株与无乳支原体PG2西班牙株的同源性进行比较,伊朗株的同源性大部分为97%,部分为80 ~ 88%,3株疫苗株的同源性为99%。根据PCR和生物信息学分析结果,伊朗6个省被确认为该效应蛋白表达不同的感染区,这表明发现特定效应蛋白的个体特征可能需要对疫苗接种进行经验检测。最后将选定的p40基因序列克隆到pgemb1克隆载体上,在T7启动子控制下,通过pET-22b+表达质粒在大肠杆菌中表达。该融合蛋白的表达被SDS-PAGE吸收并证实。重组P40蛋白在SDS-PAGE上的分子量为37 kDa。无乳支原体感染家兔血清产生多克隆抗体,进行免疫印迹。兔经心脏穿刺强化免疫后10 d出血。值得注意的是,使用重组特异性抗原代替其他工具进行疾病诊断可以改善调查地区阳性和阴性动物的区分和分离,因此可用于控制感染动物并减少经济损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Study of p40 Gene Expression of Mycoplasma Agalactiae Isolated from Iranian Provinces
Mycoplasma agalactiae pathogen is the main cause of agalactia in small ruminants and as such, results in some economic losses in Iran. Contagious agalactia disease should be regarded as a syndrome, caused by various Mycoplasmas which infect several organs. In the present study, 30 suspected samples from 11 provinces of Iran were isolated from mammary gland, joint and eyes of sheep and goats and subjected to genus and species detection via PCR technique for 2 genes. These Mycoplasma strains and three Iranian vaccinal strains of Mycoplasma agalactiae were submitted to sequence analysis of a surface lipoprotein called p40 protein. Based on a comparative study between Iranian strains and PG2 Spanish strain of Mycoplasma agalactiae, most Iranian strains presented 97% homology, whereas some strains showed 80-88% and three vaccinal strains were associated with 99% homology. According to PCR and bioinformatics analysis outcomes, 6 provinces of Iran were recognized as infection areas with different expressions of this effecter protein, suggesting that finding the individual characteristics of a particular effecter may require empirical testing for vaccination. Finally, the selected sequence of p40 gene was cloned into pGEMB1cloning vector and subsequently expressed in Escherichia coli by pET-22b+ expression plasmid under the control of the T7 promoter. The expression of this fusion protein was absorbed and confirmed by SDS-PAGE. The recombinant P40 protein was expressed with a molecular mass of 37 kDa on SDS-PAGE. The sera taken from rabbits infected with Mycoplasma agalactiae produced polyclonal antibody which was then used for westernblotting. The rabbits were bled 10 days after the booster immunization using cardiac puncture. Significantly, the use of recombinant specific antigens instead of other tools for diagnosis of a disease could improve the discrimination and separation of positive and negative animals in the area under investigation and therefore, it can be applied to control infected animals and reduce economic losses.
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