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作 者:王娜[1] 朱广艺 艾克拜尔.热合曼 崔鑫[1] 胡建军[1] 张莹钰[2] 张婉琪[2] WANG Na;ZHU Guang-yi;AIKEBAIER·Reheman;CUI Xin;HU Jian-jun;ZHANG Ying-yu;ZHANG Wan-qi(College of Animal Science,Tarim University,Alar 843300,China;College of Life Science,Tarim University,Alar 843300,China)
机构地区:[1]塔里木大学动物科学学院,阿拉尔843300 [2]塔里木大学生命科学学院,阿拉尔843300
出 处:《中国人兽共患病学报》2019年第1期85-90,共6页Chinese Journal of Zoonoses
基 金:国家自然科学基金(No.31860713;31660725);国家留学基金委(No.201805215023)资助~~
摘 要:目的快捷、准确地鉴定马鹿副结核分枝杆菌基因型和亚型,为马鹿副结核病防控工作提供理论依据。方法从疑似感染副结核病马鹿的病料样品中提取其DNA,参照副结核分枝杆菌插入序列IS900鉴定引物、亚型分型引物,PCR扩增、测序及GenBank中BLAST比对。结果所测2份病例与副结核分枝杆菌核苷酸同源性均在99%以上,属于副结核分枝杆菌,采用亚型分型鉴定,属于Ⅱ型(牛型)副结核分枝杆菌。结论结合发病马鹿的临床症状、病理变化、抗酸性染色,证实该马鹿感染牛型副结核病。The aim of this study is to identify quickly and accurately genotype of Mycobacterium avium subsp.paraenberculosis and provide reference to the prevention and control of paratuberculosis,DNA was extracted from two suspected samples of red deer paratuberculosis.Primers were designed based on IS900 of M.avium subsp.paraenberculosis according to reference.The amplified fragments were sequenced.Analysis of the nucleotide sequences and construction of phylogenetic tree were based on IS900 gene of Mycobacterium avium subsp.paraenberculosis with computer programs.The sequencing results showed that two suspected samples had 99% similarity to reference strain from GenBank.Two suspected samples were tested to infect M.avium subsp.paraenberculosis.According to DMC primers,the pathogen was genotype Ⅱ Mycobacterium avium subsp.paraenberculosis.It was confirmed that two red deer infected genotype Ⅱ paratuberculosis according to symptoms,pathological change,acid-fast stain and PCR.
分 类 号:S855.3[农业科学—临床兽医学]
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