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作 者:王祥生[1] 刘小芳[1] 刘俊华[1] 赵文忠[1] 刘全[1] 董文其[2] 曲利芝[2]
机构地区:[1]解放军农牧大学军事兽医研究所 [2]第一军医大学
出 处:《中国兽医学报》1999年第2期156-160,共5页Chinese Journal of Veterinary Science
基 金:国家自然科学基金
摘 要:为了获得伊氏锥虫次黄嘌呤鸟嘌呤磷酸核糖转化酶(HGPRT)缺陷株,用不同浓度的8-氮鸟嘌呤(8-AG)和8-AG加紫外线照射的方法,对伊氏锥虫体外培养株进行了为期60~101d诱导驯化。结果,以每毫升含8-AG40μg的培养液培养驯化,再配合紫外线照射,以及以每毫升含8-AG60μg的培养液培养驯化,均获得了伊氏锥虫HGPRT缺陷株。试验表明,培养虫体经过2~3个死亡期后逐步进入适应期,虫数升高到(1.5~2.5)×106/mL,饲养细胞通常于2~5d变黑、崩解,应适时更换。培养驯化的13株克隆虫株,经6-巯基鸟嘌呤(6-TG)抗性测定,10株存活。克隆株在3倍量氨基喋呤的HAT选择性培养液中死亡。生物学试验表明,HGPRT缺陷株在无HT的培养液中生长良好,对小鼠致病力有下隆的趋势,虫血症和小鼠死亡时间比对照组延长1倍多。抗体凝集试验表明,HGPRT缺陷株未发生抗原变异现象。超微结构显示,HGPRT缺陷株的动基体、核和核仁比对照组明显增大,核膜电子密度区也明显增宽。A HGPRT deficient Trypanosoma evansi strain (T. evansi/HGPRT -) was obtained after T. evansi in vitro culture strain had been induced with different doses of 8 AG and ultraviolet rays for 60 101 days. The results showed that the cultivated parasites had gradually adapted to the induced environment after 2 to 3 time dead periods. When the parasites reached up to (1.5 2.5)×10 6/mL the feeder layer cells got dark and disolved in 2 5 days. The parasites of 40 mg/L and 60 mg/L 8 AG groups survived by determination of anti 6 TG and then ten cloning strains were obtained respectively. The cloning strains would be died in HAT selective medium of triple aminopurine. The biological test proved that T. evansi/HGPRT - could proliferate in the medium without HT and its pathogenicity to mice declined with the parasitemia and death of the inoculated mice to be delayed double than the control group. The antibody agglutination reaction showed that the antigenity of T. evansi/HGPRT - had not been changed. The ultramicroscopic structure proved that the size of kinetoplast, nucleus, nucleolus and electron dense of nuclear membrane of the parasite were large obviousely than that of the control.
分 类 号:S852.7[农业科学—基础兽医学]
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