首页> 美国卫生研究院文献>Journal of Clinical Microbiology >A cloned DNA probe identifies Cowdria ruminantium in Amblyomma variegatum ticks.
【2h】

A cloned DNA probe identifies Cowdria ruminantium in Amblyomma variegatum ticks.

机译:克隆的DNA探针可识别变异羊草菌壁虱中的反刍柯登菌。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Heartwater, caused by Cowdria ruminantium and transmitted by ticks of the genus Amblyomma, is a constraint to ruminant animal production in sub-Saharan Africa. This rickettsial disease could spread from endemically infected areas of sub-Saharan Africa and certain Caribbean islands to other countries, including the United States, in which Amblyomma ticks exist. To detect C. ruminantium in tick vectors and animals, we made DNA probes from C. ruminantium DNA isolated from endothelial cell cultures. Two clones were evaluated; pCS20 from Crystal Springs (Zimbabwe) strain DNA had a 1,306-bp insert, and pCR9 from Kiswani (Kenya) strain DNA had a 754-bp insert. Both DNA probes detected 1 ng of Crystal Springs DNA; however, the pCS20 probe had a 10-fold-greater ability to discriminate between C. ruminantium DNA and DNA from other organisms. Also, the pCS20 probe did not hybridize to 400 ng (highest amount tested) of DNA from bovine cells, 3 protozoa, 3 rickettsiae, and 12 bacteria. In all experiments, C. ruminantium DNA was detected in midguts from 99 of 160 Amblyomma variegatum nymphs infected as larvae and in midguts from 38 of 80 adult ticks infected as nymphs but not in midguts from control nymphs and adults. The presence of C. ruminantium in nymphs and adults was confirmed by transmission of heartwater to goats. The DNA sequences of both probes were determined; synthetic oligonucleotides from pCS20 are recommended as DNA probes for C. ruminantium.
机译:由考德里亚反刍动物引起的心水,由盲肠属的tick传播,对撒哈拉以南非洲反刍动物的生产产生了限制。这种立克次氏病可能从撒哈拉以南非洲的局部感染地区和某些加勒比岛屿蔓延到其他国家,包括存在A虫tick的美国。为了检测壁虱载体和动物中的反刍动物,我们从分离自内皮细胞培养物中的反刍动物DNA制备了DNA探针。评价了两个克隆。来自Crystal Springs(津巴布韦)菌株DNA的pCS20具有1,306 bp的插入片段,来自Kiswani(肯尼亚)菌株DNA的pCR9具有754 bp的插入片段。两种DNA探针均检测到1 ng的Crystal Springs DNA。但是,pCS20探针具有十倍的区分球果反刍动物DNA和其他生物体DNA的能力。同样,pCS20探针不与牛细胞,3个原生动物,3个立克次氏体和12个细菌的400 ng DNA(最高测试量)杂交。在所有实验中,在被感染为幼虫的160株盲肠草若虫的中肠中检出了瘤胃梭状芽胞杆菌DNA,而在由对照若虫和成虫的成年s的80只成年tick的中肠中均检出了反刍动物DNA。通过将心水传播给山羊,证实了若虫和成虫中存在反刍动物。确定了两种探针的DNA序列。推荐将pCS20的合成寡核苷酸用作反刍念珠菌的DNA探针。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号