首页> 外文OA文献 >A rapid method for selecting suitable animal species for studying pathogen interactions with plasma protein ligands in vivo
【2h】

A rapid method for selecting suitable animal species for studying pathogen interactions with plasma protein ligands in vivo

机译:一种选择合适动物物种的快速方法,用于研究病原体在体内与血浆蛋白配体的相互作用

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

Species tropism constitutes a serious problem for developing relevant animal models of infection. Human pathogens can express virulence factors that show specific selectivity to human proteins, while their affinity for orthologs from other species can vary significantly. Suitable animal species must be used to analyse whether virulence factors are potential targets for drug development. We developed an assay that rapidly predicts applicable animal species for studying virulence factors binding plasma proteins. We used two well-characterized Staphylococcus aureus proteins, SSL7 and Efb, to develop an ELISA-based inhibition assay using plasma from different animal species. The interaction between SSL7 and human C5 and the binding of Efb to human fibrinogen and human C3 was studied. Affinity experiments and Western blot analyses were used to validate the assay. Human, monkey and cat plasma interfered with binding of SSL7 to human C5. Binding of Efb to human fibrinogen was blocked in human, monkey, gerbil and pig plasma, while human, monkey, gerbil, rabbit, cat and guinea pig plasma inhibited the binding of Efb to human C3. These results emphasize the importance of choosing correct animal models, and thus, our approach is a rapid and cost-effective method that can be used to prevent unnecessary animal experiments.
机译:物种嗜性是发展相关感染动物模型的严重问题。人类病原体可以表达对人类蛋白质具有特定选择性的毒力因子,而它们对其他物种直系同源物的亲和力却有很大差异。必须使用合适的动物物种来分析毒力因子是否是药物开发的潜在目标。我们开发了一种测定方法,可以快速预测可用于研究结合血浆蛋白的毒力因子的动物物种。我们使用了两个特征明确的金黄色葡萄球菌蛋白SSL7和Efb,使用来自不同动物物种的血浆开发了基于ELISA的抑制测定法。研究了SSL7与人C5之间的相互作用以及Efb与人纤维蛋白原和人C3的结合。亲和力实验和蛋白质印迹分析用于验证测定。人,猴和猫的血浆会干扰SSL7与人C5的结合。 Efb与人纤维蛋白原的结合在人,猴,沙鼠和猪的血浆中被阻断,而人,猴,沙鼠,兔,猫和豚鼠的血浆则抑制Efb与人C3​​的结合。这些结果强调了选择正确的动物模型的重要性,因此,我们的方法是一种快速且经济高效的方法,可用于防止不必要的动物实验。

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