首页> 美国卫生研究院文献>Pathogens and Disease >The Coxiella Burnetii type IVB secretion system (T4BSS) component DotA is released/secreted during infection of host cells and during in vitro growth in a T4BSS-dependent manner
【2h】

The Coxiella Burnetii type IVB secretion system (T4BSS) component DotA is released/secreted during infection of host cells and during in vitro growth in a T4BSS-dependent manner

机译:在感染宿主细胞期间和以T4BSS依赖的方式在体外生长期间柯氏杆菌IV型分泌系统(T4BSS)组分DotA释放/分泌

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

Coxiella burnetii is a Gram-negative intracellular pathogen and is the causative agent of the zoonotic disease Q fever. To cause disease, C. burnetii requires a functional type IVB secretion system (T4BSS) to transfer effector proteins required for the establishment and maintenance of a membrane-bound parasitophorous vacuole (PV) and further modulation of host cell process. However, it is not clear how the T4BSS interacts with the PV membrane since neither a secretion pilus nor an extracellular pore forming apparatus has not been described. To address this, we used the acidified citrate cysteine medium (ACCM) along with cell culture infection and immunological techniques to identify the cellular and extracellular localization of T4BSS components. Interestingly, we found that DotA and IcmX were secreted/released in a T4BSS-dependent manner into the ACCM. Analysis of C. burnetii-infected cell lines revealed that DotA colocalized with the host cell marker CD63 (LAMP3) at the PV membrane. In the absence of bacterial protein synthesis, DotA also became depleted from the PV membrane. These data are the first to identify the release/secretion of C. burnetii T4BSS components during axenic growth and the interaction of a T4BSS component with the PV membrane during infection of host cells.
机译:柯氏杆菌是革兰氏阴性细胞内病原体,是人畜共患病Q发热的病原体。为了引起疾病,伯氏梭菌需要功能性IVB分泌系统(T4BSS)来转移建立和维持膜结合的寄生虫液泡(PV)和进一步调节宿主细胞过程所需的效应蛋白。然而,尚不清楚T4BSS如何与PV膜相互作用,因为没有描述分泌菌毛或细胞外孔形成装置。为了解决这个问题,我们使用了酸化的柠檬酸半胱氨酸培养基(ACCM)以及细胞培养物感染和免疫学技术来鉴定T4BSS组件在细胞和细胞外的定位。有趣的是,我们发现DotA和IcmX以T4BSS依赖的方式分泌/释放到ACCM中。伯氏梭菌感染细胞系的分析表明,DotA与宿主细胞标记CD63(LAMP3)共定位在PV膜上。在没有细菌蛋白质合成的情况下,DotA也从PV膜中耗尽。这些数据是第一个鉴定在无性系生长过程中伯氏梭菌T4BSS组分的释放/分泌以及在宿主细胞感染期间T4BSS组分与PV膜的相互作用的数据。

著录项

相似文献

  • 外文文献
  • 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