Host Cell Remodelling and Sequestration of Malaria Transmission Stages

疟疾传播阶段的宿主细胞重塑和隔离

• 批准号: 118292138
• 负责人: Dr. Kathrin Buchholz
• 金额: --
• 依托单位: Institut für Parasitologie
• 依托单位国家: 德国
• 项目类别: Research Fellowships
• 财政年份: 2009
• 资助国家: 德国
• 起止时间: 2008-12-31 至 无数据
• 项目状态: 未结题
• 来源: https://gepris.dfg.de/gepris/projekt/118292138?language=en
• 关键词: Host; Cell; Remodelling; Sequestration; Malaria

Plasmodium falciparum causes the most severe form of human malaria with over two million deaths per year. The morbidity and mortality of the disease can be attributed exclusively to the asexual stages residing and replicating within red blood cells. Virulence of these asexual stages is linked to the unique capability of P. falciparum to induce cytoadherence of infected red blood cells to the microvascular endothelium, thereby avoiding clearance during spleen passage. While the molecular basis and the selective pressures underlying cytoadherence in asexual parasites have been studied intensively in recent years, little is known about sequestration of young transmission stages, i.e. gametocytes. Understanding the survival strategies of sexual stage parasites during their comparatively long development within the human red blood cells is a prerequisite for novel approaches to block the transmission of this devastating pathogen to its mosquito vector. This project will be supervised by Matthias Marti and aims to gain a better understanding of the molecular basis that defines the host/pathogen-interactions implicated in transmission of P. falciparum. Molecular and cellular insights into this phase of the Plasmodium lifecycle are critical to the two major tasks in malaria research, development of vaccine strategies and new drugs. Using a potent set of state-of-the-art techniques, I will address fundamental issues in malaria transmission, including discovery and validation of novel gametocyte surface antigens as potential cytoadherence determinants. I will also determine sequestration profiles of sexual stage parasites ex vivo.

恶性疟原虫引起最严重的人类疟疾，每年有200多万人死亡。该疾病的发病率和死亡率可完全归因于红细胞内的无性繁殖阶段。这些无性阶段的毒力与恶性疟原虫诱导感染的红细胞粘附于微血管内皮的独特能力有关，从而避免在脾传代期间清除。虽然在无性寄生虫的细胞粘附的分子基础和选择压力的基础上进行了深入的研究，在最近几年，鲜为人知的是年轻的传输阶段，即配子体隔离。了解性阶段寄生虫在人类红细胞内相对较长的发育过程中的生存策略是阻断这种毁灭性病原体传播给蚊子媒介的新方法的先决条件。该项目将由Matthias Marti监督，旨在更好地了解恶性疟原虫传播中涉及的宿主/病原体相互作用的分子基础。对疟原虫生命周期这一阶段的分子和细胞见解对于疟疾研究的两项主要任务至关重要，即疫苗策略和新药的开发。使用一套强大的国家的最先进的技术，我将解决疟疾传播的基本问题，包括发现和验证新的配子体表面抗原作为潜在的细胞粘附决定因素。我还将确定隔离配置文件的性阶段寄生虫离体。