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来自南美洲的恶性疟原虫野外分离株使用一种与入侵配体多态性相关的非典型红细胞入侵途径。

Plasmodium falciparum field isolates from South America use an atypical red blood cell invasion pathway associated with invasion ligand polymorphisms.

机构信息

Molecular Parasitology, Lindsley F Kimball Research Institute, New York Blood Center, New York City, New York, United States of America.

出版信息

PLoS One. 2012;7(10):e47913. doi: 10.1371/journal.pone.0047913. Epub 2012 Oct 31.

Abstract

Studies of Plasmodium falciparum invasion pathways in field isolates have been limited. Red blood cell (RBC) invasion is a complex process involving two invasion protein families; Erythrocyte Binding-Like (EBL) and the Reticulocyte Binding-Like (PfRh) proteins, which are polymorphic and not fully characterized in field isolates. To determine the various P. falciparum invasion pathways used by parasite isolates from South America, we studied the invasion phenotypes in three regions: Colombia, Peru and Brazil. Additionally, polymorphisms in three members of the EBL (EBA-181, EBA-175 and EBL-1) and five members of the PfRh (PfRh1, PfRh2a, PfRh2b, PfRh4, PfRh5) families were determined. We found that most P. falciparum field isolates from Colombia and Peru invade RBCs through an atypical invasion pathway phenotypically characterized as resistant to all enzyme treatments (NrTrCr). Moreover, the invasion pathways and the ligand polymorphisms differed substantially among the Colombian and Brazilian isolates while the Peruvian isolates represent an amalgam of those present in the Colombian and Brazilian field isolates. The NrTrCr invasion profile was associated with the presence of the PfRh2a pepC variant, the PfRh5 variant 1 and EBA-181 RVNKN variant. The ebl and Pfrh expression levels in a field isolate displaying the NrTrCr profile also pointed to PfRh2a, PfRh5 and EBA-181 as being possibly the major players in this invasion pathway. Notably, our studies demonstrate the uniqueness of the Peruvian P. falciparum field isolates in terms of their invasion profiles and ligand polymorphisms, and present a unique opportunity for studying the ability of P. falciparum parasites to expand their invasion repertoire after being reintroduced to human populations. The present study is directly relevant to asexual blood stage vaccine design focused on invasion pathway proteins, suggesting that regional invasion variants and global geographical variation are likely to preclude a simple one size fits all type of vaccine.

摘要

对野外分离株中疟原虫入侵途径的研究一直受到限制。红细胞(RBC)入侵是一个复杂的过程,涉及到两个入侵蛋白家族;红细胞结合样(EBL)和网织红细胞结合样(PfRh)蛋白,这些蛋白在野外分离株中是多态的,尚未完全表征。为了确定来自南美洲的寄生虫分离株使用的各种疟原虫入侵途径,我们在三个地区研究了入侵表型:哥伦比亚、秘鲁和巴西。此外,还确定了 EBL 家族的三个成员(EBA-181、EBA-175 和 EBL-1)和 PfRh 家族的五个成员(PfRh1、PfRh2a、PfRh2b、PfRh4 和 PfRh5)的多态性。我们发现,来自哥伦比亚和秘鲁的大多数疟原虫野外分离株通过一种非典型的入侵途径入侵 RBC,其表型特征为对所有酶处理均具有抗性(NrTrCr)。此外,哥伦比亚和巴西分离株的入侵途径和配体多态性存在显著差异,而秘鲁分离株则代表了哥伦比亚和巴西野外分离株中存在的混合体。NrTrCr 入侵谱与 PfRh2a pepC 变体、PfRh5 变体 1 和 EBA-181 RVNKN 变体的存在相关。表现出 NrTrCr 谱的野外分离株中的 ebl 和 Pfrh 表达水平也表明 PfRh2a、PfRh5 和 EBA-181 可能是该入侵途径的主要参与者。值得注意的是,我们的研究表明,秘鲁疟原虫野外分离株在其入侵谱和配体多态性方面具有独特性,为研究疟原虫寄生虫在重新引入人类种群后扩展其入侵谱的能力提供了独特的机会。本研究与针对入侵途径蛋白的无性血阶段疫苗设计直接相关,表明区域入侵变体和全球地理变异可能排除了一种简单的一刀切式的疫苗类型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d5/3485327/6b749ed669a4/pone.0047913.g001.jpg

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