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微孢子虫 Encephalitozoon cuniculi 和 Anncaliia algerae 的蓖麻 B 凝集素样蛋白参与了宿主细胞的入侵。

Ricin B lectin-like proteins of the microsporidian Encephalitozoon cuniculi and Anncaliia algerae are involved in host-cell invasion.

机构信息

Université Clermont Auvergne, CNRS, Laboratoire Microorganismes: Génomes et Environnement, F-63000 Clermont-Ferrand, France; Université Clermont Auvergne, SIGMA Clermont, Institut Pascal, F-63000 Clermont-Ferrand, France.

Université Clermont Auvergne, CNRS, Laboratoire Microorganismes: Génomes et Environnement, F-63000 Clermont-Ferrand, France.

出版信息

Parasitol Int. 2022 Apr;87:102518. doi: 10.1016/j.parint.2021.102518. Epub 2021 Nov 20.

Abstract

Microsporidia are obligate intracellular pathogens capable of infecting a wide variety of hosts ranging from invertebrates to vertebrates. The infection process requires a step of prior adherence of Microsporidia to the surface of host cells. A few studies demonstrated the involvement of proteins containing a ricin-B lectin (RBL) domain in parasite infection. In this study Anncalia algerae and Encephalitozoon cuniculi genomes were screened by bioinformatic analysis to identify proteins with an extracellular prediction and possessing RBL-type carbohydrate-binding domains, being both potentially relevant factors contributing to host cell adherence. Three proteins named AaRBLL-1 and AaRBLL-2 from A. algerae and EcRBLL-1 from E. cuniculi, were selected and comparative analysis of sequences suggested their belonging to a multigenic family, with a conserved structural RBL domain despite a significant amino acid sequence divergence. The production of recombinant proteins and antibodies against the three proteins allowed their subcellular localization on the spore wall and/or the polar tube. Adherence inhibition assays based on pre-treatments with recombinant proteins or antibodies highlighted the significant decrease of the proliferation of both E. cuniculi and A. algerae, strongly suggesting that these proteins are involved in the infection process.

摘要

微孢子虫是专性细胞内病原体,能够感染从无脊椎动物到脊椎动物等各种宿主。感染过程需要微孢子虫首先附着在宿主细胞表面。有几项研究表明,含有蓖麻毒素-B 凝集素 (RBL) 结构域的蛋白质参与寄生虫感染。在这项研究中,通过生物信息学分析筛选了 Algera anncalia 和 Encephalitozoon cuniculi 的基因组,以鉴定具有细胞外预测并具有 RBL 型碳水化合物结合结构域的蛋白质,这两种蛋白质都是可能与宿主细胞附着相关的因素。从 Algera anncalia 中选择了三种名为 AaRBLL-1 和 AaRBLL-2 的蛋白质,以及从 E. cuniculi 中选择了 EcRBLL-1,对这些序列进行比较分析表明它们属于一个多基因家族,尽管氨基酸序列存在显著差异,但具有保守的结构 RBL 结构域。重组蛋白和针对这三种蛋白质的抗体的生产允许它们在孢子壁和/或极管上的亚细胞定位。基于用重组蛋白或抗体预处理的附着抑制试验强调了 E. cuniculi 和 A. algerae 的增殖显著减少,强烈表明这些蛋白质参与了感染过程。

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