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通过对表达文库的差异筛选鉴定出的恶性疟原虫变种特异性免疫反应的新型靶抗原。

Novel target antigens of the variant-specific immune response to Plasmodium falciparum identified by differential screening of an expression library.

作者信息

Le Scanf C, Fandeur T, Bonnefoy S, Guillotte M, Mercereau-Puijalon O

机构信息

Laboratoire de Parasitologie Moléculaire, Institut Pasteur de Guyane, French Guiana.

出版信息

Infect Immun. 1999 Jan;67(1):64-73. doi: 10.1128/IAI.67.1.64-73.1999.

Abstract

A primary infection by the Plasmodium falciparum Palo Alto O and R antigenic variants induces a variant-specific immunity in the Saimiri sciureus monkey. We have shown that these variants express distinct PfEMP1 antigens and differ in their levels of expression of additional antigens, including two conserved erythrocyte membrane-associated proteins, HRP1 and PfEMP3. To identify the antigens eliciting a variant-specific response, we conducted a differential screening of a lambdagt11 library with variant-specific sera. We report here the analysis of the 46 anti-R-specific clones. Two specific targets of the anti-R response were identified: (i) PfEMP3, suggesting that immunogenicity of this antigen is modulated by its relative abundance in different variants, and (ii) Asn-rich motifs. Most anti-R-specific clones, derived from so-far-undescribed genes, were detected by a cross-reaction on poly(Asn) stretches, as indicated by elimination of the signal after absorption on Asn-rich sequences. Reverse transcription-PCR (RT-PCR) showed that expression of the gene defined by clone 13 was R specific. Pepscan analysis of clone 13 identified three Asn-rich polypeptides and one unique peptide reacting specifically with antibodies eluted from the R-infected erythrocyte surface. Antisera raised to the unique peptide reacted with an R-specific protein. Attempts to demonstrate that clone 13 was derived from a var gene by using PCRs combining clone 13 and var-derived primers were unsuccessful. The var genes expressed by O and R parasites were identified not by this strategy but by RT-PCR with var-specific primers. This work has provided novel insights into immunity to antigenic variants and has identified a novel gene switched on during antigenic variation.

摘要

恶性疟原虫帕洛阿尔托O和R抗原变异体的原发性感染在松鼠猴中诱导了变异体特异性免疫。我们已经表明,这些变异体表达不同的PfEMP1抗原,并且在包括两种保守的红细胞膜相关蛋白HRP1和PfEMP3在内的其他抗原的表达水平上存在差异。为了鉴定引发变异体特异性反应的抗原,我们用变异体特异性血清对λgt11文库进行了差异筛选。我们在此报告对46个抗R特异性克隆的分析。确定了抗R反应的两个特异性靶点:(i)PfEMP3,表明该抗原的免疫原性受其在不同变异体中的相对丰度调节,以及(ii)富含天冬酰胺的基序。大多数抗R特异性克隆来源于迄今未描述的基因,通过与聚(天冬酰胺)序列的交叉反应检测到,这在富含天冬酰胺序列上吸收后信号消除得到了证明。逆转录PCR(RT-PCR)表明,克隆13定义的基因的表达是R特异性的。对克隆13的肽扫描分析确定了三种富含天冬酰胺的多肽和一种与从感染R的红细胞表面洗脱的抗体特异性反应的独特肽。针对该独特肽产生的抗血清与一种R特异性蛋白反应。试图通过使用结合克隆13和var衍生引物的PCR来证明克隆13来源于var基因,但未成功。O和R寄生虫表达的var基因不是通过这种策略鉴定的,而是通过使用var特异性引物的RT-PCR鉴定的。这项工作为对抗抗原变异体的免疫提供了新的见解,并鉴定了一种在抗原变异过程中开启的新基因。

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