Velge-Roussel F, Dimier-Poisson I, Buzoni-Gatel D, Bout D
UMR UNIVERSITE-INRA d'Immunologie Parasitaire, UFR des Sciences Pharmaceutiques, Tours, France.
Parasitology. 2001 Sep;123(Pt 3):225-33. doi: 10.1017/s0031182001008460.
The initial attachment of Toxoplasma tachyzoites to the target host cell is an important event in the life-cycle of the parasite and a critical stage in infection. Previous studies have shown that polyclonal antibodies directed against the major surface antigen of Toxoplasma gondii (SAG1) inhibit the infection of enterocyte cell lines. Here, we demonstrate that antibodies raised against a central peptide (V41T) of SAG1 and the SAGI protein itself are able to inhibit the infection of various cell lines by the tachyzoites. Antibodies directed against SAG1 peptides were used to define a site on the SAGI antigen that interacts with the host cell. The epitope carried by V41T was identified on the tachyzoite surface by immunofluorescence. The peptide sequence seems to be conserved in all the members of the SAGI Related Sequence family (SRS). Using undifferentiated and differentiated Caco-2 cells, we found that tachyzoites enter preferentially via the basolateral side of the cell. These findings highlight the role of the SRS family members in the mediation of host cell invasion.
弓形虫速殖子与靶宿主细胞的初始附着是该寄生虫生命周期中的一个重要事件,也是感染过程中的关键阶段。先前的研究表明,针对刚地弓形虫主要表面抗原(SAG1)的多克隆抗体可抑制肠上皮细胞系的感染。在此,我们证明,针对SAG1的一个中心肽(V41T)及SAG1蛋白本身产生的抗体能够抑制速殖子对各种细胞系的感染。针对SAG1肽的抗体被用于确定SAG1抗原上与宿主细胞相互作用的位点。通过免疫荧光在速殖子表面鉴定出了V41T携带的表位。该肽序列似乎在SAG1相关序列家族(SRS)的所有成员中都是保守的。利用未分化和分化的Caco-2细胞,我们发现速殖子优先通过细胞的基底外侧进入。这些发现突出了SRS家族成员在介导宿主细胞入侵中的作用。