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Apical Membrane Antigen 1, a Major Malaria Vaccine Candidate, Mediates the Close Attachment of Invasive Merozoites to Host Red Blood Cells

机译:顶端膜抗原1,主要的疟疾疫苗候选者,介导侵入性裂殖子紧密附着在宿主红细胞中

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摘要

Apical membrane antigen 1 (AMA-1) of Plasmodium merozoites is established as a candidate molecule for inclusion in a human malaria vaccine and is strongly conserved in the genus. We have investigated its function in merozoite invasion by incubating Plasmodium knowlesi merozoites with red cells in the presence of a previously described rat monoclonal antibody (MAb R31C2) raised against an invasion-inhibitory epitope of P. knowlesi AMA-1 and then fixing the material for ultrastructural analysis. We have found that the random, initial, long-range (12 nm) contact between merozoites and red cells occurs normally in the presence of the antibody, showing that AMA-1 plays no part in this stage of attachment. Instead, inhibited merozoites fail to reorientate, so they do not bring their apices to bear on the red cell surface and do not make close junctional apical contact. We conclude that AMA-1 may be directly responsible for reorientation or that the molecule may initiate the junctional contact, which is then presumably dependent on Duffy binding proteins for its completion.
机译:疟原虫裂殖子的顶端膜抗原1(AMA-1)被确立为包含在人类疟疾疫苗中的候选分子,并且在该属中是高度保守的。我们已经研究了其在裂殖子侵袭中的功能,方法是在先前描述的针对诺氏假单胞菌AMA-1的侵袭抑制表位的大鼠单克隆抗体(MAb R31C2)存在下,将诺氏疟原虫裂殖子与红细胞一起孵育,然后将其固定用于超微结构分析。我们发现,裂殖子和红细胞之间的随机,初始,远距离(12 nm)接触通常在抗体存在下发生,这表明AMA-1在该连接阶段不起作用。取而代之的是,受抑制的裂殖子无法重新定向,因此它们不会将其顶点带到红细胞表面上,也不会形成紧密的连接顶端。我们得出的结论是,AMA-1可能直接负责重新定向,或者分子可能引发连接接触,然后其可能依赖于达菲结合蛋白的完成。

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