Soto M, Requena J M, Quijada L, Gomez L C, Guzman F, Patarroyo M E, Alonso C
Centro de Biología Molecular Severo Ochoa, Universidad Autónoma de Madrid, Spain.
Clin Exp Immunol. 1996 Dec;106(3):454-61. doi: 10.1046/j.1365-2249.1996.d01-865.x.
In the present study we show that sera from dogs naturally infected with the protozoan parasite Leishmania infantum contain antibodies that specifically react with the parasite histone H3. Using synthetic peptides covering the complete sequence of the protein we located the linear antigenic determinants within the 40 amino-terminal amino acids of the molecule. In addition to the complete form of the protein (rLiH3), two regions of the Leishmania histone H3 were expressed as recombinant proteins: the rLiH3-Nt fragment containing the 39 amino-terminal amino acids and the rLiH3-Ct fragment containing the 90 carboxyl-terminal residues. Competition experiments using the protein fragment rLiH3-Nt as competitor confirmed that the antigenic determinants of histone H3 are confined to the amino-terminal domain. This domain, which is believed to be exposed on the nucleosome surface, is also the most evolutionarily divergent region of the L. infantum histone H3. Visceral leishmaniasis (VL) sera do not react with mammalian histones, an indication that the anti-histone response elicited during Leishmania infection is triggered by the parasite histone. The results of the prevalence of anti-histone H3 antibodies in canine VL sera together with the sequence-specific characteristics of the amino-terminal region of L. infantum histone H3 indicate that the recombinant protein rLiH3-Nt may be of use for diagnosis of canine VL.
在本研究中,我们发现,自然感染原生动物寄生虫婴儿利什曼原虫的犬血清中含有能与该寄生虫组蛋白H3特异性反应的抗体。利用覆盖该蛋白完整序列的合成肽,我们确定了该分子40个氨基末端氨基酸内的线性抗原决定簇。除了完整形式的蛋白(rLiH3)外,利什曼原虫组蛋白H3的两个区域也被表达为重组蛋白:包含39个氨基末端氨基酸的rLiH3-Nt片段和包含90个羧基末端残基的rLiH3-Ct片段。使用蛋白片段rLiH3-Nt作为竞争者的竞争实验证实,组蛋白H3的抗原决定簇局限于氨基末端结构域。该结构域被认为暴露于核小体表面,也是婴儿利什曼原虫组蛋白H3在进化上差异最大的区域。内脏利什曼病(VL)血清不与哺乳动物组蛋白发生反应,这表明利什曼原虫感染期间引发的抗组蛋白反应是由寄生虫组蛋白触发的。犬VL血清中抗组蛋白H3抗体的流行率结果以及婴儿利什曼原虫组蛋白H3氨基末端区域序列特异性特征表明,重组蛋白rLiH3-Nt可用于犬VL的诊断。