Kahn S, Colbert T G, Wallace J C, Hoagland N A, Eisen H
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
Proc Natl Acad Sci U S A. 1991 May 15;88(10):4481-5. doi: 10.1073/pnas.88.10.4481.
Trypanosoma cruzi, an intracellular protozoan parasite infecting a wide variety of vertebrates, is the agent responsible for Chagas disease in humans. An estimated 15-20 million people in South and Central America are infected with the parasite. Chagas disease often results in severe autoimmune and inflammatory pathology and is the major cause of heart failure in endemic areas. Nevertheless, little is known about the host-parasite interactions that lead to this pathology. We have previously cloned several members of a large gene family (SA85-1) and shown that these genes encode 85-kDa T. cruzi, mammalian-stage-specific, surface antigens. Here we report that members of the SA85-1 family possess sialidase activity and are shed by the parasite. We suggest that the sialidases may contribute to the pathology during T. cruzi infection by cleaving sialic acid from cells of the immune system.
克氏锥虫是一种感染多种脊椎动物的细胞内原生动物寄生虫,是人类恰加斯病的病原体。南美洲和中美洲估计有1500万至2000万人感染了这种寄生虫。恰加斯病常导致严重的自身免疫和炎症病理,是流行地区心力衰竭的主要原因。然而,对于导致这种病理的宿主-寄生虫相互作用知之甚少。我们之前克隆了一个大基因家族(SA85-1)的几个成员,并表明这些基因编码85 kDa的克氏锥虫哺乳动物阶段特异性表面抗原。在此我们报告,SA85-1家族成员具有唾液酸酶活性,并被寄生虫脱落。我们认为,唾液酸酶可能通过从免疫系统细胞上切割唾液酸,在克氏锥虫感染期间促成病理过程。