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[溶组织内阿米巴致病性的最新研究发现]

[Recent findings on the pathogenicity of Entamoeba histolytica].

作者信息

Tannich E, Leippe M, Horstmann R D

机构信息

Bernhard-Nocht-Institut für Tropenmedizin, Hamburg.

出版信息

Immun Infekt. 1992 Oct;20(5):146-50.

PMID:1452192
Abstract

Entamoeba histolytica is the causative agent of human amoebiasis. During recent years, research in amoebiasis has concentrated on two subjects: 1. the dual manifestation of the infection as harmless colonization of the intestinal cavity or pathogenic tissue invasion and 2. the molecular analysis of functions of E. histolytica that are considered essential for pathogenicity. Besides epidemiological studies and isoenzyme analyses, molecular genetics have revealed additional evidence that two genetically distinct forms of E. histolytica do exist, named "pathogenic" and "nonpathogenic" forms, respectively. Both can infect humans but only the "pathogenic" form is able to invade the tissue and cause disease whereas the "nonpathogenic" is not. Questions remain open about the mechanism that triggers "pathogenic" E. histolytica to become invasive and about the molecules that are involved. Current data indicate that at least three functions of the amoebae are considered essential for pathogenic tissue invasion. Pathogenicity is viewed as a result of 1. adherence of the amoeba to host cells, predominantly mediated by a galactose- and N-acetylgalactosamine-inhibitable lectin, 2. killing of host cells by a pore-forming peptide known as amoebapore, and 3. proteolysis of the host's extracellular matrix mediated by cysteine proteinases. Structural detailed molecular analysis including cloning of the corresponding genes have led to a better understanding of the function of these proteins.

摘要

溶组织内阿米巴是人类阿米巴病的病原体。近年来,对阿米巴病的研究集中在两个方面:1. 感染的双重表现,即作为肠腔的无害定植或致病性组织侵袭;2. 对溶组织内阿米巴致病性所必需功能的分子分析。除了流行病学研究和同工酶分析外,分子遗传学还揭示了更多证据,表明确实存在两种遗传上不同的溶组织内阿米巴形式,分别称为“致病性”和“非致病性”形式。两者都可感染人类,但只有“致病性”形式能够侵袭组织并引起疾病,而“非致病性”形式则不能。关于触发“致病性”溶组织内阿米巴变得具有侵袭性的机制以及所涉及的分子,问题仍然悬而未决。目前的数据表明,至少阿米巴的三种功能被认为对致病性组织侵袭至关重要。致病性被视为以下结果:1. 阿米巴对宿主细胞的粘附,主要由一种可被半乳糖和N-乙酰半乳糖胺抑制的凝集素介导;2. 由一种称为溶组织素的成孔肽杀死宿主细胞;3. 由半胱氨酸蛋白酶介导对宿主细胞外基质的蛋白水解。包括相应基因克隆在内的详细结构分子分析,使人们对这些蛋白质的功能有了更好的理解。

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