首页> 外文期刊>The American Journal of Pathology >Identification of Enterocytozoon bieneusi-like microsporidian parasite in simian-immunodeficiency-virus-inoculated macaques with hepatobiliary disease
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Identification of Enterocytozoon bieneusi-like microsporidian parasite in simian-immunodeficiency-virus-inoculated macaques with hepatobiliary disease

机译:猿猴免疫缺陷病毒-病毒感染的猕猴肝肠疾病中的小肠虫的小孢子虫寄生虫的鉴定

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摘要

Enterocytozoon bieneusi is a common opportunistic pathogen of human patients with acquired immune deficiency syndrome (AIDS) causing significant morbidity and mortality. In a retrospective analysis utilizing conventional histochemical techniques, in situ hybridization, polymerase chain reaction, and ultrastructural examination, we identified 18 simian-immunodeficiency-virus-infected macaques (16 Macaca mulatta, 1 M. nemestrina, and 1 M. cyclopis) with Enterocytozoon infection of the hepatobiliary system and small intestine. The organisms were readily identified in the bile ducts and gall bladder by special stains and by in situ hybridization using a probe directed against the small subunit ribosomal RNA of human origin E. bieneusi. Infection of the biliary system was associated with a nonsuppurative and proliferative cholecystitis and choledochitis. Hepatic involvement was characterized by bridging portal fibrosis and nodular hepatocellular regeneration accompanied by marked bile ductular and septal duct hyperplasia. Ultrastructurally, all developmental stages of the organism were found in direct contact with the host cell cytoplasm; spores and sporoblasts contained a double layer of polar tubes. Sequencing of a 607-bp segment of the small subunit ribosomal RNA revealed 97 and 100% identity to two clones of small subunit ribosomal RNA derived from E. bieneusi of human origin. Extensive morphological and genetic similarities between the simian and human enterocytozoons suggest that experimentally infected macaques may serve as a useful model of microsporidial infection in AIDS.
机译:别氏肠杆菌是人类患者获得性免疫缺陷综合症(AIDS)的常见机会病原体,会导致大量发病和死亡。在使用常规组织化学技术,原位杂交,聚合酶链反应和超微结构检查进行的回顾性分析中,我们确定了18株被猿猴免疫缺陷病毒感染的猕猴(16猕猴,1 M. nemestrina和1 M.cyclopis)与Enterocytozozoon肝胆系统和小肠感染。通过使用特殊的染色剂,并使用针对人类起源的比氏小肠埃希菌的小亚基核糖体RNA的探针进行原位杂交,可以轻松地在胆管和胆囊中鉴定出这些生物。胆道系统感染与非化脓性和增生性胆囊炎和胆总管炎有关。肝受累的特点是桥接门脉纤维化和结节性肝细胞再生,并伴有明显的胆管和中隔导管增生。在超微结构上,发现该生物的所有发育阶段都直接与宿主细胞的细胞质接触。孢子和孢子母细胞含有两层极管。小亚基核糖体RNA 607 bp片段的测序显示与源自人源大肠杆菌的小亚基核糖体RNA的两个克隆有97%和100%的同一性。猿猴和人类小肠虫之间广泛的形态和遗传相似性表明,实验感染的猕猴可能是艾滋病微孢子感染的有用模型。

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