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腹部广州管圆线虫病:感染不同剂量……的瑞士小鼠的病理发现

Abdominal angiostrongyliasis: pathologic findings in Swiss mice infected with different doses of .

作者信息

Hermes C C, Benvegnú E, Costa M M, Rodriguez R, Vieira M I B

机构信息

Programa de Pós-graduação em Bioexperimentação, Universidade de Passo Fundo - UPF, Passo Fundo, RS, Brazil.

Instituto de Patologia de Passo Fundo, Passo Fundo, RS, Brazil.

出版信息

J Helminthol. 2020 Jul 7;94:e169. doi: 10.1017/S0022149X20000516.

Abstract

Abdominal angiostrongyliasis is caused by Angiostrongylus costaricensis, the definitive and intermediate hosts of which are wild rodents and terrestrial molluscs, respectively. Humans are accidental hosts and can be infected by ingesting the third-stage (infective) larvae (L3). It remains unclear whether the number of L3 inoculated is related to lesion severity. Our aim was to analyse histopathological alterations in Swiss mice infected with different doses of A. costaricensis. Thirty-two mice were randomly divided into four groups (n = 8/group): uninfected, control mice; mice infected with a low dose (five L3); mice infected with an intermediate dose (15 L3); and mice infected with a high dose (30 L3). The frequency of intestinal thrombi, splenitis, eggs/larvae, hepatic infarction and acute pancreatitis differed among the groups, the last being considered a significant finding. We conclude that different infective doses alter the histopathological aspects of the infection in Swiss mice, those aspects being more pronounced at medium and high doses, with no effect on the development of the disease. This experimental model shows that the parasite life cycle can be maintained in Swiss mice through the inoculation of a low dose (five L3).

摘要

腹部血管圆线虫病由哥斯达黎加血管圆线虫引起,其终宿主和中间宿主分别为野生啮齿动物和陆生软体动物。人类是偶然宿主,可因摄入第三期(感染性)幼虫(L3)而被感染。接种的L3数量是否与病变严重程度相关尚不清楚。我们的目的是分析感染不同剂量哥斯达黎加血管圆线虫的瑞士小鼠的组织病理学改变。32只小鼠随机分为四组(每组n = 8):未感染的对照小鼠;感染低剂量(5条L3)的小鼠;感染中等剂量(15条L3)的小鼠;以及感染高剂量(30条L3)的小鼠。各组之间肠道血栓、脾炎、虫卵/幼虫、肝梗死和急性胰腺炎的发生率有所不同,最后一项被认为是一项重要发现。我们得出结论,不同的感染剂量会改变瑞士小鼠感染的组织病理学表现,这些表现在中高剂量时更为明显,对疾病发展没有影响。该实验模型表明,通过接种低剂量(5条L3)可在瑞士小鼠体内维持寄生虫的生命周期。

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