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低剂量牛分枝杆菌气溶胶感染的豚鼠模型

A guinea pig model of low-dose Mycobacterium bovis aerogenic infection.

作者信息

Chambers M A, Williams A, Gavier-Widén D, Whelan A, Hughes C, Hall G, Lever M S, Marsh P D, Hewinson R G

机构信息

TB Research Group, Department of Bacterial Diseases, Veterinary Laboratories Agency Weybridge, New Haw, Addlestone, Surrey KT15 3NB, UK.

出版信息

Vet Microbiol. 2001 Jun 6;80(3):213-26. doi: 10.1016/s0378-1135(00)00378-3.

Abstract

In order to develop a model of Mycobacterium bovis infection with pathogenetical relevance, a modified version of the Henderson apparatus was used to deliver infectious aerosols directly to the snouts of guinea pigs. Aerosols generated from 10(6), 10(7), 10(8)CFU/ml M. bovis suspensions established disease in every animal, with estimated retained doses of 10, 100, 1000 CFU, respectively. For comparison, other guinea pigs were inoculated with 100 CFU M. bovis intramuscularly (i.m.). Pathology and bacterial colonisation of lungs and spleen varied according to the dose and route of inoculation. Animals inoculated i.m. gave a significant cutaneous tuberculin hypersensitivity reaction earlier after testing than those infected aerogenically. A serological response to M. bovis antigens was detected in all infected animals. Intensity of antigen recognition was dose-dependent and although the range of antigens recognised varied between animals, a 25 kDa antigen present in the cell fraction was serodominant. Thus, a reproducible guinea pig model has been defined that may be suitable for virulence, vaccination, and immunological studies.

摘要

为了建立一个具有致病相关性的牛分枝杆菌感染模型,使用改良版的亨德森装置将感染性气溶胶直接输送到豚鼠的口鼻部。由每毫升含10⁶、10⁷、10⁸CFU的牛分枝杆菌悬液产生的气溶胶使每只动物都感染发病,估计保留剂量分别为10、100、1000CFU。作为对照,其他豚鼠通过肌肉注射接种100CFU牛分枝杆菌。肺和脾的病理学及细菌定植情况因接种剂量和途径而异。肌肉注射接种的动物在检测后比经空气感染的动物更早出现明显的皮肤结核菌素超敏反应。在所有感染动物中均检测到对牛分枝杆菌抗原的血清学反应。抗原识别强度呈剂量依赖性,尽管不同动物识别的抗原范围有所不同,但细胞组分中存在的一种25kDa抗原在血清学上占主导地位。因此,已确定了一种可重复的豚鼠模型,该模型可能适用于毒力、疫苗接种和免疫学研究。

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