Suppr超能文献

卡他莫拉菌在动物模型中的肺部清除情况。

Pulmonary clearance of Moraxella catarrhalis in an animal model.

作者信息

Unhanand M, Maciver I, Ramilo O, Arencibia-Mireles O, Argyle J C, McCracken G H, Hansen E J

机构信息

Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas 75235.

出版信息

J Infect Dis. 1992 Apr;165(4):644-50. doi: 10.1093/infdis/165.4.644.

Abstract

The virulence mechanisms of Moraxella catarrhalis that are involved in producing pulmonary infection are unknown. A well-characterized murine model was used to study the pulmonary clearance of M. catarrhalis and analyze the histopathologic changes and the role of phagocytic cells in the infected lungs. Ten strains of M. catarrhalis from various isolation sites were evaluated for their ability to resist pulmonary clearance. The rates of clearance of these strains, based on the percentage of the original inoculum remaining at 6 h after challenge, varied considerably. Histopathologic examination of lungs infected with 2 strains that exhibited very different clearance rates revealed similar pathologic responses. Analysis of the phagocytic cell response to these 2 strains revealed significant alveolar recruitment of granulocytes at 3, 6, and 24 h after bacterial challenge. However, granulocyte recruitment in response to strain B22, which was cleared readily, was significantly greater than to strain 035E, which resisted pulmonary clearance. This model system should facilitate investigation of the molecular basis of the interaction between M. catarrhalis and the lower respiratory tract.

摘要

卡他莫拉菌导致肺部感染的致病机制尚不清楚。我们使用了一个特征明确的小鼠模型来研究卡他莫拉菌的肺部清除情况,并分析组织病理学变化以及吞噬细胞在受感染肺部中的作用。评估了从不同分离部位获得的10株卡他莫拉菌抵抗肺部清除的能力。基于攻毒后6小时剩余原始接种物的百分比,这些菌株的清除率差异很大。对感染了2株清除率差异很大的菌株的肺部进行组织病理学检查,发现了相似的病理反应。对这2株菌株的吞噬细胞反应分析显示,在细菌攻毒后3小时、6小时和24小时,粒细胞显著向肺泡募集。然而,对易于清除的B22菌株的粒细胞募集明显多于对抵抗肺部清除的035E菌株。该模型系统应有助于研究卡他莫拉菌与下呼吸道相互作用的分子基础。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验