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吸入类鼻疽伯克霍尔德菌诱导的小鼠肺部感染和炎症。

Murine pulmonary infection and inflammation induced by inhalation of Burkholderia pseudomallei.

机构信息

Division of Pulmonary and Critical Care Medicine, Harborview Medical Center, University of Washington, Seattle, WA 98104-2499, USA.

出版信息

Int J Exp Pathol. 2012 Dec;93(6):421-8. doi: 10.1111/j.1365-2613.2012.00842.x.

Abstract

Melioidosis is a tropical disease caused by ingestion, percutaneous inoculation or inhalation of the Gram-negative soil saprophyte Burkholderia pseudomallei. We developed a reproducible experimental murine model of pneumonic melioidosis induced by inhalation of aerosolized B. pseudomallei 1026b. In a series of experiments performed to bracket the lethal dose, we found that C57BL/6 mice were modestly more resistant than BALB/c mice (median lethal dose 334 CFU/lung vs 204 CFU/lung). We further characterized infection and pulmonary inflammation in C57BL/6 mice infected with a sublethal dose. We observed pulmonary replication and dissemination of bacteria to distant organs in the first days after infection, followed by bacterial containment by day 4 and no evidence of recrudescent infection for up to 2 months. We measured a robust host inflammatory response notable for a neutrophilic bronchoalveolar lavage fluid profile, elevated cytokines and chemokines in the lung and serum and scattered foci of neutrophilic infiltrates in the alveoli and in a perivascular distribution on histological analysis. We previously noted a similar pattern of inflammation in mice infected with aerosolized B. thailandensis. This report builds on the limited literature describing experimental murine pneumonic melioidosis induced by aerosol and characterizes pulmonary infection and resultant inflammation in C57BL/6 mice infected with aerosolized B. pseudomallei. This model has utility for the study of bacterial and host factors that contribute to the virulence of melioidosis.

摘要

类鼻疽是一种热带病,由革兰氏阴性土壤腐生菌伯克霍尔德菌假单胞菌经摄入、经皮接种或吸入引起。我们通过吸入雾化的伯克霍尔德菌假单胞菌 1026b 建立了一种可重复的实验性鼠类肺炎型类鼻疽模型。在一系列旨在确定致死剂量的实验中,我们发现 C57BL/6 小鼠比 BALB/c 小鼠具有稍高的抵抗力(中位致死剂量 334 CFU/肺 vs 204 CFU/肺)。我们进一步研究了感染亚致死剂量的 C57BL/6 小鼠的感染和肺部炎症。我们观察到感染后最初几天肺部细菌的复制和播散,随后第 4 天细菌被控制,在长达 2 个月的时间内没有证据表明复发感染。我们检测到宿主强烈的炎症反应,特征为支气管肺泡灌洗液中性粒细胞增多,肺部和血清中的细胞因子和趋化因子升高,肺泡和血管周围散在中性粒细胞浸润灶。我们之前在感染雾化的伯克霍尔德菌泰国变种的小鼠中观察到类似的炎症模式。本报告进一步描述了通过雾化诱导实验性鼠类肺炎型类鼻疽的有限文献,并对感染雾化的伯克霍尔德菌假单胞菌的 C57BL/6 小鼠肺部感染和由此产生的炎症进行了特征描述。该模型可用于研究导致类鼻疽毒力的细菌和宿主因素。

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