利用口咽抽吸法在小鼠体内建立急性铜绿假单胞菌和鲍曼不动杆菌肺部单挑战模型。

Access microbiology Pub Date : 2024-11-21 eCollection Date: 2024-01-01 DOI:10.1099/acmi.0.000860.v3
Irene Jurado-Martín, Chaoying Ma, Nouran Rezk, Maite Sainz-Mejías, Yueran Hou, John A Baugh, Siobhán McClean
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引用次数: 0

摘要

铜绿假单胞菌和鲍曼不动杆菌等耐抗菌病原体可导致易感人群发生潜在的致命感染,其中呼吸道感染是最常见的临床表现之一。目前亟需开发新型治疗或预防干预措施来对抗这些感染,这就需要建立稳健可靠的动物模型来进行临床前评估。特别是,需要在对潜在疗法进行评估前后准确测定细菌负荷,以量化治疗效果。我们利用口咽抽吸技术提供了两种可靠的、非侵入性的小鼠急性肺部铜绿假单胞菌或鲍曼不动杆菌挑战模型。在这里,我们展示了这种将悬浮液送入小鼠肺部的非手术技术不会对动物福利产生重大影响(基于福利监测和体重),而且能使细菌剂量均匀分布于双侧肺部,从而使双侧肺部的生物负荷均匀。对两种病原体进行人道处死和器官摘取的最佳时间点均为挑战后24小时,每只小鼠至少需要4×106和107 c.f.u.才能获得可重复的铜绿假单胞菌或鲍曼不动杆菌生物负荷。这些小鼠挑战模型为评估针对铜绿假单胞菌或鲍曼不动杆菌感染的治疗干预措施提供了宝贵的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of acute Pseudomonas aeruginosa and Acinetobacter baumannii lung mono-challenge models in mice using oropharyngeal aspiration.

Antimicrobial-resistant pathogens such as Pseudomonas aeruginosa and Acinetobacter baumannii can cause potentially fatal infections in susceptible individuals, with respiratory tract infections among the most common clinical presentations. The development of novel treatments or prophylactic interventions to combat these infections is urgently needed and requires robust, reliable animal models for their preclinical evaluation. In particular, the bacterial burden needs to be accurately determined before and after administration of the potential therapy under evaluation to quantify the effectiveness of the treatment. We provide two reliable, non-invasive murine acute lung challenge models with either P. aeruginosa or A. baumannii using an oropharyngeal aspiration technique, which has been widely overlooked in studies testing vaccines or treatments for these pathogens. Here, we show that this non-surgical technique to deliver suspensions into mouse lungs does not significantly impact animal welfare (based on welfare monitoring and weight) and allows uniform bilateral distribution of the bacterial dose, resulting in even bioburden in both lungs. The optimal timepoint for humane killing and organ harvest was 24 h after challenge for both pathogens, and at least 4×106 and 107 c.f.u. per mouse were needed to obtain a reproducible P. aeruginosa or A. baumannii bioburden, respectively. These mouse challenge models offer a valuable tool to assess therapeutic interventions against P. aeruginosa or A. baumannii infections.

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