首页> 美国卫生研究院文献>British Journal of Experimental Pathology >Establishment of lethal inhalational infection with Francisella tularensis (tularaemia) in the common marmoset (Callithrix jacchus)
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Establishment of lethal inhalational infection with Francisella tularensis (tularaemia) in the common marmoset (Callithrix jacchus)

机译:在普通mar猴(Callithrix jacchus)中建立了杜拉弗朗西斯菌(tularaemia)的致命吸入感染的建立。

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摘要

Susceptibility and lethality studies of inhalational tularaemia were undertaken using the common marmoset (Callithrix jacchus) to determine its suitability as a non-human primate model. Pairs of marmosets were exposed to varying challenge doses of Francisella tularensis by the airborne route and monitored for up to 14 days postchallenge (p.c.). Lethal infection was achieved following a retained dose of less than 10 bacterial colony-forming units (CFU). However, precise LD50 determination was not possible. The model was characterized using a target challenge dose of approximately 100 CFU. Increased core body temperature was the first indicator of disease, at approximately 2.5 days p.c. Overt clinical signs were first observed 12–18 h after the temperature increase. Significantly decreased activity was observed after approximately 3 days. All animals succumbed to infection between 4.5 and 7 days p.c. At postmortem examination, gross pathology was evident in the liver, spleen and lungs of all animals and high bacterial numbers were detected in all the organs assessed. Bacteraemia was demonstrated in all animals postmortem. Histopathological observations included severe suppurative bronchopneumonia, severe multifocal pyogranulomatous hepatitis, splenitis and lymphadenitis. Tularaemia disease progression in the common marmoset therefore appears to be consistent with the disease seen in humans and other animal models. The common marmoset may therefore be considered a suitable model for further studies of inhalational tularaemia.
机译:使用普通mar猴(Callithrix jacchus)进行了吸入性兔瘟的敏感性和致死性研究,以确定其是否适合作为非人类灵长类动物模型。成对的mos猴通过空中途径暴露于不同剂量的土拉弗朗西斯菌中,并在攻击后长达14天(p.c.)进行监控。保留剂量少于10个细菌菌落形成单位(CFU)后,实现了致命感染。但是,无法确定LD50。使用约100 CFU的目标激发剂量表征模型。核心体温升高是疾病的第一个指标,大约在下午2.5天左右。温度升高后12–18 h首先观察到明显的临床体征。约3天后观察到活性显着降低。在下午4.5至7天之间,所有动物都死于感染。验尸后,所有动物的肝脏,脾脏和肺部均出现明显的病理,在所有评估的器官中均发现了高细菌数。在所有动物死后均显示出细菌血症。组织病理学观察包括严重的化脓性支气管肺炎,严重的多灶性肾盂肉芽肿性肝炎,脾炎和淋巴结炎。因此,普通mar猴中的图莱拉贫血症的疾病进展似乎与人类和其他动物模型中发现的疾病一致。因此,普通mar猴可能被认为是进一步研究吸入性图拉血病的合适模型。

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