Equine Infectious Disease Laboratory, Department of Large Animal Clinical Sciences, Texas A&M University, College Station, TX, USA.
Equine Infectious Disease Laboratory, Department of Large Animal Clinical Sciences, Texas A&M University, College Station, TX, USA.
Vet Microbiol. 2018 Feb;215:18-22. doi: 10.1016/j.vetmic.2017.11.019. Epub 2017 Nov 21.
Rhodococcus equi is an opportunistic, intracellular pathogen that causes pyogranulomatous pneumonia in foals and immunocompromised people. Currently, there is no experimental model of R. equi pneumonia other than intra-bronchial experimental infection of foals with R. equi, which is labor-intensive and costly. This study's objective was to develop a guinea pig (GP) model of R. equi pneumonia that would facilitate development of novel approaches for controlling and preventing this disease. Guinea pigs were infected with either 10, 10, 10, or 10 colony forming units (CFUs) of a virulent strain of R. equi using a Madison aerosol chamber, or 10 or 10 CFUs of this strain intratracheally. Animals were monitored daily for clinical signs of pneumonia, and were euthanized and necropsied on days 1, 3, 7, or 35 post-infection (PI). Lung homogenates were plated onto selective agar to determine bacterial load. No clinical signs of disease were observed regardless of the inoculum dose or infection method. No bacteria were recovered from GPs euthanized at 35 days PI. Histology and immunostaining of T-cells, B-cells, and macrophages in lungs showed that inflammatory responses in infected GPs were similarly unremarkable irrespective of dose or route of infection. Guinea pigs appear to be resistant to pulmonary infection with virulent R. equi even at doses that reliably produce clinical pneumonia in foals.
马红球菌是一种机会性、细胞内病原体,可引起驹肺炎和免疫功能低下者的化脓性肉芽肿性肺炎。目前,除了用马红球菌对驹进行支气管内实验性感染外,尚无马红球菌肺炎的实验模型,该方法劳动强度大且成本高。本研究的目的是建立一种豚鼠(GP)马红球菌肺炎模型,以促进控制和预防这种疾病的新方法的发展。豚鼠通过 Madison 气溶胶室感染 10、10、10 或 10 个菌落形成单位(CFU)的强毒马红球菌,或通过气管内感染 10 或 10 CFU 该菌株。每天监测动物的肺炎临床症状,并在感染后第 1、3、7 或 35 天安乐死并进行尸检。肺匀浆接种于选择性琼脂平板以确定细菌载量。无论接种剂量或感染方式如何,均未观察到疾病的临床症状。在感染后 35 天处死的 GP 中未回收细菌。肺组织学和 T 细胞、B 细胞和巨噬细胞的免疫染色显示,感染 GP 中的炎症反应无论剂量或感染途径如何均无明显异常。豚鼠对强毒马红球菌的肺部感染具有抵抗力,即使在可可靠引起驹临床肺炎的剂量下也是如此。