Munder Antje, Zelmer Andrea, Schmiedl Andreas, Dittmar Kurt E J, Rohde Manfred, Dorsch Martina, Otto Klaus, Hedrich Hans-J, Tümmler Burkhard, Weiss Siegfried, Tschernig Thomas
Clinical Research Group OE 6711, Center of Pediatrics, Hannover Medical School, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany.
Microbes Infect. 2005 Apr;7(4):600-11. doi: 10.1016/j.micinf.2004.12.021. Epub 2005 Mar 16.
Murine listeriosis is a paradigm to understand host pathogen interactions. Airway infections with Listeria monocytogenes, although representing a serious problem in early onset neonatal listeriosis, has not been investigated in detail in animal models so far. Here, the susceptibility of BALB/c, DBA/2 and C57BL/6 mice towards an intratracheal (i.t.) infection with virulent L. monocytogenes EGDe and the attenuated variant L. monocytogenes EGD hlyW491A(pERL3-CMVGFP) is reported. The course of infection was characterized by determination of bacterial numbers in the organs and assessment of the health condition of the mice. The distribution and cellular localization of Listeria in the airways was assessed by immunocytochemistry and confocal and electron microscopy. The differential susceptibility of inbred mouse strains to airway infections with L. monocytogenes could be assigned to the major virulence factor listeriolysin O. Resistant C57BL/6 mice were not affected by the two listerial strains. In contrast, BALB/c and DBA/2 mice showed differential susceptibility towards L. monocytogenes EGDe and attenuated bacteria, with all the mice being killed by the wild-type bacteria but rarely by the variant that secretes a listeriolysin of only 10% activity of that of the wild-type toxin. Thus, listeriolysin is a decisive factor for differential susceptibility against Listeria. After i.t. application, bacteria were predominantly localized in the peribronchiolar space and invaded alveolar macrophages but rarely lung epithelial cells. Dissemination from the lung into the deep organs started almost immediately after application, although a pulmonary bacterial reservoir remained during the first 4 days.
小鼠李斯特菌病是理解宿主与病原体相互作用的一个范例。单核细胞增生李斯特菌引起的气道感染,尽管在早发型新生儿李斯特菌病中是一个严重问题,但目前在动物模型中尚未得到详细研究。在此,报告了BALB/c、DBA/2和C57BL/6小鼠对强毒单核细胞增生李斯特菌EGDe和减毒变体单核细胞增生李斯特菌EGD hlyW491A(pERL3-CMVGFP)气管内感染的易感性。通过测定器官中的细菌数量和评估小鼠的健康状况来表征感染过程。通过免疫细胞化学、共聚焦显微镜和电子显微镜评估李斯特菌在气道中的分布和细胞定位。近交系小鼠品系对单核细胞增生李斯特菌气道感染的不同易感性可归因于主要毒力因子李斯特菌溶血素O。抗性C57BL/6小鼠不受这两种李斯特菌菌株的影响。相比之下,BALB/c和DBA/2小鼠对单核细胞增生李斯特菌EGDe和减毒细菌表现出不同的易感性,所有小鼠都被野生型细菌杀死,但很少被分泌仅为野生型毒素活性10%的李斯特菌溶血素的变体杀死。因此,李斯特菌溶血素是对李斯特菌不同易感性的决定性因素。气管内接种后,细菌主要定位于细支气管周围间隙,并侵入肺泡巨噬细胞,但很少侵入肺上皮细胞。尽管在最初4天肺部仍有细菌储存库,但接种后几乎立即开始从肺部扩散到深部器官。