Sobotta Katharina, Bonkowski Katharina, Heydel Carsten, Henning Klaus, Menge Christian
Institute of Molecular Pathogenesis, Friedrich-Loeffler-Institut, Naumburger Strasse 96a, 07743 Jena, Germany.
Institute for Hygiene and Infectious Diseases of Animals, Justus-Liebig-University (JLU), Frankfurter Strasse 85-89, 35392 Giessen, Germany.
Pathogens. 2022 Nov 26;11(12):1422. doi: 10.3390/pathogens11121422.
Despite the high prevalence of in dairy herds and continuous shedding via milk by chronically infected cows, bovine milk is not recognized as a relevant source of human Q fever. We hypothesized that the bovine mammary gland epithelial cell line PS represents a suitable in vitro model for the identification of -strain-specific virulence properties that may account for this discrepancy. Fifteen strains were selected to represent different host species and multiple loci variable number of tandem repeat analysis (MLVA) genotypes (I, II, III and IV). The replication efficiencies of all strains were similar, even though strains of the MLVA-genotype II replicated significantly better than genotype I strains, and bovine and ovine isolates replicated better than caprine ones. Bovine milk isolates replicated with similar efficiencies to isolates from other bovine organs. One sheep isolate (Cb30/14, MLVA type I, isolated from fetal membranes) induced a remarkable up-regulation of IL-1β and TNF-α, whereas prototypic strains and bovine milk isolates tended to suppress pro-inflammatory responses. While infection with strain Nine Mile I rendered the cells partially refractory to re-stimulation with lipopolysaccharide, Cb30/14 exerted a selective suppressive effect which was restricted to IL-6 and TNF-α and spared IL-1β. PS cells support the replication of different strains of and respond in a strain-specific manner, but isolates from bovine milk did not display a common pattern, which distinguishes them from strains identified as a public health concern.
尽管Q热在奶牛群中普遍存在,且慢性感染的奶牛会通过乳汁持续排毒,但牛乳并未被视为人类Q热的相关传染源。我们推测,牛乳腺上皮细胞系PS是一种合适的体外模型,可用于鉴定可能导致这种差异的特定菌株毒力特性。选择了15株菌株,代表不同宿主物种以及多位点可变数目串联重复序列分析(MLVA)基因型(I、II、III和IV)。所有菌株的复制效率相似,尽管MLVA基因型II的菌株复制效率明显高于基因型I的菌株,并且牛和羊的分离株复制效率高于山羊分离株。牛乳分离株的复制效率与来自其他牛器官的分离株相似。一株绵羊分离株(Cb30/14,MLVA I型,从胎膜分离)诱导IL-1β和TNF-α显著上调,而原型菌株和牛乳分离株倾向于抑制促炎反应。虽然感染Nine Mile I菌株使细胞对脂多糖再次刺激部分产生抗性,但Cb30/14发挥了选择性抑制作用,仅限于IL-6和TNF-α,而对IL-1β无影响。PS细胞支持不同菌株的复制,并以菌株特异性方式做出反应,但牛乳分离株未表现出共同模式,这使其与被认定为公共卫生问题的菌株有所区别。