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Bordetella bronchiseptica promotes adherence, colonization, and cytotoxicity of Streptococcus suis in a porcine precision-cut lung slice model

机译:Bordetella Bronchiseptica在猪精密切割肺切片模型中促进链球菌Suis的粘附性,殖民和细胞毒性

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Bordetella (B.) bronchiseptica and Streptococcus (S.) suis are major pathogens in pigs, which are frequently isolated from co-infections in the respiratory tract and contribute to the porcine respiratory disease complex (PRDC). Despite the high impact of co-infections on respiratory diseases of swine (and other hosts), very little is known about pathogen-pathogen-host interactions and the mechanisms of pathogenesis. In the present study, we established a porcine precision-cut lung slice (PCLS) model to analyze the effects of B. bronchiseptica infection on adherence, colonization, and cytotoxic effects of S. suis . We hypothesized that induction of ciliostasis by a clinical isolate of B. bronchiseptica may promote subsequent infection with a virulent S. suis serotype 2 strain. To investigate this theory, we monitored the ciliary activity by light microscopy, measured the release of lactate dehydrogenase, and calculated the number of PCLS-associated bacteria. To study the role of the pore-forming toxin suilysin (SLY) in S. suis -induced cytotoxicity, we included a SLY-negative isogenic mutant and the complemented mutant strain. Furthermore, we analyzed infected PCLS by histopathology, immunofluorescence microscopy, and field emission scanning electron microscopy. Our results showed that pre-infection with B. bronchiseptica promoted adherence, colonization, and, as a consequence of the increased colonization, the cytotoxic effects of S. suis , probably by reduction of the ciliary activity. Moreover, cytotoxicity induced by S. suis is strictly dependent on the presence of SLY. Though the underlying molecular mechanisms remain to be fully clarified, our results clearly support the hypothesis that B. bronchiseptica paves the way for S. suis infection.
机译:Bordetella(B.)支气管肌肉和链球菌(S.)Suis是猪的主要病原体,其经常从呼吸道中的共感染中分离出来并有助于猪呼吸道疾病复合物(PRDC)。尽管有效地对猪(等宿主等宿主)的呼吸系统疾病影响很高,但仍然少于病原体 - 病原体 - 宿主相互作用和发病机制。在本研究中,我们建立了一种猪精密切割肺切片(PCLS)模型,用于分析B.Bronchiseptica感染对S. suis对粘附,定植和细胞毒性作用的影响。我们假设通过B.Bronchiseptica的临床分离物诱导Ciliostasis可以促进随后用毒性的S. suis血清型2株的感染。为了研究该理论,我们通过光学显微镜监测睫状体活性,测量乳酸脱氢酶的释放,并计算了PCLS相关细菌的数量。为了研究孔形成毒素的作用肠贯毒素(综合)在S. suis-诱导的细胞毒性中,我们包括含有含量的含有含量的突变突变体和互补的突变菌株。此外,我们通过组织病理学,免疫荧光显微镜和场发射扫描电子显微镜分析了感染的PCL。我们的研究结果表明,Bronchiseptica促进了粘附,定植,并且由于增加了S. suis的细胞毒性作用,可能通过降低睫状体活性而导致粘附,定植,并且可能是通过降低睫状体活性的影响。此外,S. suis诱导的细胞毒性严格依赖于含量存在。虽然潜在的分子机制仍然是完全澄清的,但我们的结果清楚地支持B. Bronchiseptica为S. suis感染铺平道路的假设。

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