首页> 外文期刊>Journal of applied microbiology >Tissue culture assays using Caco-2 cell line differentiate virulent fromnon-virulent Listeria monocytogenes strains
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Tissue culture assays using Caco-2 cell line differentiate virulent fromnon-virulent Listeria monocytogenes strains

机译:使用Caco-2细胞系进行组织培养测定可将毒力与非毒力单核细胞增生李斯特菌菌株区分开来

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Within the group of Listeria sp., only L. monacytogenes is pathogenic for humans and numerous studies oft. monocytogenes strains have described non-virulent isolates. In this study, the potential value of two tissue culture assays (TCA) was analysed to ascertain the virulence properties oft. monacytogenes strains, initially typed for virulence using the immunocompromised mouse model (ICMM). The first assay assessed both the penetration into, and multiplication within, Caco-2 cells (PM assay); the second was a plaque-forming assay (PF assay). All the clinical isolates (nine strains) were virulent in both TCA. Conversely, all the non-pathogenic species (seven strains) were non-virulent in PM and PF assays. Compared with the virulence obtained in the ICMM with 29 Listeria strains, including 12 non-virulent L. monocytogenes strains, the sensitivity of both TCA was equal to 1. Specificity was 0.89 and 0.84 for the PF and PM assays, respectively. However, a study of strains exhibiting virulence differences in three other in vivo virulence models showed that ICMM only detected highly virulent strains. The specificity of the PF test could, therefore, be higher, and close to that obtained by the enumeration of viable bacteria in the spleen of mice infected by subcutaneous injection in the footpad and by intravenous injection. Taken together, this study confirms the existence of low-virulence L. monocytogenes strains and shows that the virulence status of some non-clinical L. monocytogenes isolates depends on the virulence models used. The data suggest that the PF assay could be used as a primary test to evaluate the virulence of Listeria strains in order to reduce the cost of testing all strains in vivo.
机译:在李斯特菌属的组中,只有单核细胞增生李斯特菌对人类有致病性,并且进行了许多研究。单核细胞增生菌株已经描述了非毒力分离株。在这项研究中,分析了两种组织培养测定法(TCA)的潜在价值,以确定其毒力特性。最初使用免疫受损小鼠模型(ICMM)进行毒力鉴定的单核细胞增生菌株。第一项测定评估了Caco-2细胞的渗透性和在其中的增殖(PM测定);第二个是噬斑形成测定(PF测定)。所有临床分离株(9株)在两个TCA中均具有毒性。相反,在PM和PF分析中,所有非致病性物种(七个菌株)均无毒。与由29种李斯特菌菌株(包括12种非毒性单核细胞增生李斯特菌)在ICMM中获得的毒力相比,两种TCA的敏感性均等于1。对于PF和PM分析,特异性分别为0.89和0.84。但是,一项对在其他三个体内毒力模型中表现出毒力差异的毒株的研究表明,ICMM仅检测到高毒力的毒株。因此,PF测试的特异性可能更高,并且接近于通过足底皮下注射和静脉内注射感染的小鼠脾脏中活细菌计数所获得的特异性。综上所述,该研究证实了低毒力单核细胞增生李斯特菌菌株的存在,并表明某些非临床单核细胞增生李斯特氏菌分离株的毒力状态取决于所用的毒力模型。数据表明,PF测定法可用作评估李斯特菌菌株毒力的主要测试方法,以降低体内测试所有菌株的成本。

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