Domínguez Andrea Vila, Ledesma Marta Carretero, Domínguez Carmen Infante, Cisneros José Miguel, Lepe Jose A, Smani Younes
Institute of Biomedicine of Seville, IBiS, University Hospital Virgen del Rocio/CSIC/University of Seville, 41013 Sevilla, Spain.
Clinical Unit of Infectious Diseases, Microbiology and Parasitology, University Hospital Virgen del Rocio/CSIC/University of Seville, 41013 Sevilla, Spain.
Trop Med Infect Dis. 2023 Jan 12;8(1):58. doi: 10.3390/tropicalmed8010058.
In 2019, the biggest listeriosis outbreak by (Lm) in the South of Spain was reported, resulting in the death of three patients from 207 confirmed cases. One strain, belonging to clonal complex 388 (Lm CC388), has been isolated. We aimed to determine the Lm CC388 virulence in comparison with other highly virulent clones such as Lm CC1 and Lm CC4, in vitro and in vivo. Four strains (Lm CC388, Lm CC1, Lm CC4 and ATCC 19115) were used. Attachment to human lung epithelial cells (A549 cells) by these strains was characterized by adherence and invasion assays. Their cytotoxicities to A549 cells were evaluated by determining the cells viability. Their hemolysis activity was determined also. A murine intravenous infection model using these was performed to determine the concentration of bacteria in tissues and blood. Lm CC388 interaction with A549 cells is non-significantly higher than that of ATCC 19115 and Lm CC1, and lower than that of Lm CC4. Lm CC388 cytotoxicity is higher than that of ATCC 19115 and Lm CC1, and lower than that of Lm CC4. Moreover, Lm CC388 hemolysis activity is lower than that of the Lm CC4 strain, and higher than that of Lm CC1. Finally, in the murine intravenous infection model by Lm CC388, higher bacterial loads in tissues and at similar levels of Lm CC4 were observed. Although a lower rate of mortality of patients during the listeriosis outbreak in Spain in 2019 has been reported, the Lm CC388 strain has shown a greater or similar pathogenicity level in vitro and in an animal model, like Lm CC1 and Lm CC4.
2019年,西班牙南部报告了由单核细胞增生李斯特菌(Lm)引发的最大规模李斯特菌病疫情,207例确诊病例中有3名患者死亡。已分离出一株属于克隆复合体388(Lm CC388)的菌株。我们旨在通过体外和体内实验,确定Lm CC388与其他高毒力克隆(如Lm CC1和Lm CC4)相比的毒力。使用了四株菌株(Lm CC388、Lm CC1、Lm CC4和ATCC 19115)。通过黏附与侵袭实验对这些菌株与人肺上皮细胞(A549细胞)的黏附情况进行了表征。通过测定细胞活力评估它们对A549细胞的细胞毒性。还测定了它们的溶血活性。利用这些菌株建立了小鼠静脉感染模型,以确定组织和血液中的细菌浓度。Lm CC388与A549细胞的相互作用略高于ATCC 19115和Lm CC1,但低于Lm CC4。Lm CC388的细胞毒性高于ATCC 19115和Lm CC1,但低于Lm CC4。此外,Lm CC388的溶血活性低于Lm CC4菌株,但高于Lm CC1。最后,在Lm CC388引发的小鼠静脉感染模型中,观察到组织中的细菌载量较高,且与Lm CC4处于相似水平。尽管据报道2019年西班牙李斯特菌病疫情期间患者的死亡率较低,但Lm CC388菌株在体外和动物模型中表现出了与Lm CC1和Lm CC4相似或更高的致病水平。