Luoyang Key Laboratory of Live Carrier Biomaterial and Animal Disease Prevention and Control, College of Animal Science and Technology, Henan University of Science and Technology, Luoyang, China.
Can J Vet Res. 2020 Oct;84(4):302-309.
serovar Typhimurium (. Typhimurium) is one of the most significant zoonotic pathogens that poses a threat to humans. Previous studies have identified that -secreted effector K3 (SseK3) is a novel translated and secreted protein of . Typhimurium. The objective of this study was to determine whether deletion of the gene can attenuate the virulence of . Typhimurium. To do this, we constructed an deletion mutant using the double-exchange allele of the suicide plasmid pRE112Δ and assessed the virulence and intracellular proliferation of the mutant. The deletion mutant exhibited adhesion and invasion properties similar to those of wild-type (WT) . Typhimurium, although the virulence and intracellular proliferation of the mutant were significantly reduced compared to that of the WT strain. Furthermore, the observed increase in the median lethal dose (LD) reflects a decrease in the pathogenicity of the deletion mutant in a murine model. In summary, we concluded that disruption of can attenuate the intracellular proliferation and reduce the virulence of . Typhimurium.
鼠伤寒血清型(. Typhimurium)是对人类构成威胁的最重要的人畜共患病病原体之一。先前的研究已经确定,-分泌效应物 K3(SseK3)是鼠伤寒血清型的一种新型翻译和分泌蛋白。本研究旨在确定缺失 基因是否可以减弱鼠伤寒血清型的毒力。为此,我们使用自杀质粒 pRE112Δ 的双交换等位基因构建了一个 缺失突变体,并评估了突变体的毒力和细胞内增殖。与野生型(WT)鼠伤寒血清型相比,虽然突变体的粘附和侵袭特性与 WT 相似,但突变体的毒力和细胞内增殖明显降低。此外,观察到的半数致死剂量(LD)中位数增加反映了在小鼠模型中, 缺失突变体的致病性降低。总之,我们得出结论,破坏 可以减弱鼠伤寒血清型的细胞内增殖并降低其毒力。