Abil Olifan Zewdie, Kundu Suman, Midon Leonardo Moura, Gomes-Solecki Maria
Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, United States of America.
PLoS Negl Trop Dis. 2025 May 30;19(5):e0013163. doi: 10.1371/journal.pntd.0013163. eCollection 2025 May.
Mice are slowly being accepted as alternative models for investigation of leptospiral infection. The strain often used to analyze sublethal disease (C3H/HeJ) expresses a hyporesponsive tlr4 gene in its cells and thus the model is deemed immunocompromised. To help resolve this scientific concern we compared infection of mice expressing competent tlr4 (C3H/HeN, C57BL6) versus tlr4 hyporesponsive mice (C3H/HeJ) with Leptospira interrogans serovar Copenhageni strain Fiocruz L1-130 over a period of two weeks. We found that the two mouse strains with a functional tlr4 gene (C3H/HeN and C57BL/6) developed clinical and molecular signs of leptospirosis less pronounced but not significantly different than tlr4 hyporesponsive C3H/HeJ, as quantified by weight loss, survival curves, presence of Leptospira 16S rRNA in blood and urine and burden of viable spirochetes in kidney as compared to the respective uninfected controls. Analysis of serologic immune factors in the three strains revealed increased IgM and IgG3, and a general absence of inflammatory markers at two weeks post infection. Our data suggests that TLR4 function is not sufficient to cause susceptibility to leptospirosis. We conclude that C3H/HeN and C57BL/6 are appropriate mouse models of sublethal leptospirosis.
小鼠正逐渐被接受为钩端螺旋体感染研究的替代模型。常用于分析亚致死性疾病的品系(C3H/HeJ)在其细胞中表达反应低下的tlr4基因,因此该模型被认为存在免疫缺陷。为帮助解决这一科学问题,我们在两周时间内比较了表达有功能的tlr4的小鼠(C3H/HeN、C57BL6)与tlr4反应低下的小鼠(C3H/HeJ)感染问号钩端螺旋体哥本哈根血清型菌株Fiocruz L1-130的情况。我们发现,与各自未感染的对照相比,通过体重减轻、生存曲线、血液和尿液中钩端螺旋体16S rRNA的存在以及肾脏中活螺旋体的负荷来量化,具有功能性tlr4基因的两种小鼠品系(C3H/HeN和C57BL/6)出现钩端螺旋体病的临床和分子体征,但不如tlr4反应低下的C3H/HeJ明显,差异无统计学意义。对这三种品系血清学免疫因子的分析显示,感染后两周IgM和IgG3增加,且一般不存在炎症标志物。我们的数据表明,TLR4功能不足以导致对钩端螺旋体病的易感性。我们得出结论,C3H/HeN和C57BL/6是亚致死性钩端螺旋体病的合适小鼠模型。