Chou Li-Fang, Liu Yi-Chun, Yang Huang-Yu, Tian Ya-Chung, Lai Chih-Ho, Chang Ming-Yang, Hung Cheng-Chieh, Wang Tong-Hong, Hsu Shen-Hsing, Tsai Chung-Ying, Hung Pei-Yu, Yang Chih-Wei
Kidney Research Center, Chang Gung Memorial Hospital, Linkou,333, Taiwan.
Graduate Institute of Biomedical Sciences, Department of Microbiology and Immunology, Department of Biochemistry, Chang Gung University, Taoyuan, Taiwan.
Curr Res Microb Sci. 2024 Nov 26;8:100327. doi: 10.1016/j.crmicr.2024.100327. eCollection 2025.
Leptospirosis, a re-emerging zoonotic disease caused by spp., poses significant global health and veterinary challenges. Long-term colonization of renal tubules by in asymptomatic hosts highlights the need for sensitive detection methods. This study evaluates the chronic or latent infections in kidneys using a novel molecular approach to examine individual immune responses differences. Digital PCR strategies employing newly developed primer-probe sets targeting the flagellar gene were used to assess the presence of trace in infected murine kidneys and urine samples from laboratory-confirmed leptospirosis patients. RNA-based digital PCR detected leptospires in 58 % (targeting ) and 83 % (targeting ) of infected kidneys, demonstrating that the digital PCR strategy targeting the gene offers superior sensitivity. Notably, the newly developed -targeting assay detected as low as 20 fg of DNA, offering ten-fold greater sensitivity than traditional qPCR for trace detection. This allows for differential detection of species and facilitates monitoring of extremely low bacterial loads with greater sensitivity than conventional methods. We also observed regenerating renal tubules with mitosis and elevated cytokine expression in kidneys with transcriptionally active during chronic infection. This approach aids in identifying latent infections and offers insights into individual variations. Our research provides a powerful molecular tool for epidemiological studies and public health surveillance, contributing valuable insights into the prevalence and transmission dynamics of this pervasive zoonotic disease.
钩端螺旋体病是一种由钩端螺旋体属细菌引起的再度出现的人畜共患病,给全球健康和兽医领域带来了重大挑战。钩端螺旋体在无症状宿主的肾小管中长期定植,凸显了对灵敏检测方法的需求。本研究采用一种新颖的分子方法来评估肾脏中的慢性或潜伏性钩端螺旋体感染,以检验个体免疫反应差异。使用针对鞭毛基因开发的新型引物 - 探针组的数字PCR策略,来评估感染小鼠肾脏和实验室确诊的钩端螺旋体病患者尿液样本中微量钩端螺旋体的存在情况。基于RNA的数字PCR在58%(针对[具体基因1])和83%(针对[具体基因2])的感染肾脏中检测到钩端螺旋体,表明针对该基因的数字PCR策略具有更高的灵敏度。值得注意的是,新开发的针对[目标基因]的检测方法可检测低至20 fg的钩端螺旋体DNA,比传统定量PCR用于微量检测的灵敏度高十倍。这使得能够区分不同的钩端螺旋体物种,并以比传统方法更高的灵敏度监测极低的细菌载量。我们还观察到在慢性感染期间,肾脏中有有丝分裂的再生肾小管以及转录活跃的钩端螺旋体存在时细胞因子表达升高。这种方法有助于识别潜伏感染,并深入了解个体差异。我们的研究为流行病学研究和公共卫生监测提供了一个强大的分子工具,为这种普遍存在的人畜共患病的流行情况和传播动态提供了有价值的见解。