Jiao Yaqing, Cai Yuee, Zhang Yilin, Choy Ka-Tim, Cheng Ka-Man, Nicholls John M, Lam Pui-Kin, Yen Hui-Ling, Rainer Timothy H
Department of Emergency Medicine, Li Ka Shing Faculty of Medicine, School of Clinical Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
Lab Anim Res. 2025 Jun 4;41(1):16. doi: 10.1186/s42826-025-00248-4.
Community-acquired respiratory infections are a prevalent cause of sepsis. Current animal models simulate peritoneal rather than respiratory sepsis. This study sought to appraise an influenza model for its ability to develop sepsis.
Twenty-four six-week-old male BALB/c mice were intranasally inoculated with H1N1 strain A/PR/8/34 virus at 3.7 × 10, 3.7 × 10, 3.7 × 10, 3.7 × 10, 3.7 × 10, 3.7 × 10 median tissue culture infectious dose (TCID50) to acquire different levels of clinical severity. Murine Sepsis Score (MSS) was recorded daily over 14 days. Platelets, serum bilirubin and creatinine levels were measured to reflect coagulopathy, liver and renal dysfunction. These three parameters are from the Sequential Organ Failure Assessment (SOFA) score which is routinely used for monitoring human sepsis. The primary outcome is organ dysfunction.
Out of 24 infected mice, seven (29%) did not survive beyond 9 days. MSS predicted mortality with an AUC of 0.989 (95%CI: 0.978-1.000; P < 0.001). Liver and renal dysfunction were detected in one non-survived and six survived mice. Histological examination revealed inflammation in lung and liver but not kidney tissues.
This study demonstrates the potential of influenza to cause organ dysfunction, providing a basis for building a murine model specific for viral respiratory sepsis, and more closely simulating human viral sepsis.
社区获得性呼吸道感染是脓毒症的常见病因。目前的动物模型模拟的是腹腔脓毒症而非呼吸道脓毒症。本研究旨在评估一种流感模型引发脓毒症的能力。
将24只六周龄雄性BALB/c小鼠经鼻接种甲型H1N1流感病毒A/PR/8/34株,接种剂量分别为3.7×10、3.7×10、3.7×10、3.7×10、3.7×10、3.7×10半数组织培养感染剂量(TCID50),以获得不同程度的临床严重程度。在14天内每天记录小鼠脓毒症评分(MSS)。检测血小板、血清胆红素和肌酐水平,以反映凝血病、肝肾功能障碍。这三个参数来自序贯器官衰竭评估(SOFA)评分,该评分常用于监测人类脓毒症。主要结局是器官功能障碍。
在24只感染小鼠中,7只(29%)未存活超过9天。MSS对死亡率的预测曲线下面积为0.989(95%置信区间:0.978 - 1.000;P < 0.001)。在1只未存活和6只存活的小鼠中检测到肝肾功能障碍。组织学检查显示肺和肝组织有炎症,但肾组织无炎症。
本研究证明了流感导致器官功能障碍的可能性,为建立针对病毒性呼吸道脓毒症的小鼠模型提供了依据,且能更紧密地模拟人类病毒性脓毒症。