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纵向测温可确定 ESKAPEE 感染 BALB/c 小鼠模型的人道终点。

Longitudinal temperature measurement can determine humane endpoints in BALB/c mouse models of ESKAPEE infection.

机构信息

Veterinary Services Program, Center for Enabling Capabilities, Walter Reed Army Institute of Research, Silver Spring, MD, USA.

Wound Infections Department, Bacterial Diseases Branch, Center for Infectious Diseases Research, Walter Reed Army Institute of Research, Silver Spring, MD, USA.

出版信息

Virulence. 2023 Dec;14(1):2186331. doi: 10.1080/21505594.2023.2186331.

Abstract

Antimicrobial resistance (AMR) is a worldwide problem, which is driving more preclinical research to find new treatments and countermeasures for drug-resistant bacteria. However, translational models in the preclinical space have remained static for years. To improve animal use ethical considerations, we assessed novel methods to evaluate survival after lethal infection with ESKAPEE pathogens (, , , , , and ) in pulmonary models of infection. Consistent with published lung infection models often used for novel antimicrobial development, BALB/c mice were immunosuppressed with cyclophosphamide and inoculated intranasally with individual ESKAPEE pathogens or sterile saline. Observations were recorded at frequent intervals to determine predictive thresholds for humane endpoint decision-making. Internal temperature was measured via implanted IPTT300 microchips, and external temperature was measured using a non-contact, infrared thermometer. Additionally, clinical scores were evaluated based on animal appearance, behaviour, hydration status, respiration, and body weight. Internal temperature differences between survivors and non-survivors were statistically significant for , , , , and , and external temperature differences were statistically significant for , , , and . Internal temperature more precisely predicted mortality compared to external temperature, indicating that a threshold of 85ºF (29.4ºC) was 86.0% predictive of mortality and 98.7% predictive of survival. Based on our findings, we recommend future studies involving BALB/c mice ESKAPEE pathogen infection use temperature monitoring as a humane endpoint threshold.

摘要

抗菌药物耐药性(AMR)是一个全球性问题,促使更多的临床前研究寻找针对耐药细菌的新治疗方法和对策。然而,临床前领域的转化模型多年来一直保持不变。为了提高动物使用的伦理考虑,我们评估了新方法,以评估在感染性肺部模型中致命感染 ESKAPEE 病原体( 、 、 、 、 和 )后的存活情况。与经常用于新型抗菌药物开发的已发表的肺部感染模型一致,用环磷酰胺使 BALB/c 小鼠免疫抑制,并通过鼻腔内接种单独的 ESKAPEE 病原体或无菌盐水进行接种。频繁观察以确定用于人道终点决策的预测阈值。通过植入的 IPTT300 微芯片测量内部温度,并用非接触式红外温度计测量外部温度。此外,还根据动物的外观、行为、水合状态、呼吸和体重评估临床评分。对于 、 、 、 和 ,幸存者和非幸存者之间的内部温度差异具有统计学意义,对于 、 、 和 ,外部温度差异具有统计学意义。内部温度比外部温度更能准确预测死亡率,表明 85°F(29.4°C)的阈值对死亡率的预测准确率为 86.0%,对存活率的预测准确率为 98.7%。基于我们的发现,我们建议未来涉及 BALB/c 小鼠 ESKAPEE 病原体感染的研究使用温度监测作为人道终点阈值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/667b/10054282/0f37533bf77e/KVIR_A_2186331_F0001_OC.jpg

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