Forero Catalina, Ritter Jana M, Seixas Josilene Nascimento, Coleman-McCray JoAnn D, Brake Marie, Condrey Jillian A, Tansey Cassandra, Welch Stephen R, Genzer Sarah C, Spengler Jessica R
Comparative Medicine Branch, Division of Scientific Resources, Centers for Disease Control and Prevention, Atlanta, GA 30329, USA.
Infectious Diseases Pathology Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA 30329, USA.
Pathogens. 2022 Aug 10;11(8):898. doi: 10.3390/pathogens11080898.
Syrian hamsters are a key animal model of SARS-CoV-2 and other respiratory viruses and are useful for the evaluation of associated medical countermeasures. Delivery of an infectious agent or intervention to the respiratory tract mirrors natural routes of exposure and allows for the evaluation of clinically relevant therapeutic administration. The data to support instillation or inoculation volumes are important both for optimal experimental design and to minimize or avoid effects of diluent alone, which may compromise both data interpretation and animal welfare. Here we investigate four intranasal (IN) instillation volumes in hamsters (50, 100, 200, or 400 µL). The animals were monitored daily, and a subset were serially euthanized at one of four pre-determined time-points (1, 3, 7, and 14 days post-instillation). Weight, temperature, oxygen saturation, CBC, radiographs, and respiratory tissue histopathology were assessed to determine changes associated with instillation volume alone. With all the delivery volumes, we found no notable differences between instilled and non-instilled controls in all of the parameters assessed, except for histopathology. In the animals instilled with 200 or 400 µL, inflammation associated with foreign material was detected in the lower respiratory tract indicating that higher volumes may result in aspiration of nasal and/or oropharyngeal material in a subset of animals, resulting in IN instillation-associated histopathology.
叙利亚仓鼠是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)和其他呼吸道病毒的关键动物模型,有助于评估相关医学应对措施。将感染因子或干预措施递送至呼吸道可模拟自然暴露途径,并有助于评估临床相关的治疗给药方式。支持滴鼻或接种体积的数据对于优化实验设计以及尽量减少或避免仅稀释剂的影响非常重要,因为稀释剂可能会影响数据解读和动物福利。在此,我们研究了仓鼠的四种鼻内(IN)滴注体积(50、100、200或400微升)。每天对动物进行监测,并在四个预定时间点之一(滴注后1、3、7和14天)对一部分动物进行连续安乐死。评估体重、体温、血氧饱和度、全血细胞计数、X光片和呼吸组织组织病理学,以确定仅与滴注体积相关的变化。在所有滴注体积下,除组织病理学外,我们发现滴注组和未滴注对照组在所有评估参数上均无显著差异。在滴注200或400微升的动物中,在下呼吸道检测到与异物相关的炎症,这表明较高的滴注体积可能会导致一部分动物出现鼻腔和/或口咽物质误吸,从而导致与鼻内滴注相关的组织病理学变化。