Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, GA, United States.
Molecular Analytics R&D, GlaxoSmithKline Vaccines, Rockville, MD, United States.
Front Cell Infect Microbiol. 2022 Aug 16;12:873416. doi: 10.3389/fcimb.2022.873416. eCollection 2022.
Even with the COVID-19 pandemic, tuberculosis remains a leading cause of human death due to a single infectious agent. Until successfully treated, infected individuals may continue to transmit bacilli to contacts. As with other respiratory pathogens, such as SARS-CoV-2, modeling the process of person-to-person transmission will inform efforts to develop vaccines and therapies that specifically impede disease transmission. The ferret (), a relatively inexpensive, small animal has been successfully employed to model transmissibility, pathogenicity, and tropism of influenza and other respiratory disease agents. Ferrets can become naturally infected with and are closely related to badgers, well known in Great Britain and elsewhere as a natural transmission vehicle for bovine tuberculosis. Herein, we report results of a study demonstrating that within 7 weeks of intratracheal infection with a high dose (>5 x 10 CFU) of bacilli, ferrets develop clinical signs and pathological features similar to acute disease reported in larger animals, and ferrets infected with very-high doses (>5 x 10 CFU) develop severe signs within two to four weeks, with loss of body weight as high as 30%. Natural transmission of this pathogen was also examined. Acutely-infected ferrets transmitted bacilli to co-housed naïve sentinels; most of the sentinels tested positive for in nasal washes, while several developed variable disease symptomologies similar to those reported for humans exposed to an active tuberculosis patient in a closed setting. Transmission was more efficient when the transmitting animal had a well-established acute infection. The findings support further assessment of this model system for tuberculosis transmission including the testing of prevention measures and vaccine efficacy.
即使在 COVID-19 大流行期间,结核病仍然是单一感染源导致人类死亡的主要原因。在成功治疗之前,受感染的个体可能会继续将细菌传播给接触者。与 SARS-CoV-2 等其他呼吸道病原体一样,对人际传播过程进行建模将有助于开发专门阻碍疾病传播的疫苗和疗法。雪貂()是一种相对便宜、体型较小的动物,已成功用于模拟流感和其他呼吸道疾病病原体的传染性、致病性和嗜性。雪貂可以自然感染 ,并且与獾密切相关,獾在英国和其他地方是众所周知的牛结核病的天然传播媒介。在此,我们报告了一项研究的结果,该研究表明,在通过气管内感染高剂量(>5 x 10 CFU)的 细菌后 7 周内,雪貂会出现类似于在较大动物中报告的急性疾病的临床症状和病理特征,而感染高剂量(>5 x 10 CFU)的雪貂在两到四周内会出现严重症状,体重下降高达 30%。还研究了这种病原体的自然传播。急性感染的雪貂将 细菌传播给共同饲养的未感染哨兵;大多数哨兵在鼻腔冲洗液中检测到 呈阳性,而一些哨兵则出现了类似于在封闭环境中暴露于活动性肺结核患者的人类所报告的可变疾病症状。当传播动物有明确的急性感染时,传播效率更高。这些发现支持进一步评估该结核病传播模型系统,包括测试预防措施和疫苗的功效。