Bui Duc-Thang, Lee Yi-San, Kuo Tien-Fen, Chen Zeng-Weng, Yang Wen-Chin
Agricultural Biotechnology Research Center, Academia Sinica, Taipei City 115, Taiwan.
Institute of Biotechnology, National Taiwan University, Taipei City 106, Taiwan.
Pathogens. 2024 May 15;13(5):412. doi: 10.3390/pathogens13050412.
(APP) is a major cause of lung infections in pigs. An experimental mouse has the edge over pigs pertaining to the ease of experimental operation, disease study and therapy, abundance of genetic resources, and cost. However, it is a challenge to introduce APP into a mouse lung due to the small respiratory tract of mice and bacterial host tropism. In this study, an effective airborne transmission of APP serovar 1 (APP1) was developed in mice for lung infection. Consequently, APP1 infected BALB/c mice and caused 60% death within three days of infection at the indicated condition. APP1 seemed to enter the lung and, in turn, spread to other organs of the mice over the first 5 days after infection. Accordingly, APP1 damaged the lung as evidenced by its morphological and histological examinations. Furthermore, ampicillin fully protected mice against APP1 as shown by their survival, clinical symptoms, body weight loss, APP1 count, and lung damages. Finally, the virulence of two extra APP strains, APP2 and APP5, in the model was compared based on the survival rate of mice. Collectively, this study successfully established a fast and reliable mouse model of APP which can benefit APP research and therapy. Such a model is a potentially useful model for airway bacterial infections.
副猪嗜血杆菌(APP)是猪肺部感染的主要病因。实验小鼠在实验操作的便利性、疾病研究与治疗、丰富的遗传资源以及成本方面比猪更具优势。然而,由于小鼠呼吸道较小以及细菌宿主嗜性,将APP引入小鼠肺部具有挑战性。在本研究中,开发了一种在小鼠中有效的APP血清型1(APP1)空气传播方法用于肺部感染。因此,在所示条件下,APP1感染了BALB/c小鼠,并在感染后三天内导致60%的小鼠死亡。在感染后的前5天内,APP1似乎进入肺部,进而扩散到小鼠的其他器官。相应地,通过形态学和组织学检查证明APP1损害了肺部。此外,如小鼠的存活率、临床症状、体重减轻、APP1计数和肺部损伤所示,氨苄青霉素可完全保护小鼠免受APP1感染。最后,基于小鼠的存活率比较了另外两种APP菌株APP2和APP5在该模型中的毒力。总体而言,本研究成功建立了一种快速可靠的APP小鼠模型,这将有利于APP的研究和治疗。这样的模型是一种潜在有用的气道细菌感染模型。