Novel Experimental Mouse Model to Study the Pathogenesis and Therapy of Actinobacillus pleuropneumoniae Infection

被引:2
|
作者
Bui, Duc-Thang [1 ,2 ]
Lee, Yi-San [1 ,2 ]
Kuo, Tien-Fen [1 ]
Chen, Zeng-Weng [3 ]
Yang, Wen-Chin [1 ,2 ,4 ,5 ,6 ]
机构
[1] Acad Sinica, Agr Biotechnol Res Ctr, Taipei City 115, Taiwan
[2] Natl Taiwan Univ, Inst Biotechnol, Taipei City 106, Taiwan
[3] Agr Technol Res Inst, Anim Technol Res Ctr, Hsinchu 350, Miaoli, Taiwan
[4] Natl Taiwan Ocean Univ, Dept Life Sci, Keelung City 202, Taiwan
[5] China Med Univ, Grad Inst Integrated Med, Taichung 404, Taiwan
[6] Natl Chung Hsing Univ, Dept Life Sci, Taichung 404, Taiwan
来源
PATHOGENS | 2024年 / 13卷 / 05期
关键词
Actinobacillus pleuropneumoniae; clinical score; inflammation; lung; mouse model; pleuropneumonia; pulmonary bacterial infection; MICE;
D O I
10.3390/pathogens13050412
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Actinobacillus pleuropneumoniae (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.
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收藏
页数:10
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