New Insights into the Host-Pathogen Interaction of Mycoplasma gallisepticum and Avian Metapneumovirus in Tracheal Organ Cultures of Chicken

被引:8
|
作者
Rueger, Nancy [1 ]
Sid, Hicham [2 ]
Meens, Jochen [3 ]
Szostak, Michael P. [4 ]
Baumgaertner, Wolfgang [5 ]
Bexter, Frederik [1 ]
Rautenschlein, Silke [1 ]
机构
[1] Univ Vet Med Hannover, Clin Poultry, D-30559 Hannover, Germany
[2] Tech Univ Munich, TUM Sch Life Sci Weihenstephan, Reprod Biotechnol, D-85354 Munich, Germany
[3] Univ Vet Med Hannover, Ctr Infect Med, Inst Microbiol, D-30559 Hannover, Germany
[4] Univ Vet Med Vienna, Inst Microbiol, Dept Pathobiol, A-1210 Vienna, Austria
[5] Univ Vet Med Hannover, Dept Pathol, D-30559 Hannover, Germany
关键词
avian metapneumovirus; Mycoplasma gallisepticum; TOC; co-infection; innate immunity; interferon; INFLUENZA-A VIRUS; NITRIC-OXIDE; IN-VITRO; RESPIRATORY PATHOGENS; MOLECULAR-DETECTION; SUBTYPE-A; EX-VIVO; INFECTION; COINFECTION; POULTRY;
D O I
10.3390/microorganisms9112407
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Respiratory pathogens are a health threat for poultry. Co-infections lead to the exacerbation of clinical symptoms and lesions. Mycoplasma gallisepticum (M. gallispeticum) and Avian Metapneumovirus (AMPV) are two avian respiratory pathogens that co-circulate worldwide. The knowledge about the host-pathogen interaction of M. gallispeticum and AMPV in the chicken respiratory tract is limited. We aimed to investigate how co-infections affect the pathogenesis of the respiratory disease and whether the order of invading pathogens leads to changes in host-pathogen interaction. We used chicken tracheal organ cultures (TOC) to investigate pathogen invasion and replication, lesion development, and selected innate immune responses, such as interferon (IFN) alpha, inducible nitric oxide synthase (iNOS) and IFN lambda mRNA expression levels. We performed mono-inoculations (AMPV or M. gallispeticum) or dual-inoculations in two orders with a 24-h interval between the first and second pathogen. Dual-inoculations compared to mono-inoculations resulted in more severe host reactions. Pre-infection with AMPV followed by M. gallispeticum resulted in prolonged viral replication, more significant innate immune responses, and lesions (p < 0.05). AMPV as the secondary pathogen impaired the bacterial attachment process. Consequently, the M. gallispeticum replication was delayed, the innate immune response was less pronounced, and lesions appeared later. Our results suggest a competing process in co-infections and offer new insights in disease processes.
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页数:16
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