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Recombinant Chicken Interferon-α Inhibits H9N2 Avian Influenza Virus Replication In Vivo by Oral Administration
被引:53
作者:
Meng, Shanshan
[1
,2
]
Yang, Limin
[1
]
Xu, Chongfeng
[1
,2
]
Qin, Zhuoming
[3
]
Xu, Huaiying
[3
]
Wang, Youling
[3
]
Sun, Lei
[1
]
Liu, Wenjun
[1
,4
]
机构:
[1] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100101, Peoples R China
[3] Shandong Acad Agr Sci, Inst Poultry Sci, Jinan, Peoples R China
[4] Chinese Acad Sci, Inst Microbiol, China Japan Joint Lab Mol Immunol & Mol Microbiol, Beijing 100101, Peoples R China
关键词:
BURSAL DISEASE VIRUS;
A VIRUSES;
SOUTHEASTERN CHINA;
ANTIVIRAL ACTIVITY;
NEWCASTLE-DISEASE;
GENE-EXPRESSION;
INFECTION;
EVOLUTION;
PATHOGENICITY;
PROFILES;
D O I:
10.1089/jir.2010.0123
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Chicken interferon-alpha (ChIFN-alpha) has been demonstrated to be an important cytokine in antiviral immunity. However, the preventive or therapeutic effect of ChIFN-alpha as an oral antiviral agent on avian influenza virus (AIV) infection has not been fully clarified in chickens systemically. In the present study, we investigated the anti-H9N2 AIV effect of ChIFN-alpha on a cohort of 7- and 33-day-old specific pathogen-free (SPF) chickens by oral administration. Results showed that both the ChIFN-alpha preventive and therapeutic groups exhibited significantly reduced viral load in trachea when compared with the virus-challenged control group. The therapeutic effect was better than the preventive effect on 7-day-old SPF chickens, which is opposite to 33-day-old SPF chickens. We speculated that T-dependent lymphocyte system of 33-day-old SPF chickens might be easier to be stimulated by ChIFN-alpha than that of 7-day-old SPF chickens. In addition, there was no side effect on the body weight of chickens treated with ChIFN-alpha. We also found that IFN-stimulated genes (ISGs) (2',5'-oligoadenylate synthetase and Mx1) were upregulated in groups treated by ChIFN-alpha and/or virus, indicating that these 2 ISGs not only participated in anti-AIV response in vivo but also could be induced by oral administration of ChIFN-alpha. The present study suggested that ChIFN-alpha could be used as a potential preventive and therapeutic antiviral agent against H9N2 AIV infection by oral administration.
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页码:533 / 538
页数:6
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