Compatibility of H9N2 avian influenza surface genes and 2009 pandemic H1N1 internal genes for transmission in the ferret model

被引:120
作者
Kimble, J. Brian [1 ,2 ]
Sorrell, Erin [1 ,2 ]
Shao, Hongxia [1 ,2 ]
Martin, Philip L. [3 ]
Perez, Daniel Roberto [1 ,2 ]
机构
[1] Univ Maryland, Dept Vet Med, College Pk, MD 20742 USA
[2] Univ Maryland, Virginia Maryland Reg Coll Vet Med, College Pk, MD 20742 USA
[3] NCI, Ctr Adv Preclin Res, Sci Applicat Int Corp, Frederick, MD 21702 USA
基金
美国国家卫生研究院; 美国食品与农业研究所;
关键词
TRIG cassette; preparedness; infection; pathology; ecology; A VIRUSES; HUMAN INFECTION; HEMAGGLUTININ; ORIGIN; PATHOGENESIS; REPLICATION; POULTRY;
D O I
10.1073/pnas.1108058108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In 2009, a novel H1N1 influenza (pH1N1) virus caused the first influenza pandemic in 40 y. The virus was identified as a triple reassortant between avian, swine, and human influenza viruses, highlighting the importance of reassortment in the generation of viruses with pandemic potential. Previously, we showed that a reassortant virus composed of wild-type avian H9N2 surface genes in a seasonal human H3N2 backbone could gain efficient respiratory droplet transmission in the ferret model. Here we determine the ability of the H9N2 surface genes in the context of the internal genes of a pH1N1 virus to efficiently transmit via respiratory droplets in ferrets. We generated reassorted viruses carrying the HA gene alone or in combination with the NA gene of a prototypical H9N2 virus in the background of a pH1N1 virus. Four reassortant viruses were generated, with three of them showing efficient respiratory droplet transmission. Differences in replication efficiency were observed for these viruses; however, the results clearly indicate that H9N2 avian influenza viruses and pH1N1 viruses, both of which have occasionally infected pigs, have the potential to reassort and generate novel viruses with respiratory transmission potential in mammals.
引用
收藏
页码:12084 / 12088
页数:5
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