Isolation of influenza A(H3N2)v virus from pigs and characterization of its biological properties in pigs and mice

被引:0
|
作者
Seong-Hee Kim
Hee-Jeong Kim
Young-Hwa Jin
Jeong-Ji Yeoul
Kyoung-Ki Lee
Jae-Ku Oem
Myoung-Heon Lee
Choi-Kyu Park
机构
[1] Animal,Animal Disease Diagnostic Division
[2] Plant and Fisheries Quarantine and Inspection Agency,Department of Infectious Disease, College of Veterinary Medicine
[3] Kyungpook National University,undefined
来源
Archives of Virology | 2013年 / 158卷
关键词
Influenza; Reverse Transcription Polymerase Chain Reaction; H3N2 Virus; Hemagglutination Inhibition; Reassortant Virus;
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摘要
Recently, a novel reassortant virus, influenza A(H3N2)v [A(H3N2)v], was identified as the causative pathogen in 307 human cases of influenza in the United States. A(H3N2)v contains the matrix gene from the 2009 pandemic H1N1 (pH1N1) virus, while its other genes originate from H3N2 viruses with triple-reassorted internal genes. In this study, we isolated three A(H3N2)v viruses from commercial pigs in Korea that showed similarities with published human A(H3N2)v viruses in eight segment sequence alignments. After genetic characterization, the pathogenicity of one of these viruses was assessed in pigs and mice. Infection of pigs with this novel virus resulted in mild interstitial pneumonia with marked oronasal shedding of viral RNA for about 14 days. In mice, the virus replicated efficiently in the lungs; viral RNA was detected up to 9 days post-inoculation. However, the virus did not cause severe disease or death in mice, despite the administration of a high infectious dose (105.2 TCID50). This study demonstrates that A(H3N2)v causes a high morbidity rate with low virulence; however, global monitoring of A(H3N2)v outbreaks in mammals will be needed to determine whether this novel subtype will shift to a highly pathogenic virus.
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页码:2351 / 2357
页数:6
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