Department of Pathology, University of Georgia, Athens, GA 30602, USA.
Virology. 2010 Apr 10;399(2):280-9. doi: 10.1016/j.virol.2010.01.005. Epub 2010 Feb 2.
The direct transmission of highly pathogenic avian influenza (HPAI) viruses to humans in Eurasia and subsequent disease has sparked research efforts leading to better understanding of HPAI virus transmission and pathogenicity in mammals. There has been minimal focus on examining the capacity of circulating low pathogenic wild bird avian influenza viruses to infect mammals. We have utilized a mouse model for influenza virus infection to examine 28 North American wild bird avian influenza virus isolates that include the hemagglutinin subtypes H2, H3, H4, H6, H7, and H11. We demonstrate that many wild bird avian influenza viruses of several different hemagglutinin types replicate in this mouse model without adaptation and induce histopathologic lesions similar to other influenza virus infections but cause minimal morbidity. These findings demonstrate the potential of wild avian influenza viruses to directly infect mice without prior adaptation and support their potential role in emergence of pandemic influenza.
欧亚地区高致病性禽流感(HPAI)病毒直接传播给人类并随后引发疾病,这促使人们开展了研究工作,从而更好地了解了 HPAI 病毒在哺乳动物中的传播和致病性。人们很少关注循环的低致病性野生鸟类禽流感病毒感染哺乳动物的能力。我们利用流感病毒感染的小鼠模型,检测了 28 种北美的野生鸟类禽流感病毒分离株,这些病毒株包含血凝素亚型 H2、H3、H4、H6、H7 和 H11。我们证明,许多不同血凝素类型的野生鸟类禽流感病毒在没有适应的情况下在这种小鼠模型中复制,并诱导类似于其他流感病毒感染的组织病理学病变,但引起的发病率很低。这些发现表明,野生禽流感病毒有可能在没有事先适应的情况下直接感染小鼠,并支持它们在大流行性流感出现中的潜在作用。