Lao Guangjie, Ma Kaixiong, Qiu Ziwen, Qi Wenbao, Liao Ming, Li Huanan
National Avian Influenza Para-Reference Laboratory (Guangzhou), South China Agricultural University, Guangzhou, China.
Key Laboratory of Zoonosis, Ministry of Agriculture and Rural Affairs, Guangzhou, China.
Front Vet Sci. 2022 Feb 24;9:849178. doi: 10.3389/fvets.2022.849178. eCollection 2022.
H9N2 avian influenza viruses (AIVs) continuously cross the species barrier to infect mammalians and are repeatedly transmitted to humans, posing a significant threat to public health. Importantly, some H9N2 AIVs were found to cause lethal infection in mice, but little is known about the viral infection dynamics . To analyze the real-time infection dynamics, we described the generation of a mouse-lethal recombinant H9N2 AIV, an influenza reporter virus (V-NanoLuc virus) carrying a NanoLuc gene in the non-structural (NS) segment, which was available for imaging. Although attenuated for replication in MDCK cells, V-NanoLuc virus showed similar pathogenicity and replicative capacity in mice to its parental virus. Bioluminescent imaging of the V-NanoLuc virus permitted successive observations of viral infection and replication in infected mice, even following the viral clearance of a sublethal infection. Moreover, V-NanoLuc virus was severely restricted by the K627E mutation in PB2, as infected mice showed little weight loss and a low level of bioluminescence. In summary, we have preliminarily established a visualized tool that enables real-time observation of the infection and replication dynamics of H9N2 AIV in mice, which contributes to further understanding the mechanisms underlying the pathogenic enhancement of H9N2 AIV to mice.
H9N2禽流感病毒(AIV)不断跨越物种屏障感染哺乳动物,并多次传播给人类,对公共卫生构成重大威胁。重要的是,发现一些H9N2 AIV可在小鼠中引起致死性感染,但对病毒感染动态了解甚少。为了分析实时感染动态,我们描述了一种小鼠致死性重组H9N2 AIV的产生,这是一种在非结构(NS)片段中携带纳米荧光素酶(NanoLuc)基因的流感报告病毒(V-NanoLuc病毒),可用于成像。尽管V-NanoLuc病毒在MDCK细胞中的复制能力减弱,但其在小鼠中的致病性和复制能力与其亲本病毒相似。V-NanoLuc病毒的生物发光成像能够连续观察受感染小鼠体内的病毒感染和复制情况,即使在亚致死性感染的病毒清除后也是如此。此外,V-NanoLuc病毒受到PB2基因K627E突变的严重限制,因为受感染的小鼠体重减轻很少且生物发光水平较低。总之,我们初步建立了一种可视化工具,能够实时观察H9N2 AIV在小鼠体内的感染和复制动态,这有助于进一步了解H9N2 AIV对小鼠致病性增强的潜在机制。