Division of Avian Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, The Chinese Academy of Agricultural Sciences, Harbin 150069, PR China.
Division of Avian Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, The Chinese Academy of Agricultural Sciences, Harbin 150069, PR China; Jiangsu Co-Innovation Center for the Prevention and Control of Important Animal Infectious Disease and Zoonose, Yangzhou University, Yangzhou, 225009, PR China.
Vet Microbiol. 2019 Jan;228:32-38. doi: 10.1016/j.vetmic.2018.11.009. Epub 2018 Nov 16.
Avian metapneumovirus (aMPV), which has been reported in many countries, causes an acute upper respiratory tract disease in chickens and turkeys. Although aMPV was first detected in China in 1999, there has been no further effort to isolate and characterize the aMPV subtype B (aMPV/B) from field outbreaks. In the present study, we used Vero cells to culture a viral strain, LN16, isolated from chickens with swollen head syndrome. The results of RT-PCR, indirect immunofluorescent antibody, and G gene sequence analyses confirmed that strain LN16 corresponds to aMPV/B. We amplified and sequenced the complete genome of strain LN16 and found it to be 13,513 nucleotides in length. Nine viral protein genes of the strain were between 93.2% and 98.4% identical to those of the pathogenic field isolate VCO3/60616. However, insertions and deletions were detected in the intergenic regions. Animal experiments showed that 72.7% of chickens infected with strain LN16 had excess mucus, nasal discharge, and inflammation in the lungs and turbinate. In addition, 27.2% of chickens infected with LN16 shed progeny virions. Viral tissue distribution analysis showed that aMPV could be detected in the turbinate and occasionally in immune organs. This is the first report of the isolation of aMPV/B in China and the first complete genome sequence of aMPV/B from chicken. These findings enrich the epidemiological data on aMPV and may contribute to the development of effective measures to prevent its further spread in China.
禽偏肺病毒(aMPV)已在许多国家报道,可引起鸡和火鸡的急性上呼吸道疾病。虽然 aMPV 于 1999 年在中国首次被发现,但此后并未进一步努力从田间暴发中分离和鉴定 aMPV 亚型 B(aMPV/B)。在本研究中,我们使用 Vero 细胞培养了从患有头部肿胀综合征的鸡中分离出的病毒株 LN16。RT-PCR、间接免疫荧光抗体和 G 基因序列分析的结果证实 LN16 株对应于 aMPV/B。我们扩增和测序了 LN16 株的完整基因组,发现其长度为 13513 个核苷酸。该株的 9 种病毒蛋白基因与致病性田间分离株 VCO3/60616 的相似度在 93.2%至 98.4%之间。然而,在基因间区检测到插入和缺失。动物实验表明,感染 LN16 株的 72.7%的鸡出现过度黏液、鼻漏和肺部和鼻甲炎症。此外,27.2%的 LN16 感染鸡会排出子代病毒。病毒组织分布分析表明,aMPV 可在鼻甲中检测到,偶尔在免疫器官中也可检测到。这是中国首次分离到 aMPV/B 株,也是首次从鸡中获得 aMPV/B 的完整基因组序列。这些发现丰富了 aMPV 的流行病学数据,可能有助于制定有效的措施来防止其在中国的进一步传播。