畜牧兽医学报 ›› 2025, Vol. 56 ›› Issue (11): 5743-5757.doi: 10.11843/j.issn.0366-6964.2025.11.032

• 预防兽医 • 上一篇    下一篇

新发肠致病性重组新型禽冠状病毒的分离和鉴定

张玉杰(), 刘红祥, 宋姗姗, 薄智勇, 阮国宏, 赵成龙, 楚电峰, 杨雪, 杜元钊, 刘东*()   

  1. 青岛易邦生物工程有限公司 兽医公共卫生安全全国重点实验室, 青岛 266114
  • 收稿日期:2025-02-06 出版日期:2025-11-23 发布日期:2025-11-27
  • 通讯作者: 刘东 E-mail:ddzhang2008-2009@163.com;liudong@yebio.com
  • 作者简介:张玉杰(1986-),男,山东青岛人,兽医师,主要从事畜禽新发疫病的病原学研究,Tel:0532-85631119,E-mail:ddzhang2008-2009@163.com
  • 基金资助:
    山东省重点研发计划(竞争性创新平台)项目(2024CXPT082);2024年青岛市科技惠民示范专项(24-1-8-xdny-7-nsh)

Isolation and Identification of Novel Enteropathogenic Recombinant Avian Coronavirus

ZHANG Yujie(), LIU Hongxiang, SONG Shanshan, BO Zhiyong, RUAN Guohong, ZHAO Chenglong, CHU Dianfeng, YANG Xue, DU Yuanzhao, LIU Dong*()   

  1. State Key Laboratory of Veterinary Public Health and Safety, YEBIO Bio-engineering Co. Ltd. of Qingdao, Qingdao 266114, China
  • Received:2025-02-06 Online:2025-11-23 Published:2025-11-27
  • Contact: LIU Dong E-mail:ddzhang2008-2009@163.com;liudong@yebio.com

摘要:

2018年秋冬季以来,我国蛋鸡养殖地区新发了一种以开产蛋鸡产蛋下降和腹泻为主要特征的传染病,为查明该病的病因,作者进行了本试验。采集发病鸡肠道组织,在SPF鸡胚上连续盲传10代分离病原物;对分离毒株进行理化特性和血凝特性测定;利用设计的疑似病毒特异性引物,对提取的病毒核酸进行PCR检测、基因测序以及核苷酸同源性比对,根据比对结果设计引物获得病毒的全基因组核苷酸序列;以新型禽冠状病毒AvCoV/CH/SD/24株对SPF鸡、AA+白羽肉鸡和海兰蛋鸡进行攻毒,对发病SPF鸡肠道进行病理切片并用酶联免疫吸附试验(ELISA)测定攻毒后不同鸡血清中传染性支气管炎病毒抗体滴度。结果显示:成功分离获得4株新型禽冠状病毒AvCoV/CH/BZ/24、AvCoV/CH/JS/24、AvCoV/CH/SD/24、AvCoV/CH/HB/24,病毒无血凝活性。核酸检测结果显示,有4份样品鸡传染性支气管炎病毒NS1基因阳性,且N基因序列与数据库中鸡传染性支气管病毒相似性最高,S1基因序列与数据库中已有禽冠状病毒AvCoV/TZ/CA127/19株序列的相似性最高。全基因组扩增和测序结果显示,4株新型禽冠状病毒与2016年中国安徽省和2019年坦桑尼亚阿鲁沙发现并报道的两株禽冠状病毒全基因组核苷酸相似性高达97.1%~98.6%。系统发育分析表明,新型禽冠状病毒的S基因与类火鸡冠状病毒亲缘关系较近,处于同一进化分支的不同亚分支,而其它基因与GⅠ-19谱系传染性支气管炎病毒处于同一进化分支。动物实验表明,AvCoV/CH/SD/24株病毒能够引起SPF鸡腹泻,十二指肠绒毛脱落,绒毛顶端和黏膜固有层充血、出血,肾小管上皮细胞颗粒变性,间质充血,病毒主要通过泄殖腔排出体外,各脏器中以肠道和法氏囊的病毒载量最高,病毒不影响鸡的增重率;ELISA结果显示重组新型禽冠状病毒与鸡传染性支气管炎病毒具有血清学交叉反应;开产蛋鸡感染病毒后出现产蛋下降和腹泻,与临床发病一致。从蛋鸡产蛋下降和腹泻病例的肠道中分离获得的4株新型禽冠状病毒是类火鸡冠状病毒S基因与GⅠ-19谱系鸡传染性支气管炎病毒的重组病毒,能够引起鸡发生产蛋下降和腹泻。

关键词: 肠致病性, 重组新型禽冠状病毒, 腹泻, 产蛋下降

Abstract:

Since the autumn and winter of 2018, a newly emerged infectious disease characterized by decreased egg production and diarrhea in laying hens has been observed in China's poultry farming regions. To investigate the etiology of this condition. Intestinal tissue samples from affected chickens were collected and pathogenic agents were isolated through 10 consecutive blind passages in specific pathogen-free (SPF) chicken embryos. The isolated viral strain was characterized for physicochemical and hemagglutination properties. Suspected virus-specific primers were designed to perform PCR detegtion, gene sequencing and nucleotide homology analysis on the extracted viral nucleic acid. Based on the alignment result, primers were designed to obtain the whole genome nucleotide sequence of the virus. The novel avian coronavirus strain AvCoV/CH/SD/24 was used to challenge SPF chickens, AA+ white-feathered broilers, and Hy-Line laying hens. Intestinal tissues from infected SPF chickens were processed for histopathological sections and serum antibody titers against infectious bronchitis virus (IBV) in different chicken groups post-challenge were measured using enzyme-linked immunosorbent assay (ELISA). Four novel avian coronaviruses (AvCoV/CH/BZ/24, AvCoV/CH/JS/24, AvCoV/CH/SD/24 and AvCoV/CH/HB/24) were successfully isolated, these viruses exhibited no hemagglutinating activity.The results of nucleic acid detection showed that four samples tested positive for both the N and S1 genes of avian infectious bronchitis virus (IBV). The N gene sequences showed the highest homology with avian infectious bronchitis virus strains in the GenBank database, while the S1 gene sequences exhibited maximum identity with the avian coronavirus AvCoV/TZ/CA127/19. Whole genome amplification and sequencing revealed that the four novel avian coronaviruses demonstrated 97.1%-98.6% nucleotide homology with two previously reported avian coronavirus strains: one isolated from Anhui Province, China in 2016 and another from Arusha, Tanzania in 2019. Phylogenetic analysis revealed that the S gene of the novel avian coronavirus is closely related to a turkey coronavirus-like, forming distinct subclades within the same evolutionary branch, while its other genes clustered within the evolutionary branch of the GⅠ-19 lineage infectious bronchitis virus. Animal experiments demonstrated that the AvCoV/CH/SD/24 strain induced diarrhea in SPF chickens, accompanied by duodenal villus detachment, congestion and hemorrhage at the villus tips and lamina propria and granular degeneration of renal tubular epithelial cells with interstitial congestion. The virus was primarily excreted through the cloaca with the highest viral loads detected in the intestines and bursa of Fabricus among tested organs. Infection did not affect the weight gain rate of chickens. ELISA results indicated serological cross-reactivity between the recombinant novel avian coronavirus and infectious bronchitis virus. In laying hens, infection led to reduced egg production and diarrhea, which was consistent with the disease in the field. Four novel avian coronaviruses were isolated from the intestines of laying hens exhibiting egg production decline and diarrhea, these newly isolated avian coronaviruses are recombinant viruses capable of inducing egg production decline and diarrhea in chickens.

Key words: enteropathogenic, novel recombinant avian coronavirus, diarrhea, decline in egg production

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