High levels of virus replication and an intense inflammatory response contribute to the severe pathology in lymphoid tissues caused by Newcastle disease virus genotype VIId

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• 作者：Zenglei Hu (1)
  Jiao Hu (1) (2)
  Shunlin Hu (1) (2)
  Qingqing Song (1)
  Pingyun Ding (1)
  Jie Zhu (1)
  Xiaowen Liu (1) (2)
  Xiaoquan Wang (1) (2)
  Xiufan Liu (1) (2)
  
  1. Animal Infectious Disease Laboratory ; School of Veterinary Medicine ; Yangzhou University ; 48 East Wenhui Road ; Yangzhou ; 225009 ; Jiangsu ; China
  2. Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses ; Yangzhou University ; Yangzhou ; Jiangsu ; China
  
• 刊名：Archives of Virology
• 出版年：2015
• 出版时间：March 2015
• 年：2015
• 卷：160
• 期：3
• 页码：639-648
• 全文大小：1,837 KB
• 参考文献：1. Alexander, DJ Newcastle disease, other avian paramyxoviruses, and pneumovirus infections. In: Saif, YM eds. (2003) Diseases of poultry. Iowa State University Press, Ames, pp. 63-87
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• 刊物类别：Biomedical and Life Sciences
• 刊物主题：Biomedicine
  Virology
  Medical Microbiology
  Infectious Diseases
  
• 出版者：Springer Wien
• ISSN：1432-8798

文摘

Some strains of Newcastle disease virus (NDV) genotype VIId cause more-severe tissue damage in lymphoid organs compared to other virulent strains. In this study, we aim to define the mechanism of this distinct pathological manifestation of genotype VII viruses. Pathology, virus replication, and the innate immune response in lymphoid tissues of chickens infected with two genotype VIId NDV strains (JS5/05 and JS3/05), genotype IX NDV F48E8 and genotype IV NDV Herts/33, were compared. Histopathologic examination showed that JS5/05 and JS3/05 produced more-severe lesions in the spleen and thymus, but these four virulent strains caused comparable mild lesions in the bursa. In addition, JS3/05 and JS5/05 replicated at significantly higher levels in the lymphatic organs than F48E8 and Herts/33. A microarray assay performed on the spleens of chickens infected with JS5/05 or Herts/33 revealed that JS5/05 elicited a more potent inflammatory response by increasing the number and expression levels of activated genes. Moreover, cytokine gene expression profiling showed that JS5/05 and JS3/05 induced a stronger cytokine response in lymphoid tissues compared to F48E8 and Herts/33. Taken together, our results indicate that the severe pathology in immune organs caused by genotype VIId NDV strains is associated with high levels of virus replication and an intense inflammatory response.