National and Regional Joint Engineering Laboratory for Medicament of Zoonosis Prevention and Control, China.
Vet Microbiol. 2013 Oct 25;166(3-4):386-93. doi: 10.1016/j.vetmic.2013.06.019. Epub 2013 Jul 9.
Our previous studies have illustrated three strains of duck-origin H5N1 highly pathogenic avian influenza viruses (HPAIVs) had varying levels of pathogenicity in ducks (Sun et al., 2011). However, the host immune response of ducks infected with those of H5N1 HPAIVs was unclear. Here, we compared viral distribution and mRNA expression of immune-related genes in ducks following infection with the two HPAIV (A/Duck/Guangdong/212/2004, DK212 and A/Duck/Guangdong/383/2008, DK383). DK383 could replicate in the tested tissue of ducks (brain, spleen, lungs, cloacal bursa, kidney, and pancreas) more rapid and efficiently than DK212 at 1 and 2 days post-inoculation. Quantitative real-time PCR analysis showed that the expression levels of TLR3, IL-6, IL-8, and MHC class II in brains were higher than those of respective genes in lungs during the early stage of post infection. Furthermore, the expression levels of IL-6 and IL-8 in the brain of ducks following infection with DK383 were remarkably higher than those of ducks infected with DK212, respectively. Our results suggest that the shift in the H5N1 HPAIVs to increased virulence in ducks may be associated with efficient and rapid replication of the virus, accompanied by early destruction of host immune responses. These data are helpful to understand the underlying mechanism of the different outcome of H5N1 HPAIVs infection in ducks.
我们之前的研究表明,三种鸭源 H5N1 高致病性禽流感病毒(HPAIV)在鸭中具有不同程度的致病性(Sun 等人,2011)。然而,感染这些 H5N1 HPAIV 的鸭的宿主免疫反应尚不清楚。在这里,我们比较了感染两种 HPAIV(A/Duck/Guangdong/212/2004,DK212 和 A/Duck/Guangdong/383/2008,DK383)后鸭的病毒分布和免疫相关基因的 mRNA 表达。DK383 在感染后 1 天和 2 天比 DK212 更快、更有效地在鸭的测试组织(大脑、脾脏、肺脏、腔上囊、肾脏和胰腺)中复制。定量实时 PCR 分析表明,在感染后的早期,大脑中 TLR3、IL-6、IL-8 和 MHC 类 II 的表达水平高于肺部的相应基因。此外,感染 DK383 的鸭脑中的 IL-6 和 IL-8 表达水平明显高于感染 DK212 的鸭。我们的研究结果表明,H5N1 HPAIV 在鸭中的毒力增加可能与病毒的有效和快速复制有关,同时伴有宿主免疫反应的早期破坏。这些数据有助于了解 H5N1 HPAIV 感染鸭的不同结果的潜在机制。