| Literature DB >> 28351707 |
Changbo Ou1, Qiuxia Wang2, Yan Yu3, Yanhong Zhang3, Jinyou Ma3, Xianghui Kong4, Xingyou Liu5.
Abstract
Both CCR5 and CXCR4 are important chemokine receptors and take vital role in migration, development and distribution of T cells, however, whether they will influence the process of T cell infiltration into bursa of Fabricius during infectious bursal disease virus (IBDV) infection is unclear. In the current study, CCR5 and CXCR4 antagonists, Maraviroc and AMD3100, were administrated into chickens inoculated with IBDV, and the gene levels of IBDV VP2, CCR5, CXCR4 and related cytokines were determined by real-time PCR. The results showed that large number of T cells began to migrate into the bursae on Day 3 post infection with IBDV and the mRNA of chemokine receptors CCR5 and CXCR4 began to increase on Day 1. Moreover, antagonist treatments have increased the VP2, CCR5 and CXCR4 gene transcriptions and influenced on the gene levels of IL-2, IL-6, IL-8, IFN-γ, TGF-β4, MHC-I and MDA5. In conclusion, the chemokine receptors CCR5 and CXCR4 might influence virus replication during IBDV infection and further study would focus on the interaction between chemokine receptors and their ligands.Entities:
Keywords: CCR5; CXCR4; Infectious bursal disease virus; T cell migration
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Year: 2017 PMID: 28351707 DOI: 10.1016/j.micpath.2017.03.031
Source DB: PubMed Journal: Microb Pathog ISSN: 0882-4010 Impact factor: 3.738