期刊
CELL COMMUNICATION AND SIGNALING
卷 16, 期 -, 页码 -出版社
BMC
DOI: 10.1186/s12964-018-0283-5
关键词
Transmissible gastroenteritis virus; IPEC-J2 cells; Transferrin receptor 1
类别
资金
- National Natural Science Foundation of China [31772777]
- Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions
BackgroundTransmissible gastroenteritis virus (TGEV), the etiologic agent of transmissible gastroenteritis, infects swine of all ages causing vomiting and diarrhea, in newborn piglets the mortality rate is near 100%. Intestinal epithelial cells are the primary target cells of TGEV. Transferrin receptor 1 (TfR1), which is highly expressed in piglets with anemia, may play a role in TGEV infection. However, the underlying mechanism of TGEV invasion remains largely unknown.ResultsOur study investigated the possibility that TfR1 can serve as a receptor for TGEV infection and enables the invasion and replication of TGEV. We observed that TGEV infection promoted TfR1 internalization, clustering, and co-localization with TfR1 early in infection, while TfR1 expression was significantly down-regulated as TGEV infection proceeded. TGEV infection and replication were inhibited by occluding TfR1 with antibodies or by decreasing TfR1 expression. TGEV infection increased in TGEV-susceptible ST or IPEC-J2 cell lines and TGEV-resistant Caco-2 cells when porcine TfR1 was over-expressed. Finally, we found that the TGEV S1 protein interacts with the extracellular region of TfR1, and that pre-incubating TGEV with a protein fragment containing the extracellular region of TfR1 blocked viral infection.ConclusionsOur results support the hypothesis that TfR1 is an additional receptor for TGEV and assists TGEV invasion and replication.
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