Overexpression of bovine leukemia virus receptor SLC7A1/CAT1 enhances cellular susceptibility to BLV infection on luminescence syncytium induction assay (LuSIA)

被引:6
作者
Sato, Hirotaka [1 ,2 ]
Bai, Lanlan [2 ,3 ]
Borjigin, Liushiqi [1 ,2 ]
Aida, Yoko [1 ,2 ]
机构
[1] RIKEN, Cluster Sci Technol & Innovat Hub, Nakamura Lab, Baton Zone Program, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[2] RIKEN, Virus Infect Dis Unit, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[3] RIKEN, Ctr Adv Photon, Photon Control Technol Team, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
基金
日本学术振兴会;
关键词
Bovine leukemia virus; Receptor; CAT1; Luminescence syncytium induction assay; Infection; CELLS; ASSOCIATION; CATTLE; MILK;
D O I
10.1186/s12985-020-01324-y
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bovine leukemia virus (BLV) causes enzootic bovine leukosis, the most common neoplastic disease in cattle. We previously reported the development and protocol of the luminescence syncytium induction assay (LuSIA), a method for evaluating BLV infectivity based on CC81-GREMG cells. These cells form syncytia expressing enhanced green fluorescent protein when co-cultured with BLV-infected cells. Recently, we confirmed CAT1/SLC7A1 functions as a receptor of BLV. Here, we focused on CAT1/SLC7A1 to increase the sensitivity of LuSIA. We constructed a bovine CAT1-expressing plasmid and established a new CC81-GREMG-derived reporter cell line highly expressing bovine CAT1 (CC81-GREMG-CAT1). The new LuSIA protocol using CC81-GREMG-CAT1 cells measures cell-to-cell infectivity and cell-free infectivity of BLV faster and with greater sensitivity than the previous protocol using CC81-GREMG. The new LuSIA protocol is quantitative and more sensitive than the previous assay based on CC81-GREMG cells and will facilitate the development of several new BLV assays.
引用
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页数:6
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