Endogenous ZAP is associated with altered Zika virus infection phenotype

被引:1
|
作者
Le, Nguyen Phuong Khanh [1 ]
Singh, Prince Pal [1 ,2 ]
Sabir, Ahmad Jawad [3 ]
Trus, Ivan [4 ]
Karniychuk, Uladzimir [1 ]
机构
[1] Ohio State Univ, Coll Vet Med, Dept Vet Biosci, Columbus, OH 43210 USA
[2] Univ Saskatchewan, Sch Publ Hlth, Saskatoon, SK, Canada
[3] Univ Illinois, Coll Med, Dept Microbiol & Immunol, Chicago, IL USA
[4] Int Inst Mol & Cell Biol, Dioscuri Ctr RNA Prot Interact Human Hlth & Dis, Warsaw, Poland
基金
加拿大健康研究院;
关键词
Flavivirus; Zika virus; Zinc finger antiviral protein; ZAP; Interferon; RNA-seq; FINGER ANTIVIRAL PROTEIN; RNA HELICASE; DEFENSE;
D O I
10.1186/s12985-024-02557-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The zinc finger antiviral protein 1 (ZAP) has broad antiviral activity. ZAP is an interferon (IFN)-stimulated gene, which itself may enhance type I IFN antiviral response. In a previous study, Zika virus was identified as ZAP-resistant and not sensitive to ZAP antiviral activity. Here, we found that ZAP was associated with the inhibition of Zika virus in Vero cells, in the absence of a robust type I IFN system because Vero cells are deficient for IFN-alpha and -beta. Also, quantitative RNA-seq data indicated that endogenous ZAP is associated with altered global gene expression both in the steady state and during Zika virus infection. Further studies are warranted to elucidate this IFN-alpha and -beta independent anti-Zika virus activity and involvement of ZAP.
引用
收藏
页数:10
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