Screening of host genes regulated by ID1 and ID3 proteins during foot-and-mouth disease virus infection

•The knockout of ID1 or/and ID3 genes is beneficial to foot-and-mouth disease virus replication•There were a series of differentially expressed genes in ID gene knockout cell lines, and 17 of them were verified•Results are crucial for exploring the regulatory mechanism between ID1, ID3 gene and host...

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Veröffentlicht in:Virus research 2021-12, Vol.306, p.198597-198597, Article 198597
Hauptverfasser: Luo, Yingying, Wang, Guangxiang, Ren, Tingting, Zhang, Tianliang, Chen, Haotai, Li, Yanmin, Yin, Xiangping, Zhang, Zhidong, Sun, Yuefeng
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Sprache:eng
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Zusammenfassung:•The knockout of ID1 or/and ID3 genes is beneficial to foot-and-mouth disease virus replication•There were a series of differentially expressed genes in ID gene knockout cell lines, and 17 of them were verified•Results are crucial for exploring the regulatory mechanism between ID1, ID3 gene and host genes during FMDV infection Foot-and-mouth disease virus (FMDV) is an important pathogen that harms cloven-hoofed animals and has caused serious losses to livestock production since its discovery. Furthermore, inhibitor of DNA binding (ID) proteins have been thoroughly studied in tumorigenesis, differentiation and metastasis, but its role in viral infection is rarely known. In this study, three gene knockout cell lines ID1 KO, ID3 KO, ID1/3 KO were obtained based on BHK-21 cells. We found that ID1 and ID3 genes single or double knockout promote the replication of FMDV. Moreover, compared with negative control cells during virus infection, there were 551 up-regulated genes and 1222 down-regulated genes in the ID1 KO cell line; 916 up-regulated genes and 1845 down-regulated genes in the ID3 KO cell line; 810 up-regulated genes and 1566 down-regulated genes in ID1/3 KO cell line. Further genes expression patterns verification results also showed a good correlation between the data of RT-qRCR and RNA-seq. These findings provide a basis for studying the relevant mechanisms between host genes and ID genes during FMDV infection.
ISSN:0168-1702
1872-7492
DOI:10.1016/j.virusres.2021.198597