Gene Knockdown in Human Rhinovirus 1B Using 2'-OMe-modified siRNAs Results in the Reactivation of the Interferon Response.
- Author:
Guang Cheng XIE
1
;
Qing ZHANG
1
;
Li Li PANG
2
;
Dan Di LI
1
;
Miao JIN
1
;
Hui Ying LI
1
;
Zi Qian XU
1
;
Xiang Yu KONG
1
;
Hong WANG
1
;
Shan LU
3
;
Zhao Jun DUAN
1
Author Information
- Publication Type:Journal Article
- MeSH: Gene Knockdown Techniques; HeLa Cells; Humans; Interferons; physiology; RNA, Small Interfering; Rhinovirus; Virus Replication
- From: Biomedical and Environmental Sciences 2016;29(2):137-142
- CountryChina
- Language:English
- Abstract: The aim of this study was to investigate the knockdown efficiency of 2'-O-methylated (2'-OMe)-modified small interfering RNAs (siRNAs) on human rhinovirus 1B (HRV1B) replication and the interferon response. Thus, 24 2'-OMe-modified siRNAs were designed to target HRV1B. The RNA levels of HRV1B, Toll-like receptor 3, melanoma differentiation-associated gene 5, retinoic acid inducible gene-I, and interferons were determined in HRV1B-infected HeLa and BEAS-2B epithelial cells transfected with 2'-OMe-modified siRNAs. The results revealed that all 2'-OMe-modified siRNAs interfered with the replication of HRV1B in a cell-specific and transfection efficiency-dependent manner. Viral activation of Toll-like receptor 3, melanoma differentiation-associated gene 5, retinoic acid inducible gene-I, and the interferon response was detected. In conclusion, the 2'-OMe-modified siRNAs used in this study could interfere with HRV1B replication, possibly leading to the reactivation of the interferon response.