MicroRNA-7 Inhibits Rotavirus Replication by Targeting Viral NSP5 In Vivo and In Vitro

Rotavirus (RV) is the major causes of severe diarrhea in infants and young children under five years of age. There are no effective drugs for the treatment of rotavirus in addition to preventive live attenuated vaccine. Recent evidence demonstrates that microRNAs (miRNAs) can affect RNA virus replic...

Full description

Bibliographic Details
Main Authors: Yan Zhou, Linlin Chen, Jing Du, Xiaoqing Hu, Yuping Xie, Jinyuan Wu, Xiaochen Lin, Na Yin, Maosheng Sun, Hongjun Li
Format: Article
Language:English
Published: MDPI AG 2020-02-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/12/2/209
_version_ 1818252409521045504
author Yan Zhou
Linlin Chen
Jing Du
Xiaoqing Hu
Yuping Xie
Jinyuan Wu
Xiaochen Lin
Na Yin
Maosheng Sun
Hongjun Li
author_facet Yan Zhou
Linlin Chen
Jing Du
Xiaoqing Hu
Yuping Xie
Jinyuan Wu
Xiaochen Lin
Na Yin
Maosheng Sun
Hongjun Li
author_sort Yan Zhou
collection DOAJ
description Rotavirus (RV) is the major causes of severe diarrhea in infants and young children under five years of age. There are no effective drugs for the treatment of rotavirus in addition to preventive live attenuated vaccine. Recent evidence demonstrates that microRNAs (miRNAs) can affect RNA virus replication. However, the antiviral effect of miRNAs during rotavirus replication are largely unknown. Here, we determined that miR-7 is upregulated during RV replication and that it targets the RV NSP5 (Nonstructural protein 5). Results suggested that miR-7 affected viroplasm formation and inhibited RV replication by down-regulating RV NSP5 expression. Up-regulation of miR-7 expression is a common regulation method of different G-type RV-infected host cells. Then, we further revealed the antiviral effect of miR-7 in diarrhea suckling mice model. MiR-7 is able to inhibit rotavirus replication in vitro and in vivo. These data provide that understanding the role of cellular miR-7 during rotaviral replication may help in the identification of novel therapeutic small RNA molecule drug for anti-rotavirus.
first_indexed 2024-12-12T16:23:43Z
format Article
id doaj.art-3205225bdff540edb5c9eb4a7bf39856
institution Directory Open Access Journal
issn 1999-4915
language English
last_indexed 2024-12-12T16:23:43Z
publishDate 2020-02-01
publisher MDPI AG
record_format Article
series Viruses
spelling doaj.art-3205225bdff540edb5c9eb4a7bf398562022-12-22T00:18:56ZengMDPI AGViruses1999-49152020-02-0112220910.3390/v12020209v12020209MicroRNA-7 Inhibits Rotavirus Replication by Targeting Viral NSP5 In Vivo and In VitroYan Zhou0Linlin Chen1Jing Du2Xiaoqing Hu3Yuping Xie4Jinyuan Wu5Xiaochen Lin6Na Yin7Maosheng Sun8Hongjun Li9Institute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaInstitute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaInstitute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaInstitute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaInstitute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaInstitute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaInstitute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaInstitute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaInstitute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaInstitute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on severe Infectious Disease, Kunming 650118, ChinaRotavirus (RV) is the major causes of severe diarrhea in infants and young children under five years of age. There are no effective drugs for the treatment of rotavirus in addition to preventive live attenuated vaccine. Recent evidence demonstrates that microRNAs (miRNAs) can affect RNA virus replication. However, the antiviral effect of miRNAs during rotavirus replication are largely unknown. Here, we determined that miR-7 is upregulated during RV replication and that it targets the RV NSP5 (Nonstructural protein 5). Results suggested that miR-7 affected viroplasm formation and inhibited RV replication by down-regulating RV NSP5 expression. Up-regulation of miR-7 expression is a common regulation method of different G-type RV-infected host cells. Then, we further revealed the antiviral effect of miR-7 in diarrhea suckling mice model. MiR-7 is able to inhibit rotavirus replication in vitro and in vivo. These data provide that understanding the role of cellular miR-7 during rotaviral replication may help in the identification of novel therapeutic small RNA molecule drug for anti-rotavirus.https://www.mdpi.com/1999-4915/12/2/209rotavirusmicrorna 7non-structural protein 5gene replicationanti-viral
spellingShingle Yan Zhou
Linlin Chen
Jing Du
Xiaoqing Hu
Yuping Xie
Jinyuan Wu
Xiaochen Lin
Na Yin
Maosheng Sun
Hongjun Li
MicroRNA-7 Inhibits Rotavirus Replication by Targeting Viral NSP5 In Vivo and In Vitro
Viruses
rotavirus
microrna 7
non-structural protein 5
gene replication
anti-viral
title MicroRNA-7 Inhibits Rotavirus Replication by Targeting Viral NSP5 In Vivo and In Vitro
title_full MicroRNA-7 Inhibits Rotavirus Replication by Targeting Viral NSP5 In Vivo and In Vitro
title_fullStr MicroRNA-7 Inhibits Rotavirus Replication by Targeting Viral NSP5 In Vivo and In Vitro
title_full_unstemmed MicroRNA-7 Inhibits Rotavirus Replication by Targeting Viral NSP5 In Vivo and In Vitro
title_short MicroRNA-7 Inhibits Rotavirus Replication by Targeting Viral NSP5 In Vivo and In Vitro
title_sort microrna 7 inhibits rotavirus replication by targeting viral nsp5 in vivo and in vitro
topic rotavirus
microrna 7
non-structural protein 5
gene replication
anti-viral
url https://www.mdpi.com/1999-4915/12/2/209
work_keys_str_mv AT yanzhou microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro
AT linlinchen microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro
AT jingdu microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro
AT xiaoqinghu microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro
AT yupingxie microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro
AT jinyuanwu microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro
AT xiaochenlin microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro
AT nayin microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro
AT maoshengsun microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro
AT hongjunli microrna7inhibitsrotavirusreplicationbytargetingviralnsp5invivoandinvitro