Hypericin Inhibit Alpha-Coronavirus Replication by Targeting 3CL Protease

The porcine epidemic diarrhea virus (PEDV) is an <i>Alphacoronavirus</i> (α-CoV) that causes high mortality in infected piglets, resulting in serious economic losses in the farming industry. Hypericin is a dianthrone compound that has been shown as an antiviral activity on several viruse...

Full description

Bibliographic Details
Main Authors: Yue Zhang, Huijie Chen, Mengmeng Zou, Rick Oerlemans, Changhao Shao, Yudong Ren, Ruili Zhang, Xiaodan Huang, Guangxing Li, Yingying Cong
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/13/9/1825
_version_ 1797516917606449152
author Yue Zhang
Huijie Chen
Mengmeng Zou
Rick Oerlemans
Changhao Shao
Yudong Ren
Ruili Zhang
Xiaodan Huang
Guangxing Li
Yingying Cong
author_facet Yue Zhang
Huijie Chen
Mengmeng Zou
Rick Oerlemans
Changhao Shao
Yudong Ren
Ruili Zhang
Xiaodan Huang
Guangxing Li
Yingying Cong
author_sort Yue Zhang
collection DOAJ
description The porcine epidemic diarrhea virus (PEDV) is an <i>Alphacoronavirus</i> (α-CoV) that causes high mortality in infected piglets, resulting in serious economic losses in the farming industry. Hypericin is a dianthrone compound that has been shown as an antiviral activity on several viruses. Here, we first evaluated the antiviral effect of hypericin in PEDV and found the viral replication and egression were significantly reduced with hypericin post-treatment. As hypericin has been shown in SARS-CoV-2 that it is bound to viral 3CLpro, we thus established a molecular docking between hypericin and PEDV 3CLpro using different software and found hypericin bound to 3CLpro through two pockets. These binding pockets were further verified by another docking between hypericin and PEDV 3CLpro pocket mutants, and the fluorescence resonance energy transfer (FRET) assay confirmed that hypericin inhibits the PEDV 3CLpro activity. Moreover, the alignments of α-CoV 3CLpro sequences or crystal structure revealed that the pockets mediating hypericin and PEDV 3CLpro binding were highly conserved, especially in transmissible gastroenteritis virus (TGEV). We then validated the anti-TGEV effect of hypericin through viral replication and egression. Overall, our results push forward that hypericin was for the first time shown to have an inhibitory effect on PEDV and TGEV by targeting 3CLpro, and it deserves further attention as not only a pan-anti-α-CoV compound but potentially also as a compound of other coronaviral infections.
first_indexed 2024-03-10T07:08:31Z
format Article
id doaj.art-49bd8419c8104e0e86e27e79b75d8b86
institution Directory Open Access Journal
issn 1999-4915
language English
last_indexed 2024-03-10T07:08:31Z
publishDate 2021-09-01
publisher MDPI AG
record_format Article
series Viruses
spelling doaj.art-49bd8419c8104e0e86e27e79b75d8b862023-11-22T15:38:33ZengMDPI AGViruses1999-49152021-09-01139182510.3390/v13091825Hypericin Inhibit Alpha-Coronavirus Replication by Targeting 3CL ProteaseYue Zhang0Huijie Chen1Mengmeng Zou2Rick Oerlemans3Changhao Shao4Yudong Ren5Ruili Zhang6Xiaodan Huang7Guangxing Li8Yingying Cong9Veterinary Pathology Laboratory, College of Veterinary Medicine, Heilongjiang Key Laboratory for Animal and Comparative Medicine, Northeast Agricultural University, Harbin 150030, ChinaVeterinary Pathology Laboratory, College of Veterinary Medicine, Heilongjiang Key Laboratory for Animal and Comparative Medicine, Northeast Agricultural University, Harbin 150030, ChinaVeterinary Pathology Laboratory, College of Veterinary Medicine, Heilongjiang Key Laboratory for Animal and Comparative Medicine, Northeast Agricultural University, Harbin 150030, ChinaDepartment of Drug Design, University of Groningen, 9713 AV Groningen, The NetherlandsVeterinary Pathology Laboratory, College of Veterinary Medicine, Heilongjiang Key Laboratory for Animal and Comparative Medicine, Northeast Agricultural University, Harbin 150030, ChinaDepartment of Computer Science and Technology, College of Electrical and Information Technology, Northeast Agricultural University, Harbin 150030, ChinaVeterinary Pathology Laboratory, College of Veterinary Medicine, Heilongjiang Key Laboratory for Animal and Comparative Medicine, Northeast Agricultural University, Harbin 150030, ChinaVeterinary Pathology Laboratory, College of Veterinary Medicine, Heilongjiang Key Laboratory for Animal and Comparative Medicine, Northeast Agricultural University, Harbin 150030, ChinaVeterinary Pathology Laboratory, College of Veterinary Medicine, Heilongjiang Key Laboratory for Animal and Comparative Medicine, Northeast Agricultural University, Harbin 150030, ChinaVeterinary Pathology Laboratory, College of Veterinary Medicine, Heilongjiang Key Laboratory for Animal and Comparative Medicine, Northeast Agricultural University, Harbin 150030, ChinaThe porcine epidemic diarrhea virus (PEDV) is an <i>Alphacoronavirus</i> (α-CoV) that causes high mortality in infected piglets, resulting in serious economic losses in the farming industry. Hypericin is a dianthrone compound that has been shown as an antiviral activity on several viruses. Here, we first evaluated the antiviral effect of hypericin in PEDV and found the viral replication and egression were significantly reduced with hypericin post-treatment. As hypericin has been shown in SARS-CoV-2 that it is bound to viral 3CLpro, we thus established a molecular docking between hypericin and PEDV 3CLpro using different software and found hypericin bound to 3CLpro through two pockets. These binding pockets were further verified by another docking between hypericin and PEDV 3CLpro pocket mutants, and the fluorescence resonance energy transfer (FRET) assay confirmed that hypericin inhibits the PEDV 3CLpro activity. Moreover, the alignments of α-CoV 3CLpro sequences or crystal structure revealed that the pockets mediating hypericin and PEDV 3CLpro binding were highly conserved, especially in transmissible gastroenteritis virus (TGEV). We then validated the anti-TGEV effect of hypericin through viral replication and egression. Overall, our results push forward that hypericin was for the first time shown to have an inhibitory effect on PEDV and TGEV by targeting 3CLpro, and it deserves further attention as not only a pan-anti-α-CoV compound but potentially also as a compound of other coronaviral infections.https://www.mdpi.com/1999-4915/13/9/1825α-CoVPEDVhypericin3CL proteaseTGEV
spellingShingle Yue Zhang
Huijie Chen
Mengmeng Zou
Rick Oerlemans
Changhao Shao
Yudong Ren
Ruili Zhang
Xiaodan Huang
Guangxing Li
Yingying Cong
Hypericin Inhibit Alpha-Coronavirus Replication by Targeting 3CL Protease
Viruses
α-CoV
PEDV
hypericin
3CL protease
TGEV
title Hypericin Inhibit Alpha-Coronavirus Replication by Targeting 3CL Protease
title_full Hypericin Inhibit Alpha-Coronavirus Replication by Targeting 3CL Protease
title_fullStr Hypericin Inhibit Alpha-Coronavirus Replication by Targeting 3CL Protease
title_full_unstemmed Hypericin Inhibit Alpha-Coronavirus Replication by Targeting 3CL Protease
title_short Hypericin Inhibit Alpha-Coronavirus Replication by Targeting 3CL Protease
title_sort hypericin inhibit alpha coronavirus replication by targeting 3cl protease
topic α-CoV
PEDV
hypericin
3CL protease
TGEV
url https://www.mdpi.com/1999-4915/13/9/1825
work_keys_str_mv AT yuezhang hypericininhibitalphacoronavirusreplicationbytargeting3clprotease
AT huijiechen hypericininhibitalphacoronavirusreplicationbytargeting3clprotease
AT mengmengzou hypericininhibitalphacoronavirusreplicationbytargeting3clprotease
AT rickoerlemans hypericininhibitalphacoronavirusreplicationbytargeting3clprotease
AT changhaoshao hypericininhibitalphacoronavirusreplicationbytargeting3clprotease
AT yudongren hypericininhibitalphacoronavirusreplicationbytargeting3clprotease
AT ruilizhang hypericininhibitalphacoronavirusreplicationbytargeting3clprotease
AT xiaodanhuang hypericininhibitalphacoronavirusreplicationbytargeting3clprotease
AT guangxingli hypericininhibitalphacoronavirusreplicationbytargeting3clprotease
AT yingyingcong hypericininhibitalphacoronavirusreplicationbytargeting3clprotease