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Cepharanthine analogs mining and genomes of Stephania accelerate anti-coronavirus drug discovery

Authors :
Liang Leng
Zhichao Xu
Bixia Hong
Binbin Zhao
Ya Tian
Can Wang
Lulu Yang
Zhongmei Zou
Lingyu Li
Ke Liu
Wanjun Peng
Jiangning Liu
Zhoujie An
Yalin Wang
Baozhong Duan
Zhigang Hu
Chuan Zheng
Sanyin Zhang
Xiaodong Li
Maochen Li
Zhaoyu Liu
Zenghao Bi
Tianxing He
Baimei Liu
Huahao Fan
Chi Song
Yigang Tong
Shilin Chen
Source :
Nature Communications, Vol 15, Iss 1, Pp 1-16 (2024)
Publication Year :
2024
Publisher :
Nature Portfolio, 2024.

Abstract

Abstract Cepharanthine is a secondary metabolite isolated from Stephania. It has been reported that it has anti-conronaviruses activities including severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). Here, we assemble three Stephania genomes (S. japonica, S. yunnanensis, and S. cepharantha), propose the cepharanthine biosynthetic pathway, and assess the antiviral potential of compounds involved in the pathway. Among the three genomes, S. japonica has a near telomere-to-telomere assembly with one remaining gap, and S. cepharantha and S. yunnanensis have chromosome-level assemblies. Following by biosynthetic gene mining and metabolomics analysis, we identify seven cepharanthine analogs that have broad-spectrum anti-coronavirus activities, including SARS-CoV-2, Guangxi pangolin-CoV (GX_P2V), swine acute diarrhoea syndrome coronavirus (SADS-CoV), and porcine epidemic diarrhea virus (PEDV). We also show that two other genera, Nelumbo and Thalictrum, can produce cepharanthine analogs, and thus have the potential for antiviral compound discovery. Results generated from this study could accelerate broad-spectrum anti-coronavirus drug discovery.

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
20411723 and 54990998
Volume :
15
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.4b8b0143e0e54990998a18de425e8370
Document Type :
article
Full Text :
https://doi.org/10.1038/s41467-024-45690-5