Back to Search Start Over

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

Authors :
Leng, Liang
Xu, Zhichao
Hong, Bixia
Zhao, Binbin
Tian, Ya
Wang, Can
Yang, Lulu
Zou, Zhongmei
Li, Lingyu
Liu, Ke
Peng, Wanjun
Liu, Jiangning
An, Zhoujie
Wang, Yalin
Duan, Baozhong
Hu, Zhigang
Zheng, Chuan
Zhang, Sanyin
Li, Xiaodong
Li, Maochen
Source :
Nature Communications; 2/23/2024, Vol. 15 Issue 1, p1-16, 16p
Publication Year :
2024

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. Cepharanthine is a secondary metabolite isolated from Stephania with a variety of medicinal properties. Here, the authors assembled three Stephania genomes, propose cepharanthine biosynthetic pathway, and assess the antiviral potential of cepharanthine-related metabolites. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
15
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
175830765
Full Text :
https://doi.org/10.1038/s41467-024-45690-5