TY - JOUR
T1 - The rules in co-infection of multiple viruses across diverse lineages in a fungal host
AU - Duan, Jie
AU - Yao, Yuduo
AU - Xu, Jialing
AU - Zhang, Anmeng
AU - Kong, Xiaojing
AU - Lin, Yang
AU - Xie, Jiatao
AU - Cheng, Jiasen
AU - Fu, Yanping
AU - Chen, Tao
AU - Li, Bo
AU - Yu, Xiao
AU - Lyu, Xueliang
AU - Xiao, Xueqiong
AU - Sharon, Amir
AU - Kotta-Loizou, Ioly
AU - Jiang, Daohong
N1 - Publisher Copyright: Copyright © 2025 Duan et al.
PY - 2025/6
Y1 - 2025/6
N2 - Viruses, ubiquitous non-cellular organisms, pose significant threats to human health and to the agricultural productivity of both livestock and crops. Emerging evidence indicates that multiple viruses can infect a single host, and viral co-infection can exert a profound influence on host physiology. However, our understanding of the prevalence of co-infection and the compatibility of phylogenetically distant viruses is still limited. In this study, we surveyed 406 field strains of the plant fungal pathogen Botrytis cinerea and identified 76 mycoviruses. Strikingly, 404 strains were co-infected with two or more viruses, with some harboring up to 25 viruses simultaneously. We discerned significant preference patterns among viruses in their host. Specifically, we identified “one-to-one” and “two-to-one” rules, wherein one or two viruses could be used to reliably predict the presence or absence of other viruses in the same host, and validated these predicted rules by using five B. cinerea strains. Furthermore, through the RNA-sequencing approach, we uncovered B. cinerea genes associated with the differences caused by different sets of co-infecting viruses. These are implicated in integral components of membrane, transmembrane transporter activity, autophagy pathways, mitophagy pathway, fatty acid biosynthetic process, sphingolipid metabolism, and glycosphingolipid biosynthesis. Our findings underscore the high prevalence of co-infection by multiple viruses in a fungal host within a population and highlight compatibility dynamics among phylogenetically diverse viruses. These insights contribute to our understanding of viral ecology and hold promise for informing strategies to manage viral diseases effectively.
AB - Viruses, ubiquitous non-cellular organisms, pose significant threats to human health and to the agricultural productivity of both livestock and crops. Emerging evidence indicates that multiple viruses can infect a single host, and viral co-infection can exert a profound influence on host physiology. However, our understanding of the prevalence of co-infection and the compatibility of phylogenetically distant viruses is still limited. In this study, we surveyed 406 field strains of the plant fungal pathogen Botrytis cinerea and identified 76 mycoviruses. Strikingly, 404 strains were co-infected with two or more viruses, with some harboring up to 25 viruses simultaneously. We discerned significant preference patterns among viruses in their host. Specifically, we identified “one-to-one” and “two-to-one” rules, wherein one or two viruses could be used to reliably predict the presence or absence of other viruses in the same host, and validated these predicted rules by using five B. cinerea strains. Furthermore, through the RNA-sequencing approach, we uncovered B. cinerea genes associated with the differences caused by different sets of co-infecting viruses. These are implicated in integral components of membrane, transmembrane transporter activity, autophagy pathways, mitophagy pathway, fatty acid biosynthetic process, sphingolipid metabolism, and glycosphingolipid biosynthesis. Our findings underscore the high prevalence of co-infection by multiple viruses in a fungal host within a population and highlight compatibility dynamics among phylogenetically diverse viruses. These insights contribute to our understanding of viral ecology and hold promise for informing strategies to manage viral diseases effectively.
KW - co-infection
KW - compatibility
KW - ecology
KW - fungi
KW - virus
UR - http://www.scopus.com/inward/record.url?scp=105008833856&partnerID=8YFLogxK
U2 - 10.1128/mbio.00262-25
DO - 10.1128/mbio.00262-25
M3 - مقالة
C2 - 40391984
SN - 2161-2129
VL - 16
JO - mBio
JF - mBio
IS - 6
ER -