Maize catalases are recruited by a virus to modulate viral multiplication and infection

Author:

Tian Yiying12,Jiao Zhiyuan123,Qi Fangfang12,Ma Wendi12,Hao Yuming12,Wang Xinyu12,Xie Liyang12,Zhou Tao12ORCID,Fan Zaifeng12ORCID

Affiliation:

1. MARA‐Key Laboratory of Surveillance and Management for Plant Quarantine Pests, College of Plant Protection China Agricultural University Beijing China

2. Sanya Institute of China Agricultural University Sanya China

3. National Engineering Laboratory for Forest Tree Breeding, College of Biological Sciences and Technology Beijing Forestry University Beijing China

Abstract

AbstractGiven the detrimental effects of excessive reactive oxygen species (ROS) accumulation in plant cells, various antioxidant mechanisms have evolved to maintain cellular redox homeostasis, encompassing both enzymatic components (e.g., catalase, superoxide dismutase) and non‐enzymatic ones. Despite extensive research on the role of antioxidant systems in plant physiology and responses to abiotic stresses, the potential exploitation of antioxidant enzymes by plant viruses to facilitate viral infection remains insufficiently addressed. Herein, we demonstrate that maize catalases (ZmCATs) exhibited up‐regulated enzymatic activities upon sugarcane mosaic virus (SCMV) infection. ZmCATs played crucial roles in SCMV multiplication and infection by catalysing the decomposition of excess cellular H2O2 and promoting the accumulation of viral replication‐related cylindrical inclusion (CI) protein through interaction. Peroxisome‐localized ZmCATs were found to be distributed around SCMV replication vesicles in Nicotiana benthamiana leaves. Additionally, the helper component‐protease (HC‐Pro) of SCMV interacted with ZmCATs and enhanced catalase activities to promote viral accumulation. This study unveils a significant involvement of maize catalases in modulating SCMV multiplication and infection through interaction with two viral factors, thereby enhancing our understanding regarding viral strategies for manipulating host antioxidant mechanisms towards robust viral accumulation.

Funder

National key research and development program of China

Publisher

Wiley

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