4.6 Article

Biological and Molecular Characterization of Two Closely Related Arepaviruses and Their Antagonistic Interaction in Nicotiana benthamiana

Journal

FRONTIERS IN MICROBIOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.755156

Keywords

infectious cDNA clone; pathological properties; viral accumulation; functional compatibility; virus-virus interactions; Potyviridae

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Funding

  1. National Natural Science Foundation of China [32060603, 31860487]

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The study investigated the characteristics, functional compatibility of viral elements, and interspecies interactions of two closely related viruses from Areca catechu in the model plant Nicotiana benthamiana. It was found that one of the viruses induced more severe symptoms and rapid virus multiplication, and that specific elements were necessary for replication and systemic infection. Additionally, one of the viruses effectively excluded the other in both coinfection and super-infection assays, advancing understanding of these related arepaviruses.
Previously, our group characterized two closely related viruses from Areca catechu, areca palm necrotic ringspot virus (ANRSV) and areca palm necrotic spindle-spot virus (ANSSV). These two viruses share a distinct genomic organization of leader proteases and represent the only two species of the newly established genus Arepavirus of the family Potyviridae. The biological features of the two viruses are largely unknown. In this study, we investigated the pathological properties, functional compatibility of viral elements, and interspecies interactions in the model plant, Nicotiana benthamiana. Using a newly obtained infectious clone of ANRSV, we showed that this virus induces more severe symptoms compared with ANSSV and that this is related to a rapid virus multiplication in planta. A series of hybrid viruses were constructed via the substitution of multiple elements in the ANRSV infectious clone with the counterparts of ANSSV. The replacement of either 5 '-UTR-HCPro1-HCPro2 or CI effectively supported replication and systemic infection of ANRSV, whereas individual substitution of P3-7K, 9K-NIa, and NIb-CP-3 '-UTR abolished viral infectivity. Finally, we demonstrated that ANRSV confers effective exclusion of ANSSV both in coinfection and super-infection assays. These results advance our understanding of fundamental aspects of these two distinct but closely related arepaviruses.

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