Antiviral Activity of PD-L1 and PD-L4, Type 1 Ribosome Inactivating Proteins from Leaves of <i>Phytolacca dioica</i> L. in the Pathosystem <i>Phaseolus vulgaris–</i>Tobacco Necrosis Virus (TNV)

Using the pathosystem <i>Phaseolus vulgaris</i>–tobacco necrosis virus (TNV), we demonstrated that PD-L1 and PD-L4, type-1 ribosome inactivating proteins (RIPs) from leaves of <i>Phytolacca dioica</i> L., possess a strong antiviral activity. This activity was exerted both whe...

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Bibliographic Details
Main Authors: Daniela Bulgari, Nicola Landi, Sara Ragucci, Franco Faoro, Antimo Di Maro
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/12/8/524
Description
Summary:Using the pathosystem <i>Phaseolus vulgaris</i>–tobacco necrosis virus (TNV), we demonstrated that PD-L1 and PD-L4, type-1 ribosome inactivating proteins (RIPs) from leaves of <i>Phytolacca dioica</i> L., possess a strong antiviral activity. This activity was exerted both when the RIPs and the virus were inoculated together in the same leaf and when they were inoculated or applied separately in the adaxial and abaxial leaf surfaces. This suggests that virus inhibition would mainly occur inside plant cells at the onset of infection. Histochemical studies showed that both PD-L1 and PD-L4 were not able to induce oxidative burst and cell death in treated leaves, which were instead elicited by inoculation of the virus alone. Furthermore, when RIPs and TNV were inoculated together, no sign of H<sub>2</sub>O<sub>2</sub> deposits and cell death were detectable, indicating that the virus could have been inactivated in a very early stage of infection, before the elicitation of a hypersensitivity reaction. In conclusion, the strong antiviral activity is likely exerted inside host cells as soon the virus disassembles to start translation of the viral genome. This activity is likely directed towards both viral and ribosomal RNA, explaining the almost complete abolition of infection when virus and RIP enter together into the cells.
ISSN:2072-6651