Cargando…
Bioluminescence Production by Turnip Yellows Virus Infectious Clones: A New Way to Monitor Plant Virus Infection
We used the NanoLuc luciferase bioluminescent reporter system to detect turnip yellows virus (TuYV) in infected plants. For this, TuYV was genetically tagged by replacing the C-terminal part of the RT protein with full-length NanoLuc (TuYV-NL) or with the N-terminal domain of split NanoLuc (TuYV-N65...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692398/ https://www.ncbi.nlm.nih.gov/pubmed/36430165 http://dx.doi.org/10.3390/ijms232213685 |
_version_ | 1784837255740784640 |
---|---|
author | Boissinot, Sylvaine Ducousso, Marie Brault, Véronique Drucker, Martin |
author_facet | Boissinot, Sylvaine Ducousso, Marie Brault, Véronique Drucker, Martin |
author_sort | Boissinot, Sylvaine |
collection | PubMed |
description | We used the NanoLuc luciferase bioluminescent reporter system to detect turnip yellows virus (TuYV) in infected plants. For this, TuYV was genetically tagged by replacing the C-terminal part of the RT protein with full-length NanoLuc (TuYV-NL) or with the N-terminal domain of split NanoLuc (TuYV-N65-NL). Wild-type and recombinant viruses were agro-infiltrated in Nicotiana benthamiana, Montia perfoliata, and Arabidopsis thaliana. ELISA confirmed systemic infection and similar accumulation of the recombinant viruses in N. benthamiana and M. perfoliata but reduced systemic infection and lower accumulation in A. thaliana. RT-PCR analysis indicated that the recombinant sequences were stable in N. benthamiana and M. perfoliata but not in A. thaliana. Bioluminescence imaging detected TuYV-NL in inoculated and systemically infected leaves. For the detection of split NanoLuc, we constructed transgenic N. benthamiana plants expressing the C-terminal domain of split NanoLuc. Bioluminescence imaging of these plants after agro-infiltration with TuYV-N65-NL allowed the detection of the virus in systemically infected leaves. Taken together, our results show that NanoLuc luciferase can be used to monitor infection with TuYV. |
format | Online Article Text |
id | pubmed-9692398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96923982022-11-26 Bioluminescence Production by Turnip Yellows Virus Infectious Clones: A New Way to Monitor Plant Virus Infection Boissinot, Sylvaine Ducousso, Marie Brault, Véronique Drucker, Martin Int J Mol Sci Article We used the NanoLuc luciferase bioluminescent reporter system to detect turnip yellows virus (TuYV) in infected plants. For this, TuYV was genetically tagged by replacing the C-terminal part of the RT protein with full-length NanoLuc (TuYV-NL) or with the N-terminal domain of split NanoLuc (TuYV-N65-NL). Wild-type and recombinant viruses were agro-infiltrated in Nicotiana benthamiana, Montia perfoliata, and Arabidopsis thaliana. ELISA confirmed systemic infection and similar accumulation of the recombinant viruses in N. benthamiana and M. perfoliata but reduced systemic infection and lower accumulation in A. thaliana. RT-PCR analysis indicated that the recombinant sequences were stable in N. benthamiana and M. perfoliata but not in A. thaliana. Bioluminescence imaging detected TuYV-NL in inoculated and systemically infected leaves. For the detection of split NanoLuc, we constructed transgenic N. benthamiana plants expressing the C-terminal domain of split NanoLuc. Bioluminescence imaging of these plants after agro-infiltration with TuYV-N65-NL allowed the detection of the virus in systemically infected leaves. Taken together, our results show that NanoLuc luciferase can be used to monitor infection with TuYV. MDPI 2022-11-08 /pmc/articles/PMC9692398/ /pubmed/36430165 http://dx.doi.org/10.3390/ijms232213685 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Boissinot, Sylvaine Ducousso, Marie Brault, Véronique Drucker, Martin Bioluminescence Production by Turnip Yellows Virus Infectious Clones: A New Way to Monitor Plant Virus Infection |
title | Bioluminescence Production by Turnip Yellows Virus Infectious Clones: A New Way to Monitor Plant Virus Infection |
title_full | Bioluminescence Production by Turnip Yellows Virus Infectious Clones: A New Way to Monitor Plant Virus Infection |
title_fullStr | Bioluminescence Production by Turnip Yellows Virus Infectious Clones: A New Way to Monitor Plant Virus Infection |
title_full_unstemmed | Bioluminescence Production by Turnip Yellows Virus Infectious Clones: A New Way to Monitor Plant Virus Infection |
title_short | Bioluminescence Production by Turnip Yellows Virus Infectious Clones: A New Way to Monitor Plant Virus Infection |
title_sort | bioluminescence production by turnip yellows virus infectious clones: a new way to monitor plant virus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692398/ https://www.ncbi.nlm.nih.gov/pubmed/36430165 http://dx.doi.org/10.3390/ijms232213685 |
work_keys_str_mv | AT boissinotsylvaine bioluminescenceproductionbyturnipyellowsvirusinfectiousclonesanewwaytomonitorplantvirusinfection AT ducoussomarie bioluminescenceproductionbyturnipyellowsvirusinfectiousclonesanewwaytomonitorplantvirusinfection AT braultveronique bioluminescenceproductionbyturnipyellowsvirusinfectiousclonesanewwaytomonitorplantvirusinfection AT druckermartin bioluminescenceproductionbyturnipyellowsvirusinfectiousclonesanewwaytomonitorplantvirusinfection |