Binding immunoglobulin 2 functions as a proviral factor for potyvirus infections in Nicotiana benthamiana
Infection of viruses from the genera Bromovirus, Potyvirus, and Potexvirus in Nicotiana benthamiana induces significant up‐regulation of the genes that encode the HSP70 family, including binding immunoglobulin protein 2 (BiP2). Three up‐regulated genes were knocked down and infection assays with the...
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Published in | Molecular plant pathology Vol. 24; no. 2; pp. 179 - 187 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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England
John Wiley & Sons, Inc
01.02.2023
John Wiley and Sons Inc |
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Abstract | Infection of viruses from the genera Bromovirus, Potyvirus, and Potexvirus in Nicotiana benthamiana induces significant up‐regulation of the genes that encode the HSP70 family, including binding immunoglobulin protein 2 (BiP2). Three up‐regulated genes were knocked down and infection assays with these knockdown lines demonstrated the importance of the BiP2 gene for potyvirus infection but not for infection by the other tested viruses. Distinct symptoms of cucumber mosaic virus (CMV) and potato virus X (PVX) were observed in the BiP2 knockdown line at 10 days postagroinfiltration. Interestingly, following inoculation with either soybean mosaic virus (SMV) or pepper mottle virus (PepMoV) co‐expressing green fluorescent protein (GFP), neither crinkle symptoms nor GFP signals were observed in the BiP2 knockdown line. Subsequent reverse transcription‐quantitative PCR analysis demonstrated that knockdown of BiP2 resulted in a significant decrease of SMV and PepMoV RNA accumulation but not PVX or CMV RNA accumulation. Further yeast two‐hybrid and co‐immunoprecipitation analyses validated the interaction between BiP2 and nuclear inclusion protein b (NIb) of SMV. Together, our findings suggest the crucial role of BiP2 as a proviral host factor necessary for potyvirus infection. The interaction between BiP2 and NIb may be the critical factor determining susceptibility in N. benthamiana, but further studies are needed to elucidate the underlying mechanism.
Interaction between binding immunoglobulin protein 2 (BiP2) and NIb of potyvirus promotes virus infections, making BiP2 a good candidate for gene modification to generate a resistant cultivar against potyviruses. |
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AbstractList | Infection of viruses from the genera
Bromovirus, Potyvirus
, and
Potexvirus
in
Nicotiana benthamiana
induces significant up‐regulation of the genes that encode the HSP70 family, including binding immunoglobulin protein 2 (BiP2). Three up‐regulated genes were knocked down and infection assays with these knockdown lines demonstrated the importance of the
BiP2
gene for potyvirus infection but not for infection by the other tested viruses. Distinct symptoms of cucumber mosaic virus (CMV) and potato virus X (PVX) were observed in the
BiP2
knockdown line at 10 days postagroinfiltration. Interestingly, following inoculation with either soybean mosaic virus (SMV) or pepper mottle virus (PepMoV) co‐expressing green fluorescent protein (GFP), neither crinkle symptoms nor GFP signals were observed in the
BiP2
knockdown line. Subsequent reverse transcription‐quantitative PCR analysis demonstrated that knockdown of
BiP2
resulted in a significant decrease of SMV and PepMoV RNA accumulation but not PVX or CMV RNA accumulation. Further yeast two‐hybrid and co‐immunoprecipitation analyses validated the interaction between BiP2 and nuclear inclusion protein b (NIb) of SMV
.
Together, our findings suggest the crucial role of BiP2 as a proviral host factor necessary for potyvirus infection. The interaction between BiP2 and NIb may be the critical factor determining susceptibility in
N. benthamiana
, but further studies are needed to elucidate the underlying mechanism. Infection of viruses from the genera Bromovirus, Potyvirus, and Potexvirus in Nicotiana benthamiana induces significant up-regulation of the genes that encode the HSP70 family, including binding immunoglobulin protein 2 (BiP2). Three up-regulated genes were knocked down and infection assays with these knockdown lines demonstrated the importance of the BiP2 gene for potyvirus infection but not for infection by the other tested viruses. Distinct symptoms of cucumber mosaic virus (CMV) and potato virus X (PVX) were observed in the BiP2 knockdown line at 10 days postagroinfiltration. Interestingly, following inoculation with either soybean mosaic virus (SMV) or pepper mottle virus (PepMoV) co-expressing green fluorescent protein (GFP), neither crinkle symptoms nor GFP signals were observed in the BiP2 knockdown line. Subsequent reverse transcription-quantitative PCR analysis demonstrated that knockdown of BiP2 resulted in a significant decrease of SMV and PepMoV RNA accumulation but not PVX or CMV RNA accumulation. Further yeast two-hybrid and co-immunoprecipitation analyses validated the interaction between BiP2 and nuclear inclusion protein b (NIb) of SMV. Together, our findings suggest the crucial role of BiP2 as a proviral host factor necessary for potyvirus infection. The interaction between BiP2 and NIb may be the critical factor determining susceptibility in N. benthamiana, but further studies are needed to elucidate the underlying mechanism. Infection of viruses from the genera Bromovirus, Potyvirus , and Potexvirus in Nicotiana benthamiana induces significant up‐regulation of the genes that encode the HSP70 family, including binding immunoglobulin protein 2 (BiP2). Three up‐regulated genes were knocked down and infection assays with these knockdown lines demonstrated the importance of the BiP2 gene for potyvirus infection but not for infection by the other tested viruses. Distinct symptoms of cucumber mosaic virus (CMV) and potato virus X (PVX) were observed in the BiP2 knockdown line at 10 days postagroinfiltration. Interestingly, following inoculation with either soybean mosaic virus (SMV) or pepper mottle virus (PepMoV) co‐expressing green fluorescent protein (GFP), neither crinkle symptoms nor GFP signals were observed in the BiP2 knockdown line. Subsequent reverse transcription‐quantitative PCR analysis demonstrated that knockdown of BiP2 resulted in a significant decrease of SMV and PepMoV RNA accumulation but not PVX or CMV RNA accumulation. Further yeast two‐hybrid and co‐immunoprecipitation analyses validated the interaction between BiP2 and nuclear inclusion protein b (NIb) of SMV . Together, our findings suggest the crucial role of BiP2 as a proviral host factor necessary for potyvirus infection. The interaction between BiP2 and NIb may be the critical factor determining susceptibility in N. benthamiana , but further studies are needed to elucidate the underlying mechanism. Interaction between binding immunoglobulin protein 2 (BiP2) and NIb of potyvirus promotes virus infections, making BiP2 a good candidate for gene modification to generate a resistant cultivar against potyviruses. Infection of viruses from the genera Bromovirus, Potyvirus, and Potexvirus in Nicotiana benthamiana induces significant up-regulation of the genes that encode the HSP70 family, including binding immunoglobulin protein 2 (BiP2). Three up-regulated genes were knocked down and infection assays with these knockdown lines demonstrated the importance of the BiP2 gene for potyvirus infection but not for infection by the other tested viruses. Distinct symptoms of cucumber mosaic virus (CMV) and potato virus X (PVX) were observed in the BiP2 knockdown line at 10 days postagroinfiltration. Interestingly, following inoculation with either soybean mosaic virus (SMV) or pepper mottle virus (PepMoV) co-expressing green fluorescent protein (GFP), neither crinkle symptoms nor GFP signals were observed in the BiP2 knockdown line. Subsequent reverse transcription-quantitative PCR analysis demonstrated that knockdown of BiP2 resulted in a significant decrease of SMV and PepMoV RNA accumulation but not PVX or CMV RNA accumulation. Further yeast two-hybrid and co-immunoprecipitation analyses validated the interaction between BiP2 and nuclear inclusion protein b (NIb) of SMV. Together, our findings suggest the crucial role of BiP2 as a proviral host factor necessary for potyvirus infection. The interaction between BiP2 and NIb may be the critical factor determining susceptibility in N. benthamiana, but further studies are needed to elucidate the underlying mechanism. Infection of viruses from the genera Bromovirus, Potyvirus, and Potexvirus in Nicotiana benthamiana induces significant up‐regulation of the genes that encode the HSP70 family, including binding immunoglobulin protein 2 (BiP2). Three up‐regulated genes were knocked down and infection assays with these knockdown lines demonstrated the importance of the BiP2 gene for potyvirus infection but not for infection by the other tested viruses. Distinct symptoms of cucumber mosaic virus (CMV) and potato virus X (PVX) were observed in the BiP2 knockdown line at 10 days postagroinfiltration. Interestingly, following inoculation with either soybean mosaic virus (SMV) or pepper mottle virus (PepMoV) co‐expressing green fluorescent protein (GFP), neither crinkle symptoms nor GFP signals were observed in the BiP2 knockdown line. Subsequent reverse transcription‐quantitative PCR analysis demonstrated that knockdown of BiP2 resulted in a significant decrease of SMV and PepMoV RNA accumulation but not PVX or CMV RNA accumulation. Further yeast two‐hybrid and co‐immunoprecipitation analyses validated the interaction between BiP2 and nuclear inclusion protein b (NIb) of SMV. Together, our findings suggest the crucial role of BiP2 as a proviral host factor necessary for potyvirus infection. The interaction between BiP2 and NIb may be the critical factor determining susceptibility in N. benthamiana, but further studies are needed to elucidate the underlying mechanism. Interaction between binding immunoglobulin protein 2 (BiP2) and NIb of potyvirus promotes virus infections, making BiP2 a good candidate for gene modification to generate a resistant cultivar against potyviruses. |
Author | Widyasari, Kristin Kim, Kook‐Hyung Bwalya, John |
AuthorAffiliation | 3 Plant Genomics and Breeding Institute Seoul National University Seoul South Korea 2 Research Institute of Agriculture and Life Sciences Seoul National University Seoul South Korea 1 Department of Agricultural Biotechnology Seoul National University Seoul South Korea |
AuthorAffiliation_xml | – name: 2 Research Institute of Agriculture and Life Sciences Seoul National University Seoul South Korea – name: 3 Plant Genomics and Breeding Institute Seoul National University Seoul South Korea – name: 1 Department of Agricultural Biotechnology Seoul National University Seoul South Korea |
Author_xml | – sequence: 1 givenname: Kristin orcidid: 0000-0002-1033-734X surname: Widyasari fullname: Widyasari, Kristin organization: Seoul National University – sequence: 2 givenname: John orcidid: 0000-0003-0309-9221 surname: Bwalya fullname: Bwalya, John organization: Seoul National University – sequence: 3 givenname: Kook‐Hyung orcidid: 0000-0001-9066-6903 surname: Kim fullname: Kim, Kook‐Hyung email: kookkim@snu.ac.kr organization: Seoul National University |
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CitedBy_id | crossref_primary_10_3389_fpls_2023_1226498 crossref_primary_10_1016_j_ijbiomac_2023_124403 crossref_primary_10_1016_j_virusres_2023_199205 |
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Copyright | 2022 The Authors. published by British Society for Plant Pathology and John Wiley & Sons Ltd. 2022 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. 2023. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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Keywords | potyvirus Nicotiana benthamiana infection host factor BiP2 NIb |
Language | English |
License | Attribution-NonCommercial-NoDerivs 2022 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
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Snippet | Infection of viruses from the genera Bromovirus, Potyvirus, and Potexvirus in Nicotiana benthamiana induces significant up‐regulation of the genes that encode... Infection of viruses from the genera Bromovirus, Potyvirus , and Potexvirus in Nicotiana benthamiana induces significant up‐regulation of the genes that encode... Infection of viruses from the genera Bromovirus, Potyvirus, and Potexvirus in Nicotiana benthamiana induces significant up-regulation of the genes that encode... |
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SubjectTerms | Accumulation Binding BiP2 Bromovirus Cucumber mosaic virus Cytomegalovirus Infections Fluorescence Gene expression Gene regulation Genes Genetic engineering Green fluorescent protein heat-shock protein 70 host factor Hsp70 protein immunoglobulins Immunoprecipitation infection Infections Inoculation NIb Nicotiana Nicotiana benthamiana Pepper mottle virus Plant Diseases plant pathology Plant virus diseases Plant viruses polymerase chain reaction potatoes Potexvirus potyvirus Potyvirus - genetics precipitin tests Protein B Proteins Proviruses - genetics Reverse transcription Ribonucleic acid RNA RNA - metabolism Short Communication Soybean mosaic virus Soybeans two hybrid system techniques Viral infections Viruses Yeast |
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Title | Binding immunoglobulin 2 functions as a proviral factor for potyvirus infections in Nicotiana benthamiana |
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