Cargando…
Transient recombinant expression of highly immunogenic CagA, VacA and NapA in Nicotiana benthamiana
Interest in the plant-based transient production of recombinant immunogenic antigens has tremendously progressed because plants are cost-effective, easily selectable, free of mammalian contamination, and support complex post-translational modifications. Nicotiana benthamiana is a convenient system f...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739878/ https://www.ncbi.nlm.nih.gov/pubmed/35028298 http://dx.doi.org/10.1016/j.btre.2021.e00699 |
_version_ | 1784629194532061184 |
---|---|
author | Barzigar, Rambod Haraprasad, Nanjundappa Kumar, Basaralu Yadurappa Sathish Mehran, Mohammad Javad Fakrudin, Bashasab |
author_facet | Barzigar, Rambod Haraprasad, Nanjundappa Kumar, Basaralu Yadurappa Sathish Mehran, Mohammad Javad Fakrudin, Bashasab |
author_sort | Barzigar, Rambod |
collection | PubMed |
description | Interest in the plant-based transient production of recombinant immunogenic antigens has tremendously progressed because plants are cost-effective, easily selectable, free of mammalian contamination, and support complex post-translational modifications. Nicotiana benthamiana is a convenient system for transient expression of recombinant antigens. The present study documented a platform for rapid production of Helicobacter pylori CagA, VacA and NapA antigens three days (first harvest, FH) and six days (second harvest, SH) after agro-infiltration using a syringe. In this study, CagA, VacA and NapA antigen genes from Helicobacter pylori were cloned into the binary vector pBI121 and transformed into Nicotiana benthamiana by the Agrobacterium-mediated process. Leaves of four to five weeks old Nicotiana benthamiana plants were agroinfiltrated with EHA105 subtype of Agrobacterium tumefaciens strain containing cloned CagA (pBI121-CagA), VacA (pBI121-VacA) and NapA (pBI121-NapA) constructs. The transient expression and accumulation of the recombinant genes containing CagA, VacA and NapA expression cassettes were confirmed using qRT-PCR by comparing the relative expression at FH and SH post-infiltration with the non-infiltrated (control) samples and using ELISA at 1/5 and 1/10 dilution ratios. The qRT-PCR findings showed that Agrobacterium-mediated syringe infiltration of leaves of four to five weeks old Nicotiana benthamiana plants produced significantly higher transcript levels of CagA (about 8-fold and 7-fold), VacA (38-fold and 24-fold) and NapA (7-fold and 5-fold) genes at FH and SH compared to the control sample. Besides, the maximum amount of CagA, VacA and NapA antigens were detected at the FH stage compared to the SH stage, when the antibody concentrations of the agro-infiltrated leaf extracts containing these recombinant antigens were diluted in a 1/5 ratio. This study has developed evidence to support that recombinant CagA, VacA and NapA can be transiently produced in Nicotiana benthamiana plants. |
format | Online Article Text |
id | pubmed-8739878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-87398782022-01-12 Transient recombinant expression of highly immunogenic CagA, VacA and NapA in Nicotiana benthamiana Barzigar, Rambod Haraprasad, Nanjundappa Kumar, Basaralu Yadurappa Sathish Mehran, Mohammad Javad Fakrudin, Bashasab Biotechnol Rep (Amst) Research Article Interest in the plant-based transient production of recombinant immunogenic antigens has tremendously progressed because plants are cost-effective, easily selectable, free of mammalian contamination, and support complex post-translational modifications. Nicotiana benthamiana is a convenient system for transient expression of recombinant antigens. The present study documented a platform for rapid production of Helicobacter pylori CagA, VacA and NapA antigens three days (first harvest, FH) and six days (second harvest, SH) after agro-infiltration using a syringe. In this study, CagA, VacA and NapA antigen genes from Helicobacter pylori were cloned into the binary vector pBI121 and transformed into Nicotiana benthamiana by the Agrobacterium-mediated process. Leaves of four to five weeks old Nicotiana benthamiana plants were agroinfiltrated with EHA105 subtype of Agrobacterium tumefaciens strain containing cloned CagA (pBI121-CagA), VacA (pBI121-VacA) and NapA (pBI121-NapA) constructs. The transient expression and accumulation of the recombinant genes containing CagA, VacA and NapA expression cassettes were confirmed using qRT-PCR by comparing the relative expression at FH and SH post-infiltration with the non-infiltrated (control) samples and using ELISA at 1/5 and 1/10 dilution ratios. The qRT-PCR findings showed that Agrobacterium-mediated syringe infiltration of leaves of four to five weeks old Nicotiana benthamiana plants produced significantly higher transcript levels of CagA (about 8-fold and 7-fold), VacA (38-fold and 24-fold) and NapA (7-fold and 5-fold) genes at FH and SH compared to the control sample. Besides, the maximum amount of CagA, VacA and NapA antigens were detected at the FH stage compared to the SH stage, when the antibody concentrations of the agro-infiltrated leaf extracts containing these recombinant antigens were diluted in a 1/5 ratio. This study has developed evidence to support that recombinant CagA, VacA and NapA can be transiently produced in Nicotiana benthamiana plants. Elsevier 2021-12-29 /pmc/articles/PMC8739878/ /pubmed/35028298 http://dx.doi.org/10.1016/j.btre.2021.e00699 Text en © 2021 Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Barzigar, Rambod Haraprasad, Nanjundappa Kumar, Basaralu Yadurappa Sathish Mehran, Mohammad Javad Fakrudin, Bashasab Transient recombinant expression of highly immunogenic CagA, VacA and NapA in Nicotiana benthamiana |
title | Transient recombinant expression of highly immunogenic CagA, VacA and NapA in Nicotiana benthamiana |
title_full | Transient recombinant expression of highly immunogenic CagA, VacA and NapA in Nicotiana benthamiana |
title_fullStr | Transient recombinant expression of highly immunogenic CagA, VacA and NapA in Nicotiana benthamiana |
title_full_unstemmed | Transient recombinant expression of highly immunogenic CagA, VacA and NapA in Nicotiana benthamiana |
title_short | Transient recombinant expression of highly immunogenic CagA, VacA and NapA in Nicotiana benthamiana |
title_sort | transient recombinant expression of highly immunogenic caga, vaca and napa in nicotiana benthamiana |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739878/ https://www.ncbi.nlm.nih.gov/pubmed/35028298 http://dx.doi.org/10.1016/j.btre.2021.e00699 |
work_keys_str_mv | AT barzigarrambod transientrecombinantexpressionofhighlyimmunogeniccagavacaandnapainnicotianabenthamiana AT haraprasadnanjundappa transientrecombinantexpressionofhighlyimmunogeniccagavacaandnapainnicotianabenthamiana AT kumarbasaraluyadurappasathish transientrecombinantexpressionofhighlyimmunogeniccagavacaandnapainnicotianabenthamiana AT mehranmohammadjavad transientrecombinantexpressionofhighlyimmunogeniccagavacaandnapainnicotianabenthamiana AT fakrudinbashasab transientrecombinantexpressionofhighlyimmunogeniccagavacaandnapainnicotianabenthamiana |