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Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants

The amino acid sequence of the extracellular domain of the virus-encoded M2 matrix protein (peptide M2e) is conserved among all subtypes of influenza A strains, enabling the development of a broad-range vaccine against them. We expressed M2e from avian influenza virus A/chicken/Kurgan/5/2005 (H5N1)...

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Autores principales: Firsov, Aleksey, Tarasenko, Irina, Mitiouchkina, Tatiana, Shaloiko, Lyubov, Kozlov, Oleg, Vinokurov, Leonid, Rasskazova, Ekaterina, Murashev, Arkadii, Vainstein, Alexander, Dolgov, Sergey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816751/
https://www.ncbi.nlm.nih.gov/pubmed/29487846
http://dx.doi.org/10.3389/fchem.2018.00022
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author Firsov, Aleksey
Tarasenko, Irina
Mitiouchkina, Tatiana
Shaloiko, Lyubov
Kozlov, Oleg
Vinokurov, Leonid
Rasskazova, Ekaterina
Murashev, Arkadii
Vainstein, Alexander
Dolgov, Sergey
author_facet Firsov, Aleksey
Tarasenko, Irina
Mitiouchkina, Tatiana
Shaloiko, Lyubov
Kozlov, Oleg
Vinokurov, Leonid
Rasskazova, Ekaterina
Murashev, Arkadii
Vainstein, Alexander
Dolgov, Sergey
author_sort Firsov, Aleksey
collection PubMed
description The amino acid sequence of the extracellular domain of the virus-encoded M2 matrix protein (peptide M2e) is conserved among all subtypes of influenza A strains, enabling the development of a broad-range vaccine against them. We expressed M2e from avian influenza virus A/chicken/Kurgan/5/2005 (H5N1) in nuclear-transformed duckweed plants for further development of an avian influenza vaccine. The 30-amino acid N-terminal fragment of M2, including M2e (denoted M130), was selected for expression. The M2e DNA sequence fused in-frame to the 3′ end of ricin toxin B chain (RTB) was cloned under control of the CaMV 35S promoter into pBI121. The resulting plasmid was used for duckweed transformation, and 23 independent transgenic duckweed lines were obtained. Asialofetuin-binding ELISA of protein samples from the transgenic plants using polyclonal anti-RTB antibodies confirmed the expression of the RTB–M130 fusion protein in 20 lines. Quantitative ELISA of crude protein extracts from these lines showed RTB–M130 accumulation ranging from 0.25–2.5 μg/g fresh weight (0.0006–0.01% of total soluble protein). Affinity chromatography with immobilized asialofetuin and western blot analysis of protein samples from the transgenic plants showed expression of fusion protein RTB–M130 in the aggregate form with a molecular mass of about 70 kDa. Mice were immunized orally with a preparation of total soluble protein from transgenic plants, receiving four doses of 7 μg duckweed-derived RTB–M130 each, with no additional adjuvant. Specific IgG against M2e was detected in immunized mice, and the endpoint titer of nti-M2e IgG was 1,024. It was confirmed that oral immunization with RTB-M130 induces production of specific antibodies against peptide M2e, one of the most conserved antigens of the influenza virus. These results may provide further information for the development of a duckweed-based expression system to produce a broad-range edible vaccine against avian influenza.
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spelling pubmed-58167512018-02-27 Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants Firsov, Aleksey Tarasenko, Irina Mitiouchkina, Tatiana Shaloiko, Lyubov Kozlov, Oleg Vinokurov, Leonid Rasskazova, Ekaterina Murashev, Arkadii Vainstein, Alexander Dolgov, Sergey Front Chem Chemistry The amino acid sequence of the extracellular domain of the virus-encoded M2 matrix protein (peptide M2e) is conserved among all subtypes of influenza A strains, enabling the development of a broad-range vaccine against them. We expressed M2e from avian influenza virus A/chicken/Kurgan/5/2005 (H5N1) in nuclear-transformed duckweed plants for further development of an avian influenza vaccine. The 30-amino acid N-terminal fragment of M2, including M2e (denoted M130), was selected for expression. The M2e DNA sequence fused in-frame to the 3′ end of ricin toxin B chain (RTB) was cloned under control of the CaMV 35S promoter into pBI121. The resulting plasmid was used for duckweed transformation, and 23 independent transgenic duckweed lines were obtained. Asialofetuin-binding ELISA of protein samples from the transgenic plants using polyclonal anti-RTB antibodies confirmed the expression of the RTB–M130 fusion protein in 20 lines. Quantitative ELISA of crude protein extracts from these lines showed RTB–M130 accumulation ranging from 0.25–2.5 μg/g fresh weight (0.0006–0.01% of total soluble protein). Affinity chromatography with immobilized asialofetuin and western blot analysis of protein samples from the transgenic plants showed expression of fusion protein RTB–M130 in the aggregate form with a molecular mass of about 70 kDa. Mice were immunized orally with a preparation of total soluble protein from transgenic plants, receiving four doses of 7 μg duckweed-derived RTB–M130 each, with no additional adjuvant. Specific IgG against M2e was detected in immunized mice, and the endpoint titer of nti-M2e IgG was 1,024. It was confirmed that oral immunization with RTB-M130 induces production of specific antibodies against peptide M2e, one of the most conserved antigens of the influenza virus. These results may provide further information for the development of a duckweed-based expression system to produce a broad-range edible vaccine against avian influenza. Frontiers Media S.A. 2018-02-13 /pmc/articles/PMC5816751/ /pubmed/29487846 http://dx.doi.org/10.3389/fchem.2018.00022 Text en Copyright © 2018 Firsov, Tarasenko, Mitiouchkina, Shaloiko, Kozlov, Vinokurov, Rasskazova, Murashev, Vainstein and Dolgov. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Firsov, Aleksey
Tarasenko, Irina
Mitiouchkina, Tatiana
Shaloiko, Lyubov
Kozlov, Oleg
Vinokurov, Leonid
Rasskazova, Ekaterina
Murashev, Arkadii
Vainstein, Alexander
Dolgov, Sergey
Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants
title Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants
title_full Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants
title_fullStr Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants
title_full_unstemmed Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants
title_short Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants
title_sort expression and immunogenicity of m2e peptide of avian influenza virus h5n1 fused to ricin toxin b chain produced in duckweed plants
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816751/
https://www.ncbi.nlm.nih.gov/pubmed/29487846
http://dx.doi.org/10.3389/fchem.2018.00022
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