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Production and Characterization of Rat Monoclonal Antibodies against the PAL Antigen of Legionella spp.

The purpose of this work was to obtain genus-specific monoclonal antibodies against the Legionella spp. recombinant PAL protein, which will subsequently allow to use them as a basis for the development of new express tests for pathogenic legionella detection. A short three-week immunization protocol...

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Autores principales: Zeninskaya, N. A., Riabko, A. K., Marin, M. A., Kombarova, T. I., Mitsevich, I. P., Yeruslanov, B. V., Firstova, V. V., Shemyakin, I. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pleiades Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527138/
https://www.ncbi.nlm.nih.gov/pubmed/36213626
http://dx.doi.org/10.3103/S0891416822020082
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author Zeninskaya, N. A.
Riabko, A. K.
Marin, M. A.
Kombarova, T. I.
Mitsevich, I. P.
Yeruslanov, B. V.
Firstova, V. V.
Shemyakin, I. G.
author_facet Zeninskaya, N. A.
Riabko, A. K.
Marin, M. A.
Kombarova, T. I.
Mitsevich, I. P.
Yeruslanov, B. V.
Firstova, V. V.
Shemyakin, I. G.
author_sort Zeninskaya, N. A.
collection PubMed
description The purpose of this work was to obtain genus-specific monoclonal antibodies against the Legionella spp. recombinant PAL protein, which will subsequently allow to use them as a basis for the development of new express tests for pathogenic legionella detection. A short three-week immunization protocol for Wistar rats was used to generate rat–mouse heterohybridomas producing antibodies against PAL. Mouse myeloma cell line Sp2/0-Ag14 served as the fusion partner. Hybridization was performed using two methods: PEG-mediated fusion and electrofusion. Subsequent screening was performed by indirect solid-phase ELISA against the target protein rPAL. Specificity analysis was performed by dot-blot using a panel of lysates obtained from 39 pure cultures of different strains, which included closely related and heterologous microorganisms among others. No difference in the efficiency of stable hybridoma clones production by the two indicated cell-fusion methods was detected. Twelve clones producing specific rat monoclonal antibodies were obtained based on the screening results. The obtained rat monoclonal antibodies are highly specific towards the PAL protein of L. pneumophila of different serological groups and other pathogenic legionella and are good candidates to be used as the components of diagnostic test systems for the detection of pathogenic representatives of the Legionella genus.
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spelling pubmed-95271382022-10-03 Production and Characterization of Rat Monoclonal Antibodies against the PAL Antigen of Legionella spp. Zeninskaya, N. A. Riabko, A. K. Marin, M. A. Kombarova, T. I. Mitsevich, I. P. Yeruslanov, B. V. Firstova, V. V. Shemyakin, I. G. Mol Gen Microbiol Virol Experimental Papers The purpose of this work was to obtain genus-specific monoclonal antibodies against the Legionella spp. recombinant PAL protein, which will subsequently allow to use them as a basis for the development of new express tests for pathogenic legionella detection. A short three-week immunization protocol for Wistar rats was used to generate rat–mouse heterohybridomas producing antibodies against PAL. Mouse myeloma cell line Sp2/0-Ag14 served as the fusion partner. Hybridization was performed using two methods: PEG-mediated fusion and electrofusion. Subsequent screening was performed by indirect solid-phase ELISA against the target protein rPAL. Specificity analysis was performed by dot-blot using a panel of lysates obtained from 39 pure cultures of different strains, which included closely related and heterologous microorganisms among others. No difference in the efficiency of stable hybridoma clones production by the two indicated cell-fusion methods was detected. Twelve clones producing specific rat monoclonal antibodies were obtained based on the screening results. The obtained rat monoclonal antibodies are highly specific towards the PAL protein of L. pneumophila of different serological groups and other pathogenic legionella and are good candidates to be used as the components of diagnostic test systems for the detection of pathogenic representatives of the Legionella genus. Pleiades Publishing 2022-10-03 2022 /pmc/articles/PMC9527138/ /pubmed/36213626 http://dx.doi.org/10.3103/S0891416822020082 Text en © Allerton Press, Inc. 2022, ISSN 0891-4168, Molecular Genetics, Microbiology and Virology, 2022, Vol. 37, No. 2, pp. 65–70. © Allerton Press, Inc., 2022.Russian Text © The Author(s), 2022, published in Molekulyarnaya Genetika, Mikrobiologiya i Virusologiya, 2022, No. 2, pp. 14–20. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Experimental Papers
Zeninskaya, N. A.
Riabko, A. K.
Marin, M. A.
Kombarova, T. I.
Mitsevich, I. P.
Yeruslanov, B. V.
Firstova, V. V.
Shemyakin, I. G.
Production and Characterization of Rat Monoclonal Antibodies against the PAL Antigen of Legionella spp.
title Production and Characterization of Rat Monoclonal Antibodies against the PAL Antigen of Legionella spp.
title_full Production and Characterization of Rat Monoclonal Antibodies against the PAL Antigen of Legionella spp.
title_fullStr Production and Characterization of Rat Monoclonal Antibodies against the PAL Antigen of Legionella spp.
title_full_unstemmed Production and Characterization of Rat Monoclonal Antibodies against the PAL Antigen of Legionella spp.
title_short Production and Characterization of Rat Monoclonal Antibodies against the PAL Antigen of Legionella spp.
title_sort production and characterization of rat monoclonal antibodies against the pal antigen of legionella spp.
topic Experimental Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527138/
https://www.ncbi.nlm.nih.gov/pubmed/36213626
http://dx.doi.org/10.3103/S0891416822020082
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