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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.
Afiliação
  • Zeninskaya NA; State Scientific Center for Applied Microbiology and Biotechnology, 142279 Obolensk, Moscow oblast Russia.
  • Riabko AK; State Scientific Center for Applied Microbiology and Biotechnology, 142279 Obolensk, Moscow oblast Russia.
  • Marin MA; State Scientific Center for Applied Microbiology and Biotechnology, 142279 Obolensk, Moscow oblast Russia.
  • Kombarova TI; State Scientific Center for Applied Microbiology and Biotechnology, 142279 Obolensk, Moscow oblast Russia.
  • Mitsevich IP; State Scientific Center for Applied Microbiology and Biotechnology, 142279 Obolensk, Moscow oblast Russia.
  • Yeruslanov BV; State Scientific Center for Applied Microbiology and Biotechnology, 142279 Obolensk, Moscow oblast Russia.
  • Firstova VV; State Scientific Center for Applied Microbiology and Biotechnology, 142279 Obolensk, Moscow oblast Russia.
  • Shemyakin IG; State Scientific Center for Applied Microbiology and Biotechnology, 142279 Obolensk, Moscow oblast Russia.
Mol Gen Microbiol Virol ; 37(2): 65-70, 2022.
Article em En | MEDLINE | ID: mdl-36213626
ABSTRACT
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article