Production of monoclonal antibodies against Legionella pneumophila serogroup 1 for development of in-house immunodiagnostic assay

Introduction: It may be difficult to diagnose infection caused by Legionella pneumophila. Several studies indicate that detection of L.pneumophila urinary antigen is a promising tool for rapid diagnosis of the infection. Objective: The objectives of the study were to produce monoclonal antibodies ag...

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Published in:International Medical Journal
Main Author: Yahaya N.; Kaspan S.; Pit S.; Abdullah N.R.
Format: Article
Language:English
Published: 2006
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-33645837684&partnerID=40&md5=fb8d4ba4e91c7a35275ac43926560c0b
id 2-s2.0-33645837684
spelling 2-s2.0-33645837684
Yahaya N.; Kaspan S.; Pit S.; Abdullah N.R.
Production of monoclonal antibodies against Legionella pneumophila serogroup 1 for development of in-house immunodiagnostic assay
2006
International Medical Journal
13
1

https://www.scopus.com/inward/record.uri?eid=2-s2.0-33645837684&partnerID=40&md5=fb8d4ba4e91c7a35275ac43926560c0b
Introduction: It may be difficult to diagnose infection caused by Legionella pneumophila. Several studies indicate that detection of L.pneumophila urinary antigen is a promising tool for rapid diagnosis of the infection. Objective: The objectives of the study were to produce monoclonal antibodies against L.pneumophila serogroup 1 and to assess the potentiality of the monoclonal antibodies as diagnostic reagents to detect the bacterial antigens. Materials and Methods: Monoclonal antibodies against L.pneumophila serogroup 1 were produced by hybridoma technology using a mouse system following the technique described by Kohler and Milstein. The monoclonal antibodies were tested with antigens of L.pneumophila and other bacterial antigens by indirect ELISA using the method of Voller et al and subsequently by sandwich ELISA by the method of Zheng et al. Results: Four clones secreting monoclonal antibodies of IgM class designated as 1C7.2B, 2B2.10F, 2B2.11E and 1F4.10E had been produced against L.pneumophila serogroup 1. All the monoclonal antibodies reacted specifically with the homologous antigens of L.pneumophila serogroup 1 in the indirect ELISA as well as sandwich ELISA since no cross-reaction was detected with the other tested bacterial antigens. Conclusion: The in-house sandwich ELISA using monoclonal antibodies produced in the study detected specifically soluble antigen of L.pneumophila and hence have potential to be used as a tool to diagnose the infection caused by this pathogen. © 2006 Japan International Cultural Exchange Foundation.

13412051
English
Article

author Yahaya N.; Kaspan S.; Pit S.; Abdullah N.R.
spellingShingle Yahaya N.; Kaspan S.; Pit S.; Abdullah N.R.
Production of monoclonal antibodies against Legionella pneumophila serogroup 1 for development of in-house immunodiagnostic assay
author_facet Yahaya N.; Kaspan S.; Pit S.; Abdullah N.R.
author_sort Yahaya N.; Kaspan S.; Pit S.; Abdullah N.R.
title Production of monoclonal antibodies against Legionella pneumophila serogroup 1 for development of in-house immunodiagnostic assay
title_short Production of monoclonal antibodies against Legionella pneumophila serogroup 1 for development of in-house immunodiagnostic assay
title_full Production of monoclonal antibodies against Legionella pneumophila serogroup 1 for development of in-house immunodiagnostic assay
title_fullStr Production of monoclonal antibodies against Legionella pneumophila serogroup 1 for development of in-house immunodiagnostic assay
title_full_unstemmed Production of monoclonal antibodies against Legionella pneumophila serogroup 1 for development of in-house immunodiagnostic assay
title_sort Production of monoclonal antibodies against Legionella pneumophila serogroup 1 for development of in-house immunodiagnostic assay
publishDate 2006
container_title International Medical Journal
container_volume 13
container_issue 1
doi_str_mv
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-33645837684&partnerID=40&md5=fb8d4ba4e91c7a35275ac43926560c0b
description Introduction: It may be difficult to diagnose infection caused by Legionella pneumophila. Several studies indicate that detection of L.pneumophila urinary antigen is a promising tool for rapid diagnosis of the infection. Objective: The objectives of the study were to produce monoclonal antibodies against L.pneumophila serogroup 1 and to assess the potentiality of the monoclonal antibodies as diagnostic reagents to detect the bacterial antigens. Materials and Methods: Monoclonal antibodies against L.pneumophila serogroup 1 were produced by hybridoma technology using a mouse system following the technique described by Kohler and Milstein. The monoclonal antibodies were tested with antigens of L.pneumophila and other bacterial antigens by indirect ELISA using the method of Voller et al and subsequently by sandwich ELISA by the method of Zheng et al. Results: Four clones secreting monoclonal antibodies of IgM class designated as 1C7.2B, 2B2.10F, 2B2.11E and 1F4.10E had been produced against L.pneumophila serogroup 1. All the monoclonal antibodies reacted specifically with the homologous antigens of L.pneumophila serogroup 1 in the indirect ELISA as well as sandwich ELISA since no cross-reaction was detected with the other tested bacterial antigens. Conclusion: The in-house sandwich ELISA using monoclonal antibodies produced in the study detected specifically soluble antigen of L.pneumophila and hence have potential to be used as a tool to diagnose the infection caused by this pathogen. © 2006 Japan International Cultural Exchange Foundation.
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