Cargando…

Using recombinant Chlamydia trachomatis OMP2 as antigen in diagnostic ELISA test

BACKGROUND AND OBJECTIVES: The obligate intracellular bacterium Chlamydia trachomatis causes sexually transmissible diseases in human. Timely and sensitive detection of this pathogen is very important. There are many cross-reactions in bacteriological and serological methods in detection of this typ...

Descripción completa

Detalles Bibliográficos
Autores principales: Javaherian, Mahdieh, Sharifnia, Zarin, Taheripanah, Robabeh, Bandepour, Mojgan, Soleimani, Mohammad, Kazemi, Bahram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419049/
https://www.ncbi.nlm.nih.gov/pubmed/25954485
_version_ 1782369529415860224
author Javaherian, Mahdieh
Sharifnia, Zarin
Taheripanah, Robabeh
Bandepour, Mojgan
Soleimani, Mohammad
Kazemi, Bahram
author_facet Javaherian, Mahdieh
Sharifnia, Zarin
Taheripanah, Robabeh
Bandepour, Mojgan
Soleimani, Mohammad
Kazemi, Bahram
author_sort Javaherian, Mahdieh
collection PubMed
description BACKGROUND AND OBJECTIVES: The obligate intracellular bacterium Chlamydia trachomatis causes sexually transmissible diseases in human. Timely and sensitive detection of this pathogen is very important. There are many cross-reactions in bacteriological and serological methods in detection of this type of pathogens. The aim of this study was to achieve a more specific antigen for serological tests. MATERIALS AND METHODS: Blood samples were taken from 192 women with suspected chlamydial infection and sera were isolated. ELISA plate wells were coated with recombinant C. trachomatis OMP2 as antigen. Cut-off system was determined with 40 negative sera. The final results of this research were compared with Euroimmun commercial kit. RESULTS: The ELISA system cut-off was calculated at 0.27 using negative sera samples. ODs of positive samples were higher than 0.27 and negative samples were lower than it. We obtained 30 samples (15.62%) as positive and 162 cases (84.37%) as negative. Sensitivity and specificity of the recombinant antigen were 90% and 86%, respectively. This antigen showed no cross-reactivity with sera of patients infected with Hydatid cyst, HCV, Epstein barr virus, HBV, Helicobacter pylori, Toxoplasma gondii, Cytomegalovirus, Mycoplasma, Measles and Varicella zoster virus. CONCLUSION: The sensitivity and specificity of rOMP2 in ELISA for detection of C. trachomatis were 90% and 86%, respectively. Though the sensitivity was higher than results of Euroimmun commercial kit, its specificity was calculated lower than reference kit.
format Online
Article
Text
id pubmed-4419049
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Tehran University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-44190492015-05-07 Using recombinant Chlamydia trachomatis OMP2 as antigen in diagnostic ELISA test Javaherian, Mahdieh Sharifnia, Zarin Taheripanah, Robabeh Bandepour, Mojgan Soleimani, Mohammad Kazemi, Bahram Iran J Microbiol Medical Sciences BACKGROUND AND OBJECTIVES: The obligate intracellular bacterium Chlamydia trachomatis causes sexually transmissible diseases in human. Timely and sensitive detection of this pathogen is very important. There are many cross-reactions in bacteriological and serological methods in detection of this type of pathogens. The aim of this study was to achieve a more specific antigen for serological tests. MATERIALS AND METHODS: Blood samples were taken from 192 women with suspected chlamydial infection and sera were isolated. ELISA plate wells were coated with recombinant C. trachomatis OMP2 as antigen. Cut-off system was determined with 40 negative sera. The final results of this research were compared with Euroimmun commercial kit. RESULTS: The ELISA system cut-off was calculated at 0.27 using negative sera samples. ODs of positive samples were higher than 0.27 and negative samples were lower than it. We obtained 30 samples (15.62%) as positive and 162 cases (84.37%) as negative. Sensitivity and specificity of the recombinant antigen were 90% and 86%, respectively. This antigen showed no cross-reactivity with sera of patients infected with Hydatid cyst, HCV, Epstein barr virus, HBV, Helicobacter pylori, Toxoplasma gondii, Cytomegalovirus, Mycoplasma, Measles and Varicella zoster virus. CONCLUSION: The sensitivity and specificity of rOMP2 in ELISA for detection of C. trachomatis were 90% and 86%, respectively. Though the sensitivity was higher than results of Euroimmun commercial kit, its specificity was calculated lower than reference kit. Tehran University of Medical Sciences 2014-02 /pmc/articles/PMC4419049/ /pubmed/25954485 Text en Copyright © Iranian Journal of Microbiology & Tehran University of Medical Sciences This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Medical Sciences
Javaherian, Mahdieh
Sharifnia, Zarin
Taheripanah, Robabeh
Bandepour, Mojgan
Soleimani, Mohammad
Kazemi, Bahram
Using recombinant Chlamydia trachomatis OMP2 as antigen in diagnostic ELISA test
title Using recombinant Chlamydia trachomatis OMP2 as antigen in diagnostic ELISA test
title_full Using recombinant Chlamydia trachomatis OMP2 as antigen in diagnostic ELISA test
title_fullStr Using recombinant Chlamydia trachomatis OMP2 as antigen in diagnostic ELISA test
title_full_unstemmed Using recombinant Chlamydia trachomatis OMP2 as antigen in diagnostic ELISA test
title_short Using recombinant Chlamydia trachomatis OMP2 as antigen in diagnostic ELISA test
title_sort using recombinant chlamydia trachomatis omp2 as antigen in diagnostic elisa test
topic Medical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419049/
https://www.ncbi.nlm.nih.gov/pubmed/25954485
work_keys_str_mv AT javaherianmahdieh usingrecombinantchlamydiatrachomatisomp2asantigenindiagnosticelisatest
AT sharifniazarin usingrecombinantchlamydiatrachomatisomp2asantigenindiagnosticelisatest
AT taheripanahrobabeh usingrecombinantchlamydiatrachomatisomp2asantigenindiagnosticelisatest
AT bandepourmojgan usingrecombinantchlamydiatrachomatisomp2asantigenindiagnosticelisatest
AT soleimanimohammad usingrecombinantchlamydiatrachomatisomp2asantigenindiagnosticelisatest
AT kazemibahram usingrecombinantchlamydiatrachomatisomp2asantigenindiagnosticelisatest