Development of an indirect sandwich ELISA for detection of urinary antigen, using Legionella pneumophila PAL protein

被引:0
作者
Abolfazl Gholipour
Mojtaba Moosavian
Manoochehr Makvandi
Hamid Galehdari
Amirhooshang Alvandi
Seyyed Ali Mard
机构
[1] Shahrekord University of Medical Sciences,Department of Microbiology and Immunology, School of Medicine, Molecular and cellular Research center
[2] Ahvaz Jundishapur University of Medical Sciences,Infectious and Tropical Diseases Research Center, Department of Microbiology, School of Medicine
[3] Ahvaz Jundishapur University of Medical Science,Department of Medical Virology, School of Medicine
[4] Shahid Chamran University,Department of Genetics, Faculty of Science
[5] Kermanshah University of Medical Sciences,Department of Microbiology, Faculty of Medicine
[6] Ahvaz Jundishapur University of Medical Science,Department of Physiology, School of Medicine
来源
World Journal of Microbiology and Biotechnology | 2014年 / 30卷
关键词
Legionnaires disease (LD); Peptidoglycan-associated lipoprotein (PAL); ELISA; EIA;
D O I
暂无
中图分类号
学科分类号
摘要
Legionella pneumophila peptidoglycan-associated lipoprotein (PAL) protein is an extremely conserved antigen among Legionella species. In this study, rabbit and rat anti-PAL immunoglobulin G antibodies were produced by immunization with purified, recombinant PAL (r-PAL) protein of L. pneumophila serogroup 1 and used as capture and detection antibodies in the PAL antigen-based enzyme-linked immunosorbent assay (ELISA) to detect urinary PAL antigen. Urine samples were obtained from rats experimentally infected with L. pneumophila serogroup 1. The PAL antigen was measured in urine samples of 40 infected and 40 uninfected rats. After choosing the cut-off value of 0.192, the sensitivity and specificity of the PAL antigen-based ELISA were 87.5 and 97.5 %, respectively. The results obtained by PAL antigen base ELISA were compared with those obtained by Biotest. The PAL antigen was detected efficiently by both of the assays and all of the control human urine samples were negative by the ELISA test. The PAL antigen-based ELISA assay was relatively simple to perform, precise, highly sensitive and specific, and reproducible. Based on our data the PAL antigen-based ELISA described here is the first indirect sandwich ELISA for urinary antigen detection which could easily be applied for diagnosis of Legionnaires disease.
引用
收藏
页码:1463 / 1471
页数:8
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