Antibody response to GroEL varies in patients with acute Mycoplasma pneumoniae infection

被引:13
作者
Bencina, D [1 ]
Slavec, B [1 ]
Narat, M [1 ]
机构
[1] Univ Ljubljana, Biotech Fac, Dept Anim Sci, Domzale 1230, Slovenia
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2005年 / 43卷 / 03期
关键词
antibody response; GroEL; Mycoplasma pneumoniae;
D O I
10.1016/j.femsim.2004.10.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Although heat-shock proteins represent major antigens in a wide spectrum of bacterial infections, their immunogenicity is not known for Mycoplasma pneumoniae. M. pneumoniae is a major human respiratory pathogen and it has been suggested that its groEL gene might be dispensable in vitro. Using the specific monoclonal antibody 2C2/C3 we found an abundant synthesis of about 58 kDa GroEL in M. pneumoniae reference strains and in 15 clinical isolates examined at low and higher passages. In patients with acute respiratory disease caused by M. pneumoniae immunoblot analyses showed relatively low prevalence of systemic antibodies against its GroEL protein. Whereas all patients had strong antibody response to the P I adhesin, only 5 of 29 patients (17.2%) had antibodies to GroEL. Among them, patient RI raised an early and very strong antibody response to GroEL. During the convalescent phase, levels of his serum IgG (mainly IgG(2)) to GroEL increased and were higher than levels of IgG to P1. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:399 / 406
页数:8
相关论文
共 27 条
[1]
[Anonymous], MOL BIOL PATHOGENICI
[2]
Mycoplasmas: Sophisticated, reemerging, and burdened by their notoriety [J].
Baseman, JB ;
Tully, JG .
EMERGING INFECTIOUS DISEASES, 1997, 3 (01) :21-32
[3]
Interplay between mycoplasma surface proteins, airway cells, and the protean manifestations of mycoplasma-mediated human infections [J].
Baseman, JB ;
Reddy, SP ;
Dallo, SF .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (04) :S137-S144
[4]
VARIABLE EXPRESSION OF EPITOPES ON THE SURFACE OF MYCOPLASMA-GALLISEPTICUM DEMONSTRATED WITH MONOCLONAL-ANTIBODIES [J].
BENCINA, D ;
KLEVEN, SH ;
ELFAKI, MG ;
SNOJ, A ;
DOVC, P ;
DORRER, D ;
RUSS, I .
AVIAN PATHOLOGY, 1994, 23 (01) :19-36
[5]
Bencina D, 1999, FEMS MICROBIOL LETT, V173, P85, DOI 10.1111/j.1574-6968.1999.tb13488.x
[6]
Intrathecal synthesis of specific antibodies in patients with invasion of the central nervous system by Mycoplasma pneumoniae [J].
Bencina, D ;
Dovc, P ;
Mueller-Premru, M ;
Avsic-Zupanc, T ;
Socan, M ;
Beovic, B ;
Arnez, M ;
Narat, M .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2000, 19 (07) :521-530
[7]
BIBERFELD G, 1985, MYCOPLASMAS, V4, P293
[8]
The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis [J].
Chambaud, I ;
Heilig, R ;
Ferris, S ;
Barbe, V ;
Samson, D ;
Galisson, F ;
Moszer, I ;
Dybvig, K ;
Wróblewski, H ;
Viari, A ;
Rocha, EPC ;
Blanchard, A .
NUCLEIC ACIDS RESEARCH, 2001, 29 (10) :2145-2153
[9]
Carbohydrate recognition by Mycoplasma pneumoniae and pathologic consequences [J].
Feizi, T ;
Loveless, RW .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (04) :S133-S136
[10]
INFECTIONS CAUSED BY MYCOPLASMA-PNEUMONIAE AND POSSIBLE CARRIER STATE IN DIFFERENT POPULATIONS OF PATIENTS [J].
FOY, HM .
CLINICAL INFECTIOUS DISEASES, 1993, 17 :S37-S46