Characterization of a strain of Chlamydia pneumoniae isolated from a coronary atheroma by analysis of the omp1 gene and biological activity in human endothelial cells

被引:69
作者
Molestina, RE [1 ]
Dean, D [1 ]
Miller, RD [1 ]
Ramirez, JA [1 ]
Summersgill, JT [1 ]
机构
[1] Univ Louisville, Dept Med, Div Infect Dis, Louisville, KY 40292 USA
关键词
D O I
10.1128/IAI.66.4.1370-1376.1998
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chlamydia pneumoniae is a respiratory pathogen that has been associated with chronic inflammatory diseases such as asthma and atherosclerosis, Recent isolation of C. pneumoniae from human carotid and coronary atheromas provides additional support for a role of this organism in atherogenesis. We characterized the coronary strain C. pneumoniae A-03 by sequence analysis of the major outer membrane protein gene (omp1), In addition, the in vitro activities of A-03 and three respiratory strains of C. pneumoniae (BAL 16, TW-183, and T-2634) were examined in infected human umbilical vein endothelial cells (HUVEC) by analysis of the production of interleukin-8 (IL-8), monocyte chemotactic protein 1 (MCP-1), and soluble intercellular cell adhesion molecule 1 (sICAM-1), Sequence analysis of omp1 of C. pneumoniae A-03, compared to prototype strains TW-183 and AR-39, revealed five nucleotide changes resulting in nonsynonymous codons. Of interest was a nonconservative amino acid substitution (Ser to Pro) in position 61 of variable segment 1, In vitro, the extent of MCP-1, IL-8, and sICAM-1 production was dependent on the C. pneumoniae strain examined at low multiplicities of infection following 24 h of incubation. Strain A-03 displayed the lowest stimulatory activity in infected HUVEC, while T-2634 induced the highest levels of MCP-1, IL-8, and sICAM-1 among all strains examined, Heat-inactivated C. pneumoniae failed to stimulate production of these proteins by all strains tested, In contrast, only partial inhibition was observed by W-inactivated organisms, Results from this study demonstrate that unlike prototype respiratory strains of C. pneumoniae, the coronary strain A-03 displays divergence in the omp1 gene, In addition, the stimulation of chemokines and adhesion molecules involved in the recruitment of leukocytes to sites of inflammation by C. pneumoniae may be important in the pathogenesis of diseases associated with this organism, including atherosclerosis.
引用
收藏
页码:1370 / 1376
页数:7
相关论文
共 40 条
[1]   MAPPING ANTIGENIC DOMAINS EXPRESSED BY CHLAMYDIA-TRACHOMATIS MAJOR OUTER-MEMBRANE PROTEIN GENES [J].
BAEHR, W ;
ZHANG, YX ;
JOSEPH, T ;
SU, H ;
NANO, FE ;
EVERETT, KDE ;
CALDWELL, HD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (11) :4000-4004
[2]  
BAGGIOLINI M, 1993, ADV EXP MED BIOL, V353, P1
[3]   ANTIGENIC VARIATION AMONG STRAINS OF CHLAMYDIA-PNEUMONIAE [J].
BLACK, CM ;
JOHNSON, JE ;
FARSHY, CE ;
BROWN, TM ;
BERDAL, BP .
JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (07) :1312-1316
[4]   PARASITE-SPECIFIED PHAGOCYTOSIS OF CHLAMYDIA-PSITTACI AND CHLAMYDIA-TRACHOMATIS BY L-CELLS AND HELA-CELLS [J].
BYRNE, GI ;
MOULDER, JW .
INFECTION AND IMMUNITY, 1978, 19 (02) :598-606
[5]   STRUCTURAL AND ANTIGENIC ANALYSIS OF CHLAMYDIA-PNEUMONIAE [J].
CAMPBELL, LA ;
KUO, CC ;
GRAYSTON, JT .
INFECTION AND IMMUNITY, 1990, 58 (01) :93-97
[6]   SEROLOGICAL RESPONSE TO CHLAMYDIA-PNEUMONIAE INFECTION [J].
CAMPBELL, LA ;
KUO, CC ;
WANG, SP ;
GRAYSTON, JT .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (06) :1261-1264
[7]   MOLECULAR-IDENTIFICATION OF AN AVIAN STRAIN OF CHLAMYDIA-PSITTACI CAUSING SEVERE KERATOCONJUNCTIVITIS IN A BIRD FANCIER [J].
DEAN, D ;
SHAMA, A ;
SCHACHTER, J ;
DAWSON, CR .
CLINICAL INFECTIOUS DISEASES, 1995, 20 (05) :1179-1185
[8]  
Fryer RH, 1997, J INVEST MED, V45, P168
[9]   SIMILARITY OF CHLAMYDIA-PNEUMONIAE STRAINS IN THE VARIABLE DOMAIN-IV REGION OF THE MAJOR OUTER-MEMBRANE PROTEIN GENE [J].
GAYDOS, CA ;
QUINN, TC ;
BOBO, LD ;
EIDEN, JJ .
INFECTION AND IMMUNITY, 1992, 60 (12) :5319-5323
[10]   Replication of Chlamydia pneumoniae in vitro in human macrophages, endothelial cells, and aortic artery smooth muscle cells [J].
Gaydos, CA ;
Summersgill, JT ;
Sahney, NN ;
Ramirez, JA ;
Quinn, TC .
INFECTION AND IMMUNITY, 1996, 64 (05) :1614-1620