Molecular characterisation of Chlamydia pneumoniae associated to atherosclerosis

被引:6
作者
El Yazouli, Loubna [1 ,2 ]
Criscuolo, Alexis [3 ]
Hejaji, Hicham [4 ]
Bouazza, Mohamed [5 ]
Elmdaghri, Naima [1 ]
Alami, Aziz Aroussi [4 ]
Amraoui, Abdelouahed [5 ]
Dakka, Nadia [2 ]
Radouani, Fouzia [1 ]
机构
[1] Inst Pasteur Maroc, Chlamydiae & Mycoplasma Lab, Pl Louis Pasteur, Casablanca 20360, Morocco
[2] Univ Mohamed V Rabat, Fac Sci, Biochem & Immunol Lab, Rabat 10000, Morocco
[3] Inst Pasteur, Bioinformat & Biostat Hub C3BI, CNRS, USR 3756,IP, F-75724 Paris, France
[4] CHU Ibn Rochd, Cardiovasc Surg Dept, Casablanca 20360, Morocco
[5] CHU Ibn Rochd, Ophthalmol Dept, Casablanca 20360, Morocco
关键词
Chlamydia pneumoniae; association; atherosclerosis; strains; genotyping; phylogenetics; CORONARY-HEART-DISEASE; CHLAMYDOPHILA-PNEUMONIAE; GENOME SEQUENCES; RISK-FACTOR; INFECTION; DNA; MACROPHAGES; PERFORMANCE; PHYLOGENIES; ACCURACY;
D O I
10.1093/femspd/ftx039
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 associated with chronic inflammatory diseases such as asthma and atherosclerosis, and its detection in human carotid and coronary atheroma suggests some support for its involvement in atherogenesis. The main objective of our study was to evaluate the association between Chlamydia pneumoniae and atherosclerosis in Moroccan patients through a case-control approach and detected strain genotyping. A total of 137 cases and 124 controls were enrolled, nested PCR was performed for Chlamydia pneumoniae screening of the peripheral blood mononuclear cells (PBMCs) of both cases and controls as well as atheroma plaques from 37 cases, and positive samples were subjected to sequencing for genotyping and phylogenetic analysis. The results showed 54% and 18%, respectively, for positivity in cases and control PBMCs and 86.5% in atheroma plaques, the difference being significant between the two groups (P < 0.001, ORa = 8.580, CI, 95% [3.273-22.491]). Strain sequence analyses showed more than 98% similarity with human reference strains, and revealed various genotypes. This study supports the involvement of Chlamydia pneumoniae in atherosclerosis in the studied population and genotyping revealed that detected strains were identical to human strains circulating worldwide.
引用
收藏
页数:7
相关论文
共 46 条
[1]  
Agarwala R, 2018, NUCLEIC ACIDS RES, V46, pD8, DOI [10.1093/nar/gks1189, 10.1093/nar/gkx1095, 10.1093/nar/gkq1172]
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]   Approximate likelihood-ratio test for branches: A fast, accurate, and powerful alternative [J].
Anisimova, Maria ;
Gascuel, Olivier .
SYSTEMATIC BIOLOGY, 2006, 55 (04) :539-552
[4]   Survey of Branch Support Methods Demonstrates Accuracy, Power, and Robustness of Fast Likelihood-based Approximation Schemes [J].
Anisimova, Maria ;
Gil, Manuel ;
Dufayard, Jean-Francois ;
Dessimoz, Christophe ;
Gascuel, Olivier .
SYSTEMATIC BIOLOGY, 2011, 60 (05) :685-699
[5]  
[Anonymous], 2013, WHO REPORT WORLD HEA
[6]   No evidence of involvement of Chlamydia pneumoniae in severe cerebrovascular atherosclerosis by means of quantitative real-time polymerase chain reaction [J].
Apfalter, P ;
Barousch, W ;
Nehr, M ;
Willinger, B ;
Rotter, M ;
Hirschl, AM .
STROKE, 2004, 35 (09) :2024-2028
[7]   Association between Chlamydia pneumoniae and acute myocardial infarction in young men in the united states military:: The importance of timing of exposure measurement [J].
Arcari, CM ;
Gaydos, CA ;
Nieto, FJ ;
Krauss, M ;
Nelson, KE .
CLINICAL INFECTIOUS DISEASES, 2005, 40 (08) :1123-1130
[8]  
Assar Omid, 2015, Glob J Health Sci, V8, P260, DOI 10.5539/gjhs.v8n4p260
[9]  
Azarkar Z, 2011, ARYA ATHEROSCLER, V6, P125
[10]   Chlamydia pneumoniae, but not Bartonella quintana, is associated with coronary heart disease:: results of a French case-control study [J].
Badiaga, S ;
Paganelli, F ;
Parola, P ;
Beghin, M ;
Barrau, K ;
Eb, F ;
Brouqui, P .
CLINICAL MICROBIOLOGY AND INFECTION, 2003, 9 (04) :315-318