Prevalence of erythrovirus genotypes in the myocardium of patients with dilated cardiomyopathy

被引:64
作者
Kuehl, U. [1 ]
Lassner, D. [2 ]
Pauschinger, M. [1 ]
Gross, U. M. [2 ]
Seeberg, B. [1 ]
Noutsias, M. [1 ]
Poller, W. [1 ]
Schultheiss, H. -P. [1 ]
机构
[1] Charite, Dept Cardiol & Pneumol, D-12200 Berlin, Germany
[2] IKDT, Berlin, Germany
关键词
erythrovirus; genotypes; heart failure; dilated cardiomyopathy; prevalence;
D O I
10.1002/jmv.21187
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Parvovirus B19 (PVB19) is a member of the human erythrovirus family detected frequently in endomyocardial biopsies from patients with dilated cardiomyopathy. Human erythroviruses cluster into three genotypes 1-3 which share a high degree of homology between major structural proteins and may cause indistinguishable infections clinically and serologically. In human cardiac tissue erythrovirus genotypes other than PVB19 have not yet been reported. Three hundred seventeen consecutive patients with symptomatic dilated cardiomyopathy (median left ventricular ejection fraction: 28.6%, range 5-45%) who underwent endomyocardial biopsy for the elucidation of the etiology, were analyzed using a new consensus PCR assay designed for the detection of the three erythrovirus genotype sequences. Endomyocardial biopsies of 151 (47.6%) patients were erythrovirus-positive. Genotype 1 specific sequences were detected in 43/151 (28.5%) of positive biopsy samples, whereas genotype 2-specific sequences so far considered rare in human disease and not yet been described in human heart tissue was identified in 108/151 (71.5%) of virus-positive endomyocardial biopsies with a preference in patients above 50 years of age. In spite of younger age, systolic left ventricular dysfunction of genotype 1-positive patients was significantly reduced as compared to genotype 2-positive patients (24.4 +/- 10.4% vs. 31.0 +/- 9.5%, P=0.0001) at the initial presentation. The data show that two genetically distinct erythrovirus variants with a different age distribution are detectable in endomyocardial biopsies of patients with dilated cardiomyopathy. The erythrovirus genotype, not described previously in human heart tissue, is highly prevalent in the heart but the less prevalent genotype 1 is associated with more severe disturbed cardiac function.
引用
收藏
页码:1243 / 1251
页数:9
相关论文
共 41 条
[31]   Detection of adenoviral genome in the myocardium of adult patients with idiopathic left ventricular dysfunction [J].
Pauschinger, M ;
Bowles, NE ;
Fuentes-Garcia, FJ ;
Pham, V ;
Kühl, U ;
Schwimmbeck, PL ;
Schutheiss, HP ;
Towbin, JA .
CIRCULATION, 1999, 99 (10) :1348-1354
[32]   LightCycler consensus PCR for rapid and differential detection of human erythrovirus B19 and V9 isolates [J].
Schalasta, G ;
Schmid, M ;
Lachmund, T ;
Enders, G .
JOURNAL OF MEDICAL VIROLOGY, 2004, 73 (01) :54-59
[33]   Genetic diversity within human erythroviruses: Identification of three genotypes [J].
Servant, A ;
Laperche, S ;
Lallemand, F ;
Marinho, V ;
Saint Maur, GD ;
Meritet, JF ;
Garbarg-Chenon, A .
JOURNAL OF VIROLOGY, 2002, 76 (18) :9124-9134
[34]   NUCLEOTIDE-SEQUENCE AND GENOME ORGANIZATION OF HUMAN PARVOVIRUS B19 ISOLATED FROM THE SERUM OF A CHILD DURING APLASTIC CRISIS [J].
SHADE, RO ;
BLUNDELL, MC ;
COTMORE, SF ;
TATTERSALL, P ;
ASTELL, CR .
JOURNAL OF VIROLOGY, 1986, 58 (03) :921-936
[35]   High prevalence of cardiac parvovirus B19 infection in patients with isolated left ventricular diastolic dysfunction [J].
Tschöpe, C ;
Bock, CT ;
Kasner, M ;
Noutsias, M ;
Westermann, D ;
Schwimmbeck, PL ;
Pauschinger, M ;
Poller, WC ;
Kühl, U ;
Kandolf, R ;
Schultheiss, HP .
CIRCULATION, 2005, 111 (07) :879-886
[36]   PARTIAL NUCLEOTIDE SEQUENCING AND CHARACTERIZATION OF HUMAN PARVOVIRUS-B19 GENOME DNAS FROM DAMAGED HUMAN FETUSES AND FROM PATIENTS WITH LEUKEMIA [J].
UMENE, K ;
NUNOUE, T .
JOURNAL OF MEDICAL VIROLOGY, 1993, 39 (04) :333-339
[37]   Differential aspects of endothelial function of the coronary microcirculation considering myocardial virus persistence, endothelial activation, and myocardial leukocyte infiltrates [J].
Vallbracht, KB ;
Schwimmbeck, PL ;
Kühl, U ;
Rauch, U ;
Seeberg, B ;
Schultheiss, HP .
CIRCULATION, 2005, 111 (14) :1784-1791
[38]   Antiphospholipid antibodies in pediatric and adult patients with rheumatic disease are associated with parvovirus B19 infection [J].
von Landenberg, P ;
Lehmann, HW ;
Knöll, A ;
Dorsch, S ;
Modrow, S .
ARTHRITIS AND RHEUMATISM, 2003, 48 (07) :1939-1947
[39]   α5β1 integrin as a cellular coreceptor for human parvovirus B19:: Requirement of functional activation of β1 integrin for viral entry [J].
Weigel-Kelley, KA ;
Yoder, MC ;
Srivastava, A .
BLOOD, 2003, 102 (12) :3927-3933
[40]   A viral phospholipase A2 is required for parvovirus infectivity [J].
Zádori, Z ;
Szelei, J ;
Lacoste, MC ;
Li, Y ;
Gariépy, S ;
Raymond, P ;
Allaire, M ;
Nabi, IR ;
Tijssen, P .
DEVELOPMENTAL CELL, 2001, 1 (02) :291-302