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Can J Microbiol. 2012 Feb;58(2):200-5. doi: 10.1139/w11-119. Epub 2012 Jan 26.

Genotyping of Human parvovirus B19 among Brazilian patients with hemoglobinopathies.

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1
Regional Blood Center of Ribeirão Preto-FUNDHERP, Faculty of Medicine in Ribeirão Preto-FMRP, University of São Paulo-USP, 2051 Tenente Catão Roxo Str., Ribeirão Preto, São Paulo, Brazil. svetlyosf@yahoo.com

Abstract

Human parvovirus B19 (B19V) infection can be a life-threatening condition among patients with hereditary (chronic) hemolytic anemias. Our objective was to characterize the infection molecularly among patients with sickle cell disease and thalassemia. Forty-seven patients (37 with sickle cell disease, and 10 with β-thalassemia major) as well as 47 healthy blood donors were examined for B19V infection by anti-B19V IgG enzyme immunoassay, quantitative PCR, which detects all B19V genotypes, and DNA sequencing. B19V viremia was documented in nine patients (19.1%) as two displayed acute infection and the rest had a low titre viremia (mean 3.4 × 10(4) copies/mL). All donors were negative for B19V DNA. Anti-B19V IgG was detected in 55.3% of the patients and 57.4% among the donors. Based on partial NS1 fragments, all patient isolates were classified as genotype 1 and subgenotype 1A. The evolutionary events of the examined partial NS1 gene sequence were associated with a lack of positive selection. The quantification of all B19V genotypes by a single hydrolytic probe is a technically useful method, but it is difficult to establish relationships between B19V sequence characteristics and infection outcome.

PMID:
22280886
DOI:
10.1139/w11-119
[Indexed for MEDLINE]
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