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Updated: Feb 7, 2026

Genotypic Inference of HIV-1 Tropism Using Population-based Sequencing of V3
Published on: December 27, 2010
Prevalence and Genotypes of Parvovirus B19 Among HIV Positive Children in Ibadan, Oyo State, Nigeria
B O Aleru1, B A Olusola1, A O Faneye1
1Department of Virology, College of Medicine, University of Ibadan, Nigeria.
Insights
Human Parvovirus B19 (B19V) infection is prevalent in HIV-positive children in sub-Saharan Africa, with genotype 1 detected. This B19V infection is significantly linked to severe anemia in these children.
Area of Science:
- Virology
- Pediatrics
- Infectious Diseases
Background:
- Human Parvovirus B19 (B19V) is a widespread infection, particularly in sub-Saharan Africa.
- B19V can cause persistent anemia in immunocompromised individuals, notably complicating Human Immunodeficiency Virus (HIV) infection.
Purpose of the Study:
- To determine the prevalence and genotypes of B19V in HIV-positive children.
- To investigate the relationship between B19V infection and anemia severity in this population.
Main Methods:
- Blood samples were collected from HIV-positive children.
- Polymerase chain reaction (PCR) and gel electrophoresis were used to detect B19V DNA.
- Positive PCR products were sequenced for genotype analysis and phylogenetic comparison with HIV-negative controls.
Main Results:
- The prevalence of B19V DNA was 1.3% (2 out of 158) among HIV-positive children.
- A significant association was found between B19V infection and the severity of anemia (p=0.015).
- Phylogenetic analysis revealed all detected B19V isolates belonged to genotype 1.
Conclusions:
- B19V infection has a low prevalence but is significantly associated with anemia in HIV-positive children.
- Genotype 1 is the predominant circulating B19V genotype in this cohort.
- Findings provide insight into B19V epidemiology and its impact on anemia in HIV-infected children.
Abstract:
Human Parvovirus B19 (B19V) is a global infection with over 50% of infected children residing in sub-Saharan Africa. It causes persistent anaemia under immuno-compromised states such as HIV infection, thereby complicating the course of HIV infection. This study was therefore designed to determine the prevalence and genotypes of B19V among HIV positive children. Blood specimens were collected from HIV positive children and genomic DNA extracted and assayed for the presence of Parvovirus B19 DNA using polymerase chain reaction and the product detected by gel electrophoresis. Amplicons for positive PCR were purified and sequenced for genotype analysis. For the purpose of comparison (differences in the sequences of the NS1/VP1u region), nine HIV negative children were enrolled in this study. Two (1.3%) of the 158 HIV infected children were positive for Parvovirus B19 DNA. Analysis of the results showed a low prevalence of Parvovirus B19 among HIV positive children but a significant relationship was established between Parvovirus B19 infection and the severity of anaemia (p=0.015). Phylogenetic analysis of the sequence data showed that all the B19 virus isolates detected in this study were genotype 1. This study therefore has been able to give an insight to the prevalence and circulating genotypes of Parvovirus B19 among HIV infected children and also establishing a relationship between anaemia and parvovirus B19 infection.
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