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Inicio Porto Biomedical Journal Genetical variability of VP1 gene of BK virus in HIV-infected patients
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Vol. 2. Núm. 5.
Páginas 229 (septiembre - octubre 2017)
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Vol. 2. Núm. 5.
Páginas 229 (septiembre - octubre 2017)
PS037
Open Access
Genetical variability of VP1 gene of BK virus in HIV-infected patients
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1611
O. Lijeskić1,
Autor para correspondencia
oljalol2@gmail.com

Corresponding author.
, S. Leštarević1, D. Karalić2
1 School of Medicine, University of Belgrade, Portugal
2 Institute of Microbiology and Immunology, School of Medicine, University of Belgrade, Portugal
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Aim: The aims of this study were: to determine the prevalence of BK viruria in HIV-infected patients, to determine the distribution of BKV subtypes and the presence of nucleotide substitutions and mutations in the VP1 gene of BKV isolates.

Introduction: A broad range of diseases associated with BK virus (BKV) such as nephritis, haemorrhagic cystitis, encephalitis, retinitis and pneumonia have been reported in HIV-infected patients over the last few years. However, these diseases do not occur in all HIV-infected patients, suggesting that other factors, such as genetic variability of BKV, can contribute to their occurrence. Mutations in the BC loop of the VP1 gene may lead to selection of more aggressive variants of BKV.

Methods: The study included 50 HIV-infected patients. Seminested PCR was used for amplification of 290-nt fragment within the VP1 gene and all the positive PCR products were then directly sequenced. The sequence analysis was performed by using the appropriate bioinformatics tools.

Results: The frequency of BK viruria in HIV-infected patients was 56%. The predominant BKV subtype was I, followed by subtype IV. The majority of mutations were located within BC loop of VP1. The most frequent mutation was E82D.

Conclusion: The increased levels of BKV replication are associated with a higher incidence of mutations in the BC loop of VP1, and mutations in this domain may lead to changed tropism and the selection of more aggressive variants of BKV. Further studies are needed in order to select the patients with a higher risk of developing BKV associated-diseases.

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