Viral Hepatitis
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jul 15, 2003; 9(7): 1496-1500
Published online Jul 15, 2003. doi: 10.3748/wjg.v9.i7.1496
Acute hepatitis C in a chronically HIV-infected patient: Evolution of different viral genomic regions
Diego Flichman, Veronica Kott, Silvia Sookoian, Rodolfo Campos
Diego Flichman, Veronica Kott, Rodolfo Campos, Catedra de Virologia, Facultad de Farmacia y Bioquimica, Universidad de Buenos Aires, Argentina
Silvia Sookoian, Unidad de Higado, Hospital "Dr.Cosme Argerich", Argentina
Author contributions: All authors contributed equally to the work.
Supported by the grants from the Universidad de Buenos Aires (SECyT-UBA, TB14), Consejo Nacional de Investigaciones CientÍficas y Técnicas (CONICET, PIP723), Agencia Nacional de PromociÓn Científica y TecnolÓgica (ANPCyT, PICT 01610) and Ministerio de Salud PÚblica de la NaciÓn (Beca Carrillo-Oñativia)
Correspondence to: Dr. Rodolfo Campos, Facultad de Farmacia y Bioquimica, Junin 956, 4th floor, (1113), Capital Federal, Argentina. rcampos@ffyb.uba.ar
Telephone: +5411-49648264 Fax: +5411-45083645
Received: February 26, 2003
Revised: March 4, 2003
Accepted: March 16, 2003
Published online: July 15, 2003
Abstract

AIM: To analyze the molecular evolution of different viral genomic regions of HCV in an acute HCV infected patient chronically infected with HIV through a 42-month follow-up.

METHODS: Serum samples of a chronically HIV infected patient that seroconverted to anti HCV antibodies were sequenced, from the event of superinfection through a period of 17 mo and in a late sample (42nd month). Hypervariable genomic regions of HIV (V3 loop of the gp120) and HCV (HVR-1 on the E2 glycoprotein gene) were studied. In order to analyze genomic regions involved in different biological functions and with the cellular immune response, HCV core and NS5A were also chosen to be sequenced. Amplification of the different regions was done by RT-PCR and directly sequenced. Confirmation of sequences was done on reamplified material. Nucleotide sequences of the different time points were aligned with CLUSTAL W 1.5, and the corresponding amino acid ones were deduced.

RESULTS: Hypervariable genomic regions of both viruses (HVR1 and gp120 V3 loop) presented several nonsynonymous changes but, while in the gp120 V3 loop mutations were detected in the sample obtained right after HCV superinfection and maintained throughout, they occurred following a sequential and cumulative pattern in the HVR1. In the NS5A region of HCV, two amino acid changes were detected during the follow-up period, whereas the core region presented several amino acid replacements, once the HCV chronic infection had been established.

CONCLUSION: During the HIV-HCV superinfection, each genomic region analyzed shows a different evolutionary pattern. Most of the nucleotide substitutions observed are non-synonymous and clustered in previously described epitopes, thus suggesting an immune-driven evolutionary process.

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