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Precore/core mutations of hepatitis B virus genotype D arising in different states of infection

AIM OF THE STUDY: Precore/core variations and liver disease progression have been suggested. In this study, we aimed to determine the frequency of precore/core mutations in hepatitis B virus (HBV)-infected patients at various clinical stages. MATERIAL AND METHODS: In total, 73 HBV-infected patients...

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Detalles Bibliográficos
Autores principales: Sanaei, Neda, Hashemi, Seyed Mohammad Ali, Dehno, Seyedeh Zahra Salehi, Asl, Mozhde Mahmoudi, Moini, Maryam, Malek-Hosseini, Seyed Ali, Hosseini, Seyed Younes, Sarvari, Jamal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984791/
https://www.ncbi.nlm.nih.gov/pubmed/35415256
http://dx.doi.org/10.5114/ceh.2022.114253
Descripción
Sumario:AIM OF THE STUDY: Precore/core variations and liver disease progression have been suggested. In this study, we aimed to determine the frequency of precore/core mutations in hepatitis B virus (HBV)-infected patients at various clinical stages. MATERIAL AND METHODS: In total, 73 HBV-infected patients including 26 inactive carriers (IC), 20 chronic active (CA), and 27 patients with liver cirrhosis/hepatocellular carcinoma (C/HCC) were randomly selected. The HBV DNA was extracted from the sera and subjected to nested PCR for amplification of precore/core region. The PCR product was then sequenced by the Sanger method. RESULTS: The stop codon of W28*(G1896A) was determined as the most prevalent mutation (55%) of the precore region. The comparison of groups also demonstrated that core substitutions at residues of S21, E40 and I105 (< 0.05) correlated with the development of the inactive carrier state. Furthermore, the total substitutions in Th epitopes (117-131) were significantly higher in the C/HCC group than the IC and CA groups (p = 0.001). CONCLUSIONS: Our results indicated a high frequency of W28* mutation in HBV studied patients. Moreover, variations including S21, E40 and I105 and R151 that were mapped onto cellular epitopes might be related to inactive state development.