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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2022
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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 |
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author | Sanaei, Neda Hashemi, Seyed Mohammad Ali Dehno, Seyedeh Zahra Salehi Asl, Mozhde Mahmoudi Moini, Maryam Malek-Hosseini, Seyed Ali Hosseini, Seyed Younes Sarvari, Jamal |
author_facet | Sanaei, Neda Hashemi, Seyed Mohammad Ali Dehno, Seyedeh Zahra Salehi Asl, Mozhde Mahmoudi Moini, Maryam Malek-Hosseini, Seyed Ali Hosseini, Seyed Younes Sarvari, Jamal |
author_sort | Sanaei, Neda |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8984791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-89847912022-04-11 Precore/core mutations of hepatitis B virus genotype D arising in different states of infection Sanaei, Neda Hashemi, Seyed Mohammad Ali Dehno, Seyedeh Zahra Salehi Asl, Mozhde Mahmoudi Moini, Maryam Malek-Hosseini, Seyed Ali Hosseini, Seyed Younes Sarvari, Jamal Clin Exp Hepatol Original Paper 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. Termedia Publishing House 2022-03-23 2022-03 /pmc/articles/PMC8984791/ /pubmed/35415256 http://dx.doi.org/10.5114/ceh.2022.114253 Text en Copyright © 2022 Clinical and Experimental Hepatology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/) ) |
spellingShingle | Original Paper Sanaei, Neda Hashemi, Seyed Mohammad Ali Dehno, Seyedeh Zahra Salehi Asl, Mozhde Mahmoudi Moini, Maryam Malek-Hosseini, Seyed Ali Hosseini, Seyed Younes Sarvari, Jamal Precore/core mutations of hepatitis B virus genotype D arising in different states of infection |
title | Precore/core mutations of hepatitis B virus genotype D arising in different states of infection |
title_full | Precore/core mutations of hepatitis B virus genotype D arising in different states of infection |
title_fullStr | Precore/core mutations of hepatitis B virus genotype D arising in different states of infection |
title_full_unstemmed | Precore/core mutations of hepatitis B virus genotype D arising in different states of infection |
title_short | Precore/core mutations of hepatitis B virus genotype D arising in different states of infection |
title_sort | precore/core mutations of hepatitis b virus genotype d arising in different states of infection |
topic | Original Paper |
url | 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 |
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