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Full coding hepatitis E virus genotype 3 genome amplification method
Hepatitis E virus (HEV) genotype 3 produces zoonotic infection associated with the consumption of infected animals. HEV infections can become chronic in immunocompromised (IC) patients. The viral genome has three well defined open reading frames (ORF1, ORF2 and ORF3) within which various domains and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172825/ https://www.ncbi.nlm.nih.gov/pubmed/26784284 http://dx.doi.org/10.1016/j.jviromet.2016.01.004 |
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author | Muñoz-Chimeno, M. Forero, J.E. Echevarría, J.M. Muñoz-Bellido, J.L. Vázquez-López, L. Morago, L. García-Galera, M.C. Avellón, A. |
author_facet | Muñoz-Chimeno, M. Forero, J.E. Echevarría, J.M. Muñoz-Bellido, J.L. Vázquez-López, L. Morago, L. García-Galera, M.C. Avellón, A. |
author_sort | Muñoz-Chimeno, M. |
collection | PubMed |
description | Hepatitis E virus (HEV) genotype 3 produces zoonotic infection associated with the consumption of infected animals. HEV infections can become chronic in immunocompromised (IC) patients. The viral genome has three well defined open reading frames (ORF1, ORF2 and ORF3) within which various domains and functions have been described. This paper (i) describes a new method of complete sequencing of the HEV coding region through overlapping PCR systems, (ii) establishes a consensus sequence and polymorphic positions (PP) for each domain, and (iii) analyzes the complete coding sequence of an IC patient. With regard to the consensus, a high percentage of PP was observed in protease (PP = 19%) and the X domain (PP = 22%) within ORF1, the N-terminal region of the S domain (PP = 22%) in ORF2, and the P1 (PP = 35%) and P2 (PP = 25%) domains in ORF3. In contrast, the ORF1 Y, ORF2 S, ORF2 M and ORF3 D1 domains were conserved in the reference sequences (0.40, 1, 0.70 and 0% of PP, respectively). The sequence from the IC patient had more mutations in the RpRp (D1235G, Q1242R, S1454T, V1480I, I1502 V, K1511R, G1373 V, E1442D, V1693 M), the terminal ORF2 S- domain (F10L, S26T, G36S, S70P, A105 V, I113 V), the X domain (T938 M, T856 V, S898A) and the helicase (S1014N, S975T, Q1133 K). |
format | Online Article Text |
id | pubmed-7172825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71728252020-04-22 Full coding hepatitis E virus genotype 3 genome amplification method Muñoz-Chimeno, M. Forero, J.E. Echevarría, J.M. Muñoz-Bellido, J.L. Vázquez-López, L. Morago, L. García-Galera, M.C. Avellón, A. J Virol Methods Article Hepatitis E virus (HEV) genotype 3 produces zoonotic infection associated with the consumption of infected animals. HEV infections can become chronic in immunocompromised (IC) patients. The viral genome has three well defined open reading frames (ORF1, ORF2 and ORF3) within which various domains and functions have been described. This paper (i) describes a new method of complete sequencing of the HEV coding region through overlapping PCR systems, (ii) establishes a consensus sequence and polymorphic positions (PP) for each domain, and (iii) analyzes the complete coding sequence of an IC patient. With regard to the consensus, a high percentage of PP was observed in protease (PP = 19%) and the X domain (PP = 22%) within ORF1, the N-terminal region of the S domain (PP = 22%) in ORF2, and the P1 (PP = 35%) and P2 (PP = 25%) domains in ORF3. In contrast, the ORF1 Y, ORF2 S, ORF2 M and ORF3 D1 domains were conserved in the reference sequences (0.40, 1, 0.70 and 0% of PP, respectively). The sequence from the IC patient had more mutations in the RpRp (D1235G, Q1242R, S1454T, V1480I, I1502 V, K1511R, G1373 V, E1442D, V1693 M), the terminal ORF2 S- domain (F10L, S26T, G36S, S70P, A105 V, I113 V), the X domain (T938 M, T856 V, S898A) and the helicase (S1014N, S975T, Q1133 K). Elsevier B.V. 2016-04 2016-01-16 /pmc/articles/PMC7172825/ /pubmed/26784284 http://dx.doi.org/10.1016/j.jviromet.2016.01.004 Text en Copyright © 2016 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Muñoz-Chimeno, M. Forero, J.E. Echevarría, J.M. Muñoz-Bellido, J.L. Vázquez-López, L. Morago, L. García-Galera, M.C. Avellón, A. Full coding hepatitis E virus genotype 3 genome amplification method |
title | Full coding hepatitis E virus genotype 3 genome amplification method |
title_full | Full coding hepatitis E virus genotype 3 genome amplification method |
title_fullStr | Full coding hepatitis E virus genotype 3 genome amplification method |
title_full_unstemmed | Full coding hepatitis E virus genotype 3 genome amplification method |
title_short | Full coding hepatitis E virus genotype 3 genome amplification method |
title_sort | full coding hepatitis e virus genotype 3 genome amplification method |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172825/ https://www.ncbi.nlm.nih.gov/pubmed/26784284 http://dx.doi.org/10.1016/j.jviromet.2016.01.004 |
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