Hepatitis B and D viruses replication interference: Influence of hepatitis B genotype
AIM: To study the hepatitis B virus(HBV) and hepatitis D virus(HDV) replication interferences in patients with chronic hepatitis delta infected with different HBV genotypes.METHODS: We conducted a transversal study including 68 chronic hepatitis delta(CHD)(37 HIVpositive) patients and a control grou...
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description | AIM: To study the hepatitis B virus(HBV) and hepatitis D virus(HDV) replication interferences in patients with chronic hepatitis delta infected with different HBV genotypes.METHODS: We conducted a transversal study including 68 chronic hepatitis delta(CHD)(37 HIVpositive) patients and a control group of 49 chronic hepatitis B(CHB)(22 HIV-positive) patients. In addition, a dynamic follow-up was performed in 16 CHD patients. In all the samples, the surface antigen of hepatitis B(HBs Ag) serum titers were analyzed with the Monolisa HBs Ag Ultra system(Bio-Rad), using as quantification standard a serial dilution curve of an international HBs Ag standard. Serum HBV-DNA titers were analyzed using the Roche Cobas Taq Man(Roche, Barcelona, Spain), and the serum HDV-RNA using an in-house real-time q RT-PCR method, with Taq Man probes. HBV genotype was determined with the line immunoassay Li PA HBV genotyping system(Innogenetics, Ghent, Belgium). In those patients negative for Li PA assay, a nested PCR method of complete HBs Ag coding region, followed by sequence analysis was applied.RESULTS: No differences in the HBV-DNA levels were found in CHB patients infected with different HBV genotypes. However, in CHD patients the HBV-DNA levels were lower in those infected with HBV-A than in those with HBV-D, both in HIV negative [median(IQR): 1.25(1.00-1.35) vs 2.95(2.07-3.93) log10(copies/m L), P = 0.013] and HIV positive patients [2.63(1.24-2.69) vs 7.25(4.61-7.55) log10(copies/m L), P < 0.001]. This was confirmed in the dynamic study of the HBV/HDV patients. These differences induce an under-estimation of HBV-A incidence in patients with CHD analyzed with Li PA assay. Finally, the HBs Ag titers reflected no significant differences in CHD patients infected with HBV-A or D.CONCLUSION: Viral replication interference between HBV and HDV is HBV-genotype dependent, and more evident in patients infected with HBV-genotype A, than with HBV-D or E. |
doi_str_mv | 10.3748/wjg.v22.i11.3165 |
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In addition, a dynamic follow-up was performed in 16 CHD patients. In all the samples, the surface antigen of hepatitis B(HBs Ag) serum titers were analyzed with the Monolisa HBs Ag Ultra system(Bio-Rad), using as quantification standard a serial dilution curve of an international HBs Ag standard. Serum HBV-DNA titers were analyzed using the Roche Cobas Taq Man(Roche, Barcelona, Spain), and the serum HDV-RNA using an in-house real-time q RT-PCR method, with Taq Man probes. HBV genotype was determined with the line immunoassay Li PA HBV genotyping system(Innogenetics, Ghent, Belgium). In those patients negative for Li PA assay, a nested PCR method of complete HBs Ag coding region, followed by sequence analysis was applied.RESULTS: No differences in the HBV-DNA levels were found in CHB patients infected with different HBV genotypes. However, in CHD patients the HBV-DNA levels were lower in those infected with HBV-A than in those with HBV-D, both in HIV negative [median(IQR): 1.25(1.00-1.35) vs 2.95(2.07-3.93) log10(copies/m L), P = 0.013] and HIV positive patients [2.63(1.24-2.69) vs 7.25(4.61-7.55) log10(copies/m L), P &lt; 0.001]. This was confirmed in the dynamic study of the HBV/HDV patients. These differences induce an under-estimation of HBV-A incidence in patients with CHD analyzed with Li PA assay. Finally, the HBs Ag titers reflected no significant differences in CHD patients infected with HBV-A or D.CONCLUSION: Viral replication interference between HBV and HDV is HBV-genotype dependent, and more evident in patients infected with HBV-genotype A, than with HBV-D or E.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v22.i11.3165</identifier><identifier>PMID: 27003993</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Inc</publisher><subject>Adult ; Basic Study ; Biomarkers - blood ; Coinfection ; Cross-Sectional Studies ; DNA, Viral - blood ; DNA, Viral - genetics ; Female ; Genotype ; Hepatitis ; Hepatitis B - complications ; Hepatitis B - diagnosis ; Hepatitis B - virology ; Hepatitis B Surface Antigens - blood ; Hepatitis B virus - genetics ; Hepatitis B virus - growth & development ; Hepatitis B virus - immunology ; Hepatitis D, Chronic - complications ; Hepatitis D, Chronic - diagnosis ; Hepatitis D, Chronic - virology ; Hepatitis Delta Virus - genetics ; Hepatitis Delta Virus - growth & development ; hepatitis;Replication ; HIV Infections - complications ; HIV Infections - virology ; Humans ; interference;Viral ; Longitudinal Studies ; Male ; Middle Aged ; replication ; Retrospective Studies ; RNA, Viral - blood ; RNA, Viral - genetics ; Time Factors ; Viral Load ; Virus Replication ; virus;Delta ; virus;Hepatitis</subject><ispartof>World journal of gastroenterology : WJG, 2016-03, Vol.22 (11), p.3165-3174</ispartof><rights>The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved. 2016</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-c490cd43747ee268bd95af162ff823fc909afb4ef01ea4b8f09d37701092ceb93</citedby><cites>FETCH-LOGICAL-c440t-c490cd43747ee268bd95af162ff823fc909afb4ef01ea4b8f09d37701092ceb93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789991/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789991/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27003993$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Antonio Madejón Míriam Romero ángela Hernández Araceli García-Sánchez Marta Sánchez-Carrillo Antonio Olveira Javier García-Samaniego</creatorcontrib><title>Hepatitis B and D viruses replication interference: Influence of hepatitis B genotype</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM: To study the hepatitis B virus(HBV) and hepatitis D virus(HDV) replication interferences in patients with chronic hepatitis delta infected with different HBV genotypes.METHODS: We conducted a transversal study including 68 chronic hepatitis delta(CHD)(37 HIVpositive) patients and a control group of 49 chronic hepatitis B(CHB)(22 HIV-positive) patients. In addition, a dynamic follow-up was performed in 16 CHD patients. In all the samples, the surface antigen of hepatitis B(HBs Ag) serum titers were analyzed with the Monolisa HBs Ag Ultra system(Bio-Rad), using as quantification standard a serial dilution curve of an international HBs Ag standard. Serum HBV-DNA titers were analyzed using the Roche Cobas Taq Man(Roche, Barcelona, Spain), and the serum HDV-RNA using an in-house real-time q RT-PCR method, with Taq Man probes. HBV genotype was determined with the line immunoassay Li PA HBV genotyping system(Innogenetics, Ghent, Belgium). In those patients negative for Li PA assay, a nested PCR method of complete HBs Ag coding region, followed by sequence analysis was applied.RESULTS: No differences in the HBV-DNA levels were found in CHB patients infected with different HBV genotypes. However, in CHD patients the HBV-DNA levels were lower in those infected with HBV-A than in those with HBV-D, both in HIV negative [median(IQR): 1.25(1.00-1.35) vs 2.95(2.07-3.93) log10(copies/m L), P = 0.013] and HIV positive patients [2.63(1.24-2.69) vs 7.25(4.61-7.55) log10(copies/m L), P &lt; 0.001]. This was confirmed in the dynamic study of the HBV/HDV patients. These differences induce an under-estimation of HBV-A incidence in patients with CHD analyzed with Li PA assay. Finally, the HBs Ag titers reflected no significant differences in CHD patients infected with HBV-A or D.CONCLUSION: Viral replication interference between HBV and HDV is HBV-genotype dependent, and more evident in patients infected with HBV-genotype A, than with HBV-D or E.</description><subject>Adult</subject><subject>Basic Study</subject><subject>Biomarkers - blood</subject><subject>Coinfection</subject><subject>Cross-Sectional Studies</subject><subject>DNA, Viral - blood</subject><subject>DNA, Viral - genetics</subject><subject>Female</subject><subject>Genotype</subject><subject>Hepatitis</subject><subject>Hepatitis B - complications</subject><subject>Hepatitis B - diagnosis</subject><subject>Hepatitis B - virology</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatitis B virus - growth & development</subject><subject>Hepatitis B virus - immunology</subject><subject>Hepatitis D, Chronic - complications</subject><subject>Hepatitis D, Chronic - diagnosis</subject><subject>Hepatitis D, Chronic - virology</subject><subject>Hepatitis Delta Virus - genetics</subject><subject>Hepatitis Delta Virus - growth & development</subject><subject>hepatitis;Replication</subject><subject>HIV Infections - complications</subject><subject>HIV Infections - virology</subject><subject>Humans</subject><subject>interference;Viral</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Middle Aged</subject><subject>replication</subject><subject>Retrospective Studies</subject><subject>RNA, Viral - blood</subject><subject>RNA, Viral - genetics</subject><subject>Time Factors</subject><subject>Viral Load</subject><subject>Virus Replication</subject><subject>virus;Delta</subject><subject>virus;Hepatitis</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU1vEzEQhi0EoqFw54T2yCVh_LGxhwMSLfRDqsSFni3v7njjauPd2pug_nscNUTFI9kjzTuvx34Y-8hhJbUyX_489Ku9EKvA-Urydf2KLYTguBRGwWu24AB6iVLoM_Yu5wcAIWUt3rIzoQEkolyw-xua3BzmkKuLysWu-lHtQ9plylWiaQhtKY6xCnGm5ClRbOlrdRv9sDuk1eirzQuDnuI4P030nr3xbsj04Xies_urn78vb5Z3v65vL7_fLVulYC47Qtup8hRNJNam6bB2nq-F90ZI3yKg840iD5ycaowH7KTWwAFFSw3Kc_bt2XfaNVvqWopzcoOdUti69GRHF-z_lRg2th_3VmmDiLwYfD4apPFxR3m225BbGgYXadxly7Wu18JgrYsUnqVtGnNO5E_XcLAHGrbQsIWGLTTsgUZp-fRyvFPDv-8vAnn03IyxfwyxP2kQzGFhDcoorJXCEkaZMslfguOYEA</recordid><startdate>20160321</startdate><enddate>20160321</enddate><creator>Antonio Madejón Míriam Romero ángela Hernández Araceli García-Sánchez Marta Sánchez-Carrillo Antonio Olveira Javier García-Samaniego</creator><general>Baishideng Publishing Group Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160321</creationdate><title>Hepatitis B and D viruses replication interference: Influence of hepatitis B genotype</title><author>Antonio Madejón Míriam Romero ángela Hernández Araceli García-Sánchez Marta Sánchez-Carrillo Antonio Olveira Javier García-Samaniego</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-c490cd43747ee268bd95af162ff823fc909afb4ef01ea4b8f09d37701092ceb93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Basic Study</topic><topic>Biomarkers - blood</topic><topic>Coinfection</topic><topic>Cross-Sectional Studies</topic><topic>DNA, Viral - blood</topic><topic>DNA, Viral - genetics</topic><topic>Female</topic><topic>Genotype</topic><topic>Hepatitis</topic><topic>Hepatitis B - complications</topic><topic>Hepatitis B - diagnosis</topic><topic>Hepatitis B - virology</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Hepatitis B virus - genetics</topic><topic>Hepatitis B virus - growth & development</topic><topic>Hepatitis B virus - immunology</topic><topic>Hepatitis D, Chronic - complications</topic><topic>Hepatitis D, Chronic - diagnosis</topic><topic>Hepatitis D, Chronic - virology</topic><topic>Hepatitis Delta Virus - genetics</topic><topic>Hepatitis Delta Virus - growth & development</topic><topic>hepatitis;Replication</topic><topic>HIV Infections - complications</topic><topic>HIV Infections - virology</topic><topic>Humans</topic><topic>interference;Viral</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Middle Aged</topic><topic>replication</topic><topic>Retrospective Studies</topic><topic>RNA, Viral - blood</topic><topic>RNA, Viral - genetics</topic><topic>Time Factors</topic><topic>Viral Load</topic><topic>Virus Replication</topic><topic>virus;Delta</topic><topic>virus;Hepatitis</topic><toplevel>online_resources</toplevel><creatorcontrib>Antonio Madejón Míriam Romero ángela Hernández Araceli García-Sánchez Marta Sánchez-Carrillo Antonio Olveira Javier García-Samaniego</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Antonio Madejón Míriam Romero ángela Hernández Araceli García-Sánchez Marta Sánchez-Carrillo Antonio Olveira Javier García-Samaniego</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis B and D viruses replication interference: Influence of hepatitis B genotype</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2016-03-21</date><risdate>2016</risdate><volume>22</volume><issue>11</issue><spage>3165</spage><epage>3174</epage><pages>3165-3174</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>AIM: To study the hepatitis B virus(HBV) and hepatitis D virus(HDV) replication interferences in patients with chronic hepatitis delta infected with different HBV genotypes.METHODS: We conducted a transversal study including 68 chronic hepatitis delta(CHD)(37 HIVpositive) patients and a control group of 49 chronic hepatitis B(CHB)(22 HIV-positive) patients. In addition, a dynamic follow-up was performed in 16 CHD patients. In all the samples, the surface antigen of hepatitis B(HBs Ag) serum titers were analyzed with the Monolisa HBs Ag Ultra system(Bio-Rad), using as quantification standard a serial dilution curve of an international HBs Ag standard. Serum HBV-DNA titers were analyzed using the Roche Cobas Taq Man(Roche, Barcelona, Spain), and the serum HDV-RNA using an in-house real-time q RT-PCR method, with Taq Man probes. HBV genotype was determined with the line immunoassay Li PA HBV genotyping system(Innogenetics, Ghent, Belgium). In those patients negative for Li PA assay, a nested PCR method of complete HBs Ag coding region, followed by sequence analysis was applied.RESULTS: No differences in the HBV-DNA levels were found in CHB patients infected with different HBV genotypes. However, in CHD patients the HBV-DNA levels were lower in those infected with HBV-A than in those with HBV-D, both in HIV negative [median(IQR): 1.25(1.00-1.35) vs 2.95(2.07-3.93) log10(copies/m L), P = 0.013] and HIV positive patients [2.63(1.24-2.69) vs 7.25(4.61-7.55) log10(copies/m L), P &lt; 0.001]. This was confirmed in the dynamic study of the HBV/HDV patients. These differences induce an under-estimation of HBV-A incidence in patients with CHD analyzed with Li PA assay. Finally, the HBs Ag titers reflected no significant differences in CHD patients infected with HBV-A or D.CONCLUSION: Viral replication interference between HBV and HDV is HBV-genotype dependent, and more evident in patients infected with HBV-genotype A, than with HBV-D or E.</abstract><cop>United States</cop><pub>Baishideng Publishing Group Inc</pub><pmid>27003993</pmid><doi>10.3748/wjg.v22.i11.3165</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Basic Study Biomarkers - blood Coinfection Cross-Sectional Studies DNA, Viral - blood DNA, Viral - genetics Female Genotype Hepatitis Hepatitis B - complications Hepatitis B - diagnosis Hepatitis B - virology Hepatitis B Surface Antigens - blood Hepatitis B virus - genetics Hepatitis B virus - growth & development Hepatitis B virus - immunology Hepatitis D, Chronic - complications Hepatitis D, Chronic - diagnosis Hepatitis D, Chronic - virology Hepatitis Delta Virus - genetics Hepatitis Delta Virus - growth & development hepatitis Replication HIV Infections - complications HIV Infections - virology Humans interference Viral Longitudinal Studies Male Middle Aged replication Retrospective Studies RNA, Viral - blood RNA, Viral - genetics Time Factors Viral Load Virus Replication virus Delta virus Hepatitis |
title | Hepatitis B and D viruses replication interference: Influence of hepatitis B genotype |
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