The evolution and clinical impact of hepatitis B virus genome diversity
The global burden of hepatitis B virus (HBV) is enormous, with 257 million persons chronically infected, resulting in more than 880,000 deaths per year worldwide. HBV exists as nine different genotypes, which differ in disease progression, natural history and response to therapy. HBV is an ancient v...
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description | The global burden of hepatitis B virus (HBV) is enormous, with 257 million persons chronically infected, resulting in more than 880,000 deaths per year worldwide. HBV exists as nine different genotypes, which differ in disease progression, natural history and response to therapy. HBV is an ancient virus, with the latest reports greatly expanding the host range of the Hepadnaviridae (to include fish and reptiles) and casting new light on the origins and evolution of this viral family. Although there is an effective preventive vaccine, there is no cure for chronic hepatitis B, largely owing to the persistence of a viral minichromosome that is not targeted by current therapies. HBV persistence is also facilitated through aberrant host immune responses, possibly due to the diverse intra-host viral populations that can respond to host-mounted and therapeutic selection pressures. This Review summarizes current knowledge on the influence of HBV diversity on disease progression and treatment response and the potential effect on new HBV therapies in the pipeline. The mechanisms by which HBV diversity can occur both within the individual host and at a population level are also discussed.
Hepatitis B virus (HBV) infection remains a global public health issue. This Review provides insights into the evolution of HBV and discusses the mechanisms by which HBV and hepatitis delta virus diversity occurs and the influence of this diversity on disease progression and treatment response.
Key points
Hepatitis B virus (HBV) is an ancient virus with deep ancestry in the animal kingdom.
HBV seems to undergo very little long-term mutational variation despite multiple host–virus factors driving short-term viral variations.
Viral diversity is generated by features of the unique replication cycle of HBV as well as by cellular host factors.
A possible bottleneck in the establishment of new viral variants could be the limited number of HBV-susceptible hepatocytes in the chronically infected liver.
HBV viral diversity contributes to variations in natural history, disease progression and treatment response in those with chronic infection.
Viral diversity must be considered in the development of new therapeutic regimens. |
doi_str_mv | 10.1038/s41575-020-0296-6 |
format | Article |
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Hepatitis B virus (HBV) infection remains a global public health issue. This Review provides insights into the evolution of HBV and discusses the mechanisms by which HBV and hepatitis delta virus diversity occurs and the influence of this diversity on disease progression and treatment response.
Key points
Hepatitis B virus (HBV) is an ancient virus with deep ancestry in the animal kingdom.
HBV seems to undergo very little long-term mutational variation despite multiple host–virus factors driving short-term viral variations.
Viral diversity is generated by features of the unique replication cycle of HBV as well as by cellular host factors.
A possible bottleneck in the establishment of new viral variants could be the limited number of HBV-susceptible hepatocytes in the chronically infected liver.
HBV viral diversity contributes to variations in natural history, disease progression and treatment response in those with chronic infection.
Viral diversity must be considered in the development of new therapeutic regimens.</description><identifier>ISSN: 1759-5045</identifier><identifier>EISSN: 1759-5053</identifier><identifier>DOI: 10.1038/s41575-020-0296-6</identifier><identifier>PMID: 32467580</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/4017 ; 692/699/255/234/2513/1549 ; Animals ; Antiviral Agents - therapeutic use ; Biomedicine ; Care and treatment ; Development and progression ; Disease Progression ; Evolution ; Evolution, Molecular ; Gastroenterology ; Genetic aspects ; Genetic Variation ; Genome, Viral ; Genomes ; Genotype ; Genotypes ; Health aspects ; Hepatitis B ; Hepatitis B virus - genetics ; Hepatitis B virus - immunology ; Hepatitis B virus - pathogenicity ; Hepatitis B, Chronic - drug therapy ; Hepatitis B, Chronic - immunology ; Hepatitis B, Chronic - physiopathology ; Hepatitis B, Chronic - virology ; Hepatology ; Host range ; Host-virus relationships ; Humans ; Immune response ; Medicine ; Medicine & Public Health ; Phylogeny ; Prognosis ; Public health ; Review Article</subject><ispartof>Nature reviews. Gastroenterology & hepatology, 2020-10, Vol.17 (10), p.618-634</ispartof><rights>Springer Nature Limited 2020</rights><rights>COPYRIGHT 2020 Nature Publishing Group</rights><rights>Springer Nature Limited 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-6c66692bae68c427ba2467bbbd32c190fb7f90a38a1ed6168bc343639109a2de3</citedby><cites>FETCH-LOGICAL-c536t-6c66692bae68c427ba2467bbbd32c190fb7f90a38a1ed6168bc343639109a2de3</cites><orcidid>0000-0002-8206-2664 ; 0000-0002-0482-4387</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32467580$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Revill, Peter A.</creatorcontrib><creatorcontrib>Tu, Thomas</creatorcontrib><creatorcontrib>Netter, Hans J.</creatorcontrib><creatorcontrib>Yuen, Lilly K. W.</creatorcontrib><creatorcontrib>Locarnini, Stephen A.</creatorcontrib><creatorcontrib>Littlejohn, Margaret</creatorcontrib><title>The evolution and clinical impact of hepatitis B virus genome diversity</title><title>Nature reviews. Gastroenterology & hepatology</title><addtitle>Nat Rev Gastroenterol Hepatol</addtitle><addtitle>Nat Rev Gastroenterol Hepatol</addtitle><description>The global burden of hepatitis B virus (HBV) is enormous, with 257 million persons chronically infected, resulting in more than 880,000 deaths per year worldwide. HBV exists as nine different genotypes, which differ in disease progression, natural history and response to therapy. HBV is an ancient virus, with the latest reports greatly expanding the host range of the Hepadnaviridae (to include fish and reptiles) and casting new light on the origins and evolution of this viral family. Although there is an effective preventive vaccine, there is no cure for chronic hepatitis B, largely owing to the persistence of a viral minichromosome that is not targeted by current therapies. HBV persistence is also facilitated through aberrant host immune responses, possibly due to the diverse intra-host viral populations that can respond to host-mounted and therapeutic selection pressures. This Review summarizes current knowledge on the influence of HBV diversity on disease progression and treatment response and the potential effect on new HBV therapies in the pipeline. The mechanisms by which HBV diversity can occur both within the individual host and at a population level are also discussed.
Hepatitis B virus (HBV) infection remains a global public health issue. This Review provides insights into the evolution of HBV and discusses the mechanisms by which HBV and hepatitis delta virus diversity occurs and the influence of this diversity on disease progression and treatment response.
Key points
Hepatitis B virus (HBV) is an ancient virus with deep ancestry in the animal kingdom.
HBV seems to undergo very little long-term mutational variation despite multiple host–virus factors driving short-term viral variations.
Viral diversity is generated by features of the unique replication cycle of HBV as well as by cellular host factors.
A possible bottleneck in the establishment of new viral variants could be the limited number of HBV-susceptible hepatocytes in the chronically infected liver.
HBV viral diversity contributes to variations in natural history, disease progression and treatment response in those with chronic infection.
Viral diversity must be considered in the development of new therapeutic regimens.</description><subject>692/4017</subject><subject>692/699/255/234/2513/1549</subject><subject>Animals</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Biomedicine</subject><subject>Care and treatment</subject><subject>Development and progression</subject><subject>Disease Progression</subject><subject>Evolution</subject><subject>Evolution, Molecular</subject><subject>Gastroenterology</subject><subject>Genetic aspects</subject><subject>Genetic Variation</subject><subject>Genome, Viral</subject><subject>Genomes</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>Health aspects</subject><subject>Hepatitis B</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatitis B virus - immunology</subject><subject>Hepatitis B virus - pathogenicity</subject><subject>Hepatitis B, Chronic - drug therapy</subject><subject>Hepatitis B, Chronic - immunology</subject><subject>Hepatitis B, Chronic - physiopathology</subject><subject>Hepatitis B, Chronic - virology</subject><subject>Hepatology</subject><subject>Host range</subject><subject>Host-virus relationships</subject><subject>Humans</subject><subject>Immune response</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Phylogeny</subject><subject>Prognosis</subject><subject>Public health</subject><subject>Review Article</subject><issn>1759-5045</issn><issn>1759-5053</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kV9LHDEUxUNRqlU_gC8SEEpfRvNnkpk8qrS2IPiizyGTubMbmUnWJLPgt2-W3WqVlhASkt85uTcHoVNKLijh7WWqqWhERRgpU8lKfkKHtBGqEkTwvdd9LQ7Ql5SeCJFCcPUZHXBWy0a05BDdPiwBwzqMc3bBY-N7bEfnnTUjdtPK2IzDgJewMtlll_A1Xrs4J7wAHybAvVtDTC6_HKP9wYwJTnbrEXr88f3h5md1d3_76-bqrrKCy1xJK6VUrDMgW1uzpjObSrqu6zmzVJGhawZFDG8NhV5S2XaW11xyRYkyrAd-hL5tfVcxPM-Qsp5csjCOxkOYk2Y1aakSjSIFPf-APoU5-lJdoZpatYqp-o1amBG080PI0diNqb6S5WUpWNsU6uIfVBk9TM4GD4Mr5-8EX_8SLMGMeZl2v5zeg3QL2hhSijDoVXSTiS-aEr1JWW9T1iVlvUlZy6I523U2dxP0r4o_sRaAbYFUrvwC4lvr_3f9DZXprpU</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Revill, Peter A.</creator><creator>Tu, Thomas</creator><creator>Netter, Hans J.</creator><creator>Yuen, Lilly K. 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W.</creatorcontrib><creatorcontrib>Locarnini, Stephen A.</creatorcontrib><creatorcontrib>Littlejohn, Margaret</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Nature reviews. Gastroenterology & hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Revill, Peter A.</au><au>Tu, Thomas</au><au>Netter, Hans J.</au><au>Yuen, Lilly K. W.</au><au>Locarnini, Stephen A.</au><au>Littlejohn, Margaret</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The evolution and clinical impact of hepatitis B virus genome diversity</atitle><jtitle>Nature reviews. Gastroenterology & hepatology</jtitle><stitle>Nat Rev Gastroenterol Hepatol</stitle><addtitle>Nat Rev Gastroenterol Hepatol</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>17</volume><issue>10</issue><spage>618</spage><epage>634</epage><pages>618-634</pages><issn>1759-5045</issn><eissn>1759-5053</eissn><abstract>The global burden of hepatitis B virus (HBV) is enormous, with 257 million persons chronically infected, resulting in more than 880,000 deaths per year worldwide. HBV exists as nine different genotypes, which differ in disease progression, natural history and response to therapy. HBV is an ancient virus, with the latest reports greatly expanding the host range of the Hepadnaviridae (to include fish and reptiles) and casting new light on the origins and evolution of this viral family. Although there is an effective preventive vaccine, there is no cure for chronic hepatitis B, largely owing to the persistence of a viral minichromosome that is not targeted by current therapies. HBV persistence is also facilitated through aberrant host immune responses, possibly due to the diverse intra-host viral populations that can respond to host-mounted and therapeutic selection pressures. This Review summarizes current knowledge on the influence of HBV diversity on disease progression and treatment response and the potential effect on new HBV therapies in the pipeline. The mechanisms by which HBV diversity can occur both within the individual host and at a population level are also discussed.
Hepatitis B virus (HBV) infection remains a global public health issue. This Review provides insights into the evolution of HBV and discusses the mechanisms by which HBV and hepatitis delta virus diversity occurs and the influence of this diversity on disease progression and treatment response.
Key points
Hepatitis B virus (HBV) is an ancient virus with deep ancestry in the animal kingdom.
HBV seems to undergo very little long-term mutational variation despite multiple host–virus factors driving short-term viral variations.
Viral diversity is generated by features of the unique replication cycle of HBV as well as by cellular host factors.
A possible bottleneck in the establishment of new viral variants could be the limited number of HBV-susceptible hepatocytes in the chronically infected liver.
HBV viral diversity contributes to variations in natural history, disease progression and treatment response in those with chronic infection.
Viral diversity must be considered in the development of new therapeutic regimens.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32467580</pmid><doi>10.1038/s41575-020-0296-6</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-8206-2664</orcidid><orcidid>https://orcid.org/0000-0002-0482-4387</orcidid></addata></record> |
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subjects | 692/4017 692/699/255/234/2513/1549 Animals Antiviral Agents - therapeutic use Biomedicine Care and treatment Development and progression Disease Progression Evolution Evolution, Molecular Gastroenterology Genetic aspects Genetic Variation Genome, Viral Genomes Genotype Genotypes Health aspects Hepatitis B Hepatitis B virus - genetics Hepatitis B virus - immunology Hepatitis B virus - pathogenicity Hepatitis B, Chronic - drug therapy Hepatitis B, Chronic - immunology Hepatitis B, Chronic - physiopathology Hepatitis B, Chronic - virology Hepatology Host range Host-virus relationships Humans Immune response Medicine Medicine & Public Health Phylogeny Prognosis Public health Review Article |
title | The evolution and clinical impact of hepatitis B virus genome diversity |
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