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| __NOTOC__
| | #REDIRECT[[Hepatitis D Virus]] |
| {{Hepatitis D}}
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| {{CMG}}; {{AE}}
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| ==Overview==
| | [[Category:Emergency mdicine]] |
| | | [[Category:Disease]] |
| ==Taxonomy==
| | [[Category:Up-To-Date]] |
| ''[[Viruses]]''; ''[[Deltavirus]]''; ''[[Hepatitis delta virus]]''
| | [[Category:Infectious disease]] |
| | | [[Category:Hepatology]] |
| ==Biology==
| | [[Category:Gastroenterology]] |
| {| style="float: right;"
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| | [[File:Hep D virus.jpg|200px|thumb|none|Electron micrograph revealing the presence of hepatitis-B virus HBV "Dane particles", or virions. <SMALL>Courtesy: ''[http://www.who.int/en/ World Health Organization]''<ref>{{Cite web | title = http://www.who.int/en/ | url = http://www.who.int/en/}}</ref></SMALL>]]
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| The [[HDV]] [[genome]] is a single, negative stranded, circular [[RNA]] molecule nearly 1.7 kb in length containing about 60% C+G. A high degree of intramolecular complementarity allows about 70% of the [[nucleotides]] to be basepaired to each other to form an unbranched, double-stranded, stable, rod-shaped structure.<ref name="pmid7574482">{{cite journal| author=Lai MM| title=The molecular biology of hepatitis delta virus. | journal=Annu Rev Biochem | year= 1995 | volume= 64 | issue= | pages= 259-86 | pmid=7574482 | doi=10.1146/annurev.bi.64.070195.001355 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7574482 }} </ref><ref name="pmid2198992">{{cite journal| author=Monjardino JP, Saldanha JA| title=Delta hepatitis. The disease and the virus. | journal=Br Med Bull | year= 1990 | volume= 46 | issue= 2 | pages= 399-407 | pmid=2198992 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2198992 }} </ref> The [[genome]] of [[HDV]] is unrelated to the [[genome]]s of [[hepadnavirus]]es, of which [[hepatitis B virus]] (HBV) is a member.<ref name="pmid24843434">{{cite journal| author=Nakamura A, Osonoi T, Terauchi Y| title=Relationship between urinary sodium excretion and pioglitazone-induced edema. | journal=J Diabetes Investig | year= 2010 | volume= 1 | issue= 5 | pages= 208-11 | pmid=24843434 | doi=10.1111/j.2040-1124.2010.00046.x | pmc=PMC4020723 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24843434 }} </ref> [[HDV]] is a replication defective, helper (HBV) dependent ssRNA virus that requires the surface antigen of [[HBV]] ([[HBsAg]]) for the "encapsidation" of its own [[genome]]. The envelope [[proteins]] on the outer surface of [[HDV]] are entirely provided by [[HBV]].<ref name=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</ref><ref name="pmid3627276">{{cite journal| author=Makino S, Chang MF, Shieh CK, Kamahora T, Vannier DM, Govindarajan S et al.| title=Molecular cloning and sequencing of a human hepatitis delta (delta) virus RNA. | journal=Nature | year= 1987 | volume= 329 | issue= 6137 | pages= 343-6 | pmid=3627276 | doi=10.1038/329343a0 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3627276 }} </ref>
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| The outer envelope of [[HDV]] particles contains [[lipids]] and the three forms (S, M, and L) of [[HBsAg|HBV surface antigen]] ([[HBsAg]]), but predominantly the major form of [[HBsAg]] with very few middle (pre S1) and large (pre S2) proteins. The internal [[nucleocapsid]] structure of HDV is composed of the viral single stranded RNA [[genome]] and about 60 copies of delta antigen, the only [[HDV]]-encoded protein.<ref name=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</ref>
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| HDV does not [[infect]] established tissue culture cell lines. Complete [[viral replication]] cycles in vitro are limited to primary [[hepatocytes]] that are coinfected with a [[hepadnavirus]] or cotransfected with [[hepadnavirus]] [[cDNA]].<ref name=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</ref><ref name="pmid7574482">{{cite journal| author=Lai MM| title=The molecular biology of hepatitis delta virus. | journal=Annu Rev Biochem | year= 1995 | volume= 64 | issue= | pages= 259-86 | pmid=7574482 | doi=10.1146/annurev.bi.64.070195.001355 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7574482 }} </ref>
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| ===Life Cycle===
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| To replicate efficiently, a [[virus]] requires the cooperation of the host cell at all stages of the [[viral replication]] cycle:<ref name=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</ref> | |
| #Attachment
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| #Penetration
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| #Uncoating
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| #Provision of appropriate metabolic conditions for the synthesis of viral macromolecules
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| #Final assembly of viral subunits
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| #Release of new virions
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| *[[HDV]] also requires the presence of an helper [[hepadnavirus]] to provide the [[protein]] components for its own envelope. How HDV enters [[hepatocytes]] is still not known, but it may involve the interaction between HBsAg-L and a cellular receptor. The incoming [[HDV]] [[RNA]] is then transported into the [[nucleus]], probably by the small form of delta antigen, ''HDAg-S''. Binding of HDAg to RNA also protects the HDV RNAs from degradation.<ref name=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</ref>
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| *HDV RNA replication is carried out by cellular [[RNA]] [[polymerase]] II, without a DNA intermediate, and without the help of HBV.
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| *RNA transcription is regulated initially - [[mRNA]](s) is(are) transcribed from the incoming minus-strand genome
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| :*''Later'' - after the translation of the [[mRNA]] to make essential replication proteins, there is a switch in the mode of [[RNA]]-directed [[RNA synthesis]] to facilitate replication of the RNA [[genome]] | |
| *Three forms of [[RNA]] are made:
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| :*Circular [[genomic]] RNA | |
| :*Circular complementary antigenomic RNA
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| :*Linear polyadenylated antigenomic RNA - mRNA containing the open reading frame for the HDAg.
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| Synthesis of antigenomic RNA occurs in the nucleous, mediated by [[RNA polymerase I]], whereas synthesis of genomic RNA takes place in the nucleoplasm, mediated by RNA Pol II.<ref>{{cite journal|last=Li|first=YJ|coauthors=Macnaughton, T, Gao, L, Lai, MM|title=RNA-Templated Replication of Hepatitis Delta Virus: Genomic and Antigenomic RNAs Associate with Different Nuclear Bodies|journal=Journal of virology|date=2006 Jul|volume=80|issue=13|pages=6478–86|pmid=16775335|doi=10.1128/JVI.02650-05|pmc=1488965}}</ref>
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| *Translation of the 800 b RNA transcript yields:<ref name=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</ref><ref name="pmid9573243">{{cite journal| author=Dingle K, Bichko V, Zuccola H, Hogle J, Taylor J| title=Initiation of hepatitis delta virus genome replication. | journal=J Virol | year= 1998 | volume= 72 | issue= 6 | pages= 4783-8 | pmid=9573243 | doi= | pmc=PMC110015 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9573243 }} </ref><ref name="pmid7574482">{{cite journal| author=Lai MM| title=The molecular biology of hepatitis delta virus. | journal=Annu Rev Biochem | year= 1995 | volume= 64 | issue= | pages= 259-86 | pmid=7574482 | doi=10.1146/annurev.bi.64.070195.001355 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7574482 }} </ref><ref name="pmid1548764">{{cite journal| author=Ryu WS, Bayer M, Taylor J| title=Assembly of hepatitis delta virus particles. | journal=J Virol | year= 1992 | volume= 66 | issue= 4 | pages= 2310-5 | pmid=1548764 | doi= | pmc=PMC289026 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1548764 }} </ref>
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| :*''Small (p24) form of HDAg (HDAg-S)'' - transactivator of [[HDV]] [[RNA]] replication
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| :*''Large (p27) form of HDAg (HDAg-L)'' - inhibits [[RNA synthesis]] and initiates [[virion]] assembly with [[HBsAg]].
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| * [[HDV]] particles include:
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| :*[[HBsAg]]
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| :*HDAg-S
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| :*HDAg-L
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| :*[[RNA]]
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| These elements are only assembled in the presence of the [[hepatitis B virus]] (helper virus). [[HBsAg]] and HDAg-L are necessary and sufficient for [[virus]] assembly, whereas [[HDV]] RNA or HDAg-S are not required, but are present, in viral particles. The primary initiation event for [[HDV]] assembly is the interaction of HDAg-L with [[HBsAg]]. HDAg is localized in the [[nuclei]] while and [[HBsAg]] is present in the [[cytoplasm]] of the infected cells. The mechanism of interaction between these two proteins remains unknown. That are different models that try to explain the mechanisms of viral RNA transcription and replication.<ref name=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</ref><ref name="pmid9621000">{{cite journal| author=Modahl LE, Lai MM| title=Transcription of hepatitis delta antigen mRNA continues throughout hepatitis delta virus (HDV) replication: a new model of HDV RNA transcription and replication. | journal=J Virol | year= 1998 | volume= 72 | issue= 7 | pages= 5449-56 | pmid=9621000 | doi= | pmc=PMC110180 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9621000 }} </ref><ref>{{cite book | last = Fields | first = Bernard | title = Fields virology | publisher = Wolters Kluwer Health/Lippincott Williams & Wilkins | location = Philadelphia | year = 2013 | isbn = 1451105630 }}</ref>
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| '''The Delta Antigens'''
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| A significant difference between viroids and HDV is that, while viroids produce no proteins, HDV produces two proteins called the small and large delta antigens (HDAg-S and HDAg-L, respectively). These two proteins are produced from a single open reading frame. They are identical for 195 amino acids and differ only by the presence of an additional 19 amino acids at the C-terminus of HDAg-L. Despite having 90% identical sequences, these two proteins play diverging roles during the course of an infection. HDAg-S is produced in the early stages of an infection and is required for viral replication. HDAg-L, in contrast, is produced during the later stages of an infection, acts as an inhibitor of viral replication, and is required for assembly of viral particles.
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| '''Evolution'''
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| Three genotypes (I-III) were originally described. Genotype I has been isolated in Europe, North America, Africa and some Asia. Genotype II has been found in Japan, Taiwan, and Yakutia (Russia). Genotype III has been found exclusively in South America (Peru, Colombia, and Venezuela). Some genomes from Taiwan and the Okinawa islands have been difficult to type but have been placed in genotype 2. However it is not known that there are at least 8 genotypes of this virus (HDV-1 to HDV-8).<ref name=Celik2011>{{cite journal |author=Celik I, Karataylı E, Cevik E, ''et al.'' |title=Complete genome sequences and phylogenetic analysis of hepatitis delta viruses isolated from nine Turkish patients |journal=Arch. Virol. |volume=156 |issue=12 |pages=2215–20 |year=2011 |month=December |pmid=21984217 |doi=10.1007/s00705-011-1120-y }}</ref>Phylogenetic studies suggest an African origin for this pathogen.<ref name=Radjef2004>Radjef N, Gordien E, Ivaniushina V, Gault E, Anaïs P, Drugan T, Trinchet JC, Roulot D, Tamby M, Milinkovitch MC, Dény P (2004) Molecular phylogenetic analyses indicate a wide and ancient radiation of African hepatitis delta virus, suggesting a deltavirus genus of at least seven major clades. J Virol 78(5):2537-2544</ref>
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| ==Tropism==
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| ==Natural Reservoir==
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| ==References==
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| {{reflist|2}}
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