Hepatitis D causes: Difference between revisions

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__NOTOC__
#REDIRECT[[Hepatitis D Virus]]
{{Hepatitis D}}
{{CMG}}; {{AE}} {{JS}} {{JM}}


==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;"
| [[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>]]
|-
|}
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>
 
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>
 
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>
 
===Life Cycle===
To replicate efficiently, a [[virus]] requires the cooperation of the host cell at all stages of the [[viral replication]] cycle. These stages include:<ref name=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</ref>
#Attachment
#Penetration
#Uncoating
#Provision of appropriate [[metabolic]] conditions for the synthesis of [[viral]] macromolecules
#Final assembly of viral subunits
#Release of new [[virions]]
 
[[Hepatitis D virus]] requires the presence of an helper [[hepadnavirus]] to provide the [[protein]] components for its own envelope. How [[HDV]] enters [[hepatocytes]] is still unknown, however, 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 viral delta antigen, ''HDAg-S''. Binding of HDAg to [[RNA]] also protects the [[HDV]] [[RNA]]s from cellular degradation.<ref name=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</ref>
 
HDV RNA replication is carried out by cellular [[RNA]] [[polymerase]] II, without a DNA intermediate or help from [[HBV]]. During the replication of the HDV [[genome]] three forms of [[RNA]] are produced:
*Circular [[genomic]] [[RNA]]
*Circular complementary antigenomic [[RNA]]
*Linear polyadenylated antigenomic [[RNA]] - [[mRNA]] containing the open reading frame for the HDAg.
Synthesis of ''antigenomic [[RNA]]'' occurs in the [[nucleus]], mediated by [[RNA polymerase I]], whereas synthesis of ''genomic RNA'' takes place in the [[nucleoplasm]], mediated by RNA Polymerase 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>
*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>
:*''Small (p24) form of HDAg (HDAg-S)'' - transactivator of [[HDV]] [[RNA]] replication
:*''Large (p27) form of HDAg (HDAg-L)'' - inhibits [[RNA synthesis]] and initiates [[virion]] assembly with [[HBsAg]].
* [[HDV]] particles include:
:*[[HBsAg]]
:*HDAg-S
:*HDAg-L
:*[[RNA]]
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>
 
==Tropism==
 
==Natural Reservoir==
Humans are the only known [[natural reservoir]] of [[hepatitis D virus]], in nature. However, when in the presence of [[hepatitis B virus]], or woodchuck hepatitis virus, HDV can be experimentally transmitted to chimpanzees and woodchucks, respectively.<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=WHO>{{cite web | title = Hepatitis D | url = http://www.who.int/csr/disease/hepatitis/HepatitisD_whocdscsrncs2001_1.pdf }}</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><ref name="pmid2778877">{{cite journal| author=Sureau C, Taylor J, Chao M, Eichberg JW, Lanford RE| title=Cloned hepatitis delta virus cDNA is infectious in the chimpanzee. | journal=J Virol | year= 1989 | volume= 63 | issue= 10 | pages= 4292-7 | pmid=2778877 | doi= | pmc=PMC251044 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2778877  }} </ref>
 
==References==
{{reflist|2}}

Latest revision as of 22:06, 29 July 2020

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