Adenoviridae: Difference between revisions

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[[Image:Em_adeno.gif|thumb|200px|right|Electron micrograph of an adenovirus. From [http://www.virology.net/Big_Virology/BVDNAadeno.html Microbiology & Immunology at the University of Leicester, UK].]]
{{Curated}}
{{Viral Biorealm Family}}
 
[[Image:Vsd1 c.jpg|thumb|300px|right|Electron micrograph of adenovirus. Courtesy of [mailto:vetinfo@qub.ac.uk Prof. Stewart McNulty]. From [http://www.qub.ac.uk/afs/vs/vsd6d.html Veterinary Sciences - The Queen's University of Belfast].]]


==Baltimore Classification==
==Baltimore Classification==
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===Higher order taxa===
===Higher order taxa===


Virus; Adenoviridae (Family); ''Aviadenovirus'', ''Mastadenovirus'', ''Atadenovirus'', or ''Siadenovirus''
Virus; dsDNA viruses, no RNA stage; Adenoviridae  


===Species===
===Genera===


Numerous species and serotypes
''Aviadenovirus'', ''Mastadenovirus'', ''Atadenovirus'', and ''Siadenovirus''


==Description and Significance==
==Description and Significance==


Adenoviruses infect birds, humans, and many other mammals and other organisms. They usually cause respiratory infections, but they can also cause conjunctivitis, gastroenteritis, cystitis, and rash illness. Adenoviruses are divided into four genera: Aviadenovirus (which infects birds), Mastadenovirus (which infects mammals), Atadenovirus and Siadenovirus (which infect a variety of organisms).
Adenoviruses infect birds, humans, and many other mammals and other organisms. They usually cause respiratory infections, but they can also cause conjunctivitis, gastroenteritis, cystitis, and rash illness. Adenoviruses are divided into four genera: Aviadenovirus (which infects birds), Mastadenovirus (which infects mammals), Atadenovirus and Siadenovirus (which infect a variety of organisms). (sources: [http://www.cdc.gov/ncidod/dvrd/revb/respiratory/eadfeat.htm CDC], [http://www.socgenmicrobiol.org.uk/jgvdirect/19497/19497ft.htm Davison et al.])


Currently, research is being done to see if adenoviruses could be used as a treatment for cancer. After going through extensive engineering, adenoviruses become a promising agent for killing tumor cells.
Currently, research is being done to see if adenoviruses could be used as a treatment for cancer. After going through extensive engineering to remove the genes which control viral replication (which also creates room to insert genes which are of therapeutic interest), adenoviruses become a promising agent for killing tumor cells. (For more information on the use of adenoviruses in cancer treatment, see [http://clincancerres.aacrjournals.org/cgi/content/abstract/6/9/3395 Curiel] and [http://www.scielo.br/scielo.php?pid=S0100-879X1999000200001&script=sci_arttext&tlng=en Dani])


==Genome Structure==
==Genome Structure==


Adenoviruses have linear, non-segmented, double stranded DNA which is around 30-38kbp (though the size varies from group to group). The complete genome is 35800-36200 nucleotides long. The DNA has been fully sequenced and complete sequence is around 34000-36000 nucleotides long.A 55kD virus coded terminal protein is covalently attached 5' end of each strand. The terminal sequences of each strand are inverted repeats. Because of this, the denatured single strands can form "panhandle" structures as seen in the lower left corner of the diagram below.
Adenoviruses have linear, non-segmented, double stranded DNA which is around 30-38kbp (though the size varies from group to group). The complete genome is 35800-36200 nucleotides long. A 55kD virus coded terminal protein is covalently attached 5' end of each strand. The terminal sequences of each strand are inverted repeats. Because of this, the denatured single strands can form "panhandle" structures. (sources: [http://www.ncbi.nlm.nih.gov/ICTVdb/ICTVdB/01000000.htm ICTVdB], [http://www.socgenmicrobiol.org.uk/jgvdirect/19497/19497ft.htm Davison et al.])


==Virion Structure of a Adenovirus==
==Virion Structure of a Adenovirus==


[[Image:Adeno1.gif|thumb|100px|left|Diagram of an adenovirus virion.<br /> From [http://www-micro.msb.le.ac.uk/3035/Adenoviruses.html Microbiology & Immunology at the University of Leicester, UK].]]
Adenoviruses are non-enveloped icosahedral viruses measuring 60-90nm in diameter and containing double-stranded DNA. The structure of an adenovirus virion is simple, consisting of a capsid, fibers, a core, and associated proteins. A protein core inside the outer icosahedral protein capsid contains the genome. The capsid is comprised of 252 capsomers (12 of which are pentons, 240 of which are hexons). Trimeric fibers project from the surface and are attached to a penton. (sources: [http://www.ncbi.nlm.nih.gov/ICTVdb/ICTVdB/01000000.htm ICTVdB], [http://www.socgenmicrobiol.org.uk/jgvdirect/19497/19497ft.htm Davison et al.])
 
Adenoviruses are non-enveloped icosahedral viruses measuring 60-90nm in diameter and containing double-stranded DNA. The structure of an adenovirus virion is rather simple, consisting of a capsid, fibers, a core, and associated proteins. A protein core inside the outer icosahedral protein capsid contains the genome. The capsid is comprised of 252 capsomers (12 of which are pentons, 240 of which are hexons). Trimeric fibers project from the surface and are attached to a penton.


==Reproduction Cycle of an Adenovirus in a Host Cell==
==Reproduction Cycle of an Adenovirus in a Host Cell==
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The life cycle of an adenovirus is divided into early and late phases, separated by the DNA replication process. In the early phase, the virus attaches to a cell with its fibers. The penton base protein interacts with the host cell integrins, and the penton is internalized by the host cell through receptor-mediated endocytosis. The penton is disassembled as it is transported to the nucleus, where the viral particle releases its DNA. The viral DNA takes over as terminal protein attached to the end of the DNA strand initiates transcription. The early genes are responsible for making regulatory proteins, which alter the host proteins to prepare for DNA synthesis, activate other virus genes, and provide protection from the host's immune system. Viral DNA replication now occurs.
The life cycle of an adenovirus is divided into early and late phases, separated by the DNA replication process. In the early phase, the virus attaches to a cell with its fibers. The penton base protein interacts with the host cell integrins, and the penton is internalized by the host cell through receptor-mediated endocytosis. The penton is disassembled as it is transported to the nucleus, where the viral particle releases its DNA. The viral DNA takes over as terminal protein attached to the end of the DNA strand initiates transcription. The early genes are responsible for making regulatory proteins, which alter the host proteins to prepare for DNA synthesis, activate other virus genes, and provide protection from the host's immune system. Viral DNA replication now occurs.


The late phase begins when the late genes are expressed during DNA replication. These genes produce proteins that are involved in virus particle assembly. The host's cellular processes are shut down as transport of mRNA to the cytoplasm is blocked when the late genes are expressed. Viral mRNA is transported to the cytoplasm and translated instead. Virus assembly occurs. Finally, the host cell dies due to a build-up of adenovirus death protein. As the cell dies, the new virus particles are released from the cell.
The late phase begins when the late genes are expressed during DNA replication. These genes produce proteins that are involved in virus particle assembly. The host's cellular processes are shut down as transport of mRNA to the cytoplasm is blocked when the late genes are expressed. Viral mRNA is transported to the cytoplasm and translated instead. Virus assembly occurs. Finally, the host cell dies due to a build-up of adenovirus death protein. As the cell dies, the new virus particles are released from the cell. (sources: [http://athena.bioc.uvic.ca/bioDoc/adenoviridae/ Viral Bioinformatics Research Center], [http://www.ncbi.nlm.nih.gov/ICTVdb/ICTVdB/01000000.htm ICTVdB])


==Viral Ecology & Pathology==
==Viral Ecology & Pathology==


Adenoviruses infect many different species in many different ecosystems. According to the Centers for Diesease Control and Prevention, they can survive for long periods of time outside the body due to an unusually high resistance to chemical or physical agents and adverse pH conditions. Transmission is usually through direct contact, fecal-oral transmission, or waterborne transmission.
Adenoviruses infect many different species in many different ecosystems. According to the [http://www.cdc.gov/ncidod/dvrd/revb/respiratory/eadfeat.htm Centers for Diesease Control and Prevention], they can survive for long periods of time outside the body due to an unusually high resistance to chemical or physical agents and adverse pH conditions. Transmission is usually through direct contact, fecal-oral transmission, or waterborne transmission.


==References. Updated June 2, 2006==
==References==


[http://www.cdc.gov/ncidod/dvrd/revb/respiratory/eadfeat.htm Centers for Disease Control and Prevention: Respiratory and Enteric Viruses Branch: Adenoviruses]
[http://www.cdc.gov/ncidod/dvrd/revb/respiratory/eadfeat.htm Centers for Disease Control and Prevention: Respiratory and Enteric Viruses Branch: Adenoviruses]


[http://www.ncbi.nlm.nih.gov/ICTVdb/ICTVdB/01000000.htm ICTVdB - The Universal Virus Database, version 3. http://www.ncbi.nlm.nih.gov/ICTVdb/ICTVdB/]
[http://clincancerres.aacrjournals.org/cgi/content/abstract/6/9/3395 Curiel, David T. "The Development of Conditionally Replicative Adenoviruses for Cancer Therapy." ''Clinical Cancer Research'' 6 (2000): 3395-3399.]


[http://www-micro.msb.le.ac.uk/3035/Adenoviruses.html Microbiology @ Leicester: Virology: Adenovirus]
[http://www.scielo.br/scielo.php?pid=S0100-879X1999000200001&script=sci_arttext&tlng=en Dani, S.U. "The challenge of vector development in gene therapy." ''Brazilian Journal of Medical and Biological Research'' 32.2 (1999): 133-145.]


[http://en.wikipedia.org/wiki/Adenoviridae Wikipedia, the Free Encyclopedia: Adenoviridae]
[http://www.socgenmicrobiol.org.uk/jgvdirect/19497/19497ft.htm Davison et al.  "Genetic content and evolution of adenoviruses."  ''Journal of General Virology'' 84 (2003): 2895-2908.]
 
[http://www.ncbi.nlm.nih.gov/ICTVdb/ICTVdB/01000000.htm ICTVdB - The Universal Virus Database, version 3. http://www.ncbi.nlm.nih.gov/ICTVdb/ICTVdB/]


[http://athena.bioc.uvic.ca/bioDoc/adenoviridae/ Viral Bioinformatics Research Center - Adenoviridae]
[http://athena.bioc.uvic.ca/bioDoc/adenoviridae/ Viral Bioinformatics Research Center - Adenoviridae]
[http://clincancerres.aacrjournals.org/cgi/content/abstract/6/9/3395 Curiel, David T. "The Development of Conditionally Replicative Adenoviruses for Cancer Therapy." Clinical Cancer Research Vol.6, 3395-3399, September 2000.]
[http://www.scielo.br/scielo.php?pid=S0100-879X1999000200001&script=sci_arttext&tlng=en Dani, S.U. "The challenge of vector development in gene therapy." Brazilian Journal of Medical and Biological Research, February 1999, Volume 32(2) 133-145.]

Latest revision as of 00:17, 8 August 2010

This is a curated page. Report corrections to Microbewiki.

A Viral Biorealm page on the family Adenoviridae

Electron micrograph of adenovirus. Courtesy of Prof. Stewart McNulty. From Veterinary Sciences - The Queen's University of Belfast.

Baltimore Classification

Higher order taxa

Virus; dsDNA viruses, no RNA stage; Adenoviridae

Genera

Aviadenovirus, Mastadenovirus, Atadenovirus, and Siadenovirus

Description and Significance

Adenoviruses infect birds, humans, and many other mammals and other organisms. They usually cause respiratory infections, but they can also cause conjunctivitis, gastroenteritis, cystitis, and rash illness. Adenoviruses are divided into four genera: Aviadenovirus (which infects birds), Mastadenovirus (which infects mammals), Atadenovirus and Siadenovirus (which infect a variety of organisms). (sources: CDC, Davison et al.)

Currently, research is being done to see if adenoviruses could be used as a treatment for cancer. After going through extensive engineering to remove the genes which control viral replication (which also creates room to insert genes which are of therapeutic interest), adenoviruses become a promising agent for killing tumor cells. (For more information on the use of adenoviruses in cancer treatment, see Curiel and Dani)

Genome Structure

Adenoviruses have linear, non-segmented, double stranded DNA which is around 30-38kbp (though the size varies from group to group). The complete genome is 35800-36200 nucleotides long. A 55kD virus coded terminal protein is covalently attached 5' end of each strand. The terminal sequences of each strand are inverted repeats. Because of this, the denatured single strands can form "panhandle" structures. (sources: ICTVdB, Davison et al.)

Virion Structure of a Adenovirus

Adenoviruses are non-enveloped icosahedral viruses measuring 60-90nm in diameter and containing double-stranded DNA. The structure of an adenovirus virion is simple, consisting of a capsid, fibers, a core, and associated proteins. A protein core inside the outer icosahedral protein capsid contains the genome. The capsid is comprised of 252 capsomers (12 of which are pentons, 240 of which are hexons). Trimeric fibers project from the surface and are attached to a penton. (sources: ICTVdB, Davison et al.)

Reproduction Cycle of an Adenovirus in a Host Cell

The life cycle of an adenovirus is divided into early and late phases, separated by the DNA replication process. In the early phase, the virus attaches to a cell with its fibers. The penton base protein interacts with the host cell integrins, and the penton is internalized by the host cell through receptor-mediated endocytosis. The penton is disassembled as it is transported to the nucleus, where the viral particle releases its DNA. The viral DNA takes over as terminal protein attached to the end of the DNA strand initiates transcription. The early genes are responsible for making regulatory proteins, which alter the host proteins to prepare for DNA synthesis, activate other virus genes, and provide protection from the host's immune system. Viral DNA replication now occurs.

The late phase begins when the late genes are expressed during DNA replication. These genes produce proteins that are involved in virus particle assembly. The host's cellular processes are shut down as transport of mRNA to the cytoplasm is blocked when the late genes are expressed. Viral mRNA is transported to the cytoplasm and translated instead. Virus assembly occurs. Finally, the host cell dies due to a build-up of adenovirus death protein. As the cell dies, the new virus particles are released from the cell. (sources: Viral Bioinformatics Research Center, ICTVdB)

Viral Ecology & Pathology

Adenoviruses infect many different species in many different ecosystems. According to the Centers for Diesease Control and Prevention, they can survive for long periods of time outside the body due to an unusually high resistance to chemical or physical agents and adverse pH conditions. Transmission is usually through direct contact, fecal-oral transmission, or waterborne transmission.

References

Centers for Disease Control and Prevention: Respiratory and Enteric Viruses Branch: Adenoviruses

Curiel, David T. "The Development of Conditionally Replicative Adenoviruses for Cancer Therapy." Clinical Cancer Research 6 (2000): 3395-3399.

Dani, S.U. "The challenge of vector development in gene therapy." Brazilian Journal of Medical and Biological Research 32.2 (1999): 133-145.

Davison et al. "Genetic content and evolution of adenoviruses." Journal of General Virology 84 (2003): 2895-2908.

ICTVdB - The Universal Virus Database, version 3. http://www.ncbi.nlm.nih.gov/ICTVdb/ICTVdB/

Viral Bioinformatics Research Center - Adenoviridae