Varicella zoster virus

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Electron Micrograph Image of Varicella Zoster Virus. This [[Image:chicken pox 1.jpg|thumb|250px|]] thumb markup allows the text to wrap around the picture and the size can be reduced to a useful size.

Classification

Higher order taxa

Virus Group I, dsDNA, Family Herpesviridae, Genus Varicellovirus, Species Human herpesvirus 3 (HHV-3)


Species

Varicellovirus human herpesvirus 3 (HHV-3)

Description and significance

Herpes Zoster which causes Shingles subsequent to Varicella Infection

Varicella Zoster Virus usually comes in two forms. Upon the first infection, it produces red, leathery postules and most often appears in children. This is generally known as "Varicella virus" or chicken pox. If the infection subsequently comes back, it is then typically a painful reddish rash that encompasses most of the body. This form of the disease is known as the "Herpes zoster" or shingles part, and mainly afflicts older people, or those with weakened immune systems. The only known hosts are humans, and people have been reporting cases of Varicella since ancient civilizations.

Describe the appearance, habitat, etc. of the organism, and why it is important enough to have its genome sequenced. Describe how and where it was isolated. Include a picture or two (with sources) if you can find them.

Genome structure

The diameter of Varicella Zoster Virus is about 150-200nM, and its' MW is 125,000 base pairs,which incidentally is the smallest of the herpes virus genomes. VZV may encode up to 75 proteins, 70 of which are homologous with Herpes Simplex Virus I. [1] Being that it is an alpha herpes virus, The Varicella Virus has a latent period in the root ganglia cells, and then is reactivated as the Herpes Zoster Virus. The virion has a nucleocapsid made up of 162 capsomeres, and a protein covering separates the nucleocapsid from the lipid envelope that contains the viral glycoproteins. The core consists of a linear, double stranded DNA genome. The infection will bring out the immunoglobulin G, immunoglobulin M, and immunoglobulin A antibodies which will then bind to various viral proteins. [2]



Describe the size and content of the genome. How many chromosomes? Circular or linear? Other interesting features? What is known about its sequence? Does it have any plasmids? Are they important to the organism's lifestyle?

Cell structure and metabolism

Describe any interesting features and/or cell structures; how it gains energy; what important molecules it produces.

Ecology

Varicella Zoster interacts solely with humans, because there are no animal hosts that have been identified so far.

Describe any interactions with other organisms (included eukaryotes), contributions to the environment, effect on environment, etc.

Pathology

The Varicella Zoster Virus causes disease in human hosts by inserting its gene into the host cell at the nasopharyngeal mucosa. It is highly contangious and may be transmitted from humans by contact with chickenpox blister fluid or by airborne infection. The incubation period can be anywhere from 14- 21 days, upon which red, itchy postules develop around the hosts body. Patient symptoms include rash, itching, fever and lethargy. In serious cases, such as for small children and immunocompromised adults, it can lead to severe skin infections, pnuemonia, brain damage or even death. After the varicella infection, it has latency in the sensory ganglionic nuerons and may be reactivated years later as the Zoster virus, also known as shingles. Shingles produces painful blisters, and is chareceterized by a rash on one side of the body. Symptoms include hypersensitive skin, itching, and headache.


The Varicells Zoster Vaccine is nationally recommeded for children starting from as early as 12 months old as a way to prevent getting Varicella Zoster. The vaccine has live, attenuated virus and are based on the Oka strain of varicella. Side effects of the vaccine can range from fever, mild rash to seizure, brain reactions, low blood counts and pnuemonia, but organizations such as the Centers for Disease Control and Prevention say that these severe problems are very rare, and the benifits of immunity from VZV outweigh the risks of getting the vaccine.

How does this organism cause disease? Human, animal, plant hosts? Virulence factors, as well as patient symptoms.

Application to Biotechnology

Does this organism produce any useful compounds or enzymes? What are they and how are they used?

Current Research

Enter summaries of the most recent research here--at least three required

1. Herpes Zoster and Its Cardiovascular Complications in the Elderly – Another Look at a Dormant Virus by Tony S. Ma Tracie C. Collins Gabriel Habib Audrius Bredikis Blase A. Carabello This article mainly deals with the adverse effects of Herpes Zoster, the latent form of Varicella, on the cardiovascular healtg of geriatric patients. Numerous patients who had just suffered from Shingles subsequent heart blocks and other cardiovascular problems, and this study hoped to set up corelations between the two. Citing a previous study done by Head and Campbell, which indicates that the site of latency for zoster is in the dorsal root ganglion, they thought that it was the renal colic which stimulates the sensory ganglion to reactivate the Zoster. They continued to say that "The cardiac involvement could either be a result of a secondaryseeding of the pleural and pericardial space occurring through a cell-mediated transport of the VZV or a coincidental reactivation of VZV at the cardiac sympathetic/parasympathetic ganglia."(Tony, p. 4) In the case studies done, the researchers seemed to find that plueral and pericardial effusions were seen in a CT scan very close to when the outbreak of Zoster occured. However, further studies need to be done in order to provide a more conclusive correlation between Zoster and Cardiovascular problems.


2. http://search.ebscohost.com/login.aspx?direct=true&db=aph&AN=26916461&site=ehost-live Prevention of Varicella Recommendations of the Advisory Committee on Immunization Practices (ACIP)Mona Marin, MD, Dalya Güris, MD,* Sandra S. Chaves, MD, Scott Schmid, PhD, Jane F. Seward, MBBS [3]

References

1.Reinhart,W.J.. "Herpes Simplex Virus and Varicella Zoster Virus Anatomy, Microbiology, Epidemiology, and Diagnosis & Management of Ocular Disease" Ohio Ophthalmologic Society.2005.


2.Arvin, AM. "Varicella Zoster Virus". Clinical Microbiology Reviews. 1996. Volume 3. p.361-381.

3.[http://search.ebscohost.com/login.aspx?direct=true&db=cmedm&AN=16763386&site=ehost-live Tony S. Ma Tracie C. Collins Gabriel Habib Audrius Bredikis Blase A."Herpes Zoster and Its Cardiovascular Complications in the Elderly – Another Look at a Dormant Virus"Cardiology.2006. Volume 107. p. 63-67.]

4.Mona Marin, MD, Dalya Güris, MD,* Sandra S. Chaves, MD, Scott Schmid, PhD, Jane F. Seward, MBBS. "Prevention of Varicella". MMWR: Morbidity & Mortality Weekly Report. 2007. Colume 56. p.1-45.

[Sample reference] Takai, K., Sugai, A., Itoh, T., and Horikoshi, K. "Palaeococcus ferrophilus gen. nov., sp. nov., a barophilic, hyperthermophilic archaeon from a deep-sea hydrothermal vent chimney". International Journal of Systematic and Evolutionary Microbiology. 2000. Volume 50. p. 489-500.

  1. Reinhart,W.J.
  2. Arvin A.M.
  3. Mona Marin