Encephalomyocarditis virus: Difference between revisions
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==Genome and Structure == | ==Genome and Structure == | ||
Once humans are infected with this virus, the symptoms they may be faced with include fever, neck stiffness, lethargy, delirium, headaches, and vomiting. | |||
In primates such as gibbons and owl monkeys, ''Encephalomyocarditis Virus'' can cause necrotizing and interstitial myocarditis.[6] | |||
Transmission and pathogenesis occurs by ; incubation from nine to ten days, oral, fecal and urine contamination of food, sub clinical infections, replication in myocardial and kills them. | |||
==Cell Structure and metabolism == | ==Cell Structure and metabolism == |
Revision as of 22:10, 21 April 2009
Description and Significance
Encephalomyocarditis Virus(EMCV) is a member of the genus Cardiovirus of the family Picornaviridae. It's said that the Pacornavirusinfects many animal species, including pigs, rodents, cattle, elephants, raccons, marsupials, and primates such as baboons, monkeys, chimpanzees, as well as humans. There are two type of Encephalomyocarditis Virus. One is Encephalomyocarditis Virus type A, which causes reproductive problems. The other one is Encephalomyocarditis Virus type B, which causes heart failure in pigs. African Elephants were the first species that were infected with the virus. The first outbreak ever seen was in South Africa in 1993. Between December 1993 and August 1994, a number of acute deaths occurred in free-ranging Africa elephants in the Kruger National Park KNP. 4
Genome and Structure
Once humans are infected with this virus, the symptoms they may be faced with include fever, neck stiffness, lethargy, delirium, headaches, and vomiting. In primates such as gibbons and owl monkeys, Encephalomyocarditis Virus can cause necrotizing and interstitial myocarditis.[6] Transmission and pathogenesis occurs by ; incubation from nine to ten days, oral, fecal and urine contamination of food, sub clinical infections, replication in myocardial and kills them.
Cell Structure and metabolism
Some diagnoses may be antermorten due to rapid clinical course, gross lesions such as pale streak in the myocardium, hydrothorax, hydropericardium, pulmonary edema, froth in tracheobronchial tree. Other diagnoses are Histopathology :myocardial degeneration and necrosis with lymphocytic infiltrates, virus particles may be visible on electron microscopy, definitive diagnosis: virus isolation, PCR, mouse inoculation, serological test for antibodies available-Texas A&m. 5
Ecology and Pathology
Application to Biotechnology
There are many methods used to futher study the effects of this virus. One was the viruse isolation and serology, which consisted on inoculation of a infected tissue of the bull elephant in the Kruger National Park (KNP)into mice. Vaccine seed virus was prepared by adapting this E1-M1 isolated by passing five time on a monolayer of BHK 21 clone 13 cells which are used at the laboratory for routine foot-and-mouth disease (FMD) vaccine production. 4 Seology is the virus neutralization test that is used as antigen. Another way is the oil adjuvant which is the double suspension which was used as vaccine for pigs, elephants, and mice. Virus titrtion is flat-bottomed micro titer plates using an in-house modification and tryptose, referred to as Vac medium, for the dilution of the virus and suspension of the BHK cells. The plates where incubated at 37 Celsius for forty-eight hours in humidified chamber containing five percent of carbon dioxide and the test read with an inverted microscope. The last one mentioned in the journal was virus isolation of samples which were processed by diluting blood, ground up tissue or fecal samples and titrating the sample on microtiter plates, using BHK cells as an indicator system. Then the blood samples were diluted one over ten in medium and then diluted as described for the tissue sample. They were examined daily for cyopathogenic effect for up to seven days. 4
Current Research
The efficacy of an experimental oil-adjuvanted encephalomyocarditis vaccine in elephants, mice and pigs
The scientist in charge of preparing this vaccine found that there are many ways develop the vaccine that is most appropriate to control the virus. One of the ways of doing so was cultivation of the virus, a multiple process monolayer production system employing BHK 21 clone13 cells was used as described with the modification of freezing and defrosting the rolloer flask before harvesting to enhance the release of virus. 4
References
1 Aravindan, V., Vickraman, P. 2007. A novel gel electrolyte with lithium difluoro(oxalato) borate salt and Sb2O3 nanoparticles for lithium ion batteries. Solid State Sciences 9(11): 1069-1073
2Brewer, L.A., Lwamba, H.C.M., Murtaugh, M.P., Palamnberg, A.C., Brown, C., Njenga, M.K.2001. Porcine Encephalomyocarditis Virus Persists in Pig Myocardium and Infects Human Myocardial Cells. Journal of Virology 75(23):11621-11629
3[1] Gandolf, DVM A.R. 2003. Encephalomyocarditis Virus (EMCV):Options for Vaccation of Elephants. Retrieved 2009, from American Association of Zoo Veterinarians website:
4Hunter, P., Swanepoel, S.P., Esterhuysen,J.J., Raath,J.p., Bengis,R.G.,and Van Der Lugt,J.J.1998. The efficacy of an experimental oil-adjuvanted encephalomyocarditis vaccine in elephants, mice and pigs. Vaccine 16(1):55-61
5[2]Mikota, DVM Susan. Encephalomycarditis (EMC, EMCV). Retrieved 2009, from Elephant Care International Website:
6[3]
Encephalomyocarditis (EMCV). Retrieved 2009, from Zoologix, Inc. Website:
7[4]Encephalomyocarditis virus type A, causes reproductive problems, type B causes heart failure in pigs. Retrieved 2009, from European Bioinformatics Institute website