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EBOLA VIRUS
A Concise Presentation
By
Mr. Deepak Sarangi M.Pharm
1
CONTENTS
2
īƒ˜Introduction
īƒ˜Definition
īƒ˜Ebola virus
īƒ˜Structure
īƒ˜Classification
īƒ˜Mode of transmission
īƒ˜Mechanism of action
īƒ˜Symptoms
īƒ˜Diagnosis
īƒ˜Treatment
īƒ˜Controlling the spread of Ebola
īƒ˜Conclusion
īƒ˜References
INTRODUCTION
īƒ˜ The Ebola virus is a severe infectious often fatal
disease in human and primates.
īƒ˜ First appeared in1976 at Nzara in Sudan and at
Yambuku in the democratic republic of Congo near
the Ebola river in Africa.
īƒ˜ Second appeared in Africa 1989 in Reston.
īƒ˜ Third appeared in 2014 West Africa affecting
Guinea, Sierra, Leone, Liberia and Nigeria.
3
īƒ˜ Ebola virus is called as hemorrhagic because
bleeding will occur during the course of illness.
īƒ˜ Ebola virus causes bleeding inside and out side the
body.
īƒ˜ Ebola strikes mainly in villages of central
and west Africa but it has also spread to African
cities too.
4
īƒ˜ Ebola is a negative RNA virus.
īƒ˜ There are different species of the Ebola virus.
īƒ˜ Reston ebolavirus was first discovered in
laboratories in Reston, United States of
America (USA)
īƒ˜
5
Ebola virus is responsible for viral hemorrhagic
fevers like:
Lassa fever,
Yellow fever,
Marburg and
Dengue fever.
EBOLA OUTBREAK 1976-2014
6
DEFINITION
īƒ˜ Ebola virus disease (formally known as
Ebola hemorrhagic fever )is a disease
caused by the ebola virus in severe fatality
rate, 90% affects human and non human
primates.
7
EBOLA VIRUS
īƒ˜ Ebola virus is an infectious which kill in a short
time.
īƒ˜ Needs a host cell to survive.
īƒ˜ Considered like a non-living entity.
īƒ˜ Which is a severe, often-fatal disease caused by
infection with a species of Ebola virus.
8
STRUCTURE
9
īƒ˜ Genome 19kb long.
īƒ˜ Diameter 80nm; length 960nm to 1200nm.
īƒ˜ Four viral proteins: polymerase (L), nucleoprotein,
and proteins VP35 and VP30.
īƒ˜ Spikes formed by GP1/GP2 Complexes
(envelope glycoprotein).
īƒ˜VP24 (membrane protein) associated with envelope.
10
CLASSIFICATION
īƒ˜ Order : Mononegavirales
Enveloped, nonsegment, negative strand RNA
viruses.
īƒ˜ Family : Filoviridae, contains 3 genera :
â€ĸ Ebola virus (1976)
â€ĸ Marburg virus
â€ĸ Cueva virus
īƒ˜ Genus : Ebola virus, named after the ebola
river where it was first found.
11
MODE OF TRANSMISSION
īƒ˜ Unsterilized needles.
īƒ˜ Sub optical hospital
conditions.
īƒ˜ Personal contact.
īƒ˜ Through blood to blood
contact.
īƒ˜Human to human transmission.
īƒ˜ Reusing needles and blood
gloves in hospital.
12
īƒ˜ Ebola is introduced into the human population
through close contact with the blood, secretions,
organs or other bodily fluids of infected animals.
13
MECHANISM OF ACTION :
īƒ˜ Every tissue are affected, except bones and
muscles.
īƒ˜ The virus creates blood clots.
īƒ˜ Clots goes towards internal organs (lungs, Eyeball).
īƒ˜ It prevents oxygen to rise tissue.
īƒ˜ The virus also destroys connective tissue
(affinity with collagen).
14
INTIAL SYMPTOMS;
īƒŧ High temperature (at least 38.8c)
īƒŧ Muscle, joints, abdominal pain
īƒŧ Nausea
īƒŧ Blood stream slow down
īƒŧ Loss of appetite
īƒŧ Rashes
īƒŧ Increased liver enzyme activity
SYMPTOMS :
15
LATE SYMPTOMS:
īƒŧ Vomiting
īƒŧ Diarrhoea
īƒŧ Coughing
īƒŧ Pharyngitis
īƒŧ Prostration
īƒŧ Severe Vomiting Blood
īƒŧ Hemorrhage
īƒŧ Internal and external hemorrhages from orifices
(nose, mouth, skin, eyes).
īƒŧ Low white blood cell count.
16
DIAGNOSIS:
īƒ˜ Diagnosing Ebola can be difficult at first since early
symptoms, such as fever, are nonspecific to Ebola
infection.
īƒ˜ Samples from the patient can then be collected and
tested to confirm infection are:
1. Antibody-capture enzyme-linked immunosorbent assay
(ELISA).
17
2. Antigen-capture detection tests.
3. Serum neutralization test.
4. Reverse transcriptase polymarase chain reaction
(RT-PCR) assay.
5. Electron microscopy.
6. Virus isolation by cell culture.
18
TREATMENT
īƒ˜There are no licensed specific treatment.
īƒ˜ Patients are Frequently dehydrated and requires oral
Rehydration with solution containing electrolyte.
īƒ˜ New drug therapies are bieng evaluated.
īƒ˜ However there have been very recent development
in preventative medication.
19
Recommended care includes:
īƒ˜ Volume repletion
īƒ˜ Maintenance of blood pressure (with vasopressors if
needed)
īƒ˜ Maintenance of oxygenation
īƒ˜ Pain control
īƒ˜ Nutritional support
īƒ˜ Treating secondary bacterial infections and pre-
existing comorbidities
20
CONTROLLING THE SPREAD OF
EBOLA
a. Hospitals must follow precautionary methods, such as:
1. Wearing gloves.
2. Isolating infected individuals.
3. Practicing nurse barrier techniques.
4. Proper sterilization and disposal of all equipment.
b. Burials must be done correctly:
1. No washing or touching carcass.
2. Put into body bags and bury outside city.
c. Report any questionable illness to officials.
21
īƒ˜ Ebola virus is extremely virulent.
īƒ˜ The infected organism does not have time to
react to the virus.
īƒ˜ First symptoms appear during the critical
period.
īƒ˜ Even though scientists have recently made
breakthroughs there is still need for extensive research
to find vaccines and cures for this deadly virus.
CONCLUSION
22
REFERENCES :
īƒ˜ www.wikipidea.com.
īƒ˜ http://www.cdc.gov/ncidod/dvrd/spb/mnpages/di
spages/ebotabl.html.
īƒ˜ Hampton, Tracy, Vaccines Against Ebola and
Marburg Viruses Show Promise in Primates
Studies, Medical News and Perspectives.
JAMA, Vol. 294 No. 2 July 2005.
īƒ˜ Jones, Steven, Live attenuated recombinant
vaccine protects nonhuman primates against
Ebola and Marburg viruses, Nature Medicine,
Vol. 11 No. 7 July 2005.
23
THANKS for viewing the ppt
For more ppts
on pharma related topics plz
contact
sarangi.dipu@gmail.com
Or find me at following link
www.facebook.com/sarangi.dipu
24

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The Deadly Ebola Virus: Causes, Symptoms, and Treatment

  • 1. EBOLA VIRUS A Concise Presentation By Mr. Deepak Sarangi M.Pharm 1
  • 2. CONTENTS 2 īƒ˜Introduction īƒ˜Definition īƒ˜Ebola virus īƒ˜Structure īƒ˜Classification īƒ˜Mode of transmission īƒ˜Mechanism of action īƒ˜Symptoms īƒ˜Diagnosis īƒ˜Treatment īƒ˜Controlling the spread of Ebola īƒ˜Conclusion īƒ˜References
  • 3. INTRODUCTION īƒ˜ The Ebola virus is a severe infectious often fatal disease in human and primates. īƒ˜ First appeared in1976 at Nzara in Sudan and at Yambuku in the democratic republic of Congo near the Ebola river in Africa. īƒ˜ Second appeared in Africa 1989 in Reston. īƒ˜ Third appeared in 2014 West Africa affecting Guinea, Sierra, Leone, Liberia and Nigeria. 3
  • 4. īƒ˜ Ebola virus is called as hemorrhagic because bleeding will occur during the course of illness. īƒ˜ Ebola virus causes bleeding inside and out side the body. īƒ˜ Ebola strikes mainly in villages of central and west Africa but it has also spread to African cities too. 4
  • 5. īƒ˜ Ebola is a negative RNA virus. īƒ˜ There are different species of the Ebola virus. īƒ˜ Reston ebolavirus was first discovered in laboratories in Reston, United States of America (USA) īƒ˜ 5 Ebola virus is responsible for viral hemorrhagic fevers like: Lassa fever, Yellow fever, Marburg and Dengue fever.
  • 7. DEFINITION īƒ˜ Ebola virus disease (formally known as Ebola hemorrhagic fever )is a disease caused by the ebola virus in severe fatality rate, 90% affects human and non human primates. 7
  • 8. EBOLA VIRUS īƒ˜ Ebola virus is an infectious which kill in a short time. īƒ˜ Needs a host cell to survive. īƒ˜ Considered like a non-living entity. īƒ˜ Which is a severe, often-fatal disease caused by infection with a species of Ebola virus. 8
  • 10. īƒ˜ Genome 19kb long. īƒ˜ Diameter 80nm; length 960nm to 1200nm. īƒ˜ Four viral proteins: polymerase (L), nucleoprotein, and proteins VP35 and VP30. īƒ˜ Spikes formed by GP1/GP2 Complexes (envelope glycoprotein). īƒ˜VP24 (membrane protein) associated with envelope. 10
  • 11. CLASSIFICATION īƒ˜ Order : Mononegavirales Enveloped, nonsegment, negative strand RNA viruses. īƒ˜ Family : Filoviridae, contains 3 genera : â€ĸ Ebola virus (1976) â€ĸ Marburg virus â€ĸ Cueva virus īƒ˜ Genus : Ebola virus, named after the ebola river where it was first found. 11
  • 12. MODE OF TRANSMISSION īƒ˜ Unsterilized needles. īƒ˜ Sub optical hospital conditions. īƒ˜ Personal contact. īƒ˜ Through blood to blood contact. īƒ˜Human to human transmission. īƒ˜ Reusing needles and blood gloves in hospital. 12
  • 13. īƒ˜ Ebola is introduced into the human population through close contact with the blood, secretions, organs or other bodily fluids of infected animals. 13
  • 14. MECHANISM OF ACTION : īƒ˜ Every tissue are affected, except bones and muscles. īƒ˜ The virus creates blood clots. īƒ˜ Clots goes towards internal organs (lungs, Eyeball). īƒ˜ It prevents oxygen to rise tissue. īƒ˜ The virus also destroys connective tissue (affinity with collagen). 14
  • 15. INTIAL SYMPTOMS; īƒŧ High temperature (at least 38.8c) īƒŧ Muscle, joints, abdominal pain īƒŧ Nausea īƒŧ Blood stream slow down īƒŧ Loss of appetite īƒŧ Rashes īƒŧ Increased liver enzyme activity SYMPTOMS : 15
  • 16. LATE SYMPTOMS: īƒŧ Vomiting īƒŧ Diarrhoea īƒŧ Coughing īƒŧ Pharyngitis īƒŧ Prostration īƒŧ Severe Vomiting Blood īƒŧ Hemorrhage īƒŧ Internal and external hemorrhages from orifices (nose, mouth, skin, eyes). īƒŧ Low white blood cell count. 16
  • 17. DIAGNOSIS: īƒ˜ Diagnosing Ebola can be difficult at first since early symptoms, such as fever, are nonspecific to Ebola infection. īƒ˜ Samples from the patient can then be collected and tested to confirm infection are: 1. Antibody-capture enzyme-linked immunosorbent assay (ELISA). 17
  • 18. 2. Antigen-capture detection tests. 3. Serum neutralization test. 4. Reverse transcriptase polymarase chain reaction (RT-PCR) assay. 5. Electron microscopy. 6. Virus isolation by cell culture. 18
  • 19. TREATMENT īƒ˜There are no licensed specific treatment. īƒ˜ Patients are Frequently dehydrated and requires oral Rehydration with solution containing electrolyte. īƒ˜ New drug therapies are bieng evaluated. īƒ˜ However there have been very recent development in preventative medication. 19
  • 20. Recommended care includes: īƒ˜ Volume repletion īƒ˜ Maintenance of blood pressure (with vasopressors if needed) īƒ˜ Maintenance of oxygenation īƒ˜ Pain control īƒ˜ Nutritional support īƒ˜ Treating secondary bacterial infections and pre- existing comorbidities 20
  • 21. CONTROLLING THE SPREAD OF EBOLA a. Hospitals must follow precautionary methods, such as: 1. Wearing gloves. 2. Isolating infected individuals. 3. Practicing nurse barrier techniques. 4. Proper sterilization and disposal of all equipment. b. Burials must be done correctly: 1. No washing or touching carcass. 2. Put into body bags and bury outside city. c. Report any questionable illness to officials. 21
  • 22. īƒ˜ Ebola virus is extremely virulent. īƒ˜ The infected organism does not have time to react to the virus. īƒ˜ First symptoms appear during the critical period. īƒ˜ Even though scientists have recently made breakthroughs there is still need for extensive research to find vaccines and cures for this deadly virus. CONCLUSION 22
  • 23. REFERENCES : īƒ˜ www.wikipidea.com. īƒ˜ http://www.cdc.gov/ncidod/dvrd/spb/mnpages/di spages/ebotabl.html. īƒ˜ Hampton, Tracy, Vaccines Against Ebola and Marburg Viruses Show Promise in Primates Studies, Medical News and Perspectives. JAMA, Vol. 294 No. 2 July 2005. īƒ˜ Jones, Steven, Live attenuated recombinant vaccine protects nonhuman primates against Ebola and Marburg viruses, Nature Medicine, Vol. 11 No. 7 July 2005. 23
  • 24. THANKS for viewing the ppt For more ppts on pharma related topics plz contact sarangi.dipu@gmail.com Or find me at following link www.facebook.com/sarangi.dipu 24