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EBOLA VIRUS
A Concise Presentation
By
Mr. Deepak Sarangi M.Pharm
1
CONTENTS
2
Introduction
Definition
Ebola virus
Structure
Classification
Mode of transmission
Mechanism of action
Symptoms
Diagnosis
Treatment
Controlling the spread of Ebola
Conclusion
References
INTRODUCTION
 The Ebola virus is a severe infectious often fatal
disease in human and primates.
 First appeared in1976 at Nzara in Sudan and at
Yambuku in the democratic republic of Congo near
the Ebola river in Africa.
 Second appeared in Africa 1989 in Reston.
 Third appeared in 2014 West Africa affecting
Guinea, Sierra, Leone, Liberia and Nigeria.
3
 Ebola virus is called as hemorrhagic because
bleeding will occur during the course of illness.
 Ebola virus causes bleeding inside and out side the
body.
 Ebola strikes mainly in villages of central
and west Africa but it has also spread to African
cities too.
4
 Ebola is a negative RNA virus.
 There are different species of the Ebola virus.
 Reston ebolavirus was first discovered in
laboratories in Reston, United States of
America (USA)

5
Ebola virus is responsible for viral hemorrhagic
fevers like:
Lassa fever,
Yellow fever,
Marburg and
Dengue fever.
EBOLA OUTBREAK 1976-2014
6
DEFINITION
 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
 Ebola virus is an infectious which kill in a short
time.
 Needs a host cell to survive.
 Considered like a non-living entity.
 Which is a severe, often-fatal disease caused by
infection with a species of Ebola virus.
8
STRUCTURE
9
 Genome 19kb long.
 Diameter 80nm; length 960nm to 1200nm.
 Four viral proteins: polymerase (L), nucleoprotein,
and proteins VP35 and VP30.
 Spikes formed by GP1/GP2 Complexes
(envelope glycoprotein).
VP24 (membrane protein) associated with envelope.
10
CLASSIFICATION
 Order : Mononegavirales
Enveloped, nonsegment, negative strand RNA
viruses.
 Family : Filoviridae, contains 3 genera :
• Ebola virus (1976)
• Marburg virus
• Cueva virus
 Genus : Ebola virus, named after the ebola
river where it was first found.
11
MODE OF TRANSMISSION
 Unsterilized needles.
 Sub optical hospital
conditions.
 Personal contact.
 Through blood to blood
contact.
Human to human transmission.
 Reusing needles and blood
gloves in hospital.
12
 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 :
 Every tissue are affected, except bones and
muscles.
 The virus creates blood clots.
 Clots goes towards internal organs (lungs, Eyeball).
 It prevents oxygen to rise tissue.
 The virus also destroys connective tissue
(affinity with collagen).
14
INTIAL SYMPTOMS;
 High temperature (at least 38.8c)
 Muscle, joints, abdominal pain
 Nausea
 Blood stream slow down
 Loss of appetite
 Rashes
 Increased liver enzyme activity
SYMPTOMS :
15
LATE SYMPTOMS:
 Vomiting
 Diarrhoea
 Coughing
 Pharyngitis
 Prostration
 Severe Vomiting Blood
 Hemorrhage
 Internal and external hemorrhages from orifices
(nose, mouth, skin, eyes).
 Low white blood cell count.
16
DIAGNOSIS:
 Diagnosing Ebola can be difficult at first since early
symptoms, such as fever, are nonspecific to Ebola
infection.
 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
There are no licensed specific treatment.
 Patients are Frequently dehydrated and requires oral
Rehydration with solution containing electrolyte.
 New drug therapies are bieng evaluated.
 However there have been very recent development
in preventative medication.
19
Recommended care includes:
 Volume repletion
 Maintenance of blood pressure (with vasopressors if
needed)
 Maintenance of oxygenation
 Pain control
 Nutritional support
 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
 Ebola virus is extremely virulent.
 The infected organism does not have time to
react to the virus.
 First symptoms appear during the critical
period.
 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 :
 www.wikipidea.com.
 http://www.cdc.gov/ncidod/dvrd/spb/mnpages/di
spages/ebotabl.html.
 Hampton, Tracy, Vaccines Against Ebola and
Marburg Viruses Show Promise in Primates
Studies, Medical News and Perspectives.
JAMA, Vol. 294 No. 2 July 2005.
 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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Ebola virus ppt

  • 1. EBOLA VIRUS A Concise Presentation By Mr. Deepak Sarangi M.Pharm 1
  • 2. CONTENTS 2 Introduction Definition Ebola virus Structure Classification Mode of transmission Mechanism of action Symptoms Diagnosis Treatment Controlling the spread of Ebola Conclusion References
  • 3. INTRODUCTION  The Ebola virus is a severe infectious often fatal disease in human and primates.  First appeared in1976 at Nzara in Sudan and at Yambuku in the democratic republic of Congo near the Ebola river in Africa.  Second appeared in Africa 1989 in Reston.  Third appeared in 2014 West Africa affecting Guinea, Sierra, Leone, Liberia and Nigeria. 3
  • 4.  Ebola virus is called as hemorrhagic because bleeding will occur during the course of illness.  Ebola virus causes bleeding inside and out side the body.  Ebola strikes mainly in villages of central and west Africa but it has also spread to African cities too. 4
  • 5.  Ebola is a negative RNA virus.  There are different species of the Ebola virus.  Reston ebolavirus was first discovered in laboratories in Reston, United States of America (USA)  5 Ebola virus is responsible for viral hemorrhagic fevers like: Lassa fever, Yellow fever, Marburg and Dengue fever.
  • 7. DEFINITION  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  Ebola virus is an infectious which kill in a short time.  Needs a host cell to survive.  Considered like a non-living entity.  Which is a severe, often-fatal disease caused by infection with a species of Ebola virus. 8
  • 10.  Genome 19kb long.  Diameter 80nm; length 960nm to 1200nm.  Four viral proteins: polymerase (L), nucleoprotein, and proteins VP35 and VP30.  Spikes formed by GP1/GP2 Complexes (envelope glycoprotein). VP24 (membrane protein) associated with envelope. 10
  • 11. CLASSIFICATION  Order : Mononegavirales Enveloped, nonsegment, negative strand RNA viruses.  Family : Filoviridae, contains 3 genera : • Ebola virus (1976) • Marburg virus • Cueva virus  Genus : Ebola virus, named after the ebola river where it was first found. 11
  • 12. MODE OF TRANSMISSION  Unsterilized needles.  Sub optical hospital conditions.  Personal contact.  Through blood to blood contact. Human to human transmission.  Reusing needles and blood gloves in hospital. 12
  • 13.  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 :  Every tissue are affected, except bones and muscles.  The virus creates blood clots.  Clots goes towards internal organs (lungs, Eyeball).  It prevents oxygen to rise tissue.  The virus also destroys connective tissue (affinity with collagen). 14
  • 15. INTIAL SYMPTOMS;  High temperature (at least 38.8c)  Muscle, joints, abdominal pain  Nausea  Blood stream slow down  Loss of appetite  Rashes  Increased liver enzyme activity SYMPTOMS : 15
  • 16. LATE SYMPTOMS:  Vomiting  Diarrhoea  Coughing  Pharyngitis  Prostration  Severe Vomiting Blood  Hemorrhage  Internal and external hemorrhages from orifices (nose, mouth, skin, eyes).  Low white blood cell count. 16
  • 17. DIAGNOSIS:  Diagnosing Ebola can be difficult at first since early symptoms, such as fever, are nonspecific to Ebola infection.  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 There are no licensed specific treatment.  Patients are Frequently dehydrated and requires oral Rehydration with solution containing electrolyte.  New drug therapies are bieng evaluated.  However there have been very recent development in preventative medication. 19
  • 20. Recommended care includes:  Volume repletion  Maintenance of blood pressure (with vasopressors if needed)  Maintenance of oxygenation  Pain control  Nutritional support  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.  Ebola virus is extremely virulent.  The infected organism does not have time to react to the virus.  First symptoms appear during the critical period.  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 :  www.wikipidea.com.  http://www.cdc.gov/ncidod/dvrd/spb/mnpages/di spages/ebotabl.html.  Hampton, Tracy, Vaccines Against Ebola and Marburg Viruses Show Promise in Primates Studies, Medical News and Perspectives. JAMA, Vol. 294 No. 2 July 2005.  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