Ebola Flashcards

(29 cards)

1
Q

Define EVD and what’s it’s former name?

A
  • EVD (formerly Ebola hemorrhagic fever) is a severe, often fatal illness caused by Ebola virus, a Filovirus
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2
Q

Hosts

  • Affects humans and nonhuman primates (e.g., monkeys, gorillas, chimpanzees).
A
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3
Q

How was ebola named?

A
  • Named after the Ebola River in the Democratic Republic of Congo (formerly Zaire), site of the first recognized outbreak in 1976.
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4
Q

When was the first Ebola Outbreak?

A

First outbreaks (1976)

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5
Q
  • Two major outbreaks in Central Africa are? :
A
  • DR Congo (Zaire): near Ebola River.
  • South Sudan: \~850 km away.
  • Over 500 cases and 400 deaths.
  • Healthcare workers infected via contact with blood, excreta, and patients.
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6
Q

Subsequent outbreaks

  • Uganda: 2000
  • DR Congo: 1995, 2001, 2002, 2003
  • Gabon: 1994, 1996, 1997, 2002
  • South Africa: 1996
  • Sudan: 2004
A
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7
Q

Where had the Largest outbreak: West Africa (2013–2016)

A
  • Countries: Guinea, Liberia, Sierra Leone
  • 28,646 cases, 11,323 deaths
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8
Q

Explain the Nigeria outbreak (2014)

A
  • Index case: Patrick Sawyer, a Liberian-American, flew to Lagos on July 20, 2014
  • Became ill on arrival, died 5 days later
  • Transmission to healthcare workers:
  • Nurse Justina Ejelonu died August 5
  • Dr. Ameyo Adadevoh, who treated Sawyer, died August 19
  • 20 total cases, 8 deaths
  • 4 deaths among healthcare workers
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9
Q

What are the possible hosts for EVD? and it’s likely?

A
  • Likely natural hosts: African fruit bats (family Pteropodidae)
  • Other possible animal reservoirs:
  • Chimpanzees, gorillas, monkeys
  • Forest antelope, porcupines
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10
Q

______ Transmission (Animal to Human) happened In ebola? And how does it spread?

A

Zoonotic Transmission (Animal to Human

  • Ebola enters human population through:
  • Contact with blood, secretions, organs, or other bodily fluids of infected animals
  • Common during hunting, butchering, or consumption of bushmeat

3. Human-to-Human Transmission

Occurs via direct contact through broken skin or mucous membranes with:

  • Blood or body fluids (urine, saliva, sweat, feces, vomit, breast milk, semen) of an infected or deceased person
  • Contaminated objects (e.g., needles, bedding, clothing)
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11
Q

4. High-Risk Settings

  • Healthcare workers are at risk during:
  • Patient care without proper infection control measures
  • Funeral practices:
  • Direct contact with dead bodies during burial rituals
A
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12
Q

What’s the Classification of EVD?

A
  • Family: Filoviridae
  • Genera in family:
  • Ebolavirus
  • Marburgvirus
  • Cuevavirus
  • All cause viral hemorrhagic fever (VHF)
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13
Q

What’s the 2. Structure of EVD

A
  • Genome: Single-stranded, negative-sense RNA
  • Enclosed in:
  • Nucleocapsid
  • Lipid envelope
  • Highly virulent; requires BSL-4 containment in labs
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14
Q

Ebola virus is inactivated by?:

A
  • Heating at 60°C for 30 minutes
  • UV and gamma irradiation
  • Lipid solvents, bleach, and phenolic disinfectants
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15
Q

4. What are the Major Ebola Virus Species

A
  • Zaire ebolavirus (most virulent)
  • Sudan ebolavirus
  • Bundibugyo ebolavirus
  • Reston ebolavirus (non-pathogenic to humans)
  • Taï Forest ebolavirus
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16
Q

Whats the Pathogenesis of Ebola Virus Disease

A

1. Entry and Spread

  • Virus enters through mucous membranes, broken skin, or parenterally.
  • Early targets: monocytes, macrophages, and dendritic cells.
  • These infected immune cells carry the virus to lymph nodes, liver, spleen, and adrenal glands.

2. Cytokine Storm and Inflammation

  • Infected monocytes and macrophages release massive amounts of proinflammatory cytokines (e.g., TNF-α, IL-6).
  • This causes a cytokine storm leading to:
  • Fever
  • Vascular leakage
  • Tissue damage

3. Immune Evasion

  • Dendritic cells fail to mature → ineffective T cell activation.
  • Lymphocyte apoptosis occurs even though lymphocytes are not infected.
  • Result: Immunosuppression, viremia, and rapid viral replication.

4. Vascular Dysfunction

  • Virus infects endothelial cells, causing:
  • Loss of barrier function
  • Increased permeability
  • Widespread hemorrhage
  • Leads to hypovolemic shock and multi-organ failure.

5. Organ Damage

  • High viral loads in liver, spleen, lungs, kidneys.
  • Liver: Hepatocyte necrosis → reduced coagulation factors → worsens bleeding.
  • Adrenal glands: Damage → hypotension and electrolyte imbalance.

6. Coagulopathy

  • Disseminated intravascular coagulation (DIC) contributes to:
  • Bleeding diathesis
  • Thrombocytopenia
  • Microvascular thrombosis

Summary:

Ebola virus disables the immune system, damages blood vessels, and triggers uncontrolled inflammation. This combination causes bleeding, shock, and organ failure.

17
Q
  • Targets of EVD are? (In the immune system):
A
  • Macrophages
  • Dendritic cells
  • Fibroblasts
  • Endothelial cells
18
Q

2. Systemic Spread

  • High viral titers found in:?
A
  • Liver
  • Spleen
  • Lungs
  • Kidneys
  • Blood and body fluids

3. Immune Effects

19
Q
  • Ebola is immunosuppressive:
  • Inhibits dendritic cell function
  • Impairs humoral (antibody) response
20
Q

What are the Clinical Features of Ebola Virus Disease?
What’s the incubation period of EVD

Early symptoms

Progressive

Late

End stage sign

A

Incubation Period:

2–21 days (typically 4–10 days)

Early Symptoms (non-specific):

  • Fever
  • Fatigue
  • Muscle pain
  • Headache
  • Sore throat

Progressive Symptoms (gastrointestinal + systemic):

  • Vomiting
  • Diarrhea
  • Rash

Late Symptoms (bleeding phase):

  • Internal bleeding: GI tract, lungs, etc.
  • External bleeding:
  • Eyes, ears, nose
  • Mouth and rectum
  • Petechiae or hemorrhagic rashes

End-stage Signs:

  • Disseminated intravascular coagulation (DIC)
  • Hypovolemic shock
  • Coma
21
Q

What’s the mortality rate of EVD and which sub species has the highest?

A

Mortality:

  • 25–90% (Zaire subtype has the highest)
22
Q

Ebola Case Definitions (for surveillance and response)

1. Alert Case

  • Fever with no response to treatment for usual causes (e.g., malaria, typhoid)
  • Occurs in an endemic or outbreak area

2. Suspected Case

  • Fever + ≥3 of the following:
  • Headache
  • Anorexia
  • Lethargy
  • Muscle/joint pain
  • Vomiting or diarrhea
  • Abdominal pain
  • Breathing difficulty
  • Difficulty swallowing
  • Hiccups
  • OR any unexplained bleeding

3. Probable Case

  • Suspected case with an epidemiological link
  • Contact with a confirmed case
  • Attendance at a burial or health facility treating Ebola patients

4. Confirmed Case

  • Lab-confirmed infection (e.g., RT-PCR, antigen detection, virus isolation)
23
Q
A

Laboratory Diagnosis

Antibody-capture by ELISA

Antigen-capture detection by ELISA

Reverse transcriptase (RT-PCR)

Electron microscopy·

Virus isolation by cell culture in BSL 4

Other lab tests

FBC - Leukopaenia or leucocytosis Thrombocytopenia, Anemia or hemoconcentration

LFT - Elevated liver enzymes (AST, ALT).

E/U/Cr-

Urinalysis- Proteinuria, hematuria, and oliguria

Treatment

Supportive care - rehydration with oral or intravenous fluids - and treatment of specific symptoms improves survival

There is no standard treatment for Ebola HF.

Vaccine – Ervebo, Zabdeno-and-Mvabea under trials

Experimental therapies

Z MAPP

Immunotherapy – use of convalescent serum

Prevention and control

Outbreak control include case management, surveillance and contact tracing, a good laboratory service, safe burials and social mobilization

Reducing the risk of wildlife-to-human transmission

Reducing the risk of human-to-human transmission

Prevention and control cont’d

Safe and dignified burial of the dead

Reducing the risk of possible sexual transmission

Reducing the risk of transmission from pregnancy related fluids and tissue

Health-care workers should always take standard precautions when caring for patients

24
Q

Diagnosis of Ebola Virus Disease

Key Principle:

  • Requires high index of suspicion due to nonspecific early symptoms.

Clinical Clues

  • Recent travel to endemic areas
  • Close contact with confirmed or suspected cases
  • Unexplained fever not responding to antimalarials or antibiotics
  • History of contact with bodily fluids or burial rituals

Whatre the Immediate Actions to take?

A
  • Isolate suspected and probable cases immediately
  • Implement standard and transmission-based precautions
  • Notify public health authorities
25
**Specimen Collection** how is it done? From life and dead?
**1. From Live Patients:** * **Whole blood** * Use **EDTA bottle** * Collect during symptomatic phase **2. From Deceased or Unreachable Patients:** * **Oral fluid** (mouth swab) * Store in **universal transport medium (UTM)**
26
**Lab Confirmation** Send samples to designated **BSL-4 labs** for:
* RT-PCR (gold standard) * Antigen detection * IgM/IgG ELISA * Virus isolation (research only)
27
What are the **Laboratory Diagnosis of EVD**
**Molecular and Antigen Detection:** * **RT-PCR**: Gold standard for detecting viral RNA * **Antigen-capture ELISA**: Detects viral proteins in blood * **Antibody-capture ELISA**: Detects host antibodies (IgM, IgG) to Ebola virus **Other Diagnostic Tools:** * **Electron microscopy**: For visualizing virus particles * **Virus isolation**: Done in **BSL-4** labs using cell culture **Routine Lab Tests:** * **FBC**: Leucopenia or leukocytosis, thrombocytopenia, anemia or hemoconcentration * **Liver enzymes (AST, ALT)**: Elevated * **Electrolytes/Urea/Creatinine**: May show renal impairment * **Urinalysis**: Proteinuria, hematuria, oliguria
28
**Treatment of EVD?**
**Mainstay: Supportive Care** * **Rehydration** (oral or IV) * Correction of **electrolyte imbalances** * Management of **organ dysfunction** * **Oxygen support**, pain control, antiemetics, antibiotics for secondary infections **No universally approved antiviral therapy** **Experimental/Investigational Treatments:** * **ZMapp**: Monoclonal antibody cocktail * **Convalescent plasma**: Passive immunotherapy * **Vaccines**:   * **Ervebo** (rVSV-ZEBOV): Approved   * **Zabdeno-Mvabea**: Under trial
29
**Prevention and Control of EVD**
**Outbreak Control Measures:** * Early **case detection and isolation** * **Contact tracing** and monitoring * **Laboratory support** and safe diagnostic practices * **Safe and dignified burials** * **Community engagement** and social mobilization **Minimizing Animal-to-Human Transmission:** * Avoid contact with bushmeat, especially **fruit bats and primates** **Reducing Human-to-Human Transmission:** * Use of **personal protective equipment (PPE)** * Strict **infection control** in healthcare settings * Safe **sexual practices** after recovery * Avoid exposure to **amniotic fluid or placental tissue** from infected pregnant women