Microbiology Flashcards

1
Q

mode of infection of parvovirus B19

A
  • by respiratory secretions, blood and blood products of infected patients
    -from mother to fetus
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what types of cells are affected by parvovirus B19

A

1) RBC precursors in the bone marrow, causing aplastic anemia
2) Endothelial cells in the blood cells, accounting for the rash associated with erythema infectiosum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

clinical manifestations of parvovirus B19

A

1) TAC (transient aplastic crisis):
-temporary arrest of RBC production
- this becomes apparent only in patients with severe hemolytic anemia

2) PRCS (pure red cell aplasia):
- persistent infection in immunocompromised patients leading to severe aplastic anemia and the patient is dependent on blood transfusions.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Laboratory diagnosis of Parvovirus B19

A

Specimens: serum, blood cells

1) Direct detention:
a) ELISA for detection of viral antigen
b) PCR for detection of viral antigen. It is the most sensitive assay

2) Serology:
ELISA is used to detect B19 IgM antibodies, which indicates recent infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Treatment of B19 virus

A

symptomatic treatment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Prevention of B19 virus

A

1) Screening of blood donors
2) Standard infection control precautions

There is no vaccine available

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are Marburg and Ebola?

A

-They are severe and highly fatal diseases
-caused by viruses from the Filoviridae family.
• Though caused by different viruses, the two diseases are clinically almost indistinguishable
-Both diseases are rare but have a capacity to cause dramatic outbreaks with high fatality

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Reservoir of African Hemorrhagic fevers

A

Bats may be the reservoir
– monkeys are susceptible to infection but are not considered viable RH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Mode of Transmission of AHF

A

These are highly communicable diseases.
- Person to person transmission by intimate contact is the main route of infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Fatality of Marburg and Ebola

A
  • Marburg 25%
    -Ebola 50-90%
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Laboratory diagnosis of AHF

A

Based on symptoms and demonstration of filovirsuses in blood by ELISA and PCR

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Treatment of AHF

A

Supportive care - fluid, electrolytes and sometimes anticoagulants
- No antiviral drugs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Incubation period of AHF

A

2-21 days

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Methods of controlling EVD

A

1) Reduce bat, monkey, pig contact by handling animals with gloves
2) cook food thoroughly before consumption
3) rapid and safe burial of the dead

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Diseases presenting hemorrhage

A

Flaviviruses - yellow fever, dengue fever

Bunya viruses - rift valley fever

Arenaviruses - Lassa Fever

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is yellow fever?

16
Q

Reservoir and MOT of yellow fever

A

Jungle yellow fever:
- Primarily a monkey disease
- monkey-to-monkey transmission occurs by forest Aedes mosquito
- Man is accidental host on visiting jungle

Urban yellow fever
- involves person-to-person transmission by domestic Aedes mosquito
- It occurs when an infected person from the jungle returns to urban areas

17
Q

clinical manifestations of yellow fever

A

may be mild and unrecognized or severe and fatal
- fever, chills, headache, dizziness, jaundice or renal dysfunction

severe case - black vomititus with high mortality rate (20% or more)

18
Q

diagnosis of yellow fever

A

1) Detection of viral antigens in the blood by ELISA
2) Viral nucleic acid detection by PCR

19
Q

treatment of yellow fever

A

Supportive, depends on system involved

20
Q

General preventive measures of yellow fever

A

• Control of Aedes aegypti in urban yellow fever.
• Vector control measures:
(see Malaria)
• Aircrafts leaving an infected
area to receptive area should be disinfected
• Quarantine measures for imported monkeys at receptive areas.
• Periodic spraying of airports and surrounding receptive areas.

21
Q

specific preventive measures of yellow fever

A

-By active immunization. A single S.C. injection of a 17 D vaccine containing viable attenuated yellow fever 17 D strain virus.
Validity of the vaccine: It begins after 10 days and persists for at least 10 years. During this period of validation, no cases have been reported.

Applications:
1. Those who work in jungles.
2. Resident of endemic areas.
3. Travelers to endemic areas or between endemic and receptive areas.
-If a traveler arrives in a receptive area without a certificate, he is isolated for 6 days from the date of leaving the last infected area.
-If a traveler arrives in a receptive area before completing 10 days of vaccination, he is isolated until the certificate becomes valid, with maximum of 6 days.

22
Q

control measures for cases of yellow fever

A

-Isolation at any place (Blood and body fluid precautions). Prevent access of mosquitoes to patients for at least 3-5 days by screening the sick room, by spraying quarters with residual and insecticide, by using
insecticide-treated bed nets…

-Notification to local health office then to WHO.

-Disinfection is not required.
-Treatment is symptomatic and correction of complications.

23
Q

control measure for contacts of yellow fever

A

Family and other contacts not previously immunized should be vaccinated

24
control measure of environment (yellow fever)
Search for source of infection i.e. areas visited by patient 3-6 days before onset to locate focus of yellow fever.
25
epidemic measures of yellow fever control
- Determine the extent of the infected areas. in forest areas, restrict the movement Of animal reservoirs from the affected area. Use approved mosquito repellents for those exposed. ー Conduct a community survey to determine density of vector mosquitoes, their breeding places and effective control measures. - Identity infected animal reservoirs, prevent mosquitoes from feeding on them
26
clinical manifestations of dengue fever
Clinical manifestations: 1. Classical dengue fever (DF) -characterized by acute onset of high-grade fever, frontal headache, myalgias, arthralgias, and often a maculopapular rash. The illness may be clinically indistinguishable from influenza, measles. 2. Dengue hemorrhagic fever DHE -DHF is a potentially deadly complication of dengue. -It appears to be an immunopathological consequence of infection of a person who has already developed immunity to one serotype of Dengue virus with a virus of another serotype, although the mechanism is not fully understood. 3. Dengue shock syndrome (DSS) - The most common of these manifestations are skin hemorrhages such as petechia and purpura. -Most patients develop thrombocytopenia and hemo-concentration. These patients have DSS, which if not immediately corrected, can lead to profound shock and death.
27
diagnosis of dengue fever
Diagnosed by antigen detection in blood
28
prevention of dengue fever
a. Mosquito control is the most important strategy to prevent virus transmission to humans b. No specific treatment is available.
29
what is rift valley fever
It is a mosquito-borne zoonotic disease caused by Rift Valley Fever (RVF) virus; a member of Bunyaviridae family.
30
reservoir and MOT of rift valley fever
Primarily sheep, cattle, buffaloes, goats and camels leading to hepatitis, abortion and death Humans are secondarily affected by infected mosquito bite or blood/body fluid exposure of infected animals.
31
clinical picture of rift valley fever
-Most human cases are asymptomatic or relatively mild manifested as flu-like illness with complete recovery. • A small proportion of patients develop a much more severe disease. This generally appears as one of several recognizable syndromes: retinitis with visual loss, meningoencephalitis or hemorrhagic fever.
32
prevention of rift valley fever
Sustained program of animal vaccination. Both live attenuated and killed vaccines have been developed for veterinary use.