Viral Diagnosis Flashcards

1
Q

Purpose of viral diagnosis

A

Clinical management - treating patients who have disease

Public health management - being able to contain a disease

Health care provision - education on vaccination

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2
Q

Samples taken for viral diagnosis

A

Blood, urine, salvia, cerebrospinal fluid, nasal swab

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3
Q

Direct detection of viruses

A

Testing for the presence of a virus by testing for viral proteins or nucleic acids

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4
Q

Hemadsorption

A

Red blood cells are added to patient sample. If virus is present, red blood cells will adhere to the sample cells.

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5
Q

Hemagglutination

A

Red blood cells are added to a patient sample. If a virus is not present then the erythrocytes naturally clump together. If a virus is present, the erythrocytes are unable to clump.

After knowing a virus is present, a specific antibody can be added to the sample. If the red cells clump then that allows identification of the virus based on what antibody was used.

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6
Q

Sandwich ELISA

A
  1. Plate coated in blocking buffer and capture antibody
  2. Patient sample added (contains antigen)
  3. Plate washed to remove unbound antigen, then a defection antibody is added which has a biotin molecule bound to it
  4. Plate is washed again to remove unbound detection antibody then HRPO is added which has an avidin molecule bound to it
  5. Substrate is added, changes from colourless to yellow in presence of HRPO

2-5 times more sensitive than indirect ELISA and has high specificity

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7
Q

Indirect detection

A

Testing for the presence of specific antibodies and if we have a raised immune response.

This method doesn’t identify between past and recent exposures.

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8
Q

Indirect ELISA

A
  1. Antigen is bound to well
  2. An unlabelled primary antibody binds to the antigen
  3. A secondary antibody is bound to the first. This antibody is linked to an enzyme
  4. Substrate is added which turns the solution coloured, indicating a positive result

Economical, however takes a long time to run

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9
Q

Latex agglutination

A

Latex particles are added to a sample suspected to contain antigens.

If the antigen is present, latex beads clump together. If not, the latex beads spread out and all we can see is milky liquid.

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