diagnostic virology Flashcards

1
Q

what is detected

A

actual virus (rare)

antigens of virus, or genetic components of virus (DNA/RNA)

host response eg antibody antigen interaction

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2
Q

diagnostic methods

A

quantify antibody/antigen, or quantify genome (viral load)

serotyping eg HIV 1 or 2

genome sequencing

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3
Q

typical samples used

A

throat swob, bronchoalveolar lavage for respiratory viruses

stools/urine

CSF

blood (for serology or for viral load)

saliva

all samples used for PCR apart from for serology- PCR tests for DNA, serology tests for antibodies in blood

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4
Q

antibody testing

A

can look for IgM antibodies (last 3 months after disease onset) or IgG (last for whole life)

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5
Q

antibody avidity testing

A

those antibodies with low avidity will be washed away, as not bound strongly- avidity increases with time, so often used to DATE the disease

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6
Q

HIV testing

A

mostly use serology (elisa test)- then undergo serotyping (HIV 1 or 2), and look at viral load (amount of virus in blood)

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7
Q

point of care testing

A

done for viruses- drop of blood put on a stick (like pregnancy test)

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8
Q

electron microscopy/ culture and immunofluorescence

A

all rarely used, mainly PCR used now

detection of viral antigens- antibodies placed which are fluorescently labelled

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9
Q

CNS disease

A

meningitis/encephalitis- CSF used for PCR, STOOLS used for PCR as well, as well as BLOOD for PCR

can be HSV, VZV or enterovirus- depends on history eg travel to a certain country

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10
Q

real time PCR melt curve analysis

A

PCR products melt at different temp.s depending on virus

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11
Q

sensitivity vs specificty

A

sens- ability to correctly identify positive (ie should give few false positives)

spec- correctly identify neg (ie should give few false positives)

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12
Q

multiplex PCR

A

amplifies specific RNA/DNA sequences- multiplex can test multiple antigens from a sample ie 1st box for EBV, 2nd box for HIV

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