RLG PARASITES Flashcards

(33 cards)

1
Q

pathogen Causing dermatologic lesions

A

Cercopithifilaria
dirofilaria repens

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2
Q

Only sp. That detects antibodies

A

d. immitis

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3
Q

Causes humpsores

A

stephanofilaria

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4
Q

large sp of babesia

A

canis, vogeli

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5
Q

vector of b. vogeli

A

r. sanguineus

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6
Q

vector of b canis

A

dermacentor

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7
Q

small sp. of babesia

A

b. gibsoni

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8
Q

Causes neurologic signs
Adhere and clogs brain capillaries
Highly pathogenic

A

b. bovis

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9
Q

present in ph

A

b vogeli
b. gibsoni
b. bovis
hepatozoon canis
theileria orientalis

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10
Q

vector of t. evansi

A

tabanids

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11
Q

TAE buffer function

A

used as a running buffer in gel electrophoresis to separate nucleic acids.

based on their molecular weight and net charge, the nucleic acids move either slowly or rapidly towards the positive pole. The smaller molecules run faster than the bigger molecules during the gel electrophoresis.

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12
Q

other term for anaplasmosis

A

canine infectious cyclic thrombocytopenia

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13
Q

LAMP temperature

A

60-65C

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14
Q

sample that’s more useful when looking for babesia

A

capillary

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15
Q

stain preferred for examination of protozoan parasites and rickettsiae

A

romanowsky - wright and giemsa

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16
Q

how much blood is needed for blood smear

17
Q

angle for blood smear

18
Q

fixative for giemsa staining

19
Q

knott’s concn technique

A

mix 1 ml uncoagulated blood with 9 ml 2% formalin

invert to mix 4x

centrifuge 500g x 5min (2000 rpm)

discard supernatant
staon sediment with 1-2 drops 1% meth blue

add drop of sample and cover

20
Q

No sheath; Body curved
with hooked posterior end

A

acanthocheilonema reconditum

21
Q

Sheathed; Tail is tapered
and with cephalic space.

22
Q

size of brugia

23
Q

LAMP can amplify target DNA to what exponent

A

10 raised to 9

24
Q

LAMP utilizes a set of _- primers that recognize a total of six distinct sequences on the target DNA.

25
meaning of CFI
color fluorescent indicator
26
composition of CFI
hydroxynaphthol blue gel green
27
LAMP fluorescence is confirmed via machine called
FAM filter
28
advantages of microscopic exam
accessible can ID coinfection
29
limitations of microscopic exam
low sensitivity difficult for species lvl ID
30
advantages and disadvantages of serology
accessible, high sensitivity /// Abs take time to develop cannot distinguish past and present infection cross-reactivity
31
molecular techniques adv and disadvantages
high sensitivity and specificity multiplex PCR // not readily avail expensive may take hours false negative cases
32
LAMP meaning
loop-mediated isothermal amplification
33