Methods D Serol Flashcards

(40 cards)

1
Q

Describe Cytology testing including pros/cons

A
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2
Q

what type of lesion is this

A

Round, mass-cell granules - Mast-cell tumour

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3
Q

what does a leucogram tell us

A

Leucogram: inflammation/infection/chronic/acute/ Viral

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4
Q

Which Biochem parameters shows liver function

A

AST, ALT, AP,

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5
Q

Which Biochem parameters shows kidney function

A

Urea
Creatinine

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6
Q

Why is urinalysis used

A
  • Renal disease - RBCs, WBCs, Protein

Urine conc
pH,
Specific gravity - hydration

Cytology of urine: crystals, bacteria, bilirubin, WBCs, RBCs

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7
Q

what diagnosis can u give for
A) high glucose in blood only
B) Glycosuria and high blood glucose

A

A) hyperglycemia - Diabetes

B) Glycosuria - issues with renal filtration - Most likely kidney dx

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8
Q

When doing a necropsy, what samples must you take

A

Samples of all tissue for
-Histology
-Virology
-Bacteriology
-Toxicology

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9
Q

Give DDx for this

A
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10
Q

For Histopath, tissues are fixed in

A

10% buffered formalin

1:10 ratio

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11
Q

Define IHC
-purpose
-Steps

A

ImmunoHistoChem combines Immunology, Histology, and Chemistry to form a dx.

-can identify specific viral antigen tissue

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12
Q

What are the main cell types seen in biopsies

A
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13
Q

What is histopathology used for in disease dx

A
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14
Q

how do you use IHC to differentiate between tumor types

A
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15
Q

Describe the IHC assay step in IHC

A

if the target antigen is present, the primary antibody will bind to it and won’t wash away during the assay. Then a secondary antibody that is conjugated with an ezy will attach to the primary one. Once a substrate is added the presence of all the components in tact will cause a colour change signalling the presence of the antigen.

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16
Q

why is IHC used instead of Histo in identifying the presence of viral components in tissues

A

v difficult to see viral under H and E staining unless inclusion bodies are seen.

IHC can help target viral antigen in tissues.

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17
Q

Describe Pathology isolation for Bacteria, Toxins, and Viruses
LA

18
Q

What is pathogen isolation?
-what does it involve?
-Tissue types

A

Pathogen isolation is the process of identifying the pathogen responsible for the dx using Histo/IHC. This involves:
Staining e.g Gram-stain, Inflammation type, necrosis
Usually requires further work-up to identify genus and species of pathogen.

Fresh samples are best. Take multiple samples of key tissues and store frozen. Key tissue sites: Liver, Stomach, Urine, lung, spleen, kidney, brain.
Liver - good for toxin testing because of metabolism.
Hair - good for genetic testing

19
Q

What is usually used for molecular testing of fresh/frozen tissue and describe the methodology and cons. LA

A

PCR
- targets and amplifies small amounts of DNA from viruses, bacteria, fungi

Cons:
nucleic acid presence or not detected Not localised to a lesion or within a specific cell location

sample if homogenised

20
Q

When are samples sent for toxicology testing?
-how much tissue is submitted and from where?

A

-Toxicology testing is used when:
- unexpected or unexplained illness or death
- Muktiple animals in a group affected

-could be environmental - toxic plant growth in pasture
-approx 50mL of ingesta, feces, fresh tissue

-Collect from liver, urine, stomach

21
Q

What are serological tests and what are they used for?

A

2 types:
Direct (1only), Indirect (1 and 2 abs)

Serological tests use antigen-antibody interactions to detect antigen or antibody in body fluid such as cancer-cell specific components, infectious agents, toxins, cytokines.

These tests are easier, quicker,and cheaper compared to pathogen isolation methods.

22
Q

Define Antigen, Antibodies, Epitopes

A

Antigens are made up of multiple epitopes. Antigens are toxins/xenobiotes (foreign substances) - that illicits an immune response. This causes the production of Antibodies by the body.

Antibodies bind to the antigen at antigen-binding sites. Are Y-shaped protein called Immunoglobulins.

23
Q

Describe antibodies
-poly vs monoclonl
-primary vs secondary

24
Q

Describe the antibody production vs exposure to antigen over time.

A

First exposure: latency period

primary Abs produced and primary response

Secondary abs will only be produced in the lab.
Second exposure: secondary abs produced and secondary response

25
Describe Direct and Indirect Serology testing
26
why would IHC be preffered over immunofluorescence microscopy?
27
Describe flow cytometry - used after
28
Describe the following serology tests: -ELISA -Sandwich ELISA -SNAP -Western blot
29
Describe the following serology tests: -Indirect Western blot -Immunolabelling
30
Describe agglutination
31
Describe Haemagglutination
32
what does agglutinated vs nonagglutinated blood look like
33
Describe viral agglutination -what its used for -how can you tell?
engage the virus so that the virus won't be available to glutinate the RBC
34
what does a false positive of ab mean
35
what does a false negative of ab mean
36
you're unsure if an animal has been infected. describe the course of infection and when you would test for infection and why. LA
37
why would a single test be used for antibodies?
38
Define sensitivity and specificity
Sensitivity - true pos/all (infected) Specificity = true neg / all non-infected
39
Calculate sensitivity and specificity
40
how accurate are serolgical tests? what can we do to help make this more accurate?
Use more tests