Biology Of Disease Flashcards

1
Q

Pathogenesis is…

A
  1. Find the lesion
  2. Describe the lesion
  3. Recognize the basic process
    - -> For the MORPHOLOGIC DIAGNOSIS
  4. Explain the mechanism
    - -> Causative agent, environmental factors, host factors
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2
Q

Description

A

Describe it using lay language with the exception of correct anatomical term.

“CLASS-C”: Color, Location, Appearance, Size, Shape, Consistency

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3
Q

Morphologic Diagnosis

A
  • Interpretive- make an educated guess
  • “3D ATP”:
    3 D’s= Degree, Duration, Distribution
    A= Adjective (for inflammation usually)
    T= Tissue **
    P= Process **
  • Inflammatory= “ITIS”
  • Degenerative= “OSIS, OPATHY”
  • Disorders of Growth= “TROPHY”, “PLASIA”, “OMA”
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4
Q

Degree

A
  • Mild, mild exudative changes, little discernible tissue destruction
  • Moderate, prominent vascular and cellular exudative changes, moderate tissue destruction
  • Marked,
  • Severe, Substantial tissue destruction
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5
Q

Duration (Inflammatory vs Non-Inflammatory)

A

Peracute (immediate- hrs), few cells involved
Acute (hrs-days), primarily neutrophils in inflamm.
Subacute (5d-2wk), exudative changes diminish, cell infiltration evolves from neutrophilic to mononuclear in inflamm.
Chronic (>2-3 wks), will see mononuclear infiltration, tissue regeneration, neovascularization and fibrosis (scarring)
Chronic-Active: Recurrent bouts of active inflamm superimposed on chronic inflammation. Also seen as “flare-ups”

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6
Q

Distribution

A

Focal: 1 point
Multi-Focal: Multiple points sporadic/ parenchyma intact
Coalescing: Focal pts merging together
Locally/Regionally Extensive: Multiple points throughout certain area, broadly affected
Diffuse: All of organ affected or all repeating units of an organ affected.
Disseminated: Multiple organs affected

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10
Q

Sclerosing

A

Scarring

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11
Q

Proliferative

A

Added tissue

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12
Q

Emphysematous

A

Gas present in tissue

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13
Q

Catarrhal

A

Mucus secretion

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14
Q

Suppurative

A

Pus secretion

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15
Q

Etiologic Diagnosis

A
"Diagnosis denoting cause" 
2 elements:
- CAUSE
- TISSUE PROCESS 
Ex: Bacterial pneumonia (general) vs Streptococcal pneumonia (more specific)
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16
Q

Histopathology

A

Microscopic pathology w/ routine processing including formalin fixation, dehydration, paraffin embedding, 5 um sections, stains with H&E

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17
Q

Histo chemistry

A

Using special stains to analyze samples.

  • Trichrome -> collagen (fibrosis) visualization
  • Silver stains –> Reticular CT, some microorganisms
  • PAS –> carbohydrates (includes microbes)
  • Gram, Acid Fast, etc = Microbes
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18
Q

Immunohistochemistry

A

Use of antibody to ID specific epitope using colorimetric ID of bound Ig

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19
Q

What are potential advantages of recombinant vaccines?

A
  • Rapid development
  • Safety in manufacture and administration
  • DIVA concept: Differentiate Infected from Vaccinated Animals
20
Q

WNV Vaccines

A
  • Inactivated (Innovator)
  • DNA Vaccine (Innovator DNA)
  • Chimeric Vaccine (Prevenile/EquiNile)
  • Vectored Vaccine (Recombitek WN)
21
Q

DNA Vaccines (i.e. Innovator DNA)

  • Process
  • Specific of WNV
  • What is the primary concern for DNA vaccines?
  • How does the vaccine work once injected?
  • Pros/Cons of the vaccine
A
  1. Clone gene of interest (immunogenicity gene)
  2. Insert gene for immunogenicity protein into EXPRESSION PLASMID behind PROMOTER and CONTROL SEQUENCES, +/- ENHANCER
  3. Transform E. coli with vector and grow it.
  4. Purify the plastic DNA from lysed bacteria.
  5. Inject DNA into target population.

In the case of WNV (flavivirus) the immunogenic protein the is E CAPSULE PROTEIN.

Integration of DNA being injected and integrating into host genome.

Indicates to m cells OF ANIMAL to begin making E protein, immune response generated.

+Rapid production capacity
+Thermostable
-Expensive

22
Q

Chimeric Vaccines/Vectored Vaccines

  • Process
  • What is the primary concern for Chimeric vaccines?
  • How does the vaccine work once injected?
  • Pros/Cons of the vaccine
A
  • Combine E protein for WNV into “other” RNA genome.
  • Can still cause disease in immunocompromised
  • Infects cells with related strain?
    +DIVA discernible (ie E protein vs entire virus)
23
Q

PCR

  • Reactants needed
  • Cylces
  • Types
A

-DNA template, thermostable DNA polymerase, nucleotides, water/buggers, PRIMERS (= SPECIFICITY)
-Cycles:
Denaturation= break H bonds (95 deg)
Primer binding/reannealing (60 deg)
Primer extension and annealing= DNA SYNTH (72 deg)

24
Q

Fibrinous

A

Fibrin-forming

25
Q

Granulomatous

A

Chronic long-term inflammation

26
Q

Pyogranulomatous

A

Chronic inflammation w/ Constant Recruitment of Neutrophils