Systems For Detection Of Pathogenesis 1 Flashcards

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1
Q

What is a commensal non pathogen?

A

Present but NOT CAPABLE of causing disease in host

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2
Q

What is a zoonotic non pathogen?

A

Present but only CAPABLE of causing disease in another host

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3
Q

What is a commensal opportunist pathogen?

A

Present and capable of causing disease in the host but only in certain circumstances

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4
Q

What is a pathogen?

A

A microbe capable of causing a specific degree of host damage

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5
Q

How can a non contaminated sample be obtained?

A

Sterile sites must be free from contamination
- skin flora in blood cultures

Non sterile sites require decontamination of normal flora
- faeces, mouth, skin

Samples with higher volume or relatively low infected pathogen load require concentration

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6
Q

What are the advantages of using microscopy to identify pathogens?

A

Easy to perform

Rapid screening

Some parasites have specific morphology

Specific immunofluorescence staining possible

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7
Q

What are the disadvantages of using microscopy to identify pathogens?

A

Not sensation

Screening sputum smears requires at least 10-000 orgs per ml to be visualised

General stains are not specific

Labour intensive

Requires specialist interpretive expertise

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8
Q

What are the 3 types of media used in cell culture?

A

Non selective media

Semi selective media

Selective growth temperatures

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9
Q

What is the selective atmosphere for a cell culture?

A

Aerobic culture
- S.aureus
- catalase positive
- E.coli

Microaerophillic culture
- Respiratory pathogens - grow faster with CO2 present (lung conditions)

Anaerobic culture
- no oxygen present
- gas gangrene
- spore forming

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10
Q

How do u test for the pathogen causing food poisoning?

A

Take a stool sample

  • MacConkey agar and deoxycholate afar plate
  • direct microscopy for cyst/eggs of parasites
  • spread on campy CVA selective media plate
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11
Q

What are the ways to identify viruses?

A
  1. Culture and microscopy
    - requires permissive cell lines
    - cytopathic effect
  2. Direct antigen detection
    - ELISA
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12
Q

What are the advantages of classic cell culture and identification?

A

Cheap

Simple

Reliable reagents

Sensitive

Validated specificity

Easily achieved

Direct in vivo measurement of effectiveness of therapy

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13
Q

What are the disadvantages of classical cell culture and identification?

A

Some pathogens cannot be grown

Some pathogens cannot be well differentiated by biochemistry alone

Some pathogens grow too slowly to aid rapid diagnosis

Labour intensive (expensive)

Requires specialist interpretive expertise (more expensive)

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