Bacteriology Flashcards

1
Q

How is MIC tested?

A

least amount of antibiotics required to inhibit growth

Gradient antibiotic strips on agar - look for crossover of bacteria on the strip

Discs impregnated with different conc of antibiotic. Measure clerance zone guidelines have zone sizes on how this translated to MIC

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2
Q

What kind of investigations may be performed?

A

culture e.g. agar or a broth
Serology
Molecular techniques

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3
Q

What are the complications of starting patients on antibiotics before sending off samples?

A

The antibiotics can interfere with the test results - potential for false negatives as the dose administered may not have a clinical effect but it might have an effect at the cellular level on the agar

In meningitis or sepsis you administer anyway

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4
Q

What kind of samples might be used?

A

stool samples, mouth & vaginal swabs, taking blood

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5
Q

Describe susceptibility testing

A

Still use agar plates and MICs, takes about 18 hours

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6
Q

Describe how blood cultures are run

A

Different bottles for collection
pH indicator on bottom of bottle changes colour as pH lowered from bacteria producing CO2
takes about 18 hours

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7
Q

What kind of microbiological tests might be carried out?

A

Gram staining - double membrane are negative, single membrane are positive (peptidoglycan retains purple dye)

Microscopy - look at shape and organisation (clumping or chains)

Coagulase e.g. staf aureus is positive but other stafs are negative

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8
Q

What are the limitaions of microbiological investiagtions

A

slow - some e.g. TB can take 6 weeks to grow

MIC tests difficult to interpret

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9
Q

Explain the results of MIC

A

3 types of result resistant intermediate sensitive

guideline values for MIC enables the lab to say whether its sensitive or resistant – resistant because not enough of the drug will be able to reach the organisms. Guidelines have cross over values and zone sizes

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10
Q

What are the limitations of PCR?

A
  • need to know what looking for to design primers
  • potentially hundreds of primers needed as many genes confer resistance
  • PCR less sensitive than culture
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