CMB1003/L10 Treatment of Bacterial Infections Flashcards

1
Q

Describe late agglutination/ bead equivalent.

A

Exploiting antibody-antigen interactions for rapid diagnostics
Confirm identity of isolates
Identify known pathogen-associated antigens in specimens when isolation fails

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2
Q

What is serology? (3)

A

Relies on diagnostic identification of antibodies in the serum
E.g., latex agglutination tests
Only relevant antigens will be bound by specific antibody

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3
Q

What is serotyping? (2)

A

Determines the subtype of the organism
Allows effective treatment

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4
Q

Give 3 advantages to molecular diagnosis of infections.

A

Bacterial genomes are unique
Genetic material can be extracted from infected specimens
DNA is easy to detect and quantify
Extremely sensitive 1-10 CFU

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5
Q

Give 3 disadvantages of molecular diagnosis of infections.

A

Technology is still being developed
Some tests require bacteria to be isolated first
Some tests are too sensitive
Standardisation from lab to lab can be problematic

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6
Q

How can PCR be modified to detect DNA sequences? (2)

A

Add fluorescent DNA intercalating agent to finished reaction or other fluorescent DNA binding dyes
Add dyes to PCR without inhibiting it and detect PCR product in real-time

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7
Q

Give a successful example of RT-PCR.

A

Meningitis - pre-emptive treatment before CSF specimen collection
Whooping cough - RT-PCR diagnosis within hours rather than 3-12 days

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8
Q

Give an example of a bactericidal drug.

A

Penicillin

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9
Q

Give an example of a bacteriostatic drug.

A

Chloramphenicol

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10
Q

Give 3 antibiotic targets.

A

Cell wall
DNA/RNA synthesis
Folate synthesis
Cell membrane
Protein synthesis

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11
Q

How can bacteria become resistant to cell wall-targeting antibiotics?

A

Producing pumps to cause efflux of the antibiotic

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12
Q

How can bacteria become resistant to DNA/RNA synthesis-targeting antibiotics?

A

Producing inactivating enzymes

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13
Q

Describe the mechanism by which chloroamphenicol, macrolides and lincosamides work. (3)

A

Bind to 50S ribosomal subunit
Prevent peptide bond formation
Stop protein synthesis

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14
Q

Describe the mechanism by which aminoglycosides work. (2)

A

Bind to 30S ribosomal subunit
Impair proofreading, resulting in production of faulty proteins

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15
Q

Describe the mechanism by which tetracyclines work. (3)

A

Bind to 30S ribosomal subunit
Block binding of tRNAs
Inhibit protein synthesis

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16
Q

Define minimum inhibitory concentration (MIC).

A

The minimum concentration of antibiotic needed to inhibit growth

17
Q

How can current approaches be modified for treating infections? (3)

A

Limiting antibiotic use
Last resort antibiotics
Combination therapy
Phage therapy
Faecal transplant

18
Q

What information is required when an outbreak occurs? (4)

A

Reported by whom and where
Type of outbreak suspected
Who is affected
Population at risk

19
Q

Why is global monitoring required? (4)

A

Health education and protection can limit spread
Monitoring outbreaks can prevent an epidemic
In field diagnostics now available
Transient population and air travel mean no infection barriers

20
Q

What is Q-POC Platform?

A

A rapid multiplex PCR testing system that delivers results in approximately 30 minutes at the point of need

21
Q

What is Q-POC SARS-CoV-2 Assay?

A

A quality rapid COVID-19 PCR assay that provides results with the simplicity and hands on time of a lateral flow test