Week 8 Y Flashcards

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1
Q

Sensitivity

A

Ability to detect a true positive

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2
Q

Specificity

A

The ability to test for a true negative

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2
Q

Name types of culture methods

A

General purpose, selective, differential, chromogenic

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2
Q

Microscopy advantages and disadvantages

A

Fast, cheap specificity possible

Poor sensitivity, can’t recover organisms

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3
Q

Advantages + dis of culture

A

Cheap, shows antigen well, pathogen can be analysed further

Slow, difficult to culture some pathogens

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4
Q

Immunodiagnostics tests

A

Agglunitation
ELISA

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5
Q

Antibiotics

A

Inhibits the growth of micoorganisms

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6
Q

Bacterialcidal

A

Kills bacteria

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7
Q

Bacteriostatic

A

Stops growth, doesn’t kill bacteria, can grow back again

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8
Q

Minimum inhibitory concentration

A

lowest concentration of the antibiotic that results in
inhibition of visible growth under standard conditions.

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9
Q

Selective toxicity

A

More damage to bacterium than host

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9
Q

Synergy

A

If two antibiotics used in
combination has an antibacterial effect much
greater than either drug alone

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9
Q

How the inactivation of a drug works

A

Enzymes are produced by microbes which degrade the drug, neutralising it, e.g beta-lactamase

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9
Q

How drug targets are duplicated

A

The microbe produces additional copies of the drug target, diluting the drug’s effect as it binds to only a subset of the targets.

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9
Q

How drug permeability is reduced

A

The microbial cell reduces the uptake of the drug by altering membrane permeability or reducing the number of drug-specific porins, e.g gram negative bacteria

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9
Q

How modification of drug target works

A

Microbes alter the structure of the drug’s target site, reducing or eliminating the drug’s binding affinity

9
Q

Transformation

A

Bacteria take up free DNA from their environment, often from lysed (broken) cells, incorporated into dna

9
Q

Absence of drug target

A

The microbe naturally lacks the specific structure or pathway targeted by the drug, making it inherently resistant.

9
Q

The importance of the environment in ARGs

A

Site of Antibiotic resistance

Promotes evolution of ARGs and can create drug-resistant organisms

9
Q

Advantages of cultivation as a diagnostic tool

A

Direct observation, only living organisms, low cost, can find the CFU

10
Q

Disadvantages of cultivation as a diagnostic tool

A

Time consuming, not suitable for all organisms, labour-intensive

11
Q

What is the goal of biochemical testing

A

Identifies colonies growing, ensures it’s the right one as colonies have overlapping features e.g lactose fermenter with E.coli

12
Q

What is the goal of immunological testing with an example

A

Identifies and confirms an organism by using an antigen and antibody e.g Staphylococcus aureus on Mannitol Salt Agar

13
Q

maldi-tof stands for

A

matrix assisted laser desorption ionization-time of flight mass spectrometry

14
Q

RT-PCR

A

Stands for Reverse transcriptase Polymerase Chain reaction

Quantifies RNA using PCR

to study genes and identify viruses and pathogens

Isolate RNA, use RT enzyme to produce cDNA from RNA template, amplify to extend, identify products using gel

High sens + spec but can’t identify RNA without qRT-PCR

15
Q
A
16
Q

Therapeutic index

A

The ratio of dose toxic to host to the therapeutic dose

17
Q

MIC - Minimum inhibitory concentration

A

Lowest conc of AB that results in inhibition of growth under standard conditions

18
Q

MBC - Minimum bactericidal concentration

A

Lowest conc of the AB that kills 99.9% of the inoculum in the given time

19
Q

Synergy

A

Combining 2 AB to create a greater antibacterial affect

Trimethoprim and sulphonamides

20
Q

Antagonism

A

When 2 drugs in combination have activity less than the better of the two