Systems For Detecting Pathogens Flashcards

1
Q

What is the taxogenic ladder after species?

A

Strain
Type
Isolate

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2
Q

What are the types of pathogens?

A

Commensal non-pathogen
Zoonotic non-pathogen
Commensal opportunist

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3
Q

What is a commensal non-pathogen?

A

Present but not capable of causing disease in the host

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4
Q

What is a zoonotic non-pathogen?

A

Present but only capable of causing disease in another host

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5
Q

What is a commensal opportunist?

A

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

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6
Q

What is a pathogen?

A

Microbe capable of causing a specific degree of host damage

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7
Q

What is good sample practice?

A

Sterile sites should be free from contamination
Non-sterile sites require decontamination of normal flora
Samples with high volume or low infected pathogen load require concentration

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8
Q

What is direct light microscopy used to detect?

A

Threadworms, entamoeba histolytica, trichomonas vaginalis, schistosoma mansonii

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9
Q

What is direct electron microscopy used for?

A

Viruses

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10
Q

What colour do gram positive bacteria stain?

A

Blue

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11
Q

What colour do gram negative bacteria stain?

A

Pink

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12
Q

Are there bacteria that don’t stain?

A

Yes (TB for example)

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13
Q

What are the types of media?

A

Non-selective
Semi-selective
Selective growth temperatures

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14
Q

What are examples of non-selective media?

A

Blood, agar

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15
Q

What are examples of semi-selective media?

A

DCA, CLED

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16
Q

What are some selective atmospheres?

A

Aerobic
Microaerophilic
Anaerobic

17
Q

What are the different types of test system in bacteriology?

A

Media
Selective atmospheres
Selective temperatures
Specific haemolysis of blood

18
Q

What is a phage?

A

Virus that infect bacteria

19
Q

What is strand displacement amplification?

A

Essentially PCR

20
Q

What does molecular gene targeting aim to do?

A

Detect a gene or gene products that are pathogen specific

21
Q

What genes are suitable targets for PCR?

A
Constitutive 
Virulence
Antibiotic resistance
Pathogenic phenotype 
Repetitive
22
Q

How can you tell if the molecular test for one gene is good enough?

A
Specificity
Reliability 
Sensitivity
Accuracy
Rapidity
23
Q

How do you do bio-signature profiling?

A

Mass spectrometry
Isolate organism
Lyse with crystallising matrix
Ionise and detect time of flight for each particle
Calculate daltons for each protein produced
Compare against an archival database

24
Q

What are the advantages of MALDI-TOF profiling?

A

Rapid and specific identification

25
What are the disadvantages of MALDI-TOF profiling?
Requires pure culture Requires rigorous calibration and protocol standardisation Will only identify known profiles
26
What are biomarkers of virulence?
Looking for selected genes or gene products that drive the disease process
27
What are the advantages of serotyping?
Good specificity and sensitivity | Easily automated
28
What are the disadvantages of serotyping?
Slow Can be in response to previous exposure Some antibodies are cross-reactive Virulence is only inferred by biomarker presence Infected into an animal model can prove virulence
29
What are the advantages of molecular detection methods?
Rapid Allows fast, accurate treatment High sensitivity Can be automated/ used at point of care
30
What are the disadvantages of molecular detection methods?
``` Expensive Doesn’t screen for unknown Needs expertise Labour intensive Possibility of contamination Complex methods needed ```