Systems for detection of pathogens 1 Flashcards

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1
Q

What is taxonomy?

A

Taxonomy is the naming and classifying of organism

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2
Q

What do names of pathogens imply and not include?

A

• Names only imply capacity for pathogenicity and don’t include an assessment of virulence

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3
Q

What can pathogens be defined as?

A

Pathogen can be defined as a biological agent that causes disease or illness to its host.

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4
Q

Why is the standard definition of pathogens not the best definition?

A

○ Not the best definition as some pathogens may be latent or not at a high enough concentration to cause disease

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5
Q

What is a commensal non-pathogen?

A

• COMMENSAL NON-PATHOGEN is a pathogen which is present but not capable of causing disease in the host

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6
Q

What is a zoonotic non-pathogen?

A

• ZOONOTIC NON-PATHOGEN is a pathogen which isn’t present but only capable of causing disease in another host

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7
Q

What is a commensal opportunist?

A

• COMMENSAL OPPORTUNIST is a pathogen which is present and capable of causing disease in the host but only in certain circumstance

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8
Q

What must we make sure when obtaining a sample of the pathogen?

A

○ Sterile sites are free from contamination
○ Non sterile sites require decontamination of normal flora
○ Samples with high volume/relatively low infected pathogen load require concentration (centrifugation, filtering)

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9
Q

What is light microscopy used to identify?

A

Light microscopy can be used to quickly and easily identify large samples

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10
Q

What do we use to see viruses instead of a light microscope and why?

A

• Difficult to see viruses under a light microscope so could instead use fluorescently labelled antibodies which are complementary to viral proteins infecting our cells

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11
Q

What can electron microscopy be used to identify?

A

Electron microscopy can be used to identify the shape of smaller microorganisms

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12
Q

What is the advantage of using microscopy?

A

○ Easy to perform
○ Rapid screening
○ Some parasites have specific morphology to look out for
○ Specific immunofluorescence staining possible

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13
Q

What is the disadvantage of using microscopy?

A

○ Not very sensitive as screening sputum smears needs at least 10 000 organisms per ml to be visualised
○ General stains are not specific
○ Labour intensive hence expensive
○ Needs specialist interpretive expertise therefore becomes even more expensive

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14
Q

What do cultures rely on?

A

• This relies on the ability of the test system to be able to grow the pathogen

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15
Q

What os the classical methods of cultures?

A

Classical method: uses agar plates with different electrolytes to grow bacteria which grow quickly and form colonies

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16
Q

Why can viruses not be grown?

A

• Viruses can’t be grown as they are intracellular organisms and so require host cell mechanisms to divide as they can’t do it alone

17
Q

What do we use to grow viruses?

A

Use cell lines to grow them

18
Q

What cells is used to grow herpes simplex?

A

Vero cells used to be used to grow Herpes simplex

19
Q

What effect does herpes simplex have in cell?

A

• Herpes simplex has cytopathic effect in cell which induces changes in the way cell grows

20
Q

What do antibodies produce if it finds a specific antigen?

A

• Antibody produces colour if it finds its specific antigen on a virus

21
Q

What are the advantages of using classical systems?

A
  • Cheap and simple
  • Sensitive
  • Validated specificity as they have gold standards
  • Direct in vivo measurements of therapy effectiveness
  • Easily archived
22
Q

What are the disadvantages of using classical system?

A
  • Some pathogens cannot be grown
  • Some pathogens cannot be differentiated by biochemistry alone
  • It is slow as it needs overnight incubation and some pathogens grow too slowly
  • Labour intensive hence expensive
  • Requires specialist interpretive expertise therefore becomes even more expensive