Pathogenicity Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

What is a pathogen?

A

An organism which causes harm to it’s host through it’s own actions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is a commensal?

A

An organism which benefits from it’s host but bring neither benefit or harm to it’s host.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is an opportunistic pathogen?

A

An organism which can cause disease in it’s host but only when given the right set of conditions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is a zoonotic pathogen?

A

An organism which has an animal reservoir (either as a pathogen or commensal) and can cause disease in humans

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe disease progression

A

Pathogens infect host either causing disease or leading to an asymptomatic carrier. Disease can kill the host, be neutralized (asymptomatic carrier) or resolved entirely and the host recovers.
Pathogens use colonisation virulence factors to infect hosts such as Adhesins, Invasins, nutrient acquisition, motility, chemotaxis.
Pathogens use damage virulence factors to cause disease, such as exo/endotoxins, proteases, DNases, Lipases, Haemolysins.
Host defences include physical barriers, complement, macrophages, antimicrobial peptides and the adaptive immune response.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are kochs postulates?

A
  1. Microorganism must be found in abundance in all individuals suffering from the disease but not in healthy individuals
  2. Microorganism must be able to be isolated and grown in a pure culture
  3. Cultured microorganism must cause disease when reintroduced into a healthy experimental host.
  4. Microorganism must be reisolated from the diseased experimental host and identified as being identical to the original causative microorganism.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Describe challenges to Koch’s postulates

A
  1. Some microorganisms can cause disease without being present: Clostridium botulinum secretes toxins which can remain present after the bacteria has died.
  2. <1% of bacteria can be cultured in vitro due to complex or unknown nutritional requirements.
  3. Cultured pathogens can lose their virulence, there isn’t selective pressure against mutations in virulence factors. Puumala virus loses it’s virulence when cultured in vero cells.
  4. There’s isn’t always an animal model for reinfection. Syphilis only survives in humans or the 9-banded armadillo. Smallpox is exclusive to humans.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Tell me about strict/professional pathogens

A

They are highly adapted to their niches, unable to survive outside of their host due to nutritional requirements only satisfied through pathogenesis. They can access unique niches that yields very little competition with other microbes. They transmit efficiently between hosts and have a reduced genome.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Give some examples of strict/professional pathogens

A
  1. Helicobacter pylori - only microbe that survives in the stomach, causes stomach cancer and gastric ulcers but can protect against oesophageal adenocarcinoma and GORD.
  2. Neisseria gonorrhoeae, an STI in the genitourinary tract.
  3. Shigella dysenteriae, a gut infection that leads to dysentery.
  4. Mycobacterium tuberculosis causes TB, infects the lungs and can lead to systemic infections.
  5. Chlamydia trachomatis, intracellular STI in the genitourinary tract, can infect lungs and eyes too.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Tell me about opportunistic pathogens

A

Will only cause disease when the conditions are right, typically when the host immune system is compromised or after antibiotics when the microbiota has been disrupted. Lives in the environment or host as a commensal. Not very efficient at transmitting between hosts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Give some examples of opportunistic pathogens

A
  1. Pseudomonas aeruginosa, causes wound/burn infection, infects lungs in cystic fibrosis patients.
  2. Clostridioides difficile, inflammatory infection of large intestines. Typically occurs post-antibiotic treatment, very common in hospitals.
  3. Staphylococcus epidermis, causes skin and wound infections.
  4. Staphylococcus aureus, causes skin and wound infections, can lead to endocarditis, osteomyelitis.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Tell me about facultative pathogens

A

Well-adapted to multiple lifestyles, equally at home in a niche or as a pathogen. This flexibility is usually conferred in a large genome.
E. coli can act as a facultative pathogen, gut and UTI infections can lead to sepsis and meningitis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Tell me about the boundary between opportunistic and facultative pathogens

A

This often depends on the strain of the pathogen as some strains can be more pathogenic than others. Virulence factors are typically encoded in mobile elements or plasmids allowing them to be easily transferred via horizontal transfer. STEC, Shiga toxin-producing E. coli picked up a shigella toxin and causes bloody diarrhoea.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What’s the difference between Antiseptics, Disinfectants and Antibiotics?

A

Antiseptics and Disinfectants are too toxic for internal use, antiseptics are used on the skin while disinfectants are used on inanimate surfaces. Antibiotics are low molecular mass compounds injected or ingested into the human body with minimal side effects.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Tell me about ideal properties of antibiotics

A

Either kills or inhibits bacterial growth (bactericidal for immunocompromised individuals)
Selective toxicity; exploits differences between the pathogen and the host.
Pharmacokinetics; drug is distributed around the body.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Tell me about cycloserine

A

Acts as an analogue of D-alanine, inhibits the incorporation of Alanine into cell wall precursor

17
Q

Tell me about phosphomycin

A

Prevents UDP-NAG to UDP-NAM conversion by interacting with the enzyme MurA, key in cell wall biosynthesis

18
Q

Tell me about bacitracin

A

Stops the recycling of bacterprenol. Quite toxic, only topical use. key in cell wall biosynthesis.

19
Q

Tell me about β-lactams

A

These include penicillin, methicillin and cephalosporins. All have a 4-membered β-lactam ring, they bind to and inhibit penicillin-binding proteins. PBPs are cytoplasmic membrane proteins involved in transpeptidation & transglycosylase reactions which are key in cell wall biosynthesis

20
Q

Tell me about glycopeptides

A

These include vancomycin and teichoplanin. They bind to D-ala-D-ala and prevent transpeptidation & transglycosylase reactions.
Vancomycin is a last resort drug for MRSA.

21
Q

Tell me about sulphonamides & trimethoprim

A

They are substrate analogs and act to inhibit FH4 production which is required for nucleic acid synthesis. Mammals take up FH4 through diet

22
Q

Tell me about quinolones

A

They bind to and stabilise the topoisomerase II (DNA Gyrase) covalent complex, preventing DNA transcription and replication

23
Q

Tell me about rifampin

A

It inhibits RNA polymerase, used against Mycobacterium tuberculosis

24
Q

Tell me about Macrolides, Lincosamides and chloramphenicol

A

Erythomycin is a macrolide and clindamycin is a lincosamide. They bind the 50s subunit of the ribosome, blocking the transfer of peptides

25
Q

Tell me about Aminoglycosides

A

Some examples are kanamycin and gentamycin. They bind to the 30s subunit preventing the 50s subunit binding. Effective bactericidal but can lead to hearing loss and loss of function in kidneys

26
Q

Tell me about tetracyclines

A

They bind the 30s subunit & prevent alignment of aminoacylate tRNA with mRNA

27
Q

Tell me about gramicidin

A

Forms cation channels, H+ leaks from cell, PMF can’t be maintained

28
Q

Tell me about polymyxins

A

Act on gram negative bacteria, disrupt cytoplasmic membrane

29
Q

Tell me about synercid

A

A new antibiotic which is a mixture of dalfopristin and quinupristin. Binds to the 50s subunit to prevent peptide chain elongation. Used in animal feed, bacterial resistance is very common.

30
Q

Tell me about linezolid

A

Oxazolidinone binds to the 50s subunit preventing the initiation of protein synthesis.

31
Q

Tell me about daptomycin

A

Forms oligomeric pores, causes bacterial death with negligible cell lysis, no toxin release. Introduced in 2003, resistance found in 2005 :(