Topic 1-5 (Lecture 5) Flashcards

1
Q

What has the most impact on bacterial disease prevention?

A

Sanitation and Education

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2
Q

What are ancient/modern methods of sanitation?

A
  • slightly alcoholic beverages, having settlements near streams
  • Using natural preservation methods to keep food good (ex. spices, salt and vinegar, dehydration)
  • Getting fresh air
  • Dental and hand hygiene
  • Quarantine
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3
Q

What is an example of quarantining?

A

Sanatoriums for disease like TB or Leprosy (isolation of contagious individuals for treatment)

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4
Q

What is the main goal of education (for disease)

A

Inform the public on behavioral adaptations that can decrease risk/spread of bacteria

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5
Q

Why is education good?

A

-It’s cost-effective

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6
Q

What are the 2 levels that education can work at?

A

Personal - ex. teeth-brushing, hand sanitizer use, etc.

Political - building adequate sanitation systems

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7
Q

What are bacteriophages?

A

Viral agents that recognize and lyse bacterial pathogens

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8
Q

What are pros to using bacterophages?

A

Chepaer to make than antibiotics

Mutations can be beneficial

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9
Q

What are cons to using bacterophages?

A

Mutations can be detrimental/make viruses unsuitable for therapy
Research costs are the same in terms of cost when compared to antibiotic research

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10
Q

What are the 2 traits that are desirable in bacterophages?

A

Specificity - only targets bacteria that is causing problems (shouldn’t disrupt microbiota that much)

Lysis - Viruses that are lytic are desired (can be lytic (killing) or lysogenic (not killing))

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11
Q

What are antiseptics?

A

Chemical agents that are applied to LIVING tissue to kill or inhibit the growth of microorganisms

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12
Q

What are disinfectants?

A

Chemical agents used on INANIMATE objects to kill microorganisms

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13
Q

What is the difference between antiseptics and disinfectants?

A

One is for living tissue (antiseptics), on is for inanimate objects (disinfectants)

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14
Q

What are chemotherapeutic agents?

A

Chemical agents used to control infectious diseases internally in a body

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15
Q

What are chemotherapeutic agents that work on bacteria called?

A

Antibiotics

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16
Q

What are the two types of antibiotics?

A

Bactericidal

Bacteriostatic

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17
Q

What do bactericidal antibiotics do?

A

KILL bacteria

18
Q

What do bacteriostatic antibiotics do?

A

INHIBIT bacterial growth

19
Q

What is the difference between natural, semi-synthetic and synthetic antibioitics?

A

Natural - come from natural sources (ex. mold)
Semi-synthetic - chemically modified natural antibiotics (such that it isn’t “natural”)

Synthetic - What it means

20
Q

What is usually more sensitive to antibiotics: Gram-positive or gram-negative?

A

Gram positive

21
Q

What are the two “spectrums” of antibiotics?

A

Broad and narrow spectrum

22
Q

What is the difference between broad and narrow spectrum antibiotics?

A

Broad acts on both gram +ve and gram -ve bacteria, whereas narrow spectrum antibiotics only act on a single group of organisms

23
Q

What are optimal attributes of chemotherapeutic agents?

A

Soluble in body fluids w/ good penetration to infection site

A broad spectrum of activity (i.e. activity against broad range of bacteria)

Low frequency of resistance development

Low rate of breakdown in body

Low toicity

Well-tolerated in human body

Non-allergenic

24
Q

What are some ways how antibiotics work?

A

1) Interfere w/ bacterial cell wall biosynthesis by inhibiting peptidoglycan (only bacteria have this)
2) Destabilize cell membrane (potentially dangerous/toxic to humans, last resort)
3) interfere w/ protein synthesis by binding to ribosome and inhibiting function (doesn’t affect humans due to difference in eukaryote ribosomes)
4) interfere w/ DNA gyrase activity, disrupting replication (different in bacteria vs eukaryote)
5) interfere w/ DNA-directed RNA polymerase activity (bacterial RNAPol is different enough from humans to be OK)
6) Interfere w/ folic acid metabolism (bacteria-specific metabolic processes)

25
Q

What is antibiotic resistance?

A

Acquired ability of microorganisms to resist the effects of an antibiotic which it is normally sensitive to

26
Q

What is vertical gene transfer?

A

Transfer of mutations (ex. antibiotic resistance) to offspring during mitosis

27
Q

What are the three mechanisms of horizontal gene transfer?

A

Conjugation
Transduction
transformation

28
Q

What is conjugation (horizontal gene transfer)?

A

Transfer of plasmid DNA via cell-cell contact

29
Q

What is transduction (horizontal gene transfer)?

A

Bacterial virus picks up DNA from resistant bacteria and transfers it to sensitive cell (can be plasmid or chromosomal DNA)

30
Q

What is transformation (horizontal gene transfer)?

A

DNA w/ resistance gene taken from environment

31
Q

Are all resistance traits from mutation?

A

No, some bacteria is natural resistant (ex. lack the structural target of antibiotic; have natural physiological features such as pumps that diminish antibiotic effects)

32
Q

Why does exposure to antibiotics can result in resistant bacteria?

A

Antibiotics apply a population pressure that selects for resistant bacteria to thrive (think ecology). It is NOT exposure that results in resistance

33
Q

What are problems with antibiotics now?

A

They are overused

  • Antibiotics used for wrong illnesses (incorrect prescription or too acessible)
  • People don’t complete antibiotic course -> less-than-lethal exposure promotes antibiotic resistance to develop
  • Antibiotic misuse in agriculture (potential for zoonosis)
34
Q

What are some consequences of antibiotic use?

A
  • One may experience side-effects
  • Microbiota may also be affected (could lead to opportunistic pathogens to infect)

*Microbiota usually re-establish itself after finishing antibiotic course

35
Q

What is the problem with superbugs?

A

We cannot use antibiotics as effectively against them (the current ones) due to resistance, and developing new antibiotics are expensive

36
Q

How do biofilms contribute to antimicrobial resistance?

A

1) EPS matrix impede penetration of anitmicrobial agents
2) O2 and nutrient gradient results in some cells being less metabolically active -> metabolically active bacteria are more affected by antibiotics; thus less metabolically active = less affected by antibiotics
3) Persister cells just stay alive for some reason - hard to kill

37
Q

Approaches to anti-biofilm therapy?

A

1) Interfere w/ EPS
2) Interfere w/ biofilms from forming
3) Target autoinducers - no autoinducers, no signal; no signal, no quorum sensing and thus no biofilm formation

38
Q

How do vaccines prevent disease? *Review

A

Prevent disease by training a secondary immune response

39
Q

What materials are used to make vaccines?

A
  • killed virulent bacteria
  • avirulent mutants of pathogenic bacteria
  • outermost components of microoganisms
  • toxoids (toxins that have been deactivated)
40
Q

What are the 2 forms of immunity? *Review

A

Active and passive

41
Q

What is the difference between active and passive immunization? *Review

A

Active immunization relies on induction of immune response (trained response); passive immunization relies on injecting pre-formed antibodies (cannot train response)