Chapter 1: L3 Flashcards

(39 cards)

1
Q

refers to the ability of microorganisms—such as bacteria, fungi, viruses, and parasites—to evolve and develop resistance to the drugs that were once effective at killing or inhibiting them.

A

Antimicrobial Resistance (AMR)

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2
Q

process makes infections harder to treat,
leading to longer illness durations, increased
medical costs, and higher mortality rates

A

Antimicrobial Resistance (AMR)

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3
Q

Causes of Antimicrobial Resistance (6)

A
  • Overuse of Antibiotics
  • Incomplete Courses of Treatment
  • Self-medication:
  • Poor Infection Control:
  • Environmental Contamination
  • Genetic Mutations
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4
Q

Mechanisms Develop by Microorganisms
to become Resistant (6)

A
  1. Enzyme Production (Degradation or Modification of Antibiotics)
  2. Efflux Pumps
  3. Alteration of Target Sites
  4. Reduced Permeability (Decreased Antibiotic Uptake)
    5.Biofilm Formation
  5. Horizontal Gene Transfer (HGT)
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5
Q

some bacteria produce enzymes that degrade or chemically
modify the antibiotics, rendering them ineffective.- These enzymes can break down the molecular structure of the
antibiotic before it can act on the bacteria

A

Enzyme
Production (Degradation or
Modification of Antibiotics)

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6
Q

examples of Enzyme
Production (Degradation or
Modification of Antibiotics)

A

β-lactamase Enzymes (Extended-Spectrum Beta-Lactamases (ESBLs));
Carbapenemases:

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7
Q

: These enzymes degrade antibiotics
(e.g., penicillins, cephalosporins) by breaking the ___ ring that is
critical for the antibiotic’s function.

A

β-lactamase Enzymes; β-lactam

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8
Q

These are a more
advanced form of β-lactamase enzymes that degrade a broader
range of antibiotics.

A

Extended-Spectrum Beta-Lactamases (ESBLs):

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9
Q

These enzymes degrade carbapenems, which
are typically used as last-resort antibiotics

A

Carbapenemases:

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10
Q

are protein complexes found in the
bacterial cell membrane that actively expel harmful substances, including antibiotics, from inside the bacterial cell

A

Efflux pumps

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11
Q

This reduces the intracellular concentration of the antibiotic to sub-lethal levels, allowing the bacteria to
survive

A

Efflux pumps

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12
Q

examples of efflux pumps

A

AcrAB-TolC Efflux Pump in E. coli
MexAB-OprM Efflux Pump in Pseudomonas aeruginosa

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13
Q

This system is
responsible for expelling a variety of antibiotics,
including tetracycline, fluoroquinolones, and β-lactams.

A

AcrAB-TolC Efflux Pump in E. coli:

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14
Q

This pump is involved in the resistance to antibiotics like
ciprofloxacin.

A

MexAB-OprM Efflux Pump in Pseudomonas aeruginosa:

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15
Q

Bacteria can modify the molecular structures of the target sites
where antibiotics normally bind and exert their effects.–
These structural changes prevent the antibiotic from
recognizing or binding to its target, neutralizing its action

A

Alteration
of Target Sites

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16
Q

examples of Alteration of Target Site

A

-Penicillin-Binding Proteins (PBPs):
Methicillin-Resistant Staphylococcus aureus (MRSA)

-Modification of Ribosomal Targets:
Resistance to Macrolides (e.g., Erythromycin):

-Target Enzyme Modifications:
Fluoroquinolone Resistance

17
Q

have altered PBPs that prevent
methicillin and other β-lactam antibiotics from
binding to the bacterial cell wall.

A

MRSA bacteria

18
Q

: Bacteria can modify the ribosomal binding sites, making it impossible for macrolide antibiotics to bind and inhibit protein synthesis.

A

Resistance to Macrolides (e.g., Erythromycin)

19
Q

In some bacteria, mutations in the
gyrase or topoisomerase enzymes make the antibiotic less effective.

A

Fluoroquinolone
Resistance:

20
Q

Some bacteria alter the permeability of their cell membranes,
making it more difficult for antibiotics to enter the cell.
This can occur through mutations in membrane porins (protein
channels that allow substances to pass through the membrane).

A

Reduced
Permeability (Decreased
Antibiotic Uptake)

21
Q

Reduced
Permeability (Decreased
Antibiotic Uptake) examples

A

Pseudomonas aeruginosa Resistance to Penicillins:
Neisseria gonorrhoeae

22
Q

In ___, the bacteria can reduce the
number of porins in their outer membrane, making it harder
for penicillins (and other antibiotics) to penetrate

A

Pseudomonas aeruginosa

23
Q

certain strains of ____ can reduce the expression of porins, thus decreasing the uptake of
antibiotics like penicillin

A

Neisseria gonorrhoeae

24
Q

Manybacteria can form ___, which are clusters of bacterial cells
embedded in a self-produced matrix of ___.

A

biofilms;
extracellular polymeric
substances (EPS)

25
__act as a physical barrier, protecting bacteria from antibiotics, host immune responses, and environmental stresses
Biofilms
26
examples of biofilm formation
Staphylococcus aureus in Medical Devices: Pseudomonas aeruginosa in Cystic Fibrosis:
27
is the process by which bacteria acquire genetic material from other bacteria, even from different species.-
Horizontal Gene Transfer (HGT)
28
Types of Horizontal Gene Transfer: (3)
Conjugation: Transformation: Transduction:
29
Transfer of genetic material through direct cell-to-cell contact, often via plasmids (small DNA molecules).- Plasmids carrying resistance genes (e.g.,
Conjugation:
30
Uptake of free DNA from the environment.- Some bacteria can incorporate DNA containing resistance genes into their own genome.
Transformation:
31
Transfer of genetic material through bacteriophages (viruses that infect bacteria).- When bacteriophages infect bacteria, they can sometimes transfer resistance genes from one bacterium to another.
Transduction
32
These bacteria can acquire resistance genes via plasmids through conjugation, making them resistant to multiple antibiotics.
Shiga toxin-producing Escherichia coli (STEC):-
33
Examples of Antimicrobial Resistance: 4
1. Methicillin-Resistant Staphylococcus aureus (MRSA) 2. Multidrug-Resistant Tuberculosis (MDR-TB): 3. Carbapenem-Resistant Enterobacteriaceae (CRE): 4. Drug-Resistant Malaria
34
Challenges Posed by Antimicrobial Resistance
-Limited Treatment Options - Longer Hospital Stays and Higher Costs: - Increased Mortality: - Impact on Medical Procedures: -Global Health Threat: -Slow Development of New Antibiotics:
35
- This involves the responsible use of antibiotics, including proper dosing, avoiding unnecessary prescriptions, and completing prescribed courses
Antibiotic Stewardship:
36
- Improved hygiene, sterilization, and infection control measures in hospitals can help reduce the spread of resistant microorganisms.
Infection Prevention and Control:
37
- Investment in developing new antibiotics, vaccines, and alternative therapies is crucial for combating AMR
Research and Development:
38
- International efforts, such as the World Health Organization's Global Action Plan on AMR, are essential in tackling the problem.
Global Collaboration:
39
Educating the public on the risks of self-medication, overuse of antibiotics, and the importance of completing prescribed treatments can reduce AMR
Public Awareness:-