Co-Evolution of Antimicrobial Resistance Flashcards

(26 cards)

1
Q

How many deaths are associated with AMR globally each year

A

5.3 million deaths from bacterial infections
14 millions directly attributable to AMR

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2
Q

What regions are most affected by AMR

A

Sub-Saharan Africa followed by South Asia

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3
Q

Which infection types are most impacted by AMR

A

Lower Respiratory Infections (LRIs) > Bloodstream Infections (BSIs)

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4
Q

Name the top 3 AMR bacterial pathogens

A
  1. E. coli
  2. Staphylococcus aureus
  3. Klebsiella pneumoniae
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5
Q

What is the major challenge in tracking AMR in LMICs

A

Lack of reliable data and surveillance systems

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6
Q

What is ‘collateral damage’ in AMR

A

Unintended selection for multiple resistance mechanisms when using one antibiotic (e.g. Drug A selects for resistance to B, C, D due to gene clustering)

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7
Q

What happens when you switch antibiotics in presence of collateral resistance

A

Bacteria often remain resistant which can lead to clinical failure

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8
Q

Why can bacteria rapidly acquire resistance to multiple drug

A

Genes are physically clustered on plasmids
Spread via horizontal gene transfer (HGT)
Facilitated by homologous recombination

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9
Q

What can worsen AMR in a setting such as Dessie, Ethiopia

A

Healthcare inaccessibility, economic inflation, and limited drug availability

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10
Q

What leads to AMR in Dessie, Ethiopia

A

Shared use of meropenem
Sub-lethal doses create selection pressure
Leads to NDM-producing CRE (Carbapenem-Resistant Enterobacterales)

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11
Q

How does poor WASH contribute to AMR in Sierra Leone

A

Environmental reservoirs from human waste
Hospital-acquired infections (HAIs) due to lack of sanitation
e.g. ESBL-E. coli and K. pneumoniae

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12
Q

How does heavy metal pollution contribute to AMR

A

Resistance genes linked to metal-resistance genes, increasing selection even without antibiotics

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13
Q

What are plasmids and their role in AMR

A

Circular DNA that carry AMR genes
Transferred between bacteria by conjugation

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14
Q

What are transposons

A

Jumping genes that move within and between chromosomes/plasmids

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15
Q

What are IS (insertion sequences) elements

A

Short DNA that rearrange genomes, facilitating resistance

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16
Q

What are ICEs (Integrative & Conjugative Elements)

A

Large gene cassettes that carry multiple resistance genes and transfer between bacteria

17
Q

What maintains IS and ICEs in populations

A

Toxin-antitoxin (T/AT) systems stabilise plasmids
Balance between fitness cost and survival benefit

18
Q

How is AMR linked to livestock farming

A

AMR genes spread via food, water, and contact
Antibiotics used in animal feed select for resistance

19
Q

What lab methods are used to track AMR spread

A

Conjugation assays – track plasmid transfer
PCR-based plasmid typing – identify genes
Whole-genome sequencing (WGS) – map transmission

20
Q

What is NMD-5 resistance

A

New Delhi Metallo-beta-lactamase-5 - confers carbapenem resistance, found in clinical, environmental, and animal samples

21
Q

What causes resistance to Tigecycline

A

TetX3–8 genes
Dangerous as Tigecycline is a last-resort drug

22
Q

What is colistin resistance and how does it work

A

MCR genes (MCR-1, MCR-3.1, MCR-3.2)
Modify lipid channels in bacterial membranes

23
Q

How do G+ and G- bacteria share resistance genes

A

HGT bridges previously distinct resistance mechanisms

24
Q

How does environmental degradation impact AMR

A

Increases plasmid transfer rates, linking pollution with AMR

25
What is the fitness impact of MCR resistance genes
Alters bacterial membrane, often with fitness cost
26
What is the effect of MCR-3.2 mutations
Can decrease bacterial fitness, leading to reduced resistance when antibiotic pressure is removed