Lecture 24 Flashcards

1
Q
A
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2
Q
A
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3
Q

Life history theory

A
  • Organisms have limited resources to allocate to these different functions
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4
Q

Malaria parasites face a similar resource allocation tradeoff

A
  • Growth and reproduction
  • Malaria parasites allocate few resources to reproduction (invest little in transmission)
  • Of all infected red blood cells, only few percent (1-2%) produce transmission stages
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5
Q

Why do malaria parasites invest little in transmission

A

Hypotheses
- Greater investment means stronger transmission blocking immunity
- Greater investment means more mosquito mortality
- Within-host competition

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6
Q

What investment strategies maximize R0

A
  • Hypotheses depend on number of transmission stages produced, not relative investment
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7
Q

Co-infections

A
  • Parasites that can exploit more host red blood cells do better (low transmission investment favored)
  • In experimental co-infections, parasites reduce transmission investment as predicted
  • Where co-infections and within-host competition are common, expect more virulent parasites
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8
Q
  • Changing investment can help parasites recoup fitness lost due to drugs
A
  • At high doses, increasing transmission investment provides marginal fitness benefit (“terminal investment”)
  • At intermediate doses, decreasing transmission investment provides large fitness benefit ~90% (“reproductive restraint”)
  • Parasites do adjust investment as predicted by theory
  • More killing, less transmission
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9
Q

Does altered investment help parasites evade effects of drugs

A
  • Changing transmission investment can mitigate some effects of drugs
  • In addition to classical resistance mechanisms, drug treatment could generate selection for altered life history traits
  • By favoring parasites that invest more in proliferation vs. transmission, drugs can select for higher virulence
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10
Q

Evolutionary hypotheses for coordinated development of malaria parasites

A
  • Synchronicity is beneficial to parasites
  • Timing is beneficial to parasites
  • Synchronicity and timing both beneficial to parasites
  • Neither synchronicity nor timing are beneficial to parasites (not)
  • There is benefit to coordination
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11
Q

Disrupting rhythms of malaria parasites

A
  • In rodent malaria, ring stage parasites are most abundant during day
  • Ring stage parasites used to initiate experimental infections
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12
Q

Consequences for parasites of disrupted rhythms

A
  • Parasites do worse
  • When mismatched with host, parasites achieve ~50% lower densities (both asexual and transmission stages) compared to when matched with host
  • Jet lag is bad for malaria parasites
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13
Q

Consequences for hosts of disrupted parasite rhythms

A
  • Mismatched hosts do better (lose fewer red blood cells)
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14
Q

Potential benefit of synchronicity

A
  • For malaria parasites, synchronicity may allow bursting parasites to overcome immune responses through sheer force of number
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15
Q

Testing plausibility of hypothesis

A
  • Under what conditions do synchronous parasites perform better than asynchronous ones
  • Asynchronous parasites do best when higher # of free parasites required to trigger immune response
  • Synchronous parasites do best when lower # of free parasites required to trigger immune response
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16
Q

Potential benefit of timing

A
  • Avoiding an unfavorable environment
  • Timing may allow parasites in vulnerable stages to avoid exposure to their more damaging immune effectors
  • Timing may allow parasites to match availability of resources