TB and prions (exam 2) Flashcards

1
Q

what is the leading cause of death worldwide?

A

tuberculosis (global emergency)

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2
Q

how much of the worlds population is infected with latent TB?

A

1/4

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3
Q

what is the issue with antibiotics for TB?

A

6-9 month drug course => issue with compliance, affordability, access

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4
Q

Mycobacterium tuberculosis

A
  • aerobic
  • gram-positive
  • non-motile
  • no outer cell membrane (have to acid-fast stain)
  • cell wall is thicker than most (hydrophobic)
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5
Q

why is mycobacterium tuberculosis difficult to culture?

A

it is slow growing (24 hours)

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6
Q

mycobacterium tuberculosis complex

A

8 (sub)species form complex and cause human disease

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7
Q

what protects the bacilli of TB?

A

waxy outer coat

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8
Q

what are the two front line antibiotics used for primary infection of TB?

A

isoniazid (INH) and rifampin (RIF)

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9
Q

what is the antibiotic therapy recommended for primary active TB disease?

A

antibiotic combination for 6 to 9 months

rest, good diet

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10
Q

why is TB re-emerging?

A
  • TB and HIV co-infection (HIV victims are 800 times more likely to develop active TB)
  • Multiple Drug-Resistant (MDR) and Extremely Drug-Resistant (XDR) TB
    MDR are resistant to INH and RIF (rifampin); XDR resistant to multiple treatments
  • complacency
  • travel and immigration
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11
Q

what is the vaccine for TB?

A

BCG (bacillus Calmette-Guerin) vaccine

  • attenuated (weakened)
  • protection rate is 80% for children and <50% for adults
  • protection is not life long (5-15 years)
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12
Q

why do we not vaccinate for TB in the U.S.?

A
  • not that effective

- TB skin test will always test positive = ineffective surveillance tool

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13
Q

Ways to prevent TB

A
  • improve DOTS implementation
  • improve social conditions (poverty, water, nutrition, housing)
  • improve public health care systems
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14
Q

what are some examples of prion diseases?

A
  • scrapie (sheep)
  • kuru (humans)
  • mad cow disease
  • Creutzfeldt-Jakob disease (CJD) in humans
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15
Q

PrP^c

A

normal, “non-virulent” protein
unknown function
protein found in brain

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16
Q

PrP^sc

A

infectious prion (abnormal, misfolded)

17
Q

why are prions infectious?

A

normal prion proteins are converted to prion proteins -> neurons die and vacuolar areas form in gray matter (ultimately neurological deteriation)

18
Q

what kind of disease are prion diseases?

A

transmissible spongiform encephalopathies (TSEs)

19
Q

what are the symptoms of prion disease?

A

loss of motor coordination, dementia, other neurological symptoms, death (autopsy reveals “sponge-like” brain full of holes)

20
Q

treatment or cure for prion disease

A

NONE

21
Q

examples of animal TSEs

A
  • mad cow disease (Bovine Spongiform Encephalitis, BSE)
  • scrapie
  • TSEs in household cats, deer, elk, and mink
  • Chronic Wasting Disease (CDW) in mule deer, white-tailed deer
22
Q

what are the three ways Creutzfeldt-Jakob disease (CJD) occurs?

A

1) sporadic (85% of cases; worldwide but only 1-2 mortality cases per million people)
2) hereditary (gene mutations; 5-15%)
3) iatrogenic (via contaminated surgical equipment, corneal transplants, blood transfusions - rare)

23
Q

what age does CJD affect and what is the prognosis?

A

age 65; death within 1 year

24
Q

what TSE leads to the cannibalistic eating of brains?

A

Kuru

25
Q

what prion disease is obtained from ingesting BSE-contaminated beef? Where is this disease commonly found?

A

vCJD (variant CJD)

found in U.K.

26
Q

what are ways to prevent prion disease?

A
  • ban against animal products in livestock feed
  • increased surveillance
  • diagnosis (presence of protein in cerebrospinal fluid)