Mumps, Measles, slow Flashcards

0
Q

Measles, mumps vs flu

A

All hemagglutinate
Mumps is antigenetically similar to parainfluenza

BUT
Single strand RNA -> no genetic reassortment -> no rapid antigen shifts
Flu (ortho) and paraflu (paramyxo) both local, nonviremic
Measles, mumps (paramyxo) systemic, viremic (longer incubation, lifelong immunity via IgG)

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1
Q

Paramyxoviruses

A

Single (-) RNA
Helical, envelope
Must carry RNA polymerase in virion

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2
Q

Mumps epidemiology

A

One serotype, only in humans ->
effective vaccine has decreased cases
lifelong immunity even after subclinical infection

Transmission = respiratory (saliva)
Infectious before and after symptoms
Incubation 18-21 days

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3
Q

Mumps presentation

A

Incubation 18-21 days
Prodrome = fever, malaise, anorexia
PAROTIDITIS - unilateral or bilateral, swelling, inflamed duct
Can also have orchitis, aseptic meningitis, pancreas, ovaries
No therapy

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4
Q

Mumps vaccine

A

Live attenuated
Part of MMR
Given in two low doses to minimize side effects

Effective drop in incidence when introduced (60’s)
Still epidemics in unvaccinated pockets (UK, summer camp)
Endemic in Africa

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5
Q

Mumps pathogenesis

A

Respiratory transmission ->
obligatory viremia (IgG response) ->
parotid gland -> duct -> mouth ->
shed in saliva

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6
Q

Measles epidemiology

A

Most contagious disease known!
Exposure (resp, tears, urine) -> almost 100% infection -> 100% symptoms
Only humans, enveloped/unstable -> requires large susceptible population

Pre-vaccine: cyclical epidemics every 3 years
(no antigenetic variation -> new births susceptible-> no herd immunity -> rapid spread)

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7
Q

Measles presentation

A

Respiratory -> resp epithelium -> lymph ->
VIREMIA ->
prodrome = fever, URI, conjunctivitis = infectious shedding! ->
Koplik’s spots (red with white) on mucosa ->
rash, photophobia, fever, URI, conjunctivitis

Incubation = 14 days
No treatment

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8
Q

Measles complications

A

More likely in adult, immunocompromised (partially dt immune response)
1:20 -> bacterial pneumonia
- giant cell pneumonia - can occur without rash
frequent otitis media (bact)
acute encephalitis (1-2:1000)
deaths (1-3:1000)

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9
Q

Measles pathophysiology

A

Syncytia - viral membrane proteins -> fusion -> large multinucleated cells in lymphoid, resp

  • damage without IgG exposure
  • > giant cell pneumonia

Anergy - grows in T cells -> severely depresses cell-mediated immunity -> secondary infections -> death

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10
Q

Measles in developing world

A

Higher mortality!
5-25% vs can’t regenerate immune system)
Reduced mortality from Vitamin A (best ROI for global health!)

Eradicated from US but 50-100 cases imported each year

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11
Q

Measles vaccine

A

Live attenuated
Part of MMR -> given twice

Must maintain herd immunity due to high infectivity

How to eradicate? Vaccine not effective megadoses earlier?

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12
Q

Slow virus overview

A

Long incubation (years) -> slow death
Can have latency -> reemerge with immune compromise
Often genetic predisposition

Ex HIV, PML, SSPE, BK nephropathy (transplant failure)

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13
Q

PML

A

Progressive multifocal leukoencephalopathy
JC virus (papovavirus) -> CNS oligodendroglia ->
Immune compromise activates -> demyelination ->
Blind, dementia, coma, death

No inflammation

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14
Q

SSPE

A

Subacute sclerosing pan-encephalitis
Insidious neuro/psych -> blind -> paralysis -> death

Measles and inclusion bodies in CNS, high antibody titers
Early, subclinical infection -> ? mechanism unclear, no CTL in CNS?
Can occur after vaccine but lower risk (1:million vs 1:100K)

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15
Q

Prion definition

A
Disease-causing proteins - no nucleic acid
Long incubation (years) -> CNS -> spongiform encephalopathy
Ex
Scrapie (sheep)
Kuru
CJD, variant CJD
Gerstmann-Straussler-Scheinker (GSS)
fatal familial insomnia
16
Q

Scrapie

A
Prion disease of sheep
Genetic susceptibility (inbred lines)

Can infect mice (reproduce symptoms)
Resistant to UV, formaldehyde, alkylating -> not virus

17
Q

Kuru

A

Progressive prion disease
Spongiform encephalopathy - esp in cerebellum

50% mortality in New Guinea tribe
Transmission via ingestion of CNS

18
Q

CJD

A

Creutzfeld-Jacob disease
Most common prion disease in humans

Familial (fCJD) and inherited
Spontaneous/sporadic
Iatrogenic (cornea, GH, instruments)

19
Q

Variant CJD

A

aka mad cow disease

Infected cows and sheep meat -> cows ->
Humans eat contaminated meat