Pathogenicity Flashcards

1
Q

Streptococcus pyogenes: General information

A
  • Gram positive, thick peptidoglycan layer
  • B-hemolytic, break down red blood cells when grown in blood agar
  • Group A, Lancefield classification based on cell wall carbohydrate
  • Forms chains that resemble a ‘string of pearls’ when viewed under the microscope
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2
Q

GAS: which strains are associated with disease?

A

High encapsulated strains

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3
Q

GAS: virulence

A

See diagram in lecture slides

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4
Q

GAS: general disease info

A
  • Obligate human pathogen
  • Colonizes the throat or skin
  • Causes a broad spectrum of disease
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5
Q

GAS: Diagnosis

A
  • Bacterial swab, and labaratory culture remain gold standard, results take 48-72hrs
  • Rapid tests are now available but are less commonly used. … high false positive?
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6
Q

GAS: Transmission

A
  1. Human to human by direct contact
    * Droplet spread from pharyngeal colonisation (sneezing, coughing)
    * Touching infected skin
  2. Contaminated fomites
    * Biofilm formation may enhance survival outside the host

Rarely food source

Household crowding facilitates transmission

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7
Q

GAS: Carriage

A

The GAS carriage is poorly understood
* GAS can be carried in a benign state in the pharynx
* Carriage rates estimated to be as high as 15% in children
* Carriage rates are lower in adults, less than 5%
Carriage results in positive throat swab
* Antibiotic treatment can be prescribed for treatmnet of viral sore throat with ‘co-incidental carriage’
* GAS carriers maybe resistant to antibiotic therapy, throat swab after penicillin treatment is still positive
* UNKNOWN if GAS carriage can lead to post-infectious immune sequel (ARF and APSGN)

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8
Q

GAS: Penicillin

A

GAS is susceptible to penicillin BUT controlling disease in high burden area remains challenging.

  1. Not realising they need treatment
  2. Barriers to accessibility
  3. Not having full antibiotic course
  4. Antibiotic treatment fails in severe infections
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9
Q

GAS: M protein - general information

A
  • Encoded by the emm gene
  • Has a hypervariable N-terminus which provides the basis for emm typing
  • Comprised of a series of repeated regions
  • Conservation between GAS strains increase as you move down the protein
  • C-repeat and D-repeat are highly conserved
  • Extends from cell surface as coiled-coil (dimer)
  • Repeat regions vary depending of emm type
  • Multifunctional protein - roles in adhesion by binding fibronectin in ECM, assist in immune evasion by binding fibrinogen, factor H and immunoglobulin
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10
Q

GAS: Emm-typing

A
  • Developed by the CDC in the USA
  • Relies upon the use of the two highly conserved primers to amplify a large portion of the emm-gene
  • The hypervariable sequence lies adjacent to one of the amplifying primer sequences, allowing for direct sequencing
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11
Q

GAS: emm type distribution

A
  • emm types differ in space (geographical variation)
  • Globally, emm1 is the most common emm-type in resource rich setting
  • Diversity of emm-type is greater in resource poor setting
  • No single dominating strain-type is associated with disease in LMIC
  • emm types differ in type (temporal variation)
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12
Q

GAS: Emm-pattern type

A

Three main pattern types, A-C, D and E

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13
Q

GAS: Emm-pattern type - tissue tropism marker

A

A-C pharyngeal strains dominate in temporate climates
D pattern ‘skin’ isolates dominate in warm tropical climates
E = throat or skin

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14
Q

GAS: WGS

A
  • > 200 emm-types, but this doesn’t capture all the diversity in GAS
  • Strains of the same emm-type can have different phenotype driven by differences in other important virulence factors
  • Emm81 outbreak in NZ aged care in winter, 2014 WGS proved useful.
  • WGS not used a lot due to genome being so large and large cost
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15
Q

GAS: ARF symptoms

A

Elevated antibody titers to GAS antigens

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16
Q

GAS: ARF symptoms

A

Elevated antibody titers to GAS antigens

17
Q

GAS: Pathogenesis

A

Poorly understood - see diagram in lecture slides

18
Q

GAS: Pathogenesis

A

Poorly understood - see diagram in lecture slides

19
Q

GAS: ARF Autoimmunity Hypothesis I

A
  • Mimicry between M protein and human proteins found in heart tissue (myosin, collagen) - but myosin is intracellular so antibodies cannot access
  • Laboratory studies only, clinical data are lacking
  • Still a concern for M-protein based vaccine.
20
Q

GAS: ARF Autoimmunity Hypothesis 2

A