Streptococcus pneumoniae

Background

Microbiology

• Gram-positive, lancet-shaped diplococcus
• 90+ serotypes, based on capsular polysaccharide that is bound to peptidoglycan
• Lab identification is based on catalase negative, α hemolysis of blood agar (from pneumolysin), optochin susceptibility, and bile salt solubility
• Via transformation, bacteria can exchange genetic material with each other

Antibiotic Resistance

• Penicillin resistance
  • S. pneumoniae has 6 PBPs: 1A, 1B, 2A, 2B, 2X, and 3
  • Resistance in any of the PBPs can increase the MIC
  • Mutations in PBP 2B are associated with low-level resistance
  • Mutations in PBP 2X are associated with high-level resistance
• Macrolide resistance
  • ermB encodes an enzyme that methylates the 23S subunit, blocking macrolides and giving very high MIC ≥64
  • mefA encodes an efflux pump that gives a relatively lower MIC ≤16

Epidemiology

• Present worldwide
• Major cause of morbidity and mortality in children
  • Leading cause of under-5 mortality worldwide

Pathophysiology

• Acquired by coughing and sneezing
• Asymptomatic carriage or colonization in the nasopharynx
• Invasion through epithelial cells into the bloodstream, using the PAF and pIg receptors
• Capsule and various proteins help it to evade immune system

Clinical Manifestations

Asymptomatic Carriage

• 4-10% in the general adult population, usually lasting several weeks
• Highest in children, up to 30-60% depending on the situation, lasting up to 6 months

Pneumonia

• Acute onset of cough (92%), fatigue (63%), shortness of breath (47%), and dyspnea (23%) with documented or subjective fever (92%), chills (77%), sweats, purulent sputum, and pleuritic chest pain (79%)

Meningitis

• Most common cause of bacterial meningitis in adults
• Acquired by hematogenous spread from nasopharynx, or direct invasion from sinuses
• May be secondary to otitis media or sinusitis
• CSF leaks and other defects predispose to infection
• Diagnostic yield in CSF decrease significantly 4 hours after administration of antibiotics

Management

Scenario	Penicillin (μg/mL)			Ceftriaxone (μg/mL)
	S	I	R	S	I	R
Non-meningitic oral	≤0.06	0.12-1	≥2
Non-meningitic parenteral	≤2	4	≥8	≤1	2	≥4
Meningitic parenteral	≤0.06		≥0.12	≤0.5	1	≥2

Prevention

Vaccination

• Essentially two forms of vaccine available in Canada
• Pneu-C-20: 20-valent pneumococcal conjugate vaccine (Prevnar-20)
  • More immunogenic but slightly fewer serotypes than polysaccharide
  • Routine childhood immunization, also used for immunocompromised adults
  • Given at least 1 year after Pneu-P-23 (if given)
• Pneu-P-23: 23-valent pneumococcal polysaccharide vaccine (Pneumovax)
  • Less immunogenic than conjugate vaccine
  • Used in combination with Pneu-C-15 only when Pneu-C-20 is unavailable

Age	Status	Vaccine
<18	routine	2 to 4 doses PC-20, depending on age
18-64	healthy	no routine vaccination
	smoking, alcohol, injection drug use, homeless, long-term care facility	1 dose PC-20
	high risk for invasive disease	1 dose PC-20
≥18	immunocompromised	1 dose PC-20
	HSCT recipient	3 doses PC-20 q4wk starting 3-9 months post-transplant
≥65	healthy, regardless of prior vaccination	1 dose PC-20

• Conditions with high risk for invasive disease include (highest risk are bolded): CSF leak, chronic neurologic conditions that impair clearance of oral secretions, cochlear implants, chronic heart disease, diabetes mellitus, chronic kidney disease, chronic liver disease including cirrhosis, and chronic lung disease including asthma requiring medical care within past 12 months
• Immunocompromising conditions: hyposplenia (including sickle cell disease, asplenia, or splenic dysfunction), primary immunodeficiency, therapeutic immune suppression (including corticosteroids, chemotherapy, radiation therapy, and transplantation), HIV, HSCT, malignancy, nephrotic syndrome, solid organ transplantation

Post-Exposure Management

• Per Public Health Ontario, no specific management is required for close contacts