Gram-negativeBacilliRespiratory

Bordetella pertussis

Gram-negative coccobacillus that causes pertussis (whooping cough), characterized by severe paroxysmal coughing with inspiratory whoop, primarily in unvaccinated children.

Organism Card

DomainMust know
Identity
  • G−ve coccobacillus (small, pleomorphic) [1]
  • Strictly aerobic; fastidious; non-motile
  • Genus Bordetella; species pertussis (human-only pathogen)
  • Closely related: B. parapertussis (milder disease), B. bronchiseptica (animal pathogen)
Lab discriminator
  • Nasopharyngeal swab/aspirate is the optimal specimen (NOT throat swab in viral transport medium) [1]
  • Culture on Bordet-Gengou (potato-glycerol-blood agar) or Regan-Lowe (charcoal agar) → small, mercury-drop "bisected-pearl" colonies
  • Multiplex RT-PCR on NPA is most sensitive [1]
  • Swabs for B. pertussis culture should NOT be refrigerated/frozen — plate immediately (unlike most other bacterial swabs) [1]
  • Oxidase +, catalase +, urease − (vs B. parapertussis urease +)
Reservoir / transmission
  • Humans are the only reservoir (no animal reservoir)
  • Transmitted by respiratory droplets (highly contagious, attack rate ~80% in susceptible household contacts)
  • Infectivity highest during catarrhal stage (before the classic cough)
Key virulence
  • Pertussis toxin (PT): ADP-ribosylates Gi protein → ↑cAMP → lymphocytosis, impaired immune cell chemotaxis; causes marked lymphocytosis on CBC
  • Filamentous haemagglutinin (FHA): adhesin to ciliated respiratory epithelium
  • Tracheal cytotoxin: damages ciliated cells → impaired mucociliary clearance → paroxysmal cough
  • Adenylate cyclase toxin: inhibits phagocyte function
  • Pertactin & fimbriae: additional adhesins (vaccine targets)
Clinical syndromes
  • Classical whooping cough — 3 stages [2]:
  • Catarrhal (1-2 wk): URTI symptoms, most contagious
  • Paroxysmal (2-8 wk): spasmodic cough bursts → inspiratory "whoop"; post-tussive vomiting; cough worse at night
  • Convalescent (wks-months): gradual ↓ cough ("100-day cough")
  • Infants < 6 mo: may present with apnoea / cyanosis without classic whoop → high mortality
  • Adolescents/adults (waned immunity): prolonged non-specific cough, often undiagnosed
  • B. pertussis can cause bronchiolitis in children < 2 y [2]
  • Complications: pneumonia, seizures, encephalopathy, subconjunctival haemorrhage, rectal prolapse
Diagnosis
  • Best specimen: NPA or nasopharyngeal swab (NOT oropharyngeal) [1]
  • PCR is most sensitive diagnostic test [1]
  • Culture on Bordet-Gengou / Regan-Lowe agar (low sensitivity, especially after antibiotics started)
  • Serology (anti-PT IgG): useful in later stages when culture/PCR may be negative
  • CBC: marked lymphocytosis (WCC can be > 50 × 10⁹/L) — classic lab clue
  • Pitfall: lymphocytosis in infants can mimic leukaemia (→ d/dx with ALL in haematology context) [3]
Treatment
  • Macrolides are first-line: azithromycin (preferred, short course) or erythromycin or clarithromycin
  • Antibiotics shorten infectious period but have limited effect on cough once paroxysmal stage established
  • TMP-SMX as alternative if macrolide-intolerant
  • Supportive care for infants: O₂, suction, monitoring for apnoea
Prevention
  • DTaP-IPV vaccine: 3 doses at 2nd, 4th, 6th months (HK childhood immunisation programme) [2][4]
  • D = diphtheria toxoid, T = tetanus toxoid, aP = acellular pertussis, IPV = inactivated poliovirus [2][4]
  • Booster: Tdap (reduced-antigen) for adolescents / adults / pregnant women (cocooning strategy)
  • Post-exposure prophylaxis: macrolides for close contacts (especially household contacts of infants)
  • Notifiable disease in Hong Kong
  • Droplet precautions for hospitalised cases until 5 days of effective antibiotic therapy
Classic traps
  • Catarrhal stage most contagious but least recognisable → diagnosis often delayed
  • Marked lymphocytosis can mimic ALL in infants — check PBS for blasts [3]
  • B. pertussis swab: use bacterial transport medium, NOT viral transport medium (contains antibiotics that kill Bordetella) [1]
  • Acellular vaccine (aP) does NOT prevent colonisation/transmission as effectively as it prevents disease
  • B. parapertussis: urease +, milder illness, no pertussis toxin gene expression

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