Gram-negativeBacilliNon-fermenters

Pseudomonas aeruginosa

Obligate aerobic, oxidase-positive, non-fermenting Gram-negative bacillus that is a leading cause of nosocomial infections, particularly ventilator-associated pneumonia, burn wound infections, and opportunistic infections in immunocompromised and cystic fibrosis patients.

Organism Card

DomainMust know
Identity
  • G−ve bacillus (rod), non-fermenter [1]
  • Obligate aerobe; motile (single polar flagellum)
  • Family Pseudomonadaceae; NOT Enterobacteriaceae
  • Produces blue-green pigment (pyocyanin + pyoverdin)
Lab discriminator
  • Oxidase positive (vs Enterobacteriaceae which are oxidase −ve) [1]
  • Lactose non-fermenter on MacConkey agar (colourless colonies)
  • Grape-like / sweet fruity odour on culture plates
  • Blue-green pigment on Mueller-Hinton agar is classic
  • Grows at 42°C (vs most other non-fermenters)
Reservoir / transmission
  • Ubiquitous in moist environments: water, soil, sinks, ventilators, humidifiers
  • Hospital-acquired: introduced by hands of medical personnel, diagnostic/therapeutic procedures [2]
  • Colonises patients during hospitalisation, especially after broad-spectrum Abx suppress normal anaerobic flora [2]
  • Community: hot tubs, contact lens solutions, contaminated ear-piercing equipment
Key virulence
  • Exotoxin A → inhibits EF-2 (same mechanism as diphtheria toxin) → tissue necrosis
  • Pyocyanin → generates ROS, impairs ciliary function, damages epithelium
  • Elastase + alkaline protease → tissue destruction, corneal ulceration
  • Alginate (mucoid exopolysaccharide) → biofilm formation on devices & in CF lungs
  • Biofilm on devices (catheters, ETT) resists eradication without device removal [2]
  • Type III secretion system → injects cytotoxins directly into host cells
  • Endotoxin (lipid A / LPS) → septic shock
Clinical syndromes
  • Nosocomial pneumonia / VAP — common cause; variable presentation, no specific features [3][4]
  • Neutropenic fever / sepsis — important G−ve cause (with E. coli) post-chemotherapy [2][5]
  • Bronchiectasis acute exacerbation — especially if long-standing disease [4][6]
  • Nosocomial / complicated UTI — catheter-associated [7]
  • CAPD peritonitis — G−ve cause; requires catheter removal if refractory [8]
  • Burns & wound infection — classic G−ve pathogen in burn units
  • Otitis externa — "swimmer's ear"; malignant otitis externa in diabetic/elderly
  • Keratitis — contact lens wearers; rapidly destructive
  • Septic arthritis in IVDU [9]
  • Ecthyma gangrenosum — necrotic skin lesion virtually pathognomonic in neutropenic patients
  • Endocarditis in IVDU — right-sided; cover in critically ill IVDU IE [10]
Diagnosis
  • Specimen: sputum / BAL, blood culture, wound swab, urine, PD effluent as appropriate
  • Gram stain: G−ve rods (non-specific morphology)
  • Culture on MacConkey: NLF colonies; oxidase +ve confirms non-fermenter
  • Colonisation is common — isolation in respiratory specimens must be correlated with clinical situation [3]
  • Antibiotic susceptibility testing essential (high resistance rates)
Treatment
  • Anti-pseudomonal agents [3][4][6]:
  • (1) Anti-pseudomonal BL/BLI: piperacillin-tazobactam (Tazocin), ticarcillin-clavulanate (Timentin)
  • (2) Selected cephalosporins: ceftazidime (Fortum), cefepime, cefoperazone [3]
  • (3) Fluoroquinolones: ciprofloxacin > levofloxacin for Pseudomonas [3]
  • (4) Carbapenems: imipenem, meropenem (NOT ertapenem) [3]
  • (5) Aminoglycosides: amikacin, gentamicin
  • Single agent generally suffices; start DUAL therapy in severe infections [3]
  • If Pseudomonas likely in sepsis: Vancomycin + TWO anti-pseudomonal agents from different classes [11]
  • MRPA (multi-resistant P. aeruginosa): may need colistin, ceftazidime-avibactam (Zavicefta), ceftolozane-tazobactam (Zerbaxa), cefiderocol [3]
  • Bronchiectasis with chronic Pseudomonas: consider inhaled anti-pseudomonal agents
Prevention
  • Infection control: hand hygiene, contact precautions for MDR strains [2]
  • Antimicrobial stewardship — avoid unnecessary broad-spectrum Abx that suppress anaerobic flora and promote colonisation [2]
  • Device removal if catheter-related / PD catheter infection refractory to Abx [2][8]
  • No vaccine in routine clinical use
  • Ceftazidime-resistant Pseudomonas is a notifiable MDR organism in HK public hospitals [12]
Classic traps
  • Oxidase +ve separates Pseudomonas from Enterobacteriaceae (exam favourite)
  • Ertapenem has NO anti-pseudomonal activity — trap MCQ answer [3]
  • Colonisation ≠ infection — do not treat sputum isolate without clinical correlation [3]
  • ESBL-producing E. coli (NOT Pseudomonas) is the most common MDR organism in HK public hospitals [12]
  • Ecthyma gangrenosum + neutropenia = Pseudomonas until proven otherwise
  • Malignant otitis externa in elderly diabetic = Pseudomonas (not S. aureus)
  • Contact lens keratitis = Pseudomonas (not Acanthamoeba, which is subacute)

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