Hospital-acquired pneumonia caused by multidrug-resistant Streptococcus pneumoniae serotype 15A

Hidemasa Akazawa1, Shinnosuke Fukushima1,2, Kenta Nakamoto1

  • 1Department of Infectious Diseases, Okayama University Hospital, 2-5-1 Shikata-cho, Kitaku, Okayama, 700-8558, Japan.

Infection
|September 23, 2025
PubMed
Abstract

Insights

Multidrug-resistant Streptococcus pneumoniae can cause early hospital-acquired pneumonia, often missed by standard treatments. Surveillance of emerging strains like MDR serotype 15A is crucial for effective patient care.

Area of Science:

  • Infectious Diseases
  • Clinical Microbiology
  • Critical Care Medicine

Background:

  • Streptococcus pneumoniae is a frequent cause of community-acquired pneumonia but rarely causes hospital-acquired pneumonia (HAP).
  • Emerging global strains of multidrug-resistant (MDR) S. pneumoniae, particularly non-vaccine serotypes, increase the risk of nosocomial infections.
  • MDR S. pneumoniae poses a significant challenge due to resistance to common antibiotics.

Purpose of the Study:

  • To report a case of early-onset HAP caused by a multidrug-resistant Streptococcus pneumoniae serotype 15A.
  • To highlight the limitations of standard empiric antibiotic therapies against emerging MDR S. pneumoniae strains.
  • To emphasize the importance of antimicrobial susceptibility testing and surveillance of vaccine-escape clones.

Main Methods:

  • A case study of a 71-year-old male patient who developed HAP post-spinal fusion surgery.
  • Initial treatment with ampicillin/sulbactam, followed by empirical ceftriaxone, with subsequent adjustment to levofloxacin based on susceptibility testing.
  • Identification of the causative pathogen as S. pneumoniae serotype 15A, sequence type 63 (ST63), with detailed antimicrobial resistance profiling.

Main Results:

  • The patient experienced clinical deterioration requiring ICU admission and mechanical ventilation despite initial antibiotic treatment.
  • The S. pneumoniae isolate exhibited resistance to penicillin, ceftriaxone, meropenem, macrolides, and clindamycin.
  • Treatment with levofloxacin led to clinical improvement, indicating susceptibility to this agent.

Conclusions:

  • MDR S. pneumoniae, including serotype 15A, can cause early-onset HAP and may evade standard empiric treatment regimens.
  • Close monitoring of treatment response and prompt antimicrobial susceptibility testing are vital for managing HAP.
  • Continuous surveillance of vaccine-escape MDR S. pneumoniae clones is essential due to their growing clinical significance.

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