Evaluation of phage-based decontamination in respiratory intensive care unit environments using ddPCR and 16S rRNA targeted sequencing techniques

Front Cell Infect Microbiol. 2024 Aug 19:14:1442062. doi: 10.3389/fcimb.2024.1442062. eCollection 2024.

Abstract

Background: Klebsiella pneumoniae is a major cause of hospital-acquired infections (HAIs), primarily spread through environmental contamination in hospitals. The effectiveness of current chemical disinfectants is waning due to emerging resistance, which poses environmental hazards and fosters new resistance in pathogens. Developing environmentally friendly and effective disinfectants against multidrug-resistant organisms is increasingly important.

Methods: This study developed a bacteriophage cocktail targeting two common carbapenem-resistant Klebsiella pneumoniae (CRKP) strains, ST11 KL47 and ST11 KL64. The cocktail was used as an adjunctive disinfectant in a hospital's respiratory intensive care unit (RICU) via ultrasonic nebulization. Digital PCR was used to quantify CRKP levels post-intervention. The microbial community composition was analyzed via 16S rRNA sequencing to assess the intervention's impact on overall diversity.

Results: The phage cocktail significantly reduced CRKP levels within the first 24 hours post-treatment. While a slight increase in pathogen levels was observed after 24 hours, they remained significantly lower than those treated with conventional disinfectants. 16S rRNA sequencing showed a decrease in the target pathogens' relative abundance, while overall species diversity remained stable, confirming that phages selectively target CRKP without disrupting ecological balance.

Discussion: The findings highlight the efficacy and safety of phage-based biocleaners as a sustainable alternative to conventional disinfectants. Phages selectively reduce multidrug-resistant pathogens while preserving microbial diversity, making them a promising tool for infection control.

Keywords: 16S rRNA; bacteriophages; drug-resistant bacterial; hospital-acquired infections; targeted metagenomics in pathogen.

MeSH terms

  • Bacteriophages* / genetics
  • Cross Infection / microbiology
  • Cross Infection / prevention & control
  • Decontamination* / methods
  • Disinfectants / pharmacology
  • Humans
  • Intensive Care Units*
  • Klebsiella Infections / microbiology
  • Klebsiella Infections / prevention & control
  • Klebsiella pneumoniae* / genetics
  • Klebsiella pneumoniae* / virology
  • Polymerase Chain Reaction / methods
  • RNA, Ribosomal, 16S* / genetics
  • Sequence Analysis, DNA

Substances

  • RNA, Ribosomal, 16S
  • Disinfectants

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by grants from the National Natural Science Foundation of China (Grant No.82341119) and Beijing Municipal Natural Science Foundation (No. 7222181).