4.2 Article

Antibacterial effect of acetic acid during an outbreak of carbapenem- resistant Acinetobacter baumannii in an ICU (II)

Journal

JOURNAL OF INFECTION IN DEVELOPING COUNTRIES
Volume 15, Issue 8, Pages 1167-1172

Publisher

J INFECTION DEVELOPING COUNTRIES
DOI: 10.3855/jidc.11693

Keywords

Acetic acid; Carbapenem-resistance; Acinetobacter baumannii; loop-mediated isothermal amplification

Funding

  1. CIBNOR (PAZA)
  2. CONACyT (Mexican Council for Science andTechnology) [256927]

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This study evaluated the antibacterial effect of acetic acid (AA) during an outbreak in an ICU facility in Baja California Sur, Mexico. The results showed a significant decrease in Carbapenem-resistant A. baumannii (CRAB) before and after disinfection, suggesting the potential of AA as a cheap and efficacious disinfectant to prevent the spread of CRAB in healthcare settings. The study also demonstrated the novel application of AA with LAMP assays for detecting CRAB, revealing wide clonal dissemination of CRAB in the ICU facility.
Introduction: Acetic acid (AA) has been commonly used in medicine as an antiseptic agent for the past 6000 years. This study evaluated the antibacterial effect of AA during an outbreak in an intensive care unit (ICU) facility in Baja California Sur, Mexico. Methodology: Thirty-five environmental samples were collected, subsequently, disinfection with AA (4%) was performed, and two days later the same areas were sampled inside the ICU facility. Carbapenem-resistant A. baumannii (CRAB) was detected with loop-mediated isothermal amplification assay (Garciglia-Mercado et al. companion paper), targeting bla(OXA-23-like), bla(OXA-24-like), bla(OXA-51-like), bla(OXA-58-like), bla(IMP) and bla(VIM) genes. CRAB isolates before and after disinfection were compared by PFGE. Results: Eighteen (54.5%) and five (14.3%) of thirty-five environmental samples were identified as Acinetobacter baumannii before and after disinfection, respectively, showing a significant decrease of 85.7% (p < 0.05) both by Loop-mediated isothermal amplification (LAMP) and polymerase chain reaction (PCR). Furthermore, the presence of bla(OXA-23-like) and bla(OXA-58-like) genes significantly decreased (p < 0.05) both by LAMP and PCR methods. PFGE genotype showed high similarity among CRAB isolates before and after disinfection, suggesting wide clonal dissemination in the ICU facility. Conclusions: This study demonstrated the novel application of AA with the LAMP assays developed for detecting CRAB. AA promises to be a cheap and efficacious disinfectant alternative to both developed and especially developing countries, preventing the spread of this organism in the environment and to other susceptible patients in health care settings.

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