In-vitro archaeacidal activity of biocides against human-associated archaea

Saber Khelaifia1, Jean Michel Brunel, Jean Brunel Michel

  • 1Aix Marseille Université, URMITE, UMR63 CNRS 7278, IRD 198, Inserm 1095, Marseille, France.

Plos One
|May 10, 2013
PubMed
Abstract

Insights

A novel squalamine derivative, S1, demonstrates potent archaeacidal activity against human-associated methanogenic archaea. This finding suggests S1

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Biochemistry

Background:

  • Methanogenic archaea are present in the human gut microbiome.
  • These archaea can potentially contaminate medical devices like colonoscopes.
  • No prior biocide activity data exists for human-associated archaea.

Purpose of the Study:

  • To determine the archaeacidal activity of squalamine and its derivatives against human-associated methanogenic archaea.
  • To evaluate the potential of these compounds for medical device decontamination.

Main Methods:

  • Minimal archaeacidal concentration (MAC) was determined for peracetic acid, chlorhexidine, squalamine, and 12 synthetic squalamine derivatives.
  • Testing was conducted against five human-associated methanogenic archaea and two environmental methanogens.
  • A serial dilution technique in Hungate tubes was employed.

Main Results:

  • Squalamine derivative S1 showed significant archaeacidal activity, with MACs of 0.05 mg/L against most tested human-associated archaea.
  • Other squalamine derivatives (S2-S12) and squalamine itself exhibited higher MACs, ranging from 0.5 to ≥10 mg/L.
  • Chlorhexidine and peracetic acid had MACs of 0.2 and 1.5 mg/L, respectively.

Conclusions:

  • Squalamine derivative S1 displayed 10-200 times higher archaeacidal activity compared to other tested squalamine derivatives.
  • S1 is a promising candidate for further investigation in the decontamination of medical devices.
  • Squalamine and its derivative S1 possess broad-spectrum antimicrobial properties and low corrosivity.

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