4.6 Article

Artificial Human Sweat as a Novel Growth Condition for Clinically Relevant Pathogens on Hospital Surfaces

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MICROBIOLOGY SPECTRUM
卷 10, 期 2, 页码 -

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AMER SOC MICROBIOLOGY
DOI: 10.1128/spectrum.02137-21

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hospital surfaces; biofilms; dry surface biofilms; hospital infections; human sweat

资金

  1. Royal Commission for the Exhibition of 1851

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This study developed a novel culture medium, artificial human sweat (AHS), to mimic the biofilm formation on dry hospital surfaces. The AHS model showed similar characteristics to clinical biofilms and can be used for efficacy testing of cleaning products against dry surface biofilms. Accurate modeling of dry surface biofilms is crucial for understanding their role in hospital-acquired infections and surface contamination.
The emergence of biofilms on dry hospital surfaces has led to the development of numerous models designed to challenge the efficacious properties of common antimicrobial agents used in cleaning. This is in spite of limited research defining how dry surfaces are able to facilitate biofilm growth and formation in such desiccating and nutrient-deprived environments. While it is well established that the phenotypical response of biofilms is dependent on the conditions in which they are formed, most models incorporate a nutrient-enriched, hydrated environment dissimilar to the clinical setting. In this study, we piloted a novel culture medium, artificial human sweat (AHS), which is perceived to be more indicative of the nutrient sources available on hospital surfaces, particularly those in close proximity to patients. AHS was capable of sustaining the proliferation of four clinically relevant multidrug-resistant pathogens (Acinetobacter baumannii, Staphylococcus aureus, Enterococcus faecalis, and Pseudomonas aeruginosa) and achieved biofilm formation at concentration levels equivalent to those found in situ (average, 6.00 log(10), CFU/cm(2)) with similar visual characteristics upon microscopy. The AHS model presented here could be used for downstream applications, including efficacy testing of hospital cleaning products, due to its resemblance to clinical biofilms on dry surfaces. This may contribute to a better understanding of the true impact these products have on surface hygiene. IMPORTANCE Precise modeling of dry surface biofilms in hospitals is critical for understanding their role in hospital-acquired infection transmission and surface contamination. Using a representative culture condition which includes a nutrient source is key to developing a phenotypically accurate biofilm community. This will enable accurate laboratory testing of cleaning products and their efficacy against dry surface biofilms.

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