Efficacy of a novel antimicrobial hydrogel for eradication of Staphylococcus epidermidis, Staphylococcus aureus and Cutibacterium acnes from preformed biofilm and treatment performance in an in vivo MRSA wound model. Issue 3 (29th July 2021)
- Record Type:
- Journal Article
- Title:
- Efficacy of a novel antimicrobial hydrogel for eradication of Staphylococcus epidermidis, Staphylococcus aureus and Cutibacterium acnes from preformed biofilm and treatment performance in an in vivo MRSA wound model. Issue 3 (29th July 2021)
- Main Title:
- Efficacy of a novel antimicrobial hydrogel for eradication of Staphylococcus epidermidis, Staphylococcus aureus and Cutibacterium acnes from preformed biofilm and treatment performance in an in vivo MRSA wound model
- Authors:
- Ronco, Troels
Aragao, Maria F
Svenningsen, Søren
Christensen, Jørn B
Permin, Anders
Saaby, Lasse
Bionda, Nina
Lantz, Ellen E
Olsen, Rikke H - Abstract:
- Abstract: Background: Bacterial biofilm formation is a complicating factor in the antimicrobial treatment of bacterial infections. Objectives: In this study, we assessed the impact of a novel hydrogel with the active antimicrobial compound JBC 1847 on eradication of preformed biofilms of Staphylococcus epidermidis, Cutibacterium acnes and MRSA in vitro, and evaluated the in vivo efficacy of MRSA wound treatment. Methods: Biofilms were exposed to JBC 1847 for 24 h and subsequently the treatments were neutralized and surviving biofilm-associated bacteria recovered and enumerated. The efficacy of the hydrogel on post-treatment load of MRSA was determined in a murine model of MRSA wound infection, and skin samples of the infected mice were examined histologically to evaluate the degree of healing. Results: A concentration-dependent eradication of biofilm-embedded bacteria by JBC 1847 was observed for all three pathogens, and the hydrogel caused a greater than four log reduction of cfu in all cases. In the mouse model, treatment with the hydrogel significantly reduced the cfu/mL of MRSA compared with treatment of MRSA-infected wounds with pure hydrogel. Histopathological analysis of the wounds showed that the JBC 1847 treatment group had a lower grade of inflammation, a higher mean score of re-epithelization and higher mean scores of parameters assessing the maturity of the newly formed epidermis, compared with both the fusidic acid 2% and vehicle treatment groups. Conclusions:Abstract: Background: Bacterial biofilm formation is a complicating factor in the antimicrobial treatment of bacterial infections. Objectives: In this study, we assessed the impact of a novel hydrogel with the active antimicrobial compound JBC 1847 on eradication of preformed biofilms of Staphylococcus epidermidis, Cutibacterium acnes and MRSA in vitro, and evaluated the in vivo efficacy of MRSA wound treatment. Methods: Biofilms were exposed to JBC 1847 for 24 h and subsequently the treatments were neutralized and surviving biofilm-associated bacteria recovered and enumerated. The efficacy of the hydrogel on post-treatment load of MRSA was determined in a murine model of MRSA wound infection, and skin samples of the infected mice were examined histologically to evaluate the degree of healing. Results: A concentration-dependent eradication of biofilm-embedded bacteria by JBC 1847 was observed for all three pathogens, and the hydrogel caused a greater than four log reduction of cfu in all cases. In the mouse model, treatment with the hydrogel significantly reduced the cfu/mL of MRSA compared with treatment of MRSA-infected wounds with pure hydrogel. Histopathological analysis of the wounds showed that the JBC 1847 treatment group had a lower grade of inflammation, a higher mean score of re-epithelization and higher mean scores of parameters assessing the maturity of the newly formed epidermis, compared with both the fusidic acid 2% and vehicle treatment groups. Conclusions: The novel hydrogel shows promising results as a candidate for future wound treatment, likely to be highly effective even in the case of biofilm-complicating infected wounds. … (more)
- Is Part Of:
- JAC-antimicrobial resistance. Volume 3:Issue 3(2021)
- Journal:
- JAC-antimicrobial resistance
- Issue:
- Volume 3:Issue 3(2021)
- Issue Display:
- Volume 3, Issue 3 (2021)
- Year:
- 2021
- Volume:
- 3
- Issue:
- 3
- Issue Sort Value:
- 2021-0003-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-07-29
- Subjects:
- Anti-infective agents -- Periodicals
Chemotherapy -- Periodicals
Drug resistance in microorganisms -- Periodicals
616.9041 - Journal URLs:
- http://www.oxfordjournals.org/ ↗
https://academic.oup.com/jacamr ↗ - DOI:
- 10.1093/jacamr/dlab108 ↗
- Languages:
- English
- ISSNs:
- 2632-1823
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19755.xml