Deferiprone-Gallium-Protoporphyrin Chitogel Decreases Pseudomonas aeruginosa Biofilm Infection without Impairing Wound Healing

Author:

Kennewell Tahlia L.1ORCID,Haidari Hanif1ORCID,Mashtoub Suzanne23,Howarth Gordon S.4,Bennett Catherine56,Cooksley Clare M.56,Wormald Peter John56,Cowin Allison J.1ORCID,Vreugde Sarah56,Kopecki Zlatko1ORCID

Affiliation:

1. Future Industries Institute, University of South Australia, Mawson Lakes, SA 5095, Australia

2. School of Biomedicine, The University of Adelaide, Adelaide, SA 5005, Australia

3. Department of Gastroenterology, Women’s and Children’s Hospital, North Adelaide, SA 5006, Australia

4. School of Animal and Veterinary Sciences, The University of Adelaide, Roseworthy, SA 5371, Australia

5. Adelaide Medical School, The University of Adelaide, Adelaide, SA 5005, Australia

6. Department of Surgery Otolaryngology Head and Neck Surgery, Basil Hetzel Institute for Translational Health Research, Central Adelaide Local Health Network, Woodville South, SA 5011, Australia

Abstract

Pseudomonas aeruginosa is one of the most common pathogens encountered in clinical wound infections. Clinical studies have shown that P. aeruginosa infection results in a larger wound area, inhibiting healing, and a high prevalence of antimicrobial resistance. Hydroxypyridinone-derived iron chelator Deferiprone (Def) and heme analogue Gallium-Protoporphyrin (GaPP) in a chitosan-dextran hydrogel (Chitogel) have previously been demonstrated to be effective against PAO1 and clinical isolates of P. aeruginosa in vitro. Moreover, this combination of these two agents has been shown to improve sinus surgery outcomes by quickly reducing bleeding and preventing adhesions. In this study, the efficacy of Def-GaPP Chitogel was investigated in a P. aeruginosa biofilm-infected wound murine model over 6 days. Two concentrations of Def-GaPP Chitogel were investigated: Def-GaPP high dose (10 mM Def + 500 µg/mL GaPP) and Def-GaPP low dose (5 mM Def + 200 µg/mL GaPP). The high-dose Def-GaPP treatment reduced bacterial burden in vivo from day 2, without delaying wound closure. Additionally, Def-GaPP treatment decreased wound inflammation, as demonstrated by reduced neutrophil infiltration and increased anti-inflammatory M2 macrophage presence within the wound bed to drive wound healing progression. Def-GaPP Chitogel treatment shows promising potential in reducing P. aeruginosa cutaneous infection with positive effects observed in the progression of wound healing.

Funder

UniSA Postgraduate Research Award Scholarship

Channel 7 Children’s Research Foundation Fellowship

DEBRA Australia Research Grant

Publisher

MDPI AG

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