Cryomilled zinc sulfide: A prophylactic for Staphylococcus aureus-infected wounds

Author:

Tran Phat L1,Li Jianqiang2,Lungaro Lisa3,Ramesh Srikanthan2,Ivanov Ilia N4,Moon Ji-Won5,Graham David E5ORCID,Hamood Abdul67,Wang James8,Elfick Alistair PD3,Rivero Iris V27ORCID

Affiliation:

1. Department of Ophthalmology and Visual Sciences, Texas Tech University Health Sciences Center, School of Medicine, Lubbock, Texas, USA

2. Department of Industrial and Manufacturing Systems Engineering, Iowa State University, Ames IA, USA

3. Institute for Bioengineering, University of Edinburgh, Edinburgh, Scotland, UK

4. Center for Nanophase Materials Science, Oak Ridge National Laboratory, Oak Ridge TN, USA

5. Biosciences Division, Oak Ridge National Laboratory, Oak Ridge TN, USA

6. Department of Molecular Microbiology and Immunology, Texas Tech University Health Sciences Center, Lubbock, Texas, USA

7. Department of Surgery, Texas Tech University Health Sciences Center, Lubbock, Texas, USA

8. School of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, USA

Abstract

Bacterial pathogens that colonize wounds form biofilms, which protect the bacteria from the effect of host immune response and antibiotics. This study examined the effectiveness of newly synthesized zinc sulfide in inhibiting biofilm development by Staphylococcus aureus ( S. aureus) strains. Zinc sulfide (ZnS) was anaerobically biosynthesized to produce CompA, which was further processed by cryomilling to maximize the antibacterial properties to produce CompB. The effect of the two compounds on the S. aureus strain AH133 was compared using zone of inhibition assay. The compounds were formulated in a polyethylene glycol cream. We compared the effect of the two compounds on biofilm development by AH133 and two methicillin-resistant S. aureus clinical isolates using the in vitro model of wound infection. Zone of inhibition assay revealed that CompB is more effective than CompA. At 15 mg/application, the formulated cream of either compound inhibited biofilm development by AH133, which was confirmed using confocal laser scanning microscopy. At 20 mg/application, CompB inhibited biofilm development by the two methicillin-resistant S. aureus clinical isolates. To further validate the effectiveness of CompB, mice were treated using the murine model of wound infection. Colony forming cell assay and in vivo live imaging results strongly suggested the inhibition of S. aureus growth.

Funder

US Department of Energy

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials

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