Postbiotic lactobacilli induce cutaneous antimicrobial response and restore the barrier to inhibit the intracellular invasion of Staphylococcus aureus in vitro and ex vivo

Author:

Dinić Miroslav12ORCID,Burgess Jamie L.13ORCID,Lukić Jovanka2ORCID,Catanuto Paola1ORCID,Radojević Dušan2ORCID,Marjanović Jelena1ORCID,Verpile Rebecca1,Thaller Seth R.4ORCID,Gonzalez Tammy1ORCID,Golić Nataša2ORCID,Strahinić Ivana2ORCID,Tomic‐Canic Marjana13ORCID,Pastar Irena1ORCID

Affiliation:

1. Wound Healing and Regenerative Medicine Research Program, Dr. Phillip Frost Department of Dermatology and Cutaneous Surgery University of Miami Miller School of Medicine Miami Florida USA

2. Group for Probiotics and Microbiota‐Host Interactions, Institute of Molecular Genetics and Genetic Engineering University of Belgrade Belgrade Serbia

3. Molecular and Cellular Pharmacology Graduate Program University of Miami Miller School of Medicine Miami Florida USA

4. DeWitt Daughtry Family Department of Surgery, Division of Plastic Surgery University of Miami Miller School of Medicine Miami Florida USA

Abstract

AbstractIntracellular pathogens including Staphylococcus aureus contribute to the non‐healing phenotype of chronic wounds. Lactobacilli, well known as beneficial bacteria, are also reported to modulate the immune system, yet their role in cutaneous immunity remains largely unknown. We explored the therapeutic potential of bacteria‐free postbiotics, bioactive lysates of lactobacilli, to reduce intracellular S. aureus colonization and promote healing. Fourteen postbiotics derived from various lactobacilli species were screened, and Latilactobacillus curvatus BGMK2‐41 was selected for further analysis based on the most efficient ability to reduce intracellular infection by S. aureus diabetic foot ulcer clinical isolate and S. aureus USA300. Treatment of both infected keratinocytes in vitro and infected human skin ex vivo with BGMK2‐41 postbiotic cleared S. aureus. Keratinocytes treated in vitro with BGMK2‐41 upregulated expression of antimicrobial response genes, of which DEFB4, ANG, and RNASE7 were also found upregulated in treated ex vivo human skin together with CAMP exclusively upregulated ex vivo. Furthermore, BGMK2‐41 postbiotic treatment has a multifaceted impact on the wound healing process. Treatment of keratinocytes stimulated cell migration and the expression of tight junction proteins, while in ex vivo human skin BGMK2‐41 increased expression of anti‐inflammatory cytokine IL‐10, promoted re‐epithelialization, and restored the epidermal barrier via upregulation of tight junction proteins. Together, this provides a potential therapeutic approach for persistent intracellular S. aureus infections.

Funder

Foundation for the National Institutes of Health

Science Fund of the Republic of Serbia

Innovation Fund of the Republic of Serbia

Fulbright U.S. Scholar Program

Publisher

Wiley

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