Aug 2026· Frontiers in Microbiology· Vol 17· 0 citations· 58 references
Medicine
TL;DR
Evaluated postbiotic preparations derived from the probiotic yeast Pichia kudriavzevii isolated from a homemade kefir highlight the potential of P. kudriavzevii-derived postbiotics as multifunctional agents capable of controlling biofilm-associated infections, modulating inflammation, and supporting tissue repair.
Abstract
Atopic dermatitis (AD) is a chronic inflammatory skin disorder associated with microbial dysbiosis and persistent biofilm-forming infections, particularly involving Candida parapsilosis and Staphylococcus aureus. Postbiotics have recently emerged as promising alternatives to live probiotics due to their stability, safety, and antimicrobial properties. In this study, we evaluated the in vitro biological activity of two postbiotic preparations derived from the probiotic yeast Pichia kudriavzevii isolated from a homemade kefir: cell-free supernatant (CFS) and extracellular vesicles (EVs) against two clinical isolates of S. aureus and C. parapsilosis. While S. aureus demonstrated high vulnerability to postbiotic treatments, C. parapsilosis and the dual-species biofilm exhibited significantly higher tolerance. Results indicate a susceptibility gradient to postbiotic treatments, with S. aureus being the most vulnerable and C. parapsilosis more tolerant probably due to its structural and morphological characteristics. Treatment with CFS and EVs also reduced microbial adhesion and invasion of HaCaT keratinocytes, lowering microbial loads to 3.7–6.6 and 3.6–6.1 log10 CFU/mL, respectively. Furthermore, both postbiotics attenuated the inflammatory response by decreasing IL-6 and IL-8 production in pathogen-infected keratinocytes . Notably, EVs exhibited superior wound-healing activity by promoting keratinocyte migration and accelerating wound closure ( > 90% after 24 h). These findings highlight the potential of P. kudriavzevii-derived postbiotics as multifunctional agents capable of controlling biofilm-associated infections, modulating inflammation, and supporting tissue repair. Their application may represent a novel therapeutic approach for the management of chronic skin lesions associated with AD.
Atopic dermatitis (AD) is a common, chronic, relapsing inflammatory skin disease characterized by xerosis, pruritus and eczematous lesions, arising from the interplay between skin barrier dysfunction and a predominantly T-helper-2 (Th2)-polarized immune response. A defining and clinically important feature of AD is its...
Haidar A. Abdulamir, Dena Mohammed Alsahaf, FarisKadhim Khadir· Journal of Microbiological S...· 0 citations
Introduction Methicillin-resistant Staphylococcus aureus (MRSA) colonization is a major contributor to atopic dermatitis (AD), and its rising resistance and virulence underscore the urgent need for novel antimicrobial strategies. Methods In this study, a halotolerant strain designated Bacillus halotolerans DY299 was is...
Cai-Xia Deng, Yan Zhao, Qishi Qishi et al.· Frontiers in Microbiology· 0 citations
This study aimed to review the scientific literature on dysbiosis characterized by Staphylococcus aureus enrichment and its implications for atopic dermatitis and other dermatoses. A narrative literature review was conducted using the PubMed database with the descriptors “Staphylococcus aureus” and “dysbiosis”, coverin...
Joyce Marinho de Souza, Guilherme Bartolomeu-Gonçalves, Rafaela Moraes Leal et al.· Dermato· 0 citations
Abstract Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by epidermal barrier dysfunction, immune dysregulation, oxidative stress, microbial dysbiosis, and persistent inflammation. Although current therapies have improved disease management, long-term treatment remains challenging because of...
I. Sopyan, Endang Lukitaningsih, R. Mauludin et al.· Drug Design, Development and...· 0 citations
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