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1.
Nat Commun ; 14(1): 1005, 2023 02 22.
Article in English | MEDLINE | ID: mdl-36813793

ABSTRACT

Acne vulgaris is a common neutrophil-driven inflammatory skin disorder in which Cutibacterium acnes (C. acnes) is known to play a key role. For decades, antibiotics have been widely employed to treat acne vulgaris, inevitably resulting in increased bacterial antibiotic resistance. Phage therapy is a promising strategy to combat the growing challenge of antibiotic-resistant bacteria, utilizing viruses that specifically lyse bacteria. Herein, we explore the feasibility of phage therapy against C. acnes. Eight novel phages, isolated in our laboratory, and commonly used antibiotics eradicate 100% of clinically isolated C. acnes strains. Topical phage therapy in a C. acnes-induced acne-like lesions mouse model affords significantly superior clinical and histological scores. Moreover, the decrease in inflammatory response was reflected by the reduced expression of chemokine CXCL2, neutrophil infiltration, and other inflammatory cytokines when compared with the infected-untreated group. Overall, these findings indicate the potential of phage therapy for acne vulgaris as an additional tool to conventional antibiotics.


Subject(s)
Acne Vulgaris , Phage Therapy , Animals , Mice , Anti-Bacterial Agents/pharmacology , Skin/microbiology , Drug Resistance, Bacterial , Propionibacterium acnes
3.
Acta Derm Venereol ; 100(17): adv00295, 2020 10 20.
Article in English | MEDLINE | ID: mdl-33021324

ABSTRACT

Antibiotic-resistant Cutibacterium acnes has been reported worldwide, but data from Israeli patients with acne is currently lacking. This study evaluated the antibiotic susceptibility of C. acnes, isolated from 50 Israeli patients with acne to commonly prescribed antibiotics, using the Epsilometer test (E-test). Matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) analysis, 16S rRNA sequencing and single locus sequence typing (SLST) molecular typing were used to identify and characterize C. acnes. Among 36 strains isolated, phylotype IA1 was most common. Resistance to at least one antibiotic was found in 30.6% of tested strains. Resistance rates were highest for erythromycin (25.0%), followed by doxycycline (19.4%), clindamycin (16.7%), minocycline (11.1%) and tetracycline (8.3%). Significant correlation was found between resistance to multiple antibiotics, with 5.6% of isolates resistant to all antibiotics tested. When reviewing resistances rate worldwide antibiotic resistance was found to be prevalent in Israel. Measures to limit the emergence of antibiotic-resistant strains of Cutibacterium acnes should be taken and alternative treatments should be sought.


Subject(s)
Acne Vulgaris , Propionibacterium acnes , Acne Vulgaris/diagnosis , Acne Vulgaris/drug therapy , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/therapeutic use , Humans , Israel/epidemiology , Microbial Sensitivity Tests , Propionibacterium acnes/genetics , RNA, Ribosomal, 16S/genetics
4.
Res Microbiol ; 169(9): 531-539, 2018 Nov.
Article in English | MEDLINE | ID: mdl-29777835

ABSTRACT

Clinical applications of bacteriophage therapy have been recently gathering significant attention worldwide, used mostly as rescue therapy in cases of near-fatal antibiotic failure. Thus, clinically relevant in-vivo models presenting both short- and long-term implications of phage therapy given as rescue treatment for fulminant infections are of highest importance. In this study, a cocktail consisting of two lytic bacteriophages was used to evaluate the therapeutic efficacy of phage therapy as a rescue treatment for severe septic peritonitis in a mouse model. We established that a single injection of the bacteriophage cocktail was sufficient to completely reverse a 100% mortality trend caused by Vancomycin-Resistant Enterococcus faecalis, with significant improvement in both the clinical state and laboratory test results, and without harmful effects on the microbiome. The combination of bacteriophages with a suboptimal antibiotic regimen imparts an additional beneficial effect on the treatment success.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Bacteriophages/physiology , Enterococcus faecalis/drug effects , Gram-Positive Bacterial Infections/therapy , Phage Therapy/methods , Animals , Anti-Bacterial Agents/administration & dosage , Disease Models, Animal , Drug Therapy, Combination/methods , Enterococcus faecalis/growth & development , Female , Gastrointestinal Microbiome/drug effects , Mice , Peritonitis/microbiology , Peritonitis/therapy , Phage Therapy/adverse effects , Stem Cells
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