Bacteriophage therapy for inhibition of multi drug-resistant uropathogenic bacteria: a narrative review.


Journal

Annals of clinical microbiology and antimicrobials
ISSN: 1476-0711
Titre abrégé: Ann Clin Microbiol Antimicrob
Pays: England
ID NLM: 101152152

Informations de publication

Date de publication:
26 Apr 2021
Historique:
received: 22 01 2021
accepted: 13 04 2021
entrez: 27 4 2021
pubmed: 28 4 2021
medline: 5 10 2021
Statut: epublish

Résumé

Multi-Drug Resistant (MDR) uropathogenic bacteria have increased in number in recent years and the development of new treatment options for the corresponding infections has become a major challenge in the field of medicine. In this respect, recent studies have proposed bacteriophage (phage) therapy as a potential alternative against MDR Urinary Tract Infections (UTI) because the resistance mechanism of phages differs from that of antibiotics and few side effects have been reported for them. Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis are the most common uropathogenic bacteria against which phage therapy has been used. Phages, in addition to lysing bacterial pathogens, can prevent the formation of biofilms. Besides, by inducing or producing polysaccharide depolymerase, phages can easily penetrate into deeper layers of the biofilm and degrade it. Notably, phage therapy has shown good results in inhibiting multiple-species biofilm and this may be an efficient weapon against catheter-associated UTI. However, the narrow range of hosts limits the use of phage therapy. Therefore, the use of phage cocktail and combination therapy can form a highly attractive strategy. However, despite the positive use of these treatments, various studies have reported phage-resistant strains, indicating that phage-host interactions are more complicated and need further research. Furthermore, these investigations are limited and further clinical trials are required to make this treatment widely available for human use. This review highlights phage therapy in the context of treating UTIs and the specific considerations for this application.

Identifiants

pubmed: 33902597
doi: 10.1186/s12941-021-00433-y
pii: 10.1186/s12941-021-00433-y
pmc: PMC8077874
doi:

Substances chimiques

Glycoside Hydrolases EC 3.2.1.-
capsular-polysaccharide galactohydrolase EC 3.2.1.87

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

30

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Auteurs

Zahra Chegini (Z)

Department of Microbiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Amin Khoshbayan (A)

Department of Microbiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Soheil Vesal (S)

Department of Molecular Genetics, Faculty of Basic Sciences and Advanced Technologies in Biology, University of Science and Culture, Tehran, Iran.

Alireza Moradabadi (A)

Department of Medical Laboratory Sciences, Khomein University of Medical Sciences, Khomein, Iran.

Ali Hashemi (A)

Department of Microbiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Aref Shariati (A)

Department of Microbiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran. arefshariati0111@sbmu.ac.ir.

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Classifications MeSH