A potent enzybiotic against methicillin-resistant Staphylococcus aureus.
Alternative therapies
Bacteriophage
Endolysin
Enzybiotics
Staphylococcal infections
Journal
Virus genes
ISSN: 1572-994X
Titre abrégé: Virus Genes
Pays: United States
ID NLM: 8803967
Informations de publication
Date de publication:
Aug 2020
Aug 2020
Historique:
received:
06
11
2019
accepted:
24
04
2020
pubmed:
6
5
2020
medline:
28
1
2021
entrez:
6
5
2020
Statut:
ppublish
Résumé
Staphylococcus aureus is one of the most dreadful infectious agents, responsible for high mortality and morbidity in both humans and animals. The increased prevalence of multidrug-resistant (MDR) Staphylococcus aureus strains has limited the number of available treatment options, which calls for the development of alternative and effective modalities against MDR S. aureus. Endolysins are bacteriophage-derived antibacterials, which attack essential conserved elements of peptidoglycan that are vital for bacterial survival, making them promising alternatives or complements to existing antibiotics for tackling such infections. For developing endolysin lysin-methicillin-resistant-5 (LysMR-5) as an effective antimicrobial agent, we evaluated its physical and chemical characteristics, and its intrinsic antibacterial activity against staphylococcal strains, including methicillin-resistant Staphylococcus aureus (MRSA). In this study, we cloned, expressed, and purified LysMR-5 from S. aureus phage MR-5. In silico analysis revealed that LysMR-5 harbors two catalytic and one cell wall-binding domain. Biochemical characterization and LC-MS analysis showed that both catalytic domains were active and had no dependence on divalent ions for their action, Zn
Identifiants
pubmed: 32367411
doi: 10.1007/s11262-020-01762-4
pii: 10.1007/s11262-020-01762-4
doi:
Substances chimiques
Anti-Bacterial Agents
0
Peptidoglycan
0
Endopeptidases
EC 3.4.-
endolysin
EC 3.4.99.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM