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1.
Microb Drug Resist ; 18(3): 322-32, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22480295

ABSTRACT

Increasing antibiotic resistance of bacterial pathogens has drawn the attention to the potential use of bacteriophage endolysins as alternative antibacterial agents. Here we have identified, characterized, and studied the lytic potential of two endolysins, Lys168 and Lys170, from phages infecting Enterococcus faecalis. Lys168 and Lys170 belong to the cysteine, histidine-dependent amidohydrolases/peptidases (CHAP) and amidase-2 protein families, respectively. Lys168 is quite a unique enterococcal phage endolysin. It shares 95% amino acidic identity with the endolysin of Staphylococcus aureus phage SAP6, which in turn is distantly related to all known CHAP endolysins of S. aureus phages. Lys170 seems to be a natural chimera assembling catalytic and cell-wall-binding domains of different origin. Both endolysins showed a clear preference to act against E. faecalis and they were able to lyse a high proportion of clinical isolates of this species. Specifically, Lys168 and Lys170 lysed more than 70% and 90% of the tested isolates, respectively, which included a panel of diverse and typed strains representative of highly prevalent clonal complexes. Lys170 was active against all tested E. faecalis VRE strains. The quasi specificity toward E. faecalis is discussed considering the nature of the enzymes' functional domains and the structure of the cell wall peptidoglycan.


Subject(s)
Amidohydrolases/chemistry , Anti-Bacterial Agents/chemistry , Bacteriophages/chemistry , Enterococcus faecalis/drug effects , Viral Proteins/chemistry , Amidohydrolases/biosynthesis , Amidohydrolases/pharmacology , Amino Acid Sequence , Anti-Bacterial Agents/biosynthesis , Anti-Bacterial Agents/pharmacology , Cell Wall/chemistry , Cloning, Molecular , Enterococcus faecalis/chemistry , Enterococcus faecalis/virology , Host Specificity , Molecular Sequence Data , Peptidoglycan/chemistry , Protein Structure, Tertiary , Recombinant Proteins/biosynthesis , Recombinant Proteins/chemistry , Recombinant Proteins/pharmacology , Staphylococcus Phages/chemistry , Structure-Activity Relationship , Viral Proteins/biosynthesis , Viral Proteins/pharmacology
2.
Microb Drug Resist ; 18(3): 333-43, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22432707

ABSTRACT

Due to their bacterial lytic action, bacteriophage endolysins have recently gained great attention as a potential alternative to antibiotics in the combat of Gram-positive pathogenic bacteria, particularly those displaying multidrug resistance. However, large-scale production and purification of endolysins is frequently impaired due to their low solubility. In addition, a large number of endolysins appear to exhibit reduced lytic efficacy when compared with their action during phage infection. Here, we took advantage of the high solubility of two recently characterized enterococcal endolysins to construct chimeras targeting Staphylococcus aureus. The putative cell wall binding domain of these endolysins was substituted by that of a staphylococcal endolysin that showed poor solubility. Under appropriate conditions the resulting chimeras presented the high solubility of the parental enterococcal endolysins. In addition, they proved to be broadly active against a collection of the most relevant methicillin-resistant S. aureus epidemic clones and against other Gram-positive pathogens. Thus, fusion of endolysin domains of heterologous origin seems to be a suitable approach to design new potent endolysins with changed and/or extended lytic spectrum that are amenable to large-scale production.


Subject(s)
Amidohydrolases/chemistry , Anti-Bacterial Agents/chemistry , Enterococcus faecalis/genetics , Methicillin-Resistant Staphylococcus aureus/drug effects , Viral Proteins/chemistry , Amidohydrolases/genetics , Amidohydrolases/pharmacology , Anti-Bacterial Agents/pharmacology , Cell Wall/chemistry , Cloning, Molecular , Enterococcus faecalis/chemistry , Methicillin-Resistant Staphylococcus aureus/chemistry , Methicillin-Resistant Staphylococcus aureus/physiology , Peptidoglycan/chemistry , Protein Structure, Tertiary , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/pharmacology , Solubility , Staphylococcus Phages/chemistry , Structure-Activity Relationship , Viral Proteins/genetics , Viral Proteins/pharmacology
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