Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
J Glob Antimicrob Resist ; 8: 179-185, 2017 03.
Article in English | MEDLINE | ID: mdl-28232228

ABSTRACT

OBJECTIVES: Bacteriophages may represent a therapeutic alternative to treat infections caused by multidrug-resistant (MDR) pathogens. However, studies analysing their activity against MDR Enterobacteriaceae are limited. METHODS: The in vitro lytic activity of three commercial bacteriophage cocktails (PYO, INTESTI and Septaphage) was evaluated against 70 Escherichia coli and 31 Proteus spp. of human and non-human origin. Isolates were characterised by phenotypic and genotypic methods and included 82 MDR strains [44 extended-spectrum-ß-lactamase (ESBL)-producers (18 CTX-M-15-like, including ST131/ST648 E. coli); 27 plasmid-mediated AmpC ß-lactamase (pAmpC)-producers (23 CMY-2-like, including ST131 E. coli); 3 ESBL+pAmpC-producers; and 8 carbapenemase-producers]. Phage susceptibility was determined by the spot test. RESULTS: E. coli susceptibility to PYO, INTESTI and Septaphage was 61%, 67% and 9%, whereas that of Proteus spp. was 29%, 39% and 19%, respectively. For the subgroup of ESBL-producing E. coli/Proteus spp., the following susceptibility rates were recorded: PYO, 57%; INTESTI, 59%; and Septaphage, 11%. With regard to pAmpC-producers, 59%, 70% and 11% were susceptible to PYO, INTESTI and Septaphage, respectively. Five of eight carbapenemase-producers and three of four colistin-resistant E. coli were susceptible to PYO and INTESTI. CONCLUSIONS: This is the first study analysing the activity of the above three cocktails against well-characterised MDR E. coli and Proteus spp. The overall narrow spectrum of activity observed could be related to the absence of specific bacteriophages targeting these contemporary MDR strains that are spreading in different settings. Therefore, bacteriophages targeting emerging MDR pathogens need to be isolated and integrated in such biopreparations.


Subject(s)
Bacteriolysis , Bacteriophages/growth & development , Drug Resistance, Multiple, Bacterial , Escherichia coli Infections/microbiology , Escherichia coli/virology , Proteus Infections/microbiology , Proteus/virology , Animals , Bacteriological Techniques , Escherichia coli/isolation & purification , Escherichia coli/physiology , Escherichia coli Infections/veterinary , Humans , Proteus/isolation & purification , Proteus/physiology , Proteus Infections/veterinary
2.
Arch Virol ; 142(7): 1381-90, 1997.
Article in English | MEDLINE | ID: mdl-9267450

ABSTRACT

Out of 136 new phages, 80 (59%) are classified into 23 species according to morphology and physicochemical properties. Six new species are described and species beta 4, from a previous classification scheme, is renamed T1. The morphology of 36 phage species is schematically represented.


Subject(s)
Enterobacteriaceae/virology , Myoviridae/classification , Podoviridae/classification , Siphoviridae/classification , Coliphages/classification , Coliphages/ultrastructure , Enterobacter/virology , Klebsiella/virology , Myoviridae/ultrastructure , Podoviridae/ultrastructure , Proteus/virology , Salmonella Phages/classification , Salmonella Phages/ultrastructure , Serratia/virology , Siphoviridae/ultrastructure , Terminology as Topic , Yersinia/virology
SELECTION OF CITATIONS
SEARCH DETAIL
...