APA
Saralegui, Claudia & Herencias, Cristina & Halperin, Ana Verónica & Caballero, Juan de Dios & Pérez¿Viso, Blanca & Salgado, Sergio & Lanza, Val F. & Cantón, Rafael & Baquero, Fernando & Prieto, M.Auxiliadora & del Campo, Rosa (2022 ) .Strain-specifc predation of Bdellovibrio bacteriovorus on Pseudomonas aeruginosa with a higher range for cystic fbrosis than for bacteremia isolates.
ISO 690
Saralegui, Claudia & Herencias, Cristina & Halperin, Ana Verónica & Caballero, Juan de Dios & Pérez¿Viso, Blanca & Salgado, Sergio & Lanza, Val F. & Cantón, Rafael & Baquero, Fernando & Prieto, M.Auxiliadora & del Campo, Rosa. 2022 .Strain-specifc predation of Bdellovibrio bacteriovorus on Pseudomonas aeruginosa with a higher range for cystic fbrosis than for bacteremia isolates.
https://hdl.handle.net/20.500.12080/45115
Resumen:
This work aimed to evaluate the predatory activity of Bdellovibrio bacteriovorus 109J on clinical
isolates of Pseudomonas aeruginosa selected from well-characterized collections of cystic fbrosis
(CF) lung colonization (n= 30) and bloodstream infections (BSI) (n= 48) including strains selected by
genetic lineage (frequent and rare sequence types), antibiotic resistance phenotype (susceptible
and multidrug-resistant isolates), and colony phenotype (mucoid and non-mucoid isolates). The
intraspecies predation range (I-PR) was defned as the proportion of susceptible strains within the
entire collection. In contrast, the predation efciency (PE) is the ratio of viable prey cells remaining
after predation compared to the initial inoculum. I-PR was signifcantly higher for CF (67%) than for
BSI P. aeruginosa isolates (35%) probably related to an environmental origin of CF strains whereas
invasive strains are more adapted to humans. I-PR correlation with bacterial features such as mucoid
morphotype, genetic background, or antibiotic susceptibility profle was not detected. To test
the possibility of increasing I-PR of BSI isolates, a polyhydroxyalkanoate depolymerase defcient
B. bacteriovorus bd2637 mutant was used. Global median I-PR and PE values remained constant for
both predators, but 31.2% of 109J-resistant isolates were susceptible to the mutant, and 22.9% of
109J-susceptible isolates showed resistance to predation by the mutant, pointing to a predator¿
prey specifcity process. The potential use of predators in the clinical setting should be based on the
determination of the I-PR for each species, and the PE of each particular target strain.