University of Córdoba (Spain)

About: University of Córdoba (Spain) is a education organization based out in Cordova, Spain. It is known for research contribution in the topics: Population & Catalysis. The organization has 12006 authors who have published 22998 publications receiving 537842 citations. The organization is also known as: University of Córdoba (Spain) & Universidad de Córdoba.

Parton densities and dipole cross-sections at small x in large nuclei

Abstract: Unintegrated gluon densities in nuclei, dipole-nucleus cross-sections and quark densities are numerically investigated in the high-color limit, with the scattering on a heavy nucleus exactly described by the sum of fan diagrams of BFKL pomerons. The initial condition for the evolution in rapidity is quickly forgotten, and the gluon density presents a “supersaturation” pattern, as previous studies indicated. Both dipole-nucleus cross-sections and quark densities present the expected saturation features. Identifying the position in transverse momentum l of the maximum of the gluon distribution with the saturation momentum $Q_{\mathrm{s}}(y,b)$ , at large rapidities all distributions depend on only one variable, $l/Q_{\mathrm{s}}(y,b)$ or $rQ_{\mathrm{s}}(y,b)$ .

Mixed infections and insect–pathogen interactions

Abstract: Most studies of insect–pathogen interactions consider the direct interaction between one disease agent and one species of host. However, given that hosts are subject to challenge from many pathogen ⁄ parasite species, mixed infections are probably common. In this study, using the desert locust and two species of fungal entomopathogen, we show how mixed infection with a largely avirulent pathogen can alter the virulence and reproduction of a second, highly virulent pathogen. We find that two strains of the avirulent pathogen vary in their interaction with the virulent pathogen, depending on the order of infection and environmental conditions. We propose that avirulent pathogens, which have largely been overlooked to date, could play a significant role in host– pathogen dynamics, with implications for biological control and evolution of virulence.

Genomics and Susceptibility Profiles of Extensively Drug-Resistant Pseudomonas aeruginosa Isolates from Spain.

Abstract: This study assessed the molecular epidemiology, resistance mechanisms, and susceptibility profiles of a collection of 150 extensively drug-resistant (XDR) Pseudomonas aeruginosa clinical isolates obtained from a 2015 Spanish multicenter study, with a particular focus on resistome analysis in relation to ceftolozane-tazobactam susceptibility. Broth microdilution MICs revealed that nearly all (>95%) of the isolates were nonsusceptible to piperacillin-tazobactam, ceftazidime, cefepime, aztreonam, imipenem, meropenem, and ciprofloxacin. Most of them were also resistant to tobramycin (77%), whereas nonsusceptibility rates were lower for ceftolozane-tazobactam (31%), amikacin (7%), and colistin (2%). Pulsed-field gel electrophoresis-multilocus sequence typing (PFGE-MLST) analysis revealed that nearly all of the isolates belonged to previously described high-risk clones. Sequence type 175 (ST175) was detected in all 9 participating hospitals and accounted for 68% (n = 101) of the XDR isolates, distantly followed by ST244 (n = 16), ST253 (n = 12), ST235 (n = 8), and ST111 (n = 2), which were detected only in 1 to 2 hospitals. Through phenotypic and molecular methods, the presence of horizontally acquired carbapenemases was detected in 21% of the isolates, mostly VIM (17%) and GES enzymes (4%). At least two representative isolates from each clone and hospital (n = 44) were fully sequenced on an Illumina MiSeq. Classical mutational mechanisms, such as those leading to the overexpression of the β-lactamase AmpC or efflux pumps, OprD inactivation, and/or quinolone resistance-determining regions (QRDR) mutations, were confirmed in most isolates and correlated well with the resistance phenotypes in the absence of horizontally acquired determinants. Ceftolozane-tazobactam resistance was not detected in carbapenemase-negative isolates, in agreement with sequencing data showing the absence of ampC mutations. The unique set of mutations responsible for the XDR phenotype of ST175 clone documented 7 years earlier were found to be conserved, denoting the long-term persistence of this specific XDR lineage in Spanish hospitals. Finally, other potentially relevant mutations were evidenced, including those in penicillin-binding protein 3 (PBP3), which is involved in β-lactam (including ceftolozane-tazobactam) resistance, and FusA1, which is linked to aminoglycoside resistance.