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   <subfield code="a">Species distribution and susceptibility profile to fluconazole, voriconazole and MXP-4509 of 551 clinical yeast isolates from a Romanian multi-centre study</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[B. Minea, V. Nastasa, R. Moraru, A. Kolecka, M. Flonta, I. Marincu, A. Man, F. Toma, M. Lupse, B. Doroftei, N. Marangoci, M. Pinteala, T. Boekhout, M. Mares]</subfield>
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   <subfield code="a">This is the first multi-centre study regarding yeast infections in Romania. The aim was to determine the aetiological spectrum and susceptibility pattern to fluconazole, voriconazole and the novel compound MXP-4509. The 551 isolates were identified using routine laboratory methods, matrix-assisted laser desorption ionisation time-of-flight mass spectrometry (MALDI-TOF MS) and DNA sequence analysis. Susceptibility testing was performed using the European Committee for Antimicrobial Susceptibility Testing (EUCAST) method and breakpoints. The yeasts originated from superficial infections (SUP, 51.5%), bloodstream infections (BSI, 31.6%) and deep-seated infections (DEEP, 16.9%), from patients of all ages. Nine genera and 30 species were identified. The 20 Candida species accounted for 94.6% of all isolates. C. albicans was the overall leading pathogen (50.5%). Lodderomyces elongisporus is reported for the first time as a fungaemia cause in Europe. C. glabrata and Saccharomyces cerevisiae, as well as the non-Candida spp. and non-albicans Candida spp. groups, showed decreased fluconazole susceptibility (&lt;75%). The overall fluconazole resistance was 10.2%. C. krusei accounted for 27 of the 56 fluconazole-resistant isolates. The overall voriconazole resistance was 2.5% and was due mainly to C. glabrata and C. tropicalis isolates. Fluconazole resistance rates for the three categories of infection were similar to the overall value; voriconazole resistance rates differed: 4% for BSI, 3.2% for DEEP and 1.4% for SUP. The antifungal activity of MXP-4509 was superior to voriconazole against C. glabrata and many fluconazole-resistant isolates. There was a large percentage of non-albicans Candida isolates. A large part of the high fluconazole resistance was not acquired but intrinsic, resulting from the high percentage of C. krusei.</subfield>
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   <subfield code="u">Advanced Research Centre for Bionanoconjugates and Biopolymers, Institute of Macromolecular Chemistry &quot;Petru Poni”, 700487, Iasi, Romania</subfield>
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   <subfield code="u">Laboratory of Antimicrobial Chemotherapy, &quot;Ion Ionescu de la Brad” University, 8 Aleea Sadoveanu, P4, 1st floor, 700489, Iasi, Romania</subfield>
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   <subfield code="u">Department of Microbiology, Virology and Parasitology, University of Medicine and Pharmacy, 540139, Tirgu Mures, Romania</subfield>
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