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1.
J Clin Microbiol ; 55(11): 3210-3218, 2017 11.
Article in English | MEDLINE | ID: mdl-28814586

ABSTRACT

Aspergillus fumigatus is the main species responsible for aspergillosis in humans. The diagnosis of aspergillosis remains difficult, and the rapid emergence of azole resistance in A. fumigatus is worrisome. The aim of this study was to validate the new MycoGENIE A. fumigatus real-time PCR kit and to evaluate its performance on clinical samples for the detection of A. fumigatus and its azole resistance. This multiplex assay detects DNA from the A. fumigatus species complex by targeting the multicopy 28S rRNA gene and specific TR34 and L98H mutations in the single-copy-number cyp51A gene of A. fumigatus The specificity of cyp51A mutation detection was assessed by testing DNA samples from 25 wild-type or mutated clinical A. fumigatus isolates. Clinical validation was performed on 88 respiratory samples obtained from 62 patients and on 69 serum samples obtained from 16 patients with proven or probable aspergillosis and 13 patients without aspergillosis. The limit of detection was <1 copy for the Aspergillus 28S rRNA gene and 6 copies for the cyp51A gene harboring the TR34 and L98H alterations. No cross-reactivity was detected with various fungi and bacteria. All isolates harboring the TR34 and L98H mutations were accurately detected by quantitative PCR (qPCR) analysis. With respiratory samples, qPCR results showed a sensitivity and specificity of 92.9% and 90.1%, respectively, while with serum samples, the sensitivity and specificity were 100% and 84.6%, respectively. Our study demonstrated that this new real-time PCR kit enables sensitive and rapid detection of A. fumigatus DNA and azole resistance due to TR34 and L98H mutations in clinical samples.


Subject(s)
Antifungal Agents/pharmacology , Aspergillus fumigatus/isolation & purification , Azoles/pharmacology , Invasive Pulmonary Aspergillosis/diagnosis , Microbiological Techniques/methods , Molecular Diagnostic Techniques/methods , Real-Time Polymerase Chain Reaction/methods , Aspergillus fumigatus/drug effects , Cytochrome P-450 Enzyme System/genetics , Drug Resistance, Fungal , Fungal Proteins/genetics , Humans , Invasive Pulmonary Aspergillosis/microbiology , Multiplex Polymerase Chain Reaction/methods , RNA, Ribosomal, 28S/genetics , Reagent Kits, Diagnostic , Sensitivity and Specificity
2.
Dalton Trans ; 40(1): 44-6, 2011 Jan 07.
Article in English | MEDLINE | ID: mdl-21082145

ABSTRACT

We report the synthesis of a superparamagnetic nanoparticle MNP (γ-Fe(2)O(3)/polymer) supported dendritic catalyst based on a bulky electron-rich phosphine Pd(II) complex. The high reactivity of this catalyst is described in a copper-free Sonogashira C-C cross-coupling reaction in water, and the significant role of surfactant additives is highlighted in the recovery study.

3.
Chemistry ; 15(46): 12636-43, 2009 Nov 23.
Article in English | MEDLINE | ID: mdl-19839017

ABSTRACT

A metallodendron functionalized with dicyclohexyldiphosphino palladium complex was synthesized. The metallodendron was grafted onto core-shell superparamagnetic nanoparticles (gamma-Fe(2)O(3)/polymer, 200-500 nm) to give optimal catalytic reactivity in cross-coupling reactions. The grafted nanoparticles were used as recoverable and reusable catalysts for Suzuki C--C cross-coupling reactions. They showed remarkable reactivity towards iodo- and bromoarenes under mild conditions, and unprecedented reactivity towards chloroarenes. On completion of the catalytic reaction, the catalysts were readily recovered by using a simple magnet to attract the superparamagnetic grafted nanoparticles. Catalysts were recovered more than 25 times with almost no discernable loss of reactivity.

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