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1.
Rev. Soc. Bras. Med. Trop ; 52: e20180348, 2019.
Article Dans Anglais | LILACS | ID: biblio-1013316

Résumé

Abstract We report the occurrence in Brazil of the bla NDM-1 gene in Acinetobacter pittii, prior to the previously described first reports regarding the species Providencia rettgeri and Enterobacter hormaechei. Clinical isolates were investigated by polymerase chain reaction followed by bidirectional sequencing, and species was confirmed by 16S rDNA sequencing and matrix-assisted laser desorption-ionization time-of-flight spectrometry. A. pittii carrying bla NDM-1 was confirmed in a patient with no national or international travel history, or transfer from another hospital. The findings warn of the possibility of silent spread of bla NDM-1 to the community.


Sujets)
Humains , Femelle , Sujet âgé de 80 ans ou plus , Acinetobacter/isolement et purification , bêta-Lactamases/isolement et purification , Infections à Acinetobacter/microbiologie , Antibactériens/usage thérapeutique , bêta-Lactamases/génétique , Brésil , Infections à Acinetobacter/traitement médicamenteux , Tests de sensibilité microbienne
2.
Mem. Inst. Oswaldo Cruz ; 111(1): 37-42, Jan. 2016. tab
Article Dans Anglais | LILACS | ID: lil-771076

Résumé

Cystic fibrosis (CF) patients with Burkholderia cepacia complex (Bcc) pulmonary infections have high morbidity and mortality. The aim of this study was to compare different methods for identification of Bcc species isolated from paediatric CF patients. Oropharyngeal swabs from children with CF were used to obtain isolates of Bcc samples to evaluate six different tests for strain identification. Conventional (CPT) and automatised (APT) phenotypic tests, polymerase chain reaction (PCR)-recA, restriction fragment length polymorphism-recA, recAsequencing, and matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) were applied. Bacterial isolates were also tested for antimicrobial susceptibility. PCR-recA analysis showed that 36 out of the 54 isolates were Bcc. Kappa index data indicated almost perfect agreement between CPT and APT, CPT and PCR-recA, and APT and PCR-recA to identify Bcc, and MALDI-TOF and recAsequencing to identify Bcc species. The recAsequencing data and the MALDI-TOF data agreed in 97.2% of the isolates. Based on recA sequencing, the most common species identified were Burkholderia cenocepacia IIIA (33.4%),Burkholderia vietnamiensis (30.6%), B. cenocepaciaIIIB (27.8%), Burkholderia multivorans (5.5%), and B. cepacia (2.7%). MALDI-TOF proved to be a useful tool for identification of Bcc species obtained from CF patients, although it was not able to identify B. cenocepacia subtypes.


Sujets)
Enfant , Enfant d'âge préscolaire , Femelle , Humains , Nourrisson , Mâle , Infections à Burkholderia/virologie , Burkholderia cepacia complex/génétique , Mucoviscidose/virologie , Techniques de typage bactérien , Protéines bactériennes/génétique , Burkholderia cepacia complex/classification , ADN bactérien/génétique , Partie orale du pharynx/virologie , Phénotype , Réaction de polymérisation en chaîne , Polymorphisme de restriction , Spectrométrie de masse MALDI
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