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1.
APMIS ; 129(11): 631-640, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34561922

RESUMO

Burkholderia cenocepacia complex is associated with high transmissibility, virulence, and poor prognosis in cystic fibrosis (CF) patients. However, extrapulmonary infections are rare. We investigated the genome of a B. cenocepacia IIIA isolated from a liver abscess in a Brazilian CF patient and compared it to strain J2315. The whole genome was sequenced, and contigs were annotated by Rapid Annotation using Subsystem Technology. The Pathosystems Resource Integration Center was used to map antimicrobial and virulence genes. The genomic island (GIs) analysis was performed using two prediction methods, and the presence of putative plasmids and insertion sequences (ISs) was investigated. The isolate was confirmed as B. cenocepacia IIIA to ST-28 (ET12 lineage). A total of 64 genes for antimicrobial resistance and 47 genes related to virulence were identified. Among the virulence factors, there was a predominance of factors related to the invasion mechanism, to the flagellar biosynthesis protein, and to the RNA polymerase sigma factor for flagellar operon (cdpA). Two IS families (IS3 and IS5) and only one plasmid were found. On average 56 GIs were predicted by at least one of the methods applied. Comparative analysis showed resistance mechanisms and virulence factors revealing invasive determinants used by B. cenocepacia IIIA (ET12) in the process of disease spread to other infection sites (extrapulmonary) of highly virulent strains in CF patients.


Assuntos
Infecções por Burkholderia/microbiologia , Burkholderia cenocepacia/genética , Fibrose Cística/microbiologia , Genoma Bacteriano/genética , Abscesso Hepático/microbiologia , Adolescente , Brasil , Infecções por Burkholderia/complicações , Burkholderia cenocepacia/classificação , Burkholderia cenocepacia/isolamento & purificação , Fibrose Cística/complicações , Elementos de DNA Transponíveis/genética , DNA Bacteriano/genética , Farmacorresistência Bacteriana/genética , Feminino , Genes Bacterianos/genética , Ilhas Genômicas/genética , Humanos , Abscesso Hepático/complicações , Plasmídeos/genética , Fatores de Virulência/genética
2.
Infect Genet Evol ; 73: 411-415, 2019 09.
Artigo em Inglês | MEDLINE | ID: mdl-31121306

RESUMO

Pseudomonas aeruginosa is a major health concern globally and treating infections caused by MDR-isolates unarguably a humongous challenge that remains an unmet need in modern medicine. To determine patterns and mechanisms of antimicrobial resistance and its spread over the years in Rio de Janeiro, Brazil, 88 P. aeruginosa isolates were selected from 1995 to 2015. Phenotypic and genotypic characterization of antimicrobial resistance was evaluated and isolates were submitted to clonality by PFGE and MLST. PFGE analysis showed a great variability of clonal groups mainly over the past 10 years of this study. STs predominant in the early years (ST804, ST1860, ST487 and ST1602) associated to multidrug resistance (MDR) phenotype were replaced by ST277, ST244, ST1945, ST1791 with extensive drug resistance (XDR) in last years, with significant increase in resistance to carbapenems, fluoroquinolones and aminoglycosides. Colistin resistance was detected in 3.5%. The main mechanisms of antimicrobial resistance were mutational mechanisms (mutations in oprD, mexT and gyrA genes). We found the ESBL genes blaTEM (n = 2), blaSHV (n = 3) and blaCTX (n = 1).The carbapenemases genes was present in ST277 (blaSPM, n = 3), ST1560 (blaKPC, n = 3) and ST1944 (blaKPC, n = 2). The 16S RNA methylase gene (rmtD) was found in five isolates belonged to ST277. In conclusion, molecular epidemiological investigation reveals an increase of antimicrobial resistance in P. aeruginosa over 21 years in Rio de Janeiro with higher population structure and occurrence of high risk clone in the last years. The mutational mechanisms of resistance were present in all XDR isolates.


Assuntos
Antibacterianos/uso terapêutico , Farmacorresistência Bacteriana Múltipla/genética , Infecções por Pseudomonas/tratamento farmacológico , Infecções por Pseudomonas/epidemiologia , Pseudomonas aeruginosa/efeitos dos fármacos , Brasil/epidemiologia , Genótipo , Humanos , Testes de Sensibilidade Microbiana/métodos , Tipagem de Sequências Multilocus/métodos , Mutação/genética , Infecções por Pseudomonas/microbiologia , Pseudomonas aeruginosa/genética
3.
J Med Microbiol ; 57(Pt 2): 244-245, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18201994

RESUMO

A case of a post-surgical patient who developed a fatal bloodstream infection caused by high-level vancomycin-resistant Enterococcus gallinarum is reported. The isolate was found to carry both the vanC1 and vanA genes. This is the first report of an invasive infection associated with a vanA E. gallinarum isolate in Brazil.


Assuntos
Bacteriemia/microbiologia , Enterococcus/efeitos dos fármacos , Enterococcus/isolamento & purificação , Complicações Pós-Operatórias/microbiologia , Resistência a Vancomicina/genética , Idoso , Brasil , Enterococcus/genética , Humanos , Masculino , Vancomicina/farmacologia
4.
J Clin Microbiol ; 45(12): 4077-80, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17942657

RESUMO

Burkholderia pseudomallei is rarely isolated from cystic fibrosis patients outside known areas of endemicity. We report the recovery of B. pseudomallei from the sputum of a cystic fibrosis patient who lives in Brazil. We highlight the importance of careful attention to unusual nonfermentative gram-negative rods in cystic fibrosis patients.


Assuntos
Burkholderia pseudomallei/isolamento & purificação , Fibrose Cística/complicações , Melioidose/microbiologia , Adolescente , Antibacterianos/uso terapêutico , Brasil , Burkholderia pseudomallei/genética , Burkholderia pseudomallei/fisiologia , Feminino , Humanos , Melioidose/tratamento farmacológico , RNA Bacteriano/genética , RNA Ribossômico 16S/genética , Análise de Sequência de DNA , Escarro/microbiologia
5.
Artigo em Inglês | LILACS-Express | LILACS, VETINDEX | ID: biblio-1469429

RESUMO

Mucoid Burkholderia cepacia morphotype emerged within a nine year follow-up of a cystic fibrosis patient. Clinical data suggested a linkage between the mucoid phenotype isolation and the deterioration of the patient's condition. Despite of the phenotypic variation, molecular typing showed that the patient was chronically infected with B. cepacia complex isolates belonging to a same genetic clone.


O presente trabalho descreve a emergência de cepas mucoides do complexo B. cepacia em um paciente com Fibrose Cística dentro de um acompanhamento bacteriológico prospectivo de nove anos. Os dados clínicos sugerem a associação entre o isolamento do morfotipo mucoide e a deterioração clínica do paciente. Apesar da variação fenotípica, os testes moleculares mostraram que o paciente manteve-se cronicamente infectado por cepas de mesma origem clonal.

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