Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 10 de 10
Filtrar
Mais filtros










Intervalo de ano de publicação
1.
Front Microbiol ; 10: 593, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30967856

RESUMO

Our objective was to improve current knowledge of sporadic (Spo) nosocomial Acinetobacter calcoaceticus-Acinetobacter baumannii (Acb) complex populations, and thus better understand the epidemiology of Spo and endemoepidemic (EE) strains. Between 1999 and 2010, 133 isolates of Spo Acb complex were obtained from a single hospital. Species were identified by gyrB-PCR, and via gyrB- and rpoB-sequencing. Clonal analysis was undertaken using pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing. Susceptibility to antimicrobial agents was determined by microdilution and E-tests. Carbapenemase genes were detected by PCR. One hundred and one PFGE types were detected. A. baumannii was the most common (67/101 PFGE types), followed by Acinetobacter pittii (22/101), Acinetobacter lactucae (6/101), and Acinetobacter calcoaceticus (2/101). gyrB, rpoB1, and rpoB2 sequencing returned 49, 13, and 16 novel sequences, respectively. Sixty-three sequence types (STs) (38 new STs and 66 new alleles) were detected; the most common were ST2 (29/133 isolates) and ST132 (14/133). Twenty-six OXA-51 allelic variants were detected, nine of which were novel. The PFGE types were generally susceptible (88/101) to all the tested antimicrobials; 3/101 were carbapenem-resistant due to the presence of the genetic structure ISAba2-bla OXA-58-like-ISAba3, and 2/101 were multidrug-resistant. It can be concluded that the examined Spo Acb complex population was mainly composed of A. baumannii. Many different clones were detected (with ST2 clearly dominant), all largely susceptible to antimicrobials; multidrug resistance was rare. In contrast, a previously examined EE Acb population was composed of just four expanding, multidrug-resistant A. baumannii clones -ST2, ST3, ST15, and ST80-.

2.
BMC Microbiol ; 15: 47, 2015 Feb 25.
Artigo em Inglês | MEDLINE | ID: mdl-25887224

RESUMO

BACKGROUND: Nosocomial outbreaks of multidrug-resistant Acinetobacter baumannii are of worldwide concern. Using pulsed-field gel electrophoresis (PFGE), multilocus sequence typing (MLST), and multiple locus variable number tandem repeat sequence (VNTR) analysis (MLVA), the present work examines the genetic diversity of the endemic and epidemic A. baumannii clones isolated in a single hospital over a twelve-year period. RESULTS: PFGE analysis of 405 A. baumannii-calcoaceticus complex isolates detected 15 A. baumannii endemic/epidemic PFGE types (EE1 to EE15) that grouped into five clusters: EE1-EE8, EE9, EE10, EE11 and EE12-EE15. The MLST sequence type (ST) distributions were: international clone II (ST-2) 60%, international clone III (ST-3) 26.7%, ST-15 6.7%, and ST-80 6.7%. MLVA-8Orsay returned 17 allelic profiles. The large (L) VNTR marker profiles were fully concordant with the detected STs, and concordant with 14 up to 15 PFGE types. Imipenem resistance was detected in five PFGE types; the prevalence of the bla OXA-58-like and bla OXA-40-like genes was 60% and 40% respectively. CONCLUSIONS: PFGE proved to be a vital tool for analysis of the temporal and spatial distribution of the clones. MLST and the VNTR L-markers grouped the isolates into clonal clusters. The wide diversity of MLVA small (S)-markers, however, did not permit clustering. The present results demonstrate the persistence of several endemic PFGE types in the hospital, the involvement of some of them in outbreaks, and the inter hospital transmission of extensively drug-resistant ST-15 and ST-80.


Assuntos
Infecções por Acinetobacter/epidemiologia , Infecções por Acinetobacter/microbiologia , Acinetobacter baumannii/classificação , Acinetobacter baumannii/isolamento & purificação , Infecção Hospitalar/epidemiologia , Infecção Hospitalar/microbiologia , Genótipo , Acinetobacter baumannii/genética , DNA Bacteriano/genética , Humanos , Repetições Minissatélites , Epidemiologia Molecular , Tipagem de Sequências Multilocus , Polimorfismo de Fragmento de Restrição , Centros de Atenção Terciária
3.
Matronas prof ; 15(4): 132-136, oct.-dic. 2014.
Artigo em Espanhol | IBECS | ID: ibc-131998

RESUMO

El estreptococo del grupo B (EGB) constituye la principal causa de morbimortalidad neonatal y de morbilidad materna durante el embarazo y el posparto. Coloniza el aparato digestivo y el genitourinario en un 10-30% de las gestantes, con una tasa de transmisión vertical del 50%. De entre los recién nacidos colonizados, un 1-2% desarrollará una sepsis grave precoz. Se ha realizado una revisión bibliográfica con el objetivo de conocer las estrategias de prevención de la infección neonatal por EGB. Los resultados ponen de manifiesto que las recomendaciones para su prevención consisten en el cribado universal prenatal de colonización por EGB mediante cultivo vaginorrectal a las 35-37 semanas, y la administración de profilaxis antibiótica intraparto a todas las embarazadas portadoras


Group B streptococcus (GBS) is the leading cause of neonatal morbimortality and maternal morbidity during pregnancy and postpartum.GBS colonizes the gastrointestinal and genitourinary apparatus in 10-30% of pregnant women, having a vertical transmission rate of 50%.1-2% of the colonized newborns develop early severe sepsis. A literature review has been performed in order to find the strategies for prevention of neonatal GBS infection. The results show that recommendations for prevention consist on universal prenatal screening for GBS colonization by vaginal and rectal culture at 35-37 weeks, and the administration of intrapartum antibiotic prophylaxis to all pregnant carriers


Assuntos
Humanos , Feminino , Gravidez , Infecções Estreptocócicas/prevenção & controle , Transmissão Vertical de Doenças Infecciosas/prevenção & controle , Streptococcus agalactiae/isolamento & purificação , Programas de Rastreamento/métodos , Antibioticoprofilaxia
4.
Med. clín (Ed. impr.) ; 140(2): 49-52, ene. 2013. tab
Artigo em Espanhol | IBECS | ID: ibc-109871

RESUMO

Fundamento y objetivo Estudios genéticos y farmacológicos sugieren que algunas vías de neurotransmisores influyen en la dependencia nicotínica. En esta línea se investigó el rol de 4 polimorfismos genéticos en genes relacionados con el control de impulsos: OPRM1, TPH1, ADRA2A y HTR1B. Se analizó el genotipo de una población de 490 individuos no emparentados de Cataluña y se compararon las frecuencias génicas de fumadores, ex fumadores y no fumadores con el fin de descubrir correlaciones. Material y método Todos los polimorfismos se genotiparon en cada grupo de población y se analizaron estadísticamente. Resultados Los datos obtenidos muestran que existe una relación entre el sexo, la edad y el locus TPH1, que indica una tendencia hacia una menor frecuencia del genotipo AA en los ex fumadores. Conclusiones El polimorfismo del triptófano «TPH1» parece desempeñar un papel como indicador de pronóstico en la deshabituación al tabaquismo (AU)


Background and objectives In line with genetic and pharmacological studies suggesting that neurotransmitter pathways play a role in nicotine dependence, research was conducted in connection with 4 genetic polymorphisms: OPRM1, TPH1, ADRA2A and HTR1B. This study compares the genotype and allele frequencies in 3 groups (non-smokers, former smokers and smokers) of unrelated individuals (n=490) from Catalonia (north east Spain) in order to find any relationship. Material and methods All polymorphisms were genotyped in each population group and statistical analysis was performed. Results Data obtained show that there is a relationship between sex, age and the TPH1 locus, indicating a trend towards a lower frequency of the AA genotype in former smokers for the TPH1 locus. Conclusions The results indicate that a role is played by the TPH1 polymorphism as an indicator of therapeutic failure in smoking cessation (AU)


Assuntos
Humanos , Polimorfismo Genético/genética , Fumar/genética , Genótipo , Predisposição Genética para Doença , Receptores Adrenérgicos/análise , Triptofano/genética
5.
Antimicrob Agents Chemother ; 57(1): 254-60, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23114769

RESUMO

Fourteen fluoroquinolone-resistant streptococcal isolates with recombinant DNA topoisomerase genes, preliminarily identified as pneumococci, were further characterized using phenotypic and genotypic approaches. Phenotypic tests classified them as atypical pneumococci. Phylogenetic relationships were analyzed by using the sequences of seven housekeeping alleles from these isolates and from isolates of Streptococcus pneumoniae, Streptococcus mitis, Streptococcus oralis, and Streptococcus pseudopneumoniae. Four isolates grouped with S. pneumoniae, seven grouped with S. pseudopneumoniae, and three grouped with S. mitis. These results generally agreed with those obtained with an optochin susceptibility test and with the organization of the atp operon chromosomal region, encoding the F(o)F(1) H(+)-ATPase (the target of optochin). All seven isolates grouping with S. pseudopneumoniae share the same spr1368-atpC-atpA gene order; all four grouping with S. pneumoniae share the spr1368-IS1239-atpC-atpA order, and two out of the three grouping with S. mitis share the spr1284-atpC-atpA order. In addition, evidence for recombination within the seven housekeeping alleles of the S. pseudopneumoniae population was provided by several methods: the index of association (0.4598, P < 0.001), the pairwise homoplasy index, and the split-decomposition method. This study confirms the existence of pneumococci among the alpha-hemolytic streptococci with DNA topoisomerase genes showing a mosaic structure and reveals a close relationship between atypical pneumococci and S. pseudopneumoniae.


Assuntos
Antibacterianos/farmacologia , Proteínas de Bactérias/genética , Cromossomos Bacterianos , Quinina/análogos & derivados , Recombinação Genética , Streptococcus/genética , Alelos , Proteínas de Bactérias/metabolismo , Técnicas de Tipagem Bacteriana , Mapeamento Cromossômico , DNA Topoisomerases/genética , DNA Topoisomerases/metabolismo , Genes Essenciais , Genótipo , Óperon , Fenótipo , Filogenia , ATPases Translocadoras de Prótons/genética , ATPases Translocadoras de Prótons/metabolismo , Quinina/farmacologia , Streptococcus/efeitos dos fármacos , Streptococcus/isolamento & purificação , Streptococcus mitis/efeitos dos fármacos , Streptococcus mitis/genética , Streptococcus mitis/isolamento & purificação , Streptococcus oralis/efeitos dos fármacos , Streptococcus oralis/genética , Streptococcus oralis/isolamento & purificação , Streptococcus pneumoniae/efeitos dos fármacos , Streptococcus pneumoniae/genética , Streptococcus pneumoniae/isolamento & purificação
6.
Med Clin (Barc) ; 140(2): 49-52, 2013 Jan 19.
Artigo em Espanhol | MEDLINE | ID: mdl-23177301

RESUMO

BACKGROUND AND OBJECTIVES: In line with genetic and pharmacological studies suggesting that neurotransmitter pathways play a role in nicotine dependence, research was conducted in connection with 4 genetic polymorphisms: OPRM1, TPH1, ADRA2A and HTR1B. This study compares the genotype and allele frequencies in 3 groups (non-smokers, former smokers and smokers) of unrelated individuals (n=490) from Catalonia (north east Spain) in order to find any relationship. MATERIAL AND METHODS: All polymorphisms were genotyped in each population group and statistical analysis was performed. RESULTS: Data obtained show that there is a relationship between sex, age and the TPH1 locus, indicating a trend towards a lower frequency of the AA genotype in former smokers for the TPH1 locus. CONCLUSIONS: The results indicate that a role is played by the TPH1 polymorphism as an indicator of therapeutic failure in smoking cessation.


Assuntos
Polimorfismo de Nucleotídeo Único , Fumar/genética , Tabagismo/genética , Triptofano Hidroxilase/fisiologia , Adulto , Idade de Início , Alelos , Feminino , Frequência do Gene , Predisposição Genética para Doença , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Neurotransmissores/fisiologia , Receptor 5-HT1B de Serotonina/genética , Receptores Adrenérgicos alfa 2/genética , Receptores Opioides mu/genética , Fumar/epidemiologia , Abandono do Hábito de Fumar , Espanha/epidemiologia , Tabagismo/epidemiologia , Tabagismo/fisiopatologia , Falha de Tratamento , Triptofano Hidroxilase/genética
7.
Environ Manage ; 48(1): 168-76, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21442293

RESUMO

Habitat fragmentation due to human activities is one of the most important causes of biodiversity loss. In Mediterranean areas the species have co-evolved with traditional farming, which has recently been replaced for more severe and aggressive practices. We use a methodological approach that enables the evaluation of the impact that agriculture and land use changes have for the conservation of sensitive species. As model species, we selected Linaria nigricans, a critically endangered plant from arid and semiarid ecosystems in south-eastern Spain. A chronosequence of the evolution of the suitable habitat for the species over more than 50 years has been reconstructed and several geometrical fragmentation indices have been calculated. A new index called fragmentation cadence (FC) is proposed to quantify the historical evolution of habitat fragmentation regardless of the habitat size. The application of this index has provided objective forecasting of the changes of each remnant population of L. nigricans. The results indicate that greenhouses and construction activities (mainly for tourist purposes) exert a strong impact on the populations of this endangered species. The habitat depletion showed peaks that constitute the destruction of 85% of the initial area in only 20 years for some populations of L. nigricans. According to the forecast established by the model, a rapid extinction could take place and some populations may disappear as early as the year 2030. Fragmentation-cadence analysis can help identify population units of primary concern for its conservation, by means of the adoption of improved management and regulatory measures.


Assuntos
Ecossistema , Espécies em Perigo de Extinção/tendências , Linaria , Extinção Biológica , Espanha
10.
J Clin Microbiol ; 43(4): 1694-8, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15814987

RESUMO

More than 50% of the nontypeable (NT) pneumococcal strains received in our laboratory for reference purposes are isolated in sporadic cases of conjunctivitis. To determine the genetic structure of the population of these NT conjunctival strains, we analyzed 75 pneumococci (40 NT and 35 typeable) isolated from conjunctivas and 30 (15 NT and 15 typeable) isolated from other sources. The NT and typeable conjunctival strains grouped in separate clusters, whereas NT and typeable pneumococci isolated from other sources were similarly distributed. NT conjunctival strains belonged to two well-differentiated clonal lineages. The first, represented by three newly described sequence types, featured fully antibiotic susceptible strains and appeared to be characteristic of conjunctival tissue; the second, represented by the previously described ST344, had a pattern of multiresistance to penicillin, tetracycline, and erythromycin and shared a genetic background with some NT strains isolated from other sources.


Assuntos
Túnica Conjuntiva/microbiologia , Conjuntivite Bacteriana/microbiologia , Infecções Pneumocócicas/microbiologia , Streptococcus pneumoniae/classificação , Streptococcus pneumoniae/genética , Técnicas de Tipagem Bacteriana , Eletroforese em Gel de Campo Pulsado , Sorotipagem , Streptococcus pneumoniae/isolamento & purificação
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...