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1.
Front Microbiol ; 10: 1446, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31333599

RESUMO

The Elizabethkingia are a genetically diverse genus of emerging pathogens that exhibit multidrug resistance to a range of common antibiotics. Two representative species, Elizabethkingia bruuniana and E. meningoseptica, were phenotypically tested to determine minimum inhibitory concentrations (MICs) for five antibiotics. Ultra-long read sequencing with Oxford Nanopore Technologies (ONT) and subsequent de novo assembly produced complete, gapless circular genomes for each strain. Alignment based annotation with Prokka identified 5,480 features in E. bruuniana and 5,203 features in E. meningoseptica, where none of these identified genes or gene combinations corresponded to observed phenotypic resistance values. Pan-genomic analysis, performed with an additional 19 Elizabethkingia strains, identified a core-genome size of 2,658,537 bp, 32 uniquely identifiable intrinsic chromosomal antibiotic resistance core-genes and 77 antibiotic resistance pan-genes. Using core-SNPs and pan-genes in combination with six machine learning (ML) algorithms, binary classification of clindamycin and vancomycin resistance achieved f1 scores of 0.94 and 0.84, respectively. Performance on the more challenging multiclass problem for fusidic acid, rifampin and ciprofloxacin resulted in f1 scores of 0.70, 0.75, and 0.54, respectively. By producing two sets of quality biological predictors, pan-genome genes and core-genome SNPs, from long-read sequence data and applying an ensemble of ML techniques, our results demonstrated that accurate phenotypic inference, at multiple AMR resolutions, can be achieved.

2.
J Microbiol Methods ; 159: 138-147, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30849421

RESUMO

Disruptive innovations in long-range, cost-effective direct template nucleic acid sequencing are transforming clinical and diagnostic medicine. A multidrug resistant strain and a pan-susceptible strain of Mannheimia haemolytica, isolated from pneumonic bovine lung samples, were sequenced at 146× and 111× coverage, respectively with Oxford Nanopore Technologies MinION. De novo assembly produced a complete genome for the non-resistant strain and a nearly complete assembly for the drug resistant strain. Functional annotation using RAST (Rapid Annotations using Subsystems Technology), CARD (Comprehensive Antibiotic Resistance Database) and ResFinder databases identified genes conferring resistance to different classes of antibiotics including ß-lactams, tetracyclines, lincosamides, phenicols, aminoglycosides, sulfonamides and macrolides. Resistance phenotypes of the M. haemolytica strains were determined by minimum inhibitory concentration (MIC) of the antibiotics. Sequencing with a highly portable MinION device corresponded to MIC assays with most of the antimicrobial resistant determinants being identified with as few as 5437 reads, except for the genes responsible for resistance to Fluoroquinolones. The resulting quality assemblies and AMR gene annotation highlight the efficiency of ultra-long read, whole-genome sequencing (WGS) as a valuable tool in diagnostic veterinary medicine.


Assuntos
Farmacorresistência Bacteriana , Mannheimia haemolytica/efeitos dos fármacos , Mannheimia haemolytica/genética , Sequenciamento por Nanoporos/métodos , Pneumonia Enzoótica dos Bezerros/microbiologia , Animais , Antibacterianos/farmacologia , Bovinos , Genoma Bacteriano , Mannheimia haemolytica/isolamento & purificação , Testes de Sensibilidade Microbiana , Pneumonia Enzoótica dos Bezerros/diagnóstico , Análise de Sequência de DNA , Sequenciamento Completo do Genoma
3.
Appl Environ Microbiol ; 75(16): 5417-20, 2009 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-19542340

RESUMO

We have developed a tool for controlled expression of heterologous or ectopic genes in the chestnut pathogen Cryphonectria parasitica using the promoter region from a putative copper-regulated transporter gene. In addition, we have found that expression control via this system is not affected by the virulence-attenuating hypovirus CHV1-EP713.


Assuntos
Ascomicetos , Cobre/farmacologia , Proteínas Fúngicas/genética , Regulação Fúngica da Expressão Gênica/efeitos dos fármacos , Doenças das Plantas/virologia , Ascomicetos/genética , Ascomicetos/metabolismo , Ascomicetos/patogenicidade , Ascomicetos/virologia , Proteínas Fúngicas/metabolismo , Proteínas de Fluorescência Verde/genética , Proteínas de Fluorescência Verde/metabolismo , Interações Hospedeiro-Patógeno , Dados de Sequência Molecular , Regiões Promotoras Genéticas , Vírus de RNA/fisiologia , Análise de Sequência de DNA , Virulência
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