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Genomics ; 96(5): 290-302, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20654709

ABSTRACT

Here we report the use of a multi-genome DNA microarray to elucidate the genomic events associated with the emergence of the clonal variants of Haemophilus influenzae biogroup aegyptius causing Brazilian Purpuric Fever (BPF), an important pediatric disease with a high mortality rate. We performed directed genome sequencing of strain HK1212 unique loci to construct a species DNA microarray. Comparative genome hybridization using this microarray enabled us to determine and compare gene complements, and infer reliable phylogenomic relationships among members of the species. The higher genomic variability observed in the genomes of BPF-related strains (clones) and their close relatives may be characterized by significant gene flux related to a subset of functional role categories. We found that the acquisition of a large number of virulence determinants featuring numerous cell membrane proteins coupled to the loss of genes involved in transport, central biosynthetic pathways and in particular, energy production pathways to be characteristics of the BPF genomic variants.


Subject(s)
Fever/microbiology , Genetic Variation , Genome, Bacterial , Haemophilus influenzae/classification , Phylogeny , Purpura/microbiology , Bacterial Proteins/genetics , Brazil , Comparative Genomic Hybridization , Haemophilus Infections/microbiology , Haemophilus influenzae/genetics , Haemophilus influenzae/pathogenicity , Humans , Molecular Sequence Data , Oligonucleotide Array Sequence Analysis , Sequence Analysis, DNA , Virulence Factors/genetics
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