Tracing phylogenomic events leading to diversity of Haemophilus influenzae and the emergence of Brazilian Purpuric Fever (BPF)-associated clones

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 di...

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Veröffentlicht in:Genomics (San Diego, Calif.) Calif.), 2010-11, Vol.96 (5), p.290-302
Hauptverfasser: Papazisi, Leka, Ratnayake, Shashikala, Remortel, Brian G., Bock, Geoffrey R., Liang, Wei, Saeed, Alexander I., Liu, Jia, Fleischmann, Robert D., Kilian, Mogens, Peterson, Scott N.
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container_issue 5
container_start_page 290
container_title Genomics (San Diego, Calif.)
container_volume 96
creator Papazisi, Leka
Ratnayake, Shashikala
Remortel, Brian G.
Bock, Geoffrey R.
Liang, Wei
Saeed, Alexander I.
Liu, Jia
Fleischmann, Robert D.
Kilian, Mogens
Peterson, Scott N.
description 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.
doi_str_mv 10.1016/j.ygeno.2010.07.005
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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. 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subjects Bacterial Proteins - genetics
Biological and medical sciences
Brazil
Brazilian Purpuric Fever
Cell membranes
Comparative Genomic Hybridization
Comparative genomics
Fever - microbiology
Fundamental and applied biological sciences. Psychology
Genes. Genome
Genetic Variation
Genetics of eukaryotes. Biological and molecular evolution
Genome, Bacterial
Haemophilus
Haemophilus Infections - microbiology
Haemophilus influenzae
Haemophilus influenzae - classification
Haemophilus influenzae - genetics
Haemophilus influenzae - pathogenicity
Humans
Microarray
Molecular and cellular biology
Molecular genetics
Molecular Sequence Data
Oligonucleotide Array Sequence Analysis
Pathogen emergence
Phylogeny
Purpura - microbiology
Sequence Analysis, DNA
Virulence
Virulence Factors - genetics
title Tracing phylogenomic events leading to diversity of Haemophilus influenzae and the emergence of Brazilian Purpuric Fever (BPF)-associated clones
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