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Defining the phylogenomics of Shigella species: a pathway to diagnostics.
Sahl, Jason W; Morris, Carolyn R; Emberger, Jennifer; Fraser, Claire M; Ochieng, John Benjamin; Juma, Jane; Fields, Barry; Breiman, Robert F; Gilmour, Matthew; Nataro, James P; Rasko, David A.
Affiliation
  • Sahl JW; University of Maryland School of Medicine, Institute for Genome Sciences, Department of Microbiology and Immunology, Baltimore, Maryland, USA Translational Genomics Research Institute, Flagstaff, Arizona, USA Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona
  • Morris CR; University of Maryland School of Medicine, Institute for Genome Sciences, Department of Microbiology and Immunology, Baltimore, Maryland, USA.
  • Emberger J; University of Maryland School of Medicine, Institute for Genome Sciences, Department of Microbiology and Immunology, Baltimore, Maryland, USA.
  • Fraser CM; University of Maryland School of Medicine, Institute for Genome Sciences, Department of Microbiology and Immunology, Baltimore, Maryland, USA.
  • Ochieng JB; KEMRI-CDC Kisumu, Kisumu, Kenya.
  • Juma J; KEMRI-CDC Kisumu, Kisumu, Kenya.
  • Fields B; CDC Kenya, KEMRI Headquarters, Nairobi, Kenya.
  • Breiman RF; CDC Kenya, KEMRI Headquarters, Nairobi, Kenya.
  • Gilmour M; National Microbiology, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
  • Nataro JP; Department of Pediatrics, University of Virginia, Charlottesville, Virginia, USA.
  • Rasko DA; University of Maryland School of Medicine, Institute for Genome Sciences, Department of Microbiology and Immunology, Baltimore, Maryland, USA drasko@som.umaryland.edu.
J Clin Microbiol ; 53(3): 951-60, 2015 Mar.
Article in En | MEDLINE | ID: mdl-25588655
ABSTRACT
Shigellae cause significant diarrheal disease and mortality in humans, as there are approximately 163 million episodes of shigellosis and 1.1 million deaths annually. While significant strides have been made in the understanding of the pathogenesis, few studies on the genomic content of the Shigella species have been completed. The goal of this study was to characterize the genomic diversity of Shigella species through sequencing of 55 isolates representing members of each of the four Shigella species S. flexneri, S. sonnei, S. boydii, and S. dysenteriae. Phylogeny inferred from 336 available Shigella and Escherichia coli genomes defined exclusive clades of Shigella; conserved genomic markers that can identify each clade were then identified. PCR assays were developed for each clade-specific marker, which was combined with an amplicon for the conserved Shigella invasion antigen, IpaH3, into a multiplex PCR assay. This assay demonstrated high specificity, correctly identifying 218 of 221 presumptive Shigella isolates, and sensitivity, by not identifying any of 151 diverse E. coli isolates incorrectly as Shigella. This new phylogenomics-based PCR assay represents a valuable tool for rapid typing of uncharacterized Shigella isolates and provides a framework that can be utilized for the identification of novel genomic markers from genomic data.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phylogeny / Shigella / Genetic Variation / Genome, Bacterial / Dysentery, Bacillary / Multiplex Polymerase Chain Reaction Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: J Clin Microbiol Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phylogeny / Shigella / Genetic Variation / Genome, Bacterial / Dysentery, Bacillary / Multiplex Polymerase Chain Reaction Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: J Clin Microbiol Year: 2015 Document type: Article