Evidence map›Paper›PMID 21335389›Full record

ArticleApplied and environmental microbiology2011

Development of a DNA microarray for enterococcal species, virulence, and antibiotic resistance gene determinations among isolates from poultry.

J Champagne, M S Diarra, H Rempel, E Topp, C W Greer, J Harel, L Masson

Abstract read
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Article in Applied and environmental microbiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

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0cells of the map it votes in
9citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Presence of Virulence Genes inBioMed research international · 2019
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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

J ChampagneBiotechnology Research Institute, National Research Council of Canada, 6100 Royalmount Ave., Montreal, Quebec H4P 2R2, Canada.
M S Diarra
H Rempel
E Topp
C W Greer
J Harel
L Masson

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A DNA microarray (Enteroarray) was designed with probes targeting four species-specific taxonomic identifiers to discriminate among 18 different enterococcal species, while other probes were designed to identify 18 virulence factors and 174 antibiotic resistance genes. In total, 262 genes were utilized for rapid species identification of enterococcal isolates, while characterizing their virulence potential through the simultaneous identification of endogenous antibiotic resistance and virulence genes. Enterococcal isolates from broiler chicken farms were initially identified by using the API 20 Strep system, and the results were compared to those obtained with the taxonomic genes atpA, recA, pheS, and ddl represented on our microarray. Among the 171 isolates studied, five different enterococcal species were identified by using the API 20 Strep system: Enterococcus faecium, E. faecalis, E. durans, E. gallinarum, and E. avium. The Enteroarray detected the same species as API 20 Strep, as well as two more: E. casseliflavus and E. hirae. Species comparisons resulted in 15% (27 isolates) disagreement between the two methods among the five API 20 Strep identifiable species and 24% (42 isolates) disagreement when considering the seven Enteroarray identified species. The species specificity of key antibiotic and virulence genes identified by the Enteroarray were consistent with the literature adding further robustness to the redundant taxonomic probe data. Sequencing of the cpn60 gene further confirmed the complete accuracy of the microarray results. The new Enteroarray should prove to be a useful tool to accurately genotype strains of enterococci and assess their virulence potential.

Indexed as

Drug Resistance, BacterialAnimalsBacterial Typing TechniquesBase SequenceChickensDNA, BacterialEnterococcusEscherichia coli ProteinsFimbriae ProteinsOligonucleotide Array Sequence AnalysisPeptide SynthasesPolymerase Chain ReactionRec A RecombinasesSequence Analysis, DNAVirulenceVirulence FactorsAtpA protein, E coliD-alanylalanine synthetaseDNA, BacterialEscherichia coli ProteinsFimbriae ProteinsPeptide SynthasesRec A RecombinasesVirulence Factors

Identifiers

PMID21335389
PMCPMC3126350

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.