Evidence map›Paper›PMID 19889901›Full record

ArticleJournal of clinical microbiology2010

Diversity of Staphylococcus species strains based on partial kat (catalase) gene sequences and design of a PCR-restriction fragment length polymorphism assay for identification and differentiation of coagulase-positive species (S. aureus, S. delphini, S. hyicus, S. intermedius, S. pseudintermedius, and S. schleiferi subsp. coagulans).

Giuseppe Blaiotta, Vincenzina Fusco, Danilo Ercolini, Olimpia Pepe, Salvatore Coppola

Abstract readEvaluation Study
In one paragraph

Article in Journal of clinical microbiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Article
  2. Review
  3. Antimicrobial Resistance of Coagulase-PositiveAntibiotics (Basel, Switzerland) · 2020
    Article
  4. Article
  5. Article
  6. High Occurrence ofJournal of environmental and public health · 2018
    Article
  7. Evolution of the Population Structure ofFrontiers in microbiology · 2018
    Article
  8. Review
  9. Molecular Epidemiology of Methicillin-ResistantFrontiers in microbiology · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Staphylococcal response to oxidative stress.Frontiers in cellular and infection microbiology · 2012
    Review
  17. Comparative genomics of the Staphylococcus intermedius group of animal pathogens.Frontiers in cellular and infection microbiology · 2012
    Article
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Giuseppe BlaiottaDepartment of Food Science, School of Agriculture, University of Naples Federico II, Via Università 100, 80055 Portici, Italy. blaiotta@unina.it
Vincenzina Fusco
Danilo Ercolini
Olimpia Pepe
Salvatore Coppola

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A set of degenerate PCR primers was designed and used to amplify and sequence about 75% of the catalase (kat) gene from each of 49 staphylococcal strains. In some strains of Staphylococcus xylosus, S. saprophyticus, and S. equorum, two catalase genes, katA and katB, were found. A phylogenetic tree was generated and showed diversities among 66 partial (about 900-bp) staphylococcal kat nucleotide sequences (including 17 sequences found in GenBank) representing 26 different species. The topology of this tree showed a distribution of staphylococcal species similar, but not identical, to those reported previously based on 16S rRNA, hsp60, sodA, rpoB, tuf, and gap genes. The kat gene sequences were less conserved than those of 16S rRNA, rpoB, hsp60, and tuf genes and slightly more conserved than those of the gap gene. Therefore, kat gene sequence analysis may provide an additional marker for inferring phylogenetic relationships of staphylococci. Moreover, the discrete nucleotide polymorphism revealed in this gene could be exploited for rapid, low-cost identification of staphylococcal species through PCR-restriction fragment length polymorphism (RFLP) analysis. In this study, a PCR-RFLP assay performed by using only the TaqI restriction enzyme was successfully developed for rapid unequivocal identification/differentiation, at species and subspecies levels, of coagulase-positive staphylococci (CPS). The assay was validated by testing the DNA from 100 staphylococcal strains, including reference and wild CPS strains isolated from different environments. This reliable, rapid, and low-cost approach (requiring about 6 h from DNA isolation to the achievement of results and <5 Euros for each strain tested) allowed unambiguous identification of all the strains assayed, including the newly described S. delphini and S. pseudintermedius CPS species.

Indexed as

Polymorphism, Restriction Fragment LengthBacteriological TechniquesCatalaseCluster AnalysisCoagulaseDNA, BacterialDNA FingerprintingDNA PrimersHumansMolecular Sequence DataPhylogenyPolymerase Chain ReactionPolymorphism, GeneticSequence Analysis, DNASequence HomologyStaphylococcal InfectionsCatalaseCoagulaseDNA, BacterialDNA Primers

Identifiers

PMID19889901
PMCPMC2812296

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.