Kate E Dingle

Summary

Affiliation: University of Oxford
Country: UK

Publications

  1. ncbi Molecular characterization of Campylobacter jejuni clones: a basis for epidemiologic investigation
    Kate E Dingle
    Department of Zoology, University of Oxford, United Kingdom
    Emerg Infect Dis 8:949-55. 2002
  2. ncbi Sequence typing and comparison of population biology of Campylobacter coli and Campylobacter jejuni
    Kate E Dingle
    Nuffield Department of Clinical Sciences, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom
    J Clin Microbiol 43:340-7. 2005
  3. ncbi Multilocus sequence typing of Clostridium difficile
    David Griffiths
    Nuffield Department of Clinical Medicine, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom
    J Clin Microbiol 48:770-8. 2010
  4. ncbi Clinical Clostridium difficile: clonality and pathogenicity locus diversity
    Kate E Dingle
    Nuffield Department of Clinical Laboratory Sciences, Oxford University, John Radcliffe Hospital, Oxford, United Kingdom
    PLoS ONE 6:e19993. 2011
  5. ncbi Genetic relationships among reptilian and mammalian Campylobacter fetus strains determined by multilocus sequence typing
    Kate E Dingle
    Nuffield Department of Clinical Laboratory Sciences, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom
    J Clin Microbiol 48:977-80. 2010
  6. ncbi Stable and noncompetitive RNA internal control for routine clinical diagnostic reverse transcription-PCR
    Kate E Dingle
    Nuffield Department of Clinical Sciences, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom
    J Clin Microbiol 42:1003-11. 2004
  7. ncbi Mutation in a Lordsdale norovirus epidemic strain as a potential indicator of transmission routes
    Kate E Dingle
    Nuffield Department of Clinical Sciences, Oxford University, John Radcliffe Hospital, Oxford, United Kingdom, OX3 9DU
    J Clin Microbiol 42:3950-7. 2004
  8. ncbi Predictors of first recurrence of Clostridium difficile infection: implications for initial management
    David W Eyre
    NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK
    Clin Infect Dis 55:S77-87. 2012
  9. ncbi Molecular epidemiology of Clostridium difficile strains in children compared with that of strains circulating in adults with Clostridium difficile-associated infection
    Nicole Stoesser
    Nuffield Department of Clinical Medicine, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, UK
    J Clin Microbiol 49:3994-6. 2011
  10. ncbi Clostridium difficile mixed infection and reinfection
    David W Eyre
    NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom
    J Clin Microbiol 50:142-4. 2012

Collaborators

Detail Information

Publications17

  1. ncbi Molecular characterization of Campylobacter jejuni clones: a basis for epidemiologic investigation
    Kate E Dingle
    Department of Zoology, University of Oxford, United Kingdom
    Emerg Infect Dis 8:949-55. 2002
    ..These data demonstrate that the clonal complex, as defined by MLST, is an epidemiologically relevant unit for both long and short-term investigations of C. jejuni epidemiology...
  2. ncbi Sequence typing and comparison of population biology of Campylobacter coli and Campylobacter jejuni
    Kate E Dingle
    Nuffield Department of Clinical Sciences, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom
    J Clin Microbiol 43:340-7. 2005
    ..The use of a common MLST scheme allows direct comparisons of the population biology and molecular epidemiology of these two closely related human pathogens...
  3. ncbi Multilocus sequence typing of Clostridium difficile
    David Griffiths
    Nuffield Department of Clinical Medicine, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom
    J Clin Microbiol 48:770-8. 2010
    ..difficile in total stool DNA extracts without isolate culture. The direct (nonculture) MLST approach may prove useful as a rapid genotyping method, potentially benefiting individual patients and informing hospital infection control...
  4. ncbi Clinical Clostridium difficile: clonality and pathogenicity locus diversity
    Kate E Dingle
    Nuffield Department of Clinical Laboratory Sciences, Oxford University, John Radcliffe Hospital, Oxford, United Kingdom
    PLoS ONE 6:e19993. 2011
    ....
  5. ncbi Genetic relationships among reptilian and mammalian Campylobacter fetus strains determined by multilocus sequence typing
    Kate E Dingle
    Nuffield Department of Clinical Laboratory Sciences, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom
    J Clin Microbiol 48:977-80. 2010
    ..fetus, and there was evidence of recombination among members of these two groups. The reptile group represents a possible separate genomospecies capable of infecting humans...
  6. ncbi Stable and noncompetitive RNA internal control for routine clinical diagnostic reverse transcription-PCR
    Kate E Dingle
    Nuffield Department of Clinical Sciences, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom
    J Clin Microbiol 42:1003-11. 2004
    ..During routine testing of 324 consecutive unselected respiratory samples, the presence of the internal control ensured that genuine and false-negative results were distinguishable, thus increasing the diagnostic confidence in the assay...
  7. ncbi Mutation in a Lordsdale norovirus epidemic strain as a potential indicator of transmission routes
    Kate E Dingle
    Nuffield Department of Clinical Sciences, Oxford University, John Radcliffe Hospital, Oxford, United Kingdom, OX3 9DU
    J Clin Microbiol 42:3950-7. 2004
    ..4 to 13.6% in the outer P2 domain of the capsid, which also had a single-amino-acid insertion. Alterations to the capsid structure compared to previous noroviruses may explain the increased number of outbreaks during 2002 and 2003...
  8. ncbi Predictors of first recurrence of Clostridium difficile infection: implications for initial management
    David W Eyre
    NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK
    Clin Infect Dis 55:S77-87. 2012
    ..Risk factors, including increasing age, initial disease severity, and hospital exposure, predict CDI recurrence and identify patients likely to benefit from enhanced initial CDI treatment...
  9. ncbi Molecular epidemiology of Clostridium difficile strains in children compared with that of strains circulating in adults with Clostridium difficile-associated infection
    Nicole Stoesser
    Nuffield Department of Clinical Medicine, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, UK
    J Clin Microbiol 49:3994-6. 2011
    ..difficile-associated infections studied (n = 83). No children carried hypervirulent PCR ribotype 027. Children could participate in the transmission of some adult disease-causing genotypes...
  10. ncbi Clostridium difficile mixed infection and reinfection
    David W Eyre
    NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom
    J Clin Microbiol 50:142-4. 2012
    ..Of 109 sample pairs taken on the same day, 3 (3%) had different genotypes. Considering samples 0 to 7 days apart as the same CDI, 7% of cases had mixed infections with >1 genotype...
  11. ncbi Characterisation of Clostridium difficile hospital ward-based transmission using extensive epidemiological data and molecular typing
    A Sarah Walker
    National Institute for Health Research Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom
    PLoS Med 9:e1001172. 2012
    ..This study aimed to investigate ward-based transmission of C. difficile, by subdividing outbreaks into distinct lineages defined by multi-locus sequence typing (MLST)...
  12. ncbi Extended sequence typing of Campylobacter spp., United Kingdom
    Kate E Dingle
    John Radcliffe Hospital, Oxford, UK
    Emerg Infect Dis 14:1620-2. 2008
    ..975 to 0.992 among 620 clinical isolates from Oxfordshire, United Kingdom. This enhanced typing scheme enabled identification of clusters and retained data required for long-range epidemiologic comparisons of isolates...
  13. ncbi Host-associated genetic import in Campylobacter jejuni
    Noel D McCarthy
    Department of Zoology, University of Oxford, Oxford, United Kingdom
    Emerg Infect Dis 13:267-72. 2007
    ..Assignment using this signature enables improved prediction of source for pathogens that undergo frequent genetic recombination...
  14. ncbi A longitudinal 6-year study of the molecular epidemiology of clinical campylobacter isolates in Oxfordshire, United kingdom
    Alison J Cody
    Department of Zoology, University of Oxford, Oxford, UK
    J Clin Microbiol 50:3193-201. 2012
    ..These data also demonstrated that detailed surveillance at a single site captures information which reflects that observed nationally...
  15. ncbi Clonal nature of Campylobacter fetus as defined by multilocus sequence typing
    Marcel A P Van Bergen
    Animal Sciences Group, Division of Infectious Diseases, P.O. Box 65, 8200 AB Lelystad, The Netherlands
    J Clin Microbiol 43:5888-98. 2005
    ..Congruence was observed among C. fetus subspecies, sap type, and ST; therefore, MLST confirms that mammalian C. fetus is genetically stable, probably as result of the introduction of a single ancestral clone into a mammalian niche...
  16. ncbi Molecular evidence for dissemination of unique Campylobacter jejuni clones in CuraƧao, Netherlands Antilles
    Birgitta Duim
    Department of Medical Microbiology, Academic Medical Center, Amsterdam, The Netherlands
    J Clin Microbiol 41:5593-7. 2003
    ..Furthermore, given the observation that C. jejuni-associated diseases appear to be more severe from November to February, it can be speculated that this may be due to the presence of virulent clones with a limited span of circulation...
  17. ncbi Comparative genotyping of Campylobacter jejuni by amplified fragment length polymorphism, multilocus sequence typing, and short repeat sequencing: strain diversity, host range, and recombination
    Leo M Schouls
    Research Laboratory for Infectious Diseases, National Institute of Public Health and the Environment, Bilthoven, The Netherlands
    J Clin Microbiol 41:15-26. 2003
    ....