Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Comparative genomic hybridization of Clostridium difficile strains to identify markers of different ribotypes


ABSTRACT: Clostridium  difficile  (C. difficile) strains belonging to PCR ribotype 027, PFGE type NAP1, REA type B1 and toxinotype III, termed NAP1/027, have been implicated in the increased frequency of outbreaks of Clostridium difficile-associated diarrhoea (CDAD) in North America and Europe. The NAP1/027 strains appears to be more virulent with an increased mortality and frequency of relapse. Current  European C. difficile microarrays are designed to the first sequenced and annotated C. difficile complete genome  - strain 630 (ribotype 12). A high density oligonucleotide microarray was designed to C. difficile 630 (CD630) sequence  and extra probes  corresponding to two PCR ribotypes O27 strains C. difficile R20291 and QCD-32g58 were also included.  Comparative genomic hybridisation was used to identify markers of  ribotype 027 strains  and markers to identify CD630.  Strains hybridised to the array included the most prevalent ribotypes found in the UK and Europe (106 and 001) as well as the emerging hypervirulent ribotype 078.

ORGANISM(S): Clostridium difficile

SUBMITTER: Gemma Marsden 

PROVIDER: E-MTAB-162 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Array comparative hybridisation reveals a high degree of similarity between UK and European clinical isolates of hypervirulent Clostridium difficile.

Marsden Gemma L GL   Davis Ian J IJ   Wright Victoria J VJ   Sebaihia Mohammed M   Kuijper Ed J EJ   Minton Nigel P NP  

BMC genomics 20100621


<h4>Background</h4>Clostridium difficile is a Gram-positive, anaerobic, spore-forming bacterium that is responsible for C. difficile associated disease in humans and is currently the most common cause of nosocomial diarrhoea in the western world. This current status has been linked to the emergence of a highly virulent PCR-ribotype 027 strain. The aim of this work was to identify regions of sequence divergence that may be used as genetic markers of hypervirulent PCR-ribotype 027 strains and mark  ...[more]

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