Publication:
Microarray identification of Clostridium difficile core components and divergent regions associated with host origin

dc.contributor.authorTavan Janvilisrien_US
dc.contributor.authorJoy Scariaen_US
dc.contributor.authorAngela D. Thompsonen_US
dc.contributor.authorAinsley Nicholsonen_US
dc.contributor.authorBrandi M. Limbagoen_US
dc.contributor.authorLuis G. Arroyoen_US
dc.contributor.authorJ. Glenn Songeren_US
dc.contributor.authorYrjö T. Gröhnen_US
dc.contributor.authorYung Fu Changen_US
dc.contributor.otherCornell Universityen_US
dc.contributor.otherNational Center for Emerging and Zoonotic Infectious Diseasesen_US
dc.contributor.otherOntario Veterinary Collegeen_US
dc.contributor.otherUniversity of Arizonaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-13T06:24:25Z
dc.date.available2018-09-13T06:24:25Z
dc.date.issued2009-06-01en_US
dc.description.abstractClostridium difficile is a gram-positive, spore-forming enteric anaerobe which can infect humans and a wide variety of animal species. Recently, the incidence and severity of human C. difficile infection has markedly increased. In this study, we evaluated the genomic content of 73 C. difficile strains isolated from humans, horses, cattle, and pigs by comparative genomic hybridization with microarrays containing coding sequences from C. difficile strains 630 and QCD-32g58. The sequenced genome of C. difficile strain 630 was used as a reference to define a candidate core genome of C. difficile and to explore correlations between host origins and genetic diversity. Approximately 16% of the genes in strain 630 were highly conserved among all strains, representing the core complement of functional genes defining C. difficile. Absent or divergent genes in the tested strains were distributed across the entire C. difficile 630 genome and across all the predicted functional categories. Interestingly, certain genes were conserved among strains from a specific host species, but divergent in isolates with other host origins. This information provides insight into the genomic changes which might contribute to host adaptation. Due to a high degree of divergence among C. difficile strains, a core gene list from this study offers the first step toward the construction of diagnostic arrays for C. difficile. Copyright © 2009, American Society for Microbiology. All Rights Reserved.en_US
dc.identifier.citationJournal of Bacteriology. Vol.191, No.12 (2009), 3881-3891en_US
dc.identifier.doi10.1128/JB.00222-09en_US
dc.identifier.issn00219193en_US
dc.identifier.other2-s2.0-67549102416en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/27217
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67549102416&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.titleMicroarray identification of Clostridium difficile core components and divergent regions associated with host originen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67549102416&origin=inwarden_US

Files

Collections