Corynebacterium lowii sp. nov. and Corynebacterium oculi sp. nov., derived from human clinical disease and an emended description of Corynebacterium mastitidis

Kathryn Bernard(University of Manitoba), Ana Luisa Pacheco(Canadian Science Centre for Human and Animal Health), Courtney Loomer(Canadian Science Centre for Human and Animal Health), Tamara Burdz(Public Health Agency of Canada), Deborah Wiebe(Public Health Agency of Canada), Chris Huynh(Public Health Agency of Canada), Brynn Kaplen(Public Health Agency of Canada), Adam B. Olson(Canadian Science Centre for Human and Animal Health), Margo Cnockaert(Ghent University), Hiroshi Eguchi(Kindai University), Tomomi Kuwahara(Kagawa University), Haruyuki Nakayama‐Imaohji(Kagawa University), Hiroshi Shiota(Osaka Kaisei Hospital), Michaël Boudewijns(AZ Groeninge), Frederik Van Hoecke(AZ Sint-Lucas), Peter Vandamme(Ghent University)
INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY
April 5, 2016
Cited by 37

Abstract

Strains of members of the genus Corynebacterium derived from ophthalmologic patients in Japan, Belgium and Switzerland and found to be closely related to-, but distinguishable from Corynebacterium mastitidis by 16S rRNA gene sequencing, were characterized using biochemical, chemotaxonomic, MALDI-TOF mass spectrometry and antimicrobial susceptibility methods and DNA-DNA hybridization as well as by whole-genome sequencing (WGS). Based on this investigation, we describe Corynebacterium lowii sp. nov. and Corynebacterium oculi sp. nov., derived from human ocular specimens, as well as emend the description of Corynebacterium mastitidis. Type strains for these species are: C. lowii R-50085T (=LMG 28276T =CCUG 65815T) and C. oculi R-50187T (=LMG 28277T =CCUG 65816T). DNA G+C content was found to be 62.2 % (by HPLC) and 62.8 % (by WGS) for C. lowii R-50085T, 64.1 % (HPLC) and 64.8 % (WGS) for C. oculi R-50187T and 67.8 % (HPLC) for C. mastitidis LMG 19040T [=S-8T =CCUG 38654T =CECT 4843T =CIP 105509T =DSM 44356T =IFO (NBRC)16160T =JCM 12269T].


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