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Gardnerella vaginalis Subgroups Defined by cpn60 Sequencing and Sialidase Activity in Isolates from Canada, Belgium and Kenya.
Schellenberg, John J; Paramel Jayaprakash, Teenus; Withana Gamage, Niradha; Patterson, Mo H; Vaneechoutte, Mario; Hill, Janet E.
Afiliação
  • Schellenberg JJ; Department of Veterinary Microbiology, University of Saskatchewan, Saskatoon, Canada.
  • Paramel Jayaprakash T; Department of Veterinary Microbiology, University of Saskatchewan, Saskatoon, Canada.
  • Withana Gamage N; Department of Veterinary Microbiology, University of Saskatchewan, Saskatoon, Canada.
  • Patterson MH; Department of Veterinary Microbiology, University of Saskatchewan, Saskatoon, Canada.
  • Vaneechoutte M; Laboratory for Bacteriology Research, Ghent University, Ghent, Belgium.
  • Hill JE; Department of Veterinary Microbiology, University of Saskatchewan, Saskatoon, Canada.
PLoS One ; 11(1): e0146510, 2016.
Article em En | MEDLINE | ID: mdl-26751374
Increased abundance of Gardnerella vaginalis and sialidase activity in vaginal fluid is associated with bacterial vaginosis (BV), a common but poorly understood clinical entity associated with poor reproductive health outcomes. Since most women are colonized with G. vaginalis, its status as a normal member of the vaginal microbiota or pathogen causing BV remains controversial, and numerous classification schemes have been described. Since 2005, sequencing of the chaperonin-60 universal target (cpn60 UT) has distinguished four subgroups in isolate collections, clone libraries and deep sequencing datasets. To clarify potential clinical and diagnostic significance of cpn60 subgroups, we undertook phenotypic and molecular characterization of 112 G. vaginalis isolates from three continents. A total of 36 subgroup A, 33 B, 35 C and 8 D isolates were identified through phylogenetic analysis of cpn60 sequences as corresponding to four "clades" identified in a recently published study, based on sequencing 473 genes across 17 isolates. cpn60 subgroups were compared with other previously described molecular methods for classification of Gardnerella subgroups, including amplified ribosomal DNA restriction analysis (ARDRA) and real-time PCR assays designed to quantify subgroups in vaginal samples. Although two ARDRA patterns were observed in isolates, each was observed in three cpn60 subgroups (A/B/D and B/C/D). Real-time PCR assays corroborated cpn60 subgroups overall, but 13 isolates from subgroups A, B and D were negative in all assays. A putative sialidase gene was detected in all subgroup B, C and D isolates, but only in a single subgroup A isolate. In contrast, sialidase activity was observed in all subgroup B isolates, 3 (9%) subgroup C isolates and no subgroup A or D isolates. These observations suggest distinct roles for G. vaginalis subgroups in BV pathogenesis. We conclude that cpn60 UT sequencing is a robust approach for defining G. vaginalis subgroups within the vaginal microbiome.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gardnerella vaginalis / Vaginose Bacteriana / Chaperonina 60 / Neuraminidase Limite: Female / Humans País/Região como assunto: Africa / America do norte / Europa Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gardnerella vaginalis / Vaginose Bacteriana / Chaperonina 60 / Neuraminidase Limite: Female / Humans País/Região como assunto: Africa / America do norte / Europa Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá País de publicação: Estados Unidos