Cloning of 16S rRNA genes amplified from normal and disturbed vaginal microflora suggests a strong association between <it>Atopobium vaginae</it>, <it>Gardnerella vaginalis </it>and bacterial vaginosis

<p>Abstract</p> <p>Background</p> <p>The pathogenesis of bacterial vaginosis remains largely elusive, although some microorganisms, including <it>Gardnerella vaginalis</it>, are suspected of playing a role in the etiology of this disorder. Recently culture-i...

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Main Authors: De Ganck Catharine, Van Simaey Leen, Delanghe Joris, Verschraegen Gerda, Claeys Geert, Verstraelen Hans, Verhelst Rita, Temmerman Marleen, Vaneechoutte Mario
Format: Article
Language:English
Published: BMC 2004-04-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/4/16
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spelling doaj-7859f7dcdb254782a82c11ca9006a33d2020-11-25T00:14:39ZengBMCBMC Microbiology1471-21802004-04-01411610.1186/1471-2180-4-16Cloning of 16S rRNA genes amplified from normal and disturbed vaginal microflora suggests a strong association between <it>Atopobium vaginae</it>, <it>Gardnerella vaginalis </it>and bacterial vaginosisDe Ganck CatharineVan Simaey LeenDelanghe JorisVerschraegen GerdaClaeys GeertVerstraelen HansVerhelst RitaTemmerman MarleenVaneechoutte Mario<p>Abstract</p> <p>Background</p> <p>The pathogenesis of bacterial vaginosis remains largely elusive, although some microorganisms, including <it>Gardnerella vaginalis</it>, are suspected of playing a role in the etiology of this disorder. Recently culture-independent analysis of microbial ecosystems has proven its efficacy in characterizing the diversity of bacterial populations. Here, we report on the results obtained by combining culture and PCR-based methods to characterize the normal and disturbed vaginal microflora.</p> <p>Results</p> <p>A total of 150 vaginal swab samples from healthy women (115 pregnant and 35 non-pregnant) were categorized on the basis of Gram stain of direct smear as grade I (n = 112), grade II (n = 26), grade III (n = 9) or grade IV (n = 3). The composition of the vaginal microbial community of eight of these vaginal swabs (three grade I, two grade II and three grade III), all from non-pregnant women, were studied by culture and by cloning of the 16S rRNA genes obtained after direct amplification. Forty-six cultured isolates were identified by tDNA-PCR, 854 cloned 16S rRNA gene fragments were analysed of which 156 by sequencing, yielding a total of 38 species, including 9 presumptively novel species with at least five species that have not been isolated previously from vaginal samples. Interestingly, cloning revealed that <it>Atopobium vaginae </it>was abundant in four out of the five non-grade I specimens. Finally, species specific PCR for <it>A. vaginae </it>and <it>Gardnerella vaginalis </it>pointed to a statistically significant co-occurrence of both species in the bacterial vaginosis samples.</p> <p>Conclusions</p> <p>Although historically the literature regarding bacterial vaginosis has largely focused on <it>G. vaginalis </it>in particular, several findings of this study – like the abundance of <it>A. vaginae </it>in disturbed vaginal microflora and the presence of several novel species – indicate that much is to be learned about the composition of the vaginal microflora and its relation to the etiology of BV.</p> http://www.biomedcentral.com/1471-2180/4/16
collection DOAJ
language English
format Article
sources DOAJ
author De Ganck Catharine
Van Simaey Leen
Delanghe Joris
Verschraegen Gerda
Claeys Geert
Verstraelen Hans
Verhelst Rita
Temmerman Marleen
Vaneechoutte Mario
spellingShingle De Ganck Catharine
Van Simaey Leen
Delanghe Joris
Verschraegen Gerda
Claeys Geert
Verstraelen Hans
Verhelst Rita
Temmerman Marleen
Vaneechoutte Mario
Cloning of 16S rRNA genes amplified from normal and disturbed vaginal microflora suggests a strong association between <it>Atopobium vaginae</it>, <it>Gardnerella vaginalis </it>and bacterial vaginosis
BMC Microbiology
author_facet De Ganck Catharine
Van Simaey Leen
Delanghe Joris
Verschraegen Gerda
Claeys Geert
Verstraelen Hans
Verhelst Rita
Temmerman Marleen
Vaneechoutte Mario
author_sort De Ganck Catharine
title Cloning of 16S rRNA genes amplified from normal and disturbed vaginal microflora suggests a strong association between <it>Atopobium vaginae</it>, <it>Gardnerella vaginalis </it>and bacterial vaginosis
title_short Cloning of 16S rRNA genes amplified from normal and disturbed vaginal microflora suggests a strong association between <it>Atopobium vaginae</it>, <it>Gardnerella vaginalis </it>and bacterial vaginosis
title_full Cloning of 16S rRNA genes amplified from normal and disturbed vaginal microflora suggests a strong association between <it>Atopobium vaginae</it>, <it>Gardnerella vaginalis </it>and bacterial vaginosis
title_fullStr Cloning of 16S rRNA genes amplified from normal and disturbed vaginal microflora suggests a strong association between <it>Atopobium vaginae</it>, <it>Gardnerella vaginalis </it>and bacterial vaginosis
title_full_unstemmed Cloning of 16S rRNA genes amplified from normal and disturbed vaginal microflora suggests a strong association between <it>Atopobium vaginae</it>, <it>Gardnerella vaginalis </it>and bacterial vaginosis
title_sort cloning of 16s rrna genes amplified from normal and disturbed vaginal microflora suggests a strong association between <it>atopobium vaginae</it>, <it>gardnerella vaginalis </it>and bacterial vaginosis
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2004-04-01
description <p>Abstract</p> <p>Background</p> <p>The pathogenesis of bacterial vaginosis remains largely elusive, although some microorganisms, including <it>Gardnerella vaginalis</it>, are suspected of playing a role in the etiology of this disorder. Recently culture-independent analysis of microbial ecosystems has proven its efficacy in characterizing the diversity of bacterial populations. Here, we report on the results obtained by combining culture and PCR-based methods to characterize the normal and disturbed vaginal microflora.</p> <p>Results</p> <p>A total of 150 vaginal swab samples from healthy women (115 pregnant and 35 non-pregnant) were categorized on the basis of Gram stain of direct smear as grade I (n = 112), grade II (n = 26), grade III (n = 9) or grade IV (n = 3). The composition of the vaginal microbial community of eight of these vaginal swabs (three grade I, two grade II and three grade III), all from non-pregnant women, were studied by culture and by cloning of the 16S rRNA genes obtained after direct amplification. Forty-six cultured isolates were identified by tDNA-PCR, 854 cloned 16S rRNA gene fragments were analysed of which 156 by sequencing, yielding a total of 38 species, including 9 presumptively novel species with at least five species that have not been isolated previously from vaginal samples. Interestingly, cloning revealed that <it>Atopobium vaginae </it>was abundant in four out of the five non-grade I specimens. Finally, species specific PCR for <it>A. vaginae </it>and <it>Gardnerella vaginalis </it>pointed to a statistically significant co-occurrence of both species in the bacterial vaginosis samples.</p> <p>Conclusions</p> <p>Although historically the literature regarding bacterial vaginosis has largely focused on <it>G. vaginalis </it>in particular, several findings of this study – like the abundance of <it>A. vaginae </it>in disturbed vaginal microflora and the presence of several novel species – indicate that much is to be learned about the composition of the vaginal microflora and its relation to the etiology of BV.</p>
url http://www.biomedcentral.com/1471-2180/4/16
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