Quantitation of all Four Gardnerella vaginalis Clades Detects Abnormal Vaginal Microbiota Characteristic of Bacterial Vaginosis More Accurately than Putative G. vaginalis Sialidase A Gene Count.


Journal

Molecular diagnosis & therapy
ISSN: 1179-2000
Titre abrégé: Mol Diagn Ther
Pays: New Zealand
ID NLM: 101264260

Informations de publication

Date de publication:
02 2019
Historique:
pubmed: 6 2 2019
medline: 21 6 2019
entrez: 6 2 2019
Statut: ppublish

Résumé

Bacterial vaginosis (BV) is a vaginal disorder characterized by a depletion of the normal lactobacillus-dominant microbiota and overgrowth of mainly anaerobic bacteria. The study aimed to evaluate the distribution and abundance of the Gardnerella vaginalis clades and sialidase A gene in vaginal samples from Russian women, and investigate if the G. vaginalis sialidase A gene count detects an abnormal vaginal microbiota characteristic of BV more accurately than G. vaginalis load. Vaginal samples from 299 non-pregnant patients of gynecological clinics were examined using Nugent scores and G. vaginalis clade and sialidase A gene quantitative real-time polymerase chain reactions (PCRs). Discriminatory power for BV microbiota was evaluated with receiver operating characteristic (ROC) analysis. The vaginal microbiota was characterized by Nugent scores as normal, intermediate, and BV microbiota in 162, 58, and 79 women, respectively. G. vaginalis clades 1, 2, 3, 4, and the sialidase A gene were detected in 56% (51-62%), 40% (34-45%), 20% (16-25%), 94% (91-96%), and 70% (64-75%) of vaginal samples, respectively. The frequency and abundance of clades 1, 2, 4, and the sialidase A gene as well as clade multiplicity were significantly associated with abnormal microbiota. The sialidase A gene was present in all multi-clade samples, in all single-clade samples comprising clades 1, 2, and 3, and in four of 84 (5% [2-12%]) samples comprising clade 4 only. Total G. vaginalis load showed significantly higher discriminatory power for abnormal microbiota than sialidase A gene count (areas under ROC curves 0.933 vs. 0.881; p = 0.0306). Quantifying all four G. vaginalis clades discriminates between BV microbiota and normal microbiota more accurately than measuring G. vaginalis sialidase A gene. Clade 4 is strongly associated with BV microbiota, despite most clade 4 strains lacking the sialidase A gene.

Sections du résumé

BACKGROUND
Bacterial vaginosis (BV) is a vaginal disorder characterized by a depletion of the normal lactobacillus-dominant microbiota and overgrowth of mainly anaerobic bacteria.
OBJECTIVES
The study aimed to evaluate the distribution and abundance of the Gardnerella vaginalis clades and sialidase A gene in vaginal samples from Russian women, and investigate if the G. vaginalis sialidase A gene count detects an abnormal vaginal microbiota characteristic of BV more accurately than G. vaginalis load.
METHODS
Vaginal samples from 299 non-pregnant patients of gynecological clinics were examined using Nugent scores and G. vaginalis clade and sialidase A gene quantitative real-time polymerase chain reactions (PCRs). Discriminatory power for BV microbiota was evaluated with receiver operating characteristic (ROC) analysis.
RESULTS
The vaginal microbiota was characterized by Nugent scores as normal, intermediate, and BV microbiota in 162, 58, and 79 women, respectively. G. vaginalis clades 1, 2, 3, 4, and the sialidase A gene were detected in 56% (51-62%), 40% (34-45%), 20% (16-25%), 94% (91-96%), and 70% (64-75%) of vaginal samples, respectively. The frequency and abundance of clades 1, 2, 4, and the sialidase A gene as well as clade multiplicity were significantly associated with abnormal microbiota. The sialidase A gene was present in all multi-clade samples, in all single-clade samples comprising clades 1, 2, and 3, and in four of 84 (5% [2-12%]) samples comprising clade 4 only. Total G. vaginalis load showed significantly higher discriminatory power for abnormal microbiota than sialidase A gene count (areas under ROC curves 0.933 vs. 0.881; p = 0.0306).
CONCLUSIONS
Quantifying all four G. vaginalis clades discriminates between BV microbiota and normal microbiota more accurately than measuring G. vaginalis sialidase A gene. Clade 4 is strongly associated with BV microbiota, despite most clade 4 strains lacking the sialidase A gene.

Identifiants

pubmed: 30721449
doi: 10.1007/s40291-019-00382-5
pii: 10.1007/s40291-019-00382-5
pmc: PMC6394432
doi:

Substances chimiques

RNA, Ribosomal, 16S 0
NEU1 protein, human EC 3.2.1.18
Neuraminidase EC 3.2.1.18

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

139-147

Références

Clin Infect Dis. 2001 Oct 1;33(7):1022-7
pubmed: 11528575
J Clin Microbiol. 1992 Mar;30(3):663-6
pubmed: 1551983
J Clin Microbiol. 2005 Mar;43(3):1304-8
pubmed: 15750100
J Clin Microbiol. 1991 Feb;29(2):297-301
pubmed: 1706728
Sex Transm Dis. 2007 Nov;34(11):864-9
pubmed: 17621244
J Clin Microbiol. 2007 Oct;45(10):3270-6
pubmed: 17687006
Clin Infect Dis. 2008 Jul 1;47(1):33-43
pubmed: 18513147
Bosn J Basic Med Sci. 2008 Aug;8(3):270-6
pubmed: 18816262
J Clin Microbiol. 2009 Mar;47(3):721-6
pubmed: 19144794
Semin Fetal Neonatal Med. 2009 Aug;14(4):200-3
pubmed: 19362525
Microbiology. 2010 Feb;156(Pt 2):392-9
pubmed: 19910411
Arch Gynecol Obstet. 2010 Apr;281(4):589-600
pubmed: 19967381
BMC Genomics. 2010 Jun 11;11:375
pubmed: 20540756
PLoS One. 2010 Aug 26;5(8):e12411
pubmed: 20865041
Gynecol Obstet Invest. 2010;70(4):256-63
pubmed: 21051845
Am J Obstet Gynecol. 2011 Feb;204(2):142.e1-9
pubmed: 21055720
J Clin Microbiol. 1990 Mar;28(3):422-5
pubmed: 2108991
Am J Obstet Gynecol. 2011 May;204(5):450.e1-7
pubmed: 21444061
Am J Obstet Gynecol. 2011 Aug;205(2):113.e1-6
pubmed: 21514555
Indian J Med Microbiol. 2011 Apr-Jun;29(2):165-8
pubmed: 21654113
FEMS Immunol Med Microbiol. 2012 Jun;65(1):69-77
pubmed: 22309200
Cell Microbiol. 2012 Aug;14(8):1174-82
pubmed: 22519819
J Bacteriol. 2012 Aug;194(15):3922-37
pubmed: 22609915
J Clin Microbiol. 1990 Dec;28(12):2761-4
pubmed: 2280007
PLoS One. 2012;7(8):e43009
pubmed: 22900080
Sex Transm Dis. 2013 Feb;40(2):117-22
pubmed: 23324974
Eur J Obstet Gynecol Reprod Biol. 2013 Apr;167(2):205-9
pubmed: 23375395
J Biol Chem. 2013 Apr 26;288(17):12067-79
pubmed: 23479734
PLoS One. 2013 Apr 09;8(4):e60670
pubmed: 23585843
J Med Microbiol. 2014 Feb;63(Pt 2):162-75
pubmed: 24200640
J Infect Dis. 2014 Aug 1;210(3):338-43
pubmed: 24511102
J Infect Dis. 2014 Aug 15;210(4):593-6
pubmed: 24596283
Sci Rep. 2015 Jun 26;5:11640
pubmed: 26113465
Diagn Microbiol Infect Dis. 2016 Jan;84(1):1-3
pubmed: 26514076
PLoS One. 2016 Jan 11;11(1):e0146510
pubmed: 26751374
APMIS. 2016 Dec;124(12):1099-1108
pubmed: 27714844
Eur J Clin Microbiol Infect Dis. 2017 Jul;36(7):1269-1278
pubmed: 28197729
PLoS One. 2017 Feb 24;12(2):e0171856
pubmed: 28234976
PLoS One. 2017 Feb 27;12(2):e0172522
pubmed: 28241058
BMC Infect Dis. 2017 Jun 5;17(1):394
pubmed: 28583109
PLoS One. 2018 Jul 12;13(7):e0200625
pubmed: 30001418
J Med Microbiol. 1986 Jun;21(4):357-9
pubmed: 3088281
J Clin Microbiol. 1984 Oct;20(4):677-9
pubmed: 6333436
FEMS Immunol Med Microbiol. 1997 May;18(1):61-6
pubmed: 9215588

Auteurs

Elena Shipitsyna (E)

Laboratory of Microbiology, D.O. Ott Research Institute of Obstetrics, Gynaecology and Reproductology, 3 Mendeleyevskaya Lane, 199034, St. Petersburg, Russia.

Anna Krysanova (A)

Laboratory of Microbiology, D.O. Ott Research Institute of Obstetrics, Gynaecology and Reproductology, 3 Mendeleyevskaya Lane, 199034, St. Petersburg, Russia.

Guzel Khayrullina (G)

Laboratory of Molecular Diagnostics and Epidemiology of Reproductive Tract Infections, Federal Budget Institute of Science "Central Research Institute for Epidemiology", 3a Novogireyevskaya St, 111123, Moscow, Russia.

Kira Shalepo (K)

Laboratory of Microbiology, D.O. Ott Research Institute of Obstetrics, Gynaecology and Reproductology, 3 Mendeleyevskaya Lane, 199034, St. Petersburg, Russia.

Alevtina Savicheva (A)

Laboratory of Microbiology, D.O. Ott Research Institute of Obstetrics, Gynaecology and Reproductology, 3 Mendeleyevskaya Lane, 199034, St. Petersburg, Russia.

Alexander Guschin (A)

Laboratory of Molecular Diagnostics and Epidemiology of Reproductive Tract Infections, Federal Budget Institute of Science "Central Research Institute for Epidemiology", 3a Novogireyevskaya St, 111123, Moscow, Russia.

Magnus Unemo (M)

WHO Collaborating Centre for Gonorrhoea and other STIs, Department of Laboratory Medicine, Microbiology, Örebro University Hospital, Södra Grevrosengatan 2, 701 85, Örebro, Sweden. magnus.unemo@regionorebrolan.se.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH