Mycoplasma hominis and Gardnerella vaginalis display a significant synergistic relationship in bacterial vaginosis
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  • 作者:C. Cox ; A. P. Watt ; J. P. McKenna…
  • 刊名:European Journal of Clinical Microbiology & Infectious Diseases
  • 出版年:2016
  • 出版时间:March 2016
  • 年:2016
  • 卷:35
  • 期:3
  • 页码:481-487
  • 全文大小:332 KB
  • 参考文献:1.Mania-Pramanik J, Kerkar SC, Salvi VS (2009) Bacterial vaginosis: a cause of infertility? Int J STD AIDS 20(11):778–781CrossRef PubMed
    2.Oakeshott P, Hay P, Hay S, Steinke F, Rink E, Kerry S (2002) Association between bacterial vaginosis or chlamydial infection and miscarriage before 16 weeks’ gestation: prospective community based cohort study. BMJ (Clin Res Ed) 325(7376):1334CrossRef
    3.Leitich H, Kiss H (2007) Asymptomatic bacterial vaginosis and intermediate flora as risk factors for adverse pregnancy outcome. Best Pract Res Clin Obstet Gynaecol 21(3):375–390CrossRef PubMed
    4.Balashov SV, Mordechai E, Adelson ME, Gygax SE (2014) Identification, quantification and subtyping of Gardnerella vaginalis in noncultured clinical vaginal samples by quantitative PCR. J Med Microbiol 63(Pt 2):162–175CrossRef PubMed
    5.Fredricks DN, Fiedler TL, Marrazzo JM (2005) Molecular identification of bacteria associated with bacterial vaginosis. N Engl J Med 353(18):1899–1911CrossRef PubMed
    6.Lamont RF, Sobel JD, Akins RA, Hassan SS, Chaiworapongsa T, Kusanovic JP, Romero R (2011) The vaginal microbiome: new information about genital tract flora using molecular based techniques. BJOG: Int J Obstet Gynaecol 118(5):533–549CrossRef
    7.Cox C, McKenna JP, Watt AP, Coyle PV (2015) New assay for Gardnerella vaginalis loads correlates with Nugent scores and has potential in the diagnosis of bacterial vaginosis. J Med Microbiol 64(9):978–984. doi:10.​1099/​jmm.​0.​000118 CrossRef PubMed
    8.Ling Z, Kong J, Liu F, Zhu H, Chen X, Wang Y, Li L, Nelson KE, Xia Y, Xiang C (2010) Molecular analysis of the diversity of vaginal microbiota associated with bacterial vaginosis. BMC Genomics 11:488PubMedCentral CrossRef PubMed
    9.Haggerty CL, Totten PA, Ferris M, Martin DH, Hoferka S, Astete SG, Ondondo R, Norori J, Ness RB (2009) Clinical characteristics of bacterial vaginosis among women testing positive for fastidious bacteria. Sex Transm Infect 85(4):242–248PubMedCentral CrossRef PubMed
    10.Africa CW, Nel J, Stemmet M (2014) Anaerobes and bacterial vaginosis in pregnancy: virulence factors contributing to vaginal colonisation. Int J Environ Res Public Health 11(7):6979–7000PubMedCentral CrossRef PubMed
    11.Swidsinski A, Mendling W, Loening-Baucke V, Ladhoff A, Swidsinski S, Hale LP, Lochs H (2005) Adherent biofilms in bacterial vaginosis. Obstet Gynecol 106(5 Pt 1):1013–1023CrossRef PubMed
    12.Swidsinski A, Doerffel Y, Loening-Baucke V, Swidsinski S, Verstraelen H, Vaneechoutte M, Lemm V, Schilling J, Mendling W (2010) Gardnerella biofilm involves females and males and is transmitted sexually. Gynecol Obstet Invest 70(4):256–263CrossRef PubMed
    13.Eren AM, Zozaya M, Taylor CM, Dowd SE, Martin DH, Ferris MJ (2011) Exploring the diversity of Gardnerella vaginalis in the genitourinary tract microbiota of monogamous couples through subtle nucleotide variation. PLoS One 6(10):e26732PubMedCentral CrossRef PubMed
    14.Muzny CA, Schwebke JR (2015) Accuracy of self-report of sexual activity among adolescent girls: implications for interpretation of vaginal flora patterns. mBio 6(3):e00819. doi:10.​1128/​mBio.​00819-15 PubMedCentral CrossRef PubMed
    15.Swidsinski A, Loening-Baucke V, Swidsinski S, Verstraelen H (2015) Polymicrobial Gardnerella biofilm resists repeated intravaginal antiseptic treatment in a subset of women with bacterial vaginosis: a preliminary report. Arch Gynecol Obstet 291(3):605–609CrossRef PubMed
    16.Swidsinski A, Verstraelen H, Loening-Baucke V, Swidsinski S, Mendling W, Halwani Z (2013) Presence of a polymicrobial endometrial biofilm in patients with bacterial vaginosis. PLoS One 8(1):e53997PubMedCentral CrossRef PubMed
    17.Patterson JL, Girerd PH, Karjane NW, Jefferson KK (2007) Effect of biofilm phenotype on resistance of Gardnerella vaginalis to hydrogen peroxide and lactic acid. Am J Obstet Gynecol 197(2):170.e1–170.e7CrossRef
    18.Nugent RP, Krohn MA, Hillier SL (1991) Reliability of diagnosing bacterial vaginosis is improved by a standardized method of gram stain interpretation. J Clin Microbiol 29(2):297–301PubMedCentral PubMed
    19.Mohammadzadeh F, Dolatian M, Jorjani M, Alavi Majd H (2014) Diagnostic value of Amsel’s clinical criteria for diagnosis of bacterial vaginosis. Glob J Health Sci 7(3):8–14PubMed
    20.Rodrigues FS, Peixoto S, Adami F, da Costa Aguiar Alves B, de Sousa Gehrke F, Azzalis LA, de Campos Junqueira VB, Fonseca FL (2015) Proposal of a new cutoff for Nugent criteria in the diagnosis of bacterial vaginosis. J Microbiol Methods 115:144–146CrossRef PubMed
    21.Menard JP, Fenollar F, Henry M, Bretelle F, Raoult D (2008) Molecular quantification of Gardnerella vaginalis and Atopobium vaginae loads to predict bacterial vaginosis. Clin Infect Dis 47(1):33–43CrossRef PubMed
    22.Begum N, Muazzam N, Shamsuzzaman SM, Chowdhury A, Rashid A, Islam D (2010) Diagnosis of bacterial vaginosis by Acridine orange staining and its comparison to conventional methods and association of Gardnerella vaginalis with bacterial vaginosis. Bangladesh J Med Microbiol 4(1):37–42
    23.Oakeshott P, Aghaizu A, Hay P, Reid F, Kerry S, Atherton H, Simms I, Taylor-Robinson D, Dohn B, Jensen JS (2010) Is Mycoplasma genitalium in women the “New Chlamydia?” a community-based prospective cohort study. Clin Infect Dis: Off Publ Infect Dis Soc Am 51(10):1160–1166CrossRef
    24.Owen MK, Clenney TL (2004) Management of vaginitis. Am Fam Physician 70(11):2125–2132PubMed
    25.Lawton BA, Rose SB, Bromhead C, Gaitanos LA, MacDonald EJ, Lund KA (2008) High prevalence of Mycoplasma genitalium in women presenting for termination of pregnancy. Contraception 77(4):294–298CrossRef PubMed
    26.Manhart LE, Holmes KK, Hughes JP, Houston LS, Totten PA (2007) Mycoplasma genitalium among young adults in the United States: an emerging sexually transmitted infection. Am J Public Health 97(6):1118–1125PubMedCentral CrossRef PubMed
    27.Keane FE, Thomas BJ, Gilroy CB, Renton A, Taylor-Robinson D (2000) The association of Chlamydia trachomatis and Mycoplasma genitalium with non-gonococcal urethritis: observations on heterosexual men and their female partners. Int J STD AIDS 11(7):435–439CrossRef PubMed
    28.Lee SE, Romero R, Kim EC, Yoon BH (2009) A high Nugent score but not a positive culture for genital mycoplasmas is a risk factor for spontaneous preterm birth. J Matern Fetal Neonatal Med: Off J Eur Assoc Perinat Med Fed Asia Ocean Perinatal Soc Int Soc Perinat Obstetricians 22(3):212–217CrossRef
    29.Rosenstein IJ, Morgan DJ, Sheehan M, Lamont RF, Taylor-Robinson D (1996) Bacterial vaginosis in pregnancy: distribution of bacterial species in different gram-stain categories of the vaginal flora. J Med Microbiol 45(2):120–126CrossRef PubMed
    30.Thorsen E, Aanderud L, Aasen TB (1998) Effects of a standard hyperbaric oxygen treatment protocol on pulmonary function. Eur Respir J 12(6):1442–1445CrossRef PubMed
    31.Vancutsem E, Soetens O, Breugelmans M, Foulon W, Naessens A (2011) Modified real-time PCR for detecting, differentiating, and quantifying Ureaplasma urealyticum and Ureaplasma parvum. J Mol Diagn: JMD 13(2):206–212PubMedCentral CrossRef PubMed
    32.Chalker VJ, Jordan K, Ali T, Ison C (2009) Real-time PCR detection of the mg219 gene of unknown function of Mycoplasma genitalium in men with and without non-gonococcal urethritis and their female partners in England. J Med Microbiol 58(Pt 7):895–899CrossRef PubMed
    33.Pascual A, Jaton K, Ninet B, Bille J, Greub G (2010) New diagnostic real-time PCR for specific detection of mycoplasma hominis DNA. Int J Microbiol. doi:10.​1155/​2010/​317512 PubMedCentral PubMed
    34.Hay P, Ugwumadu A (2009) Detecting and treating common sexually transmitted diseases. Best Pract Res Clin Obstet Gynaecol 23(5):647–660CrossRef PubMed
    35.Liu CM, Hungate BA, Tobian AA, Ravel J, Prodger JL, Serwadda D, Kigozi G, Galiwango RM, Nalugoda F, Keim P, Wawer MJ, Price LB, Gray RH (2015) Penile microbiota and female partner bacterial vaginosis in Rakai, Uganda. mBio 6(3):e00589. doi:10.​1128/​mBio.​00589-15 PubMedCentral CrossRef PubMed
    36.Liu CM, Hungate BA, Tobian AA, Serwadda D, Ravel J, Lester R, Kigozi G, Aziz M, Galiwango RM, Nalugoda F, Contente-Cuomo TL, Wawer MJ, Keim P, Gray RH, Price LB (2013) Male circumcision significantly reduces prevalence and load of genital anaerobic bacteria. mBio 4(2):e00076PubMedCentral CrossRef PubMed
    37.Fethers K, Marks C, Mindel A, Estcourt CS (2000) Sexually transmitted infections and risk behaviours in women who have sex with women. Sex Transm Infect 76(5):345–349PubMedCentral CrossRef PubMed
    38.Bradshaw CS, Walker SM, Vodstrcil LA, Bilardi JE, Law M, Hocking JS, Fethers KA, Fehler G, Petersen S, Tabrizi SN, Chen MY, Garland SM, Fairley CK (2014) The influence of behaviors and relationships on the vaginal microbiota of women and their female partners: the WOW Health Study. J Infect Dis 209(10):1562–1572CrossRef PubMed
    39.Marrazzo JM, Antonio M, Agnew K, Hillier SL (2009) Distribution of genital Lactobacillus strains shared by female sex partners. J Infect Dis 199(5):680–683PubMedCentral CrossRef PubMed
    40.Schwebke JR, Desmond R (2007) Natural history of asymptomatic bacterial vaginosis in a high-risk group of women. Sex Transm Dis 34(11):876–877CrossRef PubMed
    41.Verstraelen H, Verhelst R, Vaneechoutte M, Temmerman M (2010) The epidemiology of bacterial vaginosis in relation to sexual behaviour. BMC Infect Dis 10:81PubMedCentral CrossRef PubMed
    42.Gray RH, Kigozi G, Serwadda D, Makumbi F, Nalugoda F, Watya S, Moulton L, Chen MZ, Sewankambo NK, Kiwanuka N, Sempijja V, Lutalo T, Kagayii J, Wabwire-Mangen F, Ridzon R, Bacon M, Wawer MJ (2009) The effects of male circumcision on female partners’ genital tract symptoms and vaginal infections in a randomized trial in Rakai, Uganda. Am J Obstet Gynecol 200(1):42.e1-42.e7PubMedCentral
    43.Castro J, Alves P, Sousa C, Cereija T, França Â, Jefferson KK, Cerca N (2015) Using an in-vitro biofilm model to assess the virulence potential of bacterial vaginosis or non-bacterial vaginosis Gardnerella vaginalis isolates. Sci Rep 5:11640PubMedCentral CrossRef PubMed
  • 作者单位:C. Cox (1) (2)
    A. P. Watt (1)
    J. P. McKenna (1)
    P. V. Coyle (1)

    1. Regional Virus Laboratory, Belfast Health and Social Care Trust, Belfast, Northern Ireland, UK
    2. Centre for Infection and Immunity, Queen’s University Belfast, Belfast, Northern Ireland, UK
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Biomedicine
    Medical Microbiology
    Internal Medicine
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1435-4373
文摘
Gardnerella vaginalis plays an important role in bacterial vaginosis (BV,) while the role of genital Mollicutes is less obvious. The diagnosis of BV by use of the current Gram stain Nugent score is also suboptimal for defining the role of Mollicutes that lack a cell wall. Since bacterial load and diversity is an important prerequisite for BV, real-time quantitative polymerase chain reaction (qPCR) assays enable these to be assessed. The purpose of this study was to define the role of genital Mollicutes and potential patterns of synergy with G. vaginalis in women with BV. Vaginal swabs from 130 women categorised by Nugent score as BV (n = 28), intermediate (n = 22) and non-BV (n = 80) were tested against four qPCR TaqMan assays targeting G. vaginalis, Mycoplasma hominis, M. genitalium, Ureaplasma urealyticum and U. parvum. Statistical analyses were used to compare bacterial prevalence and load between the three groups of women. Mycoplasma hominis and G. vaginalis co-infection was significantly more common in BV (60.7 %) compared to intermediate (36.4 %) and non-BV (8.8 %) Nugent scores (p < 0.001). Significantly higher loads of M. hominis (p = 0.001) and G. vaginalis (p < 0.001) were detected in women with BV and the respective loads in M. hominis and G. vaginalis co-infections displayed a significant positive correlation (p < 0.001; r = 0.60). No significant associations were seen with the other Mollicutes. The findings strengthen the evidence of a role for M. hominis in BV and a potential synergy with G. vaginalis. This synergy could be an important trigger of the condition and sexual contact the conduit for the transmission of an otherwise commensal bacterium that could initiate it.

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