Dynamics and diversity of vaginal microbiota in bacterial vaginosis among Thai patients treated with metronidazole

被引:0
作者
Sirichoat, Auttawit [1 ,2 ]
Buppasiri, Pranom [3 ]
Faksri, Kiatichai [1 ,2 ]
Lulitanond, Viraphong [1 ,2 ]
机构
[1] Khon Kaen Univ, Fac Med, Dept Microbiol, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Res & Diagnost Ctr Emerging Infect Dis RCEID, Khon Kaen, Thailand
[3] Khon Kaen Univ, Fac Med, Dept Obstet & Gynecol, Khon Kaen, Thailand
关键词
Bacterial vaginosis; Vaginal microbiota; Metronidazole; 16S rRNA gene; Next-generation sequencing; Ion Torrent PGM; PREGNANCY OUTCOMES; PREVALENCE; WOMEN; ASSOCIATION; ACQUISITION; RECURRENCE; RISK;
D O I
10.1016/j.jiph.2024.102646
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Bacterial vaginosis (BV) is a significant global public health issue due to its high recurrence rate and association with various adverse health effects. Understanding the composition and dynamics of the vaginal microbiota (VMB) is essential for better understanding of vaginal health and for developing effective strategies to improve BV management. The study aimed to determine the composition and diversity of the VMB in Thai women with BV before and after metronidazole (MTZ) treatment, and in healthy women. Methods: Vaginal samples were collected from 20 women with BV (each sampled at three time points: preMTZ treatment, post-MTZ treatment and follow-up) and from 20 healthy women (each sampled once). The VMB was analyzed using 16S rRNA gene sequencing via next-generation sequencing on the Ion Torrent PGM platform. Results: The VMB in Thai women with BV was predominantly composed of Gardnerella, Prevotella and Fannyhessea (formerly Atopobium), while Lactobacillus dominated in healthy controls. Women with BV exhibited greater bacterial diversity and higher prevalence of anaerobic species compared to healthy women. There was higher diversity and abundance in the VMB from pre-MTZ samples, while post-MTZ and follow-up samples displayed lower diversity. In the follow-up stage, the VMB was divided into two subgroups: the larger cured subgroup, which shifted towards a Lactobacillus- dominated composition resembling healthy controls, and the small treatment-failure subgroup, which exhibited a Gardnerella-dominated profile similar to pre-MTZ. Conclusions: This study provides valuable insights into the structure and dynamics of the VMB in Thai women with BV before and after treatment, offering potential markers for predicting treatment outcomes. (c) 2025 The Author(s). Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/ 4.0/).
引用
收藏
页数:10
相关论文
共 50 条
  • [1] Prevalent bacterial vaginosis infection - a risk factor for incident sexually transmitted infections in women in Durban, South Africa
    Abbai, Nathlee S.
    Reddy, Tarylee
    Ramjee, Gita
    [J]. INTERNATIONAL JOURNAL OF STD & AIDS, 2016, 27 (14) : 1283 - 1288
  • [2] Anaerobes and Bacterial Vaginosis in Pregnancy: Virulence Factors Contributing to Vaginal Colonisation
    Africa, Charlene W. J.
    Nel, Janske
    Stemmet, Megan
    [J]. INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2014, 11 (07) : 6979 - 7000
  • [3] NONSPECIFIC VAGINITIS - DIAGNOSTIC-CRITERIA AND MICROBIAL AND EPIDEMIOLOGIC ASSOCIATIONS
    AMSEL, R
    TOTTEN, PA
    SPIEGEL, CA
    CHEN, KCS
    ESCHENBACH, D
    HOLMES, KK
    [J]. AMERICAN JOURNAL OF MEDICINE, 1983, 74 (01) : 14 - 22
  • [4] Mageeibacillus indolicus gen. nov., sp nov.: A novel bacterium isolated from the female genital tract
    Austin, Michele N.
    Rabe, Lorna K.
    Srinivasan, Sujatha
    Fredricks, David N.
    Wiesenfeld, Harold C.
    Hillier, Sharon L.
    [J]. ANAEROBE, 2015, 32 : 37 - 42
  • [5] Bacterial Vaginosis and the Risk of Trichomonas vaginalis Acquisition Among HIV-1-Negative Women
    Balkus, Jennifer E.
    Richardson, Barbra A.
    Rabe, Lorna K.
    Taha, Taha E.
    Mgodi, Nyaradzo
    Kasaro, Margaret Phiri
    Ramjee, Gita
    Hoffman, Irving F.
    Karim, Salim S. Abdool
    [J]. SEXUALLY TRANSMITTED DISEASES, 2014, 41 (02) : 123 - 128
  • [6] Bacterial vaginosis: A synthesis of the literature on etiology, prevalence, risk factors, and relationship with chlamydia and gonorrhea infections
    Bautista C.T.
    Wurapa E.
    Sateren W.B.
    Morris S.
    Hollingsworth B.
    Sanchez J.L.
    [J]. Military Medical Research, 3 (1)
  • [7] Recurrence of Bacterial Vaginosis Is Significantly Associated With Posttreatment Sexual Activities and Hormonal Contraceptive Use
    Bradshaw, Catriona S.
    Vodstrcil, Lenka A.
    Hocking, Jane S.
    Law, Matthew
    Pirotta, Marie
    Garland, Suzanne M.
    De Guingand, Deborah
    Morton, Anna N.
    Fairley, Christopher K.
    [J]. CLINICAL INFECTIOUS DISEASES, 2013, 56 (06) : 777 - 786
  • [8] High recurrence rates of bacterial vaginosis over the course of 12 months after oral metronidazole therapy and factors associated with recurrence
    Bradshaw, CS
    Morton, AN
    Hocking, J
    Garland, SM
    Morris, MB
    Moss, LM
    Horvath, LB
    Kuzevska, I
    Fairley, CK
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2006, 193 (11) : 1478 - 1486
  • [9] QIIME allows analysis of high-throughput community sequencing data
    Caporaso, J. Gregory
    Kuczynski, Justin
    Stombaugh, Jesse
    Bittinger, Kyle
    Bushman, Frederic D.
    Costello, Elizabeth K.
    Fierer, Noah
    Pena, Antonio Gonzalez
    Goodrich, Julia K.
    Gordon, Jeffrey I.
    Huttley, Gavin A.
    Kelley, Scott T.
    Knights, Dan
    Koenig, Jeremy E.
    Ley, Ruth E.
    Lozupone, Catherine A.
    McDonald, Daniel
    Muegge, Brian D.
    Pirrung, Meg
    Reeder, Jens
    Sevinsky, Joel R.
    Tumbaugh, Peter J.
    Walters, William A.
    Widmann, Jeremy
    Yatsunenko, Tanya
    Zaneveld, Jesse
    Knight, Rob
    [J]. NATURE METHODS, 2010, 7 (05) : 335 - 336
  • [10] Association between acquisition of herpes simplex virus type 2 in women and bacterial vaginosis
    Cherpes, TL
    Meyn, LA
    Krohn, MA
    Lurie, JG
    Hillier, SL
    [J]. CLINICAL INFECTIOUS DISEASES, 2003, 37 (03) : 319 - 325