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Mycoplasma and Ureaplasma in HIV-positive pregnant women
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Keywords

Pregnancy
HIV
Preterm birth
Mycoplasma
Ureaplasma

How to Cite

Mycoplasma and Ureaplasma in HIV-positive pregnant women. (2024). Electronic Journal Collection Health, 24(12), e18230. https://doi.org/10.25248/reas.e18230.2024

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Abstract

Objective: To compare the cervicovaginal prevalence of the Mollicutes species: Mycoplasma genitalium, M. hominis, Ureaplasma parvum, and U. urealyticum in pregnant women according to HIV infection status. Methods: This was a prospective longitudinal study that included 29 HIV-positive and 34 HIV-negative pregnant women. All participants completed a questionnaire to obtain sociodemographic and behavioral data. Cervicovaginal samples were collected and molecularly tested for the four Mollicutes species. Prevalence rates were compared between the study groups utilizing Fisher's exact test or Chi-square test. Results: The prevalence of Mollicutes was superior in HIV-positive participants (51.7%; n=15), when compared to the HIV-negative group (12.0%; n=4), (p<0.001). The most frequently species detected was U. parvum, present in 12 (41.4%) samples from HIV-positive pregnant women and 2 (6.0%) HIV-negative participant (p<0.01). The longitudinal analysis showed that pregnant women with HIV had a higher number of positive moments for Mollicutes compared to HIV-negative women (p = 0.01). Conclusion: The prevalence rates of Mollicutes reported in this study may guide new diagnostic strategies for these microorganisms, if clinically indicated.

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References

ALLANSON B, et al. Infection and foetal loss in the mid-second trimester of pregnancy. Aust NZJ Obstet Ginecol. 2010; 50: 221–5.

BOUJEMAA S, et al. Association between genital mycoplasmas (Ureaplasma urealyticum and Mycoplasma hominis) and HIV infection: a systematic review and meta-analysis. Aids reviwes. 2023; 25: 1-10.

BRAZIL. Ministry of Health. Department of Health Surveillance. Department of STDs, AIDS, and Viral Hepatitis. Clinical Protocol and Therapeutic Guidelines for Comprehensive Care for People with Sexually Transmitted Infections / Ministry of Health, Department of Health Surveillance, Department of STDs, AIDS, and Viral Hepatitis. – Brasília: Ministry of Health, 2015; 120: 55-61.

CARNEIRO FP, et al. Cervical Cytology of Samples with Ureaplasma urealyticum, Ureaplasma parvum, Chlamydia trachomatis, Trichomonas vaginalis, Mycoplasma hominis, and Neisseria gonorrhoeae Detected by Multiplex PCR. Biomed Res Int. 2020; 7045217.

CHANG-HUI S. Chapter 10 - Amplification of nucleic acids, Editor(s): Chang-Hui Shen, Diagnostic Molecular Biology (Second Edition), Academic Press, 2023; 259-293.

CHRISTOFOLINI DM, et al. Prevalence of cases of Mycoplasma hominis, Mycoplasma genitalium, Ureaplasma urealyticum and Chlamydia trachomatis in women with no gynecologic complaints. Reprod Med Biol. 2012; 11(4): 201-205.

DJIGMA F, et al. HIV-infected women of Burkina Faso: a “reservoir” of mycoplasma infection. J Infect Dev Ctries. 2011; 5: 176-8.

DONDERS GG, et al. Relationship of bacterial vaginosis and mycoplasmas to the risk of spontaneous abortion. Am J Obstet Gynaecol. 2000; 183: 431-7.

DURSKI M, et al. Comparison of two microscopic interpretations of vaginal microbiota with molecular profiling. Diagn Microbiol Infect Dis. 2022; 104: 115728.

EROGLU S e ASGIN N. Bacterial vaginosis and Mycoplasma infections in reproductive-age women: Clarifying the association with risk factors, Clínica e Investigación en Ginecología y Obstetricia. 2022; 49(4).

FOESSLEITNER P, et al. HIV infection as a risk factor for vaginal dysbiosis, bacterial vaginosis, and candidosis in pregnancy: A matched case-control study. Birth. 2021; 48(1): 139-146.

GALLO MF, et al. Bacterial vaginosis, gonorrhea, and chlamydial infection among women attending a sexually transmitted disease clinic: a longitudinal analysis of possible causal links. Ann Epidemiol. 2012; 22: 213-20.

GOLDENBERG RL, et al. Epidemiologia e causas de nascimento prematuro. Lancet. 2008; 371: 75 -84.

GÓMEZ-LOPEZ N, et al. A imunobiologia do trabalho de parto e nascimento pré-termo: inflamação intra-amniótica ou quebra da homeostase materno-fetal. Reprodução. 2022; 164(2): R11-R45.

GOVENDER L, et al. Bacterial vaginosis and associated infections in pregnancy. Int J Gynaecol Obstet. 1996; 55: 23-28.

HORNER P, et al. Should we be testing for urogenital Mycoplasma hominis, Ureaplasma parvum and Ureaplasma urealyticum in men and women? - a position statement from the European STI Guidelines Editorial Board. J Eur Acad Dermatol Venereol. 2018; 32(11): 1845-1851.

LARSEN B e HWANG J. Mycoplasma, Ureaplasma and Adverse PregnancyOutcomes: A fresh Look. Infectious Diseases in Obstetrics and Gynecology, 2010; 52: 521921.

LIMA LM, et al. Sexually Transmitted Infections Detected by Multiplex Real Time PCR in Asymptomatic Women and Association with Cervical Intraepithelial Neoplasia. Rev Bras Ginecol Obstet. 2018; 40(9): 540-546.

LINHARES IM, et al. Ureaplasma urealyticum colonization in the vaginal introitus and cervix of human immunodeficiency virus-infected women. Int J STD AIDS. 2000; 11(3): 176-9.

LIS R, et al. Mycoplasma genitalium Infection and Female Reproductive Tract Disease: A Meta-Analysis. Clinical Infectious Diseases Advance. 2015; 61: 418-26.

LOBÃO TN, et al. Ureaplasma urealyticum e U. parvum em mulheres sexualmente ativas atendidas em postos de saúde públicos no Brasil. Epidemiol Infect. 2017; 145: 2341-235.

MARCONI C, et al. Líquido amniótico Interleucina-1 beta e interleucina-6, mas não interleucina-8, correlacionam-se com a invasão microbiana da cavidade amniótica no trabalho de parto prematuro. Jornal Americano de Imunologia Reprodutiva. 2011; 65: 549-556.

MARSCHALKÓ M e AMBRUS L. A női alsó genitalis traktus mikrobiom tulajdonságai és szerepe [Characteristics and physiologic role of female lower genital microbiome]. Orv Hetil. 2023; 164(24): 923-930.

MATOS MS, et al. Clinical and uterine cervix characteristics of women with Mycoplasma and Ureaplasma in genital discharge. Rev Assoc Med Bras (1992). 2024; 70(6): 20240045.

MBU ER, et al. “Gynecological morbidity between HIV Positive Pregnant Women in Cameroon,” Reproductive Health. 2008; 5: 1-5.

MOHANTY T, et al. Effect of bacterial vaginosis on preterm birth: a meta-analysis. Arch Gynecol Obstet. 2023 Oct;308(4):1247-1255. doi: 10.1007/s00404-022-06817-5. Epub 2022; 36251068.

MUZNY CA, et al. State of the Art for Diagnosis of Bacterial Vaginosis. J Clin Microbiol. 2023; 61(8): 0083722.

NUGENT RP, et al. Reliability of diagnosing bacterial vaginosis is improved by a standardized method of gram stain interpretation. J Clin Microbiol. 1991; 29(2): 297-301.

NYEMBA DC, et al. Prevalence of curable STIs and bacterial vaginosis during pregnancy in sub-Saharan Africa: a systematic review and meta-analysis. Sex Transm Infect. 2022; 98(7): 484-491.

OLIVEIRA CNT, et al. Associação de aborto espontâneo e Ureaplasma parvum detectado no tecido placentário. Epidemiologia e Infecção. 2020; 148: 126.

PENNA IA, et al. Freqüência de infecção pelo Mycoplasma hominis e Ureaplasma urealyticum em mulheres inférteis e relação com repercussões clínicas. Rev. Bras. Ginecol. Obstet. 2005; 27(2): 64-8.

RUZMAN N, et al. The prevalence and the risk factors of the cervical colonization by the genital mycoplasmas among pregnant women from Eastern Croatia. Coll Antropol. 2013; 37(1): 135-40.

SARAF VS, et al. Microbioma vaginal: normalidade vs disbiose. Arco Microbiol. setembro de 2021; 203(7): 3793-3802.

SILVA J, et al. Genital mycoplasmas and ureaplasmas in cervicovaginal self-collected samples of reproductive-age women: prevalence and risk factors. International Journal of STD & AIDS. 2018; 29(10): 999-1006.

SMULLIN CP, et al. Prevalence and incidence of Mycoplasma genitalium in a cohort of HIV-infected and HIV-uninfected pregnant women in Cape Town, South Africa. Sex Transm Infect. 2020 ; 96(7): 501-508.

TIBALDI C, et al. Maternal risk factors for abnormal vaginal flora during pregnancy. Int J Gynaecol Obstet. 2016; 133(1): 89-93.

TRAVASSOS AGA et al. Prevalence of sexually transmitted infections among HIV-infected women in Brazil, The Brazilian Journal of Infectious Diseases. 2012; 16(6): 581-585.

TUDDENHAM S, et al. Association of Pregnancy and HIV Status With Molecular-Bacterial Vaginosis in Indian Women. J Acquir Immune Defic Syndr. 2023; 93(5): 422-430.

WORKOWSKI KA, et al. Sexually Transmitted Infections Treatment Guidelines, 2021. MMWR Recomm Rep. 2021; 70(4): 1-192.

YALEW GT, et al. Prevalence of bacterial vaginosis and aerobic vaginitis and their associated risk factors among pregnant women from northern Ethiopia: A cross-sectional study. PLoS One. 2022; 17(2): 0262692.