Yi, J, Yoon, BH, Kim, EC. Detection and biovar discrimination of Ureaplasma urealyticum by real-time PCR. Molecular and Cellular Probes
2005; 19(4): 255–260.
Volgmann, T, Ohlinger, R, Panzig, B.
Ureaplasma urealyticum-harmless commensal or underestimated enemy of human reproduction? A review. Archives of Gynecology and Obstetrics
2005; 273(3): 133–139.
Waites, KB, et al.
Congenital and opportunistic infections: ureaplasma species and Mycoplasma hominis
. Seminars in Fetal & Neonatal Medicine
2009; 14(4): 190–199.
Xiao, L, et al.
Detection and characterization of human Ureaplasma species and serovars by real-time PCR. Journal of Clinical Microbiology
2010; 48(8): 2715–2723.
Ureaplasma infections in pre-term infants: recent information regarding the role of Ureaplasma species as neonatal pathogens. Korean Journal of Pediatrics
2010; 53(12): 989–993.
Doh, K, et al.
Differential vaginal expression of interleukin-1 system cytokines in the presence of Mycoplasma hominis and Ureaplasma urealyticum in pregnant women. Infectious Diseases in Obstetrics and Gynecology
2004; 12(2): 79–85.
Ryckman, KK, Williams, SM, Kalinka, J. Correlations of selected vaginal cytokine levels with pregnancy-related traits in women with bacterial vaginosis and mycoplasmas. Journal of Reproductive Immunology
2008; 78(2): 172–180.
Garcia, J, et al.
A Mycoplasma fermentans-derived synthetic lipopeptide induces AP-1 and NF-kappaB activity and cytokine secretion in macrophages via the activation of mitogen-activated protein kinase pathways. The Journal of Biological Chemistry
1998; 273(51): 34391–34398.
Kacerovsky, M, et al.
Amniotic fluid protein profiles of intraamniotic inflammatory response to Ureaplasma spp. and other bacteria. PloS One
2013; 8(3): e60399.
Ureaplasma species: role in neonatal morbidities and outcomes. Archives of Disease in Childhood Fetal and Neonatal Edition
2014; 99(1): F87–F92.
Campos, GB, et al.
Prevalence of Mycoplasma genitalium and Mycoplasma hominis in urogenital tract of Brazilian women. BMC Infectious Diseases
2015; 15: 60.
Busolo, F, et al.
Survival of genital mycoplasma on various bacteriological swabs and transport media. Bollettino Dell'istituto Sieroterapico Milanese
1981; 60(1): 31–40.
van Kuppeveld, FJ, et al.
Genus- and species-specific identification of mycoplasmas by 16S rRNA amplification. Applied and Environmental Microbiology
1992; 58(8): 2606–2615.
Cao, X, et al.
Two multiplex real-time TaqMan polymerase chain reaction systems for simultaneous detecting and serotyping of Ureaplasma parvum
. Diagnostic Microbiology and Infectious Disease
2007; 59(1): 109–111.
De Francesco, MA, et al.
Detection of Ureaplasma biovars and polymerase chain reaction-based subtyping of Ureaplasma parvum in women with or without symptoms of genital infections. European Journal of Clinical Microbiology & Infectious Diseases
2009; 28(6): 641–646.
Mgone, CS, Lupiwa, T, Yeka, W. High prevalence of Neisseria gonorrhoeae and multiple sexually transmitted diseases among rural women in the Eastern Highlands Province of Papua New Guinea, detected by polymerase chain reaction. Sexually Transmitted Diseases
2002; 29(12): 775–779.
Riley, DE, et al.
Development of a polymerase chain reaction-based diagnosis of Trichomonas vaginalis
. Journal of Clinical Microbiology
1992; 30(2): 465–472.
Zariffard, MR, et al.
Detection of bacterial vaginosis-related organisms by real-time PCR for Lactobacilli, Gardnerella vaginalis and Mycoplasma hominis
. FEMS Immunology and Medical Microbiology
2002; 34(4): 277–281.
Rodrigues, MM, et al.
Frequency of Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, Mycoplasma hominis and Ureaplasma species in cervical samples. Journal of Obstetrics and Gynaecology
2011; 31(3): 237–241.
Bao, T, et al.
Simultaneous detection of Ureaplasma parvum, Ureaplasma urealyticum, Mycoplasma genitalium and Mycoplasma hominis by fluorescence polarization. Journal of Biotechnology
2010; 150(1): 41–43.
Gupta, V, et al.
Detection and biovar discrimination of Ureaplasma urealyticum in Indian patients with genital tract infections. Diagnostic Microbiology and Infectious Disease
2008; 60(1): 95–97.
Humburg, J, et al.
Accuracy of urethral swab and urine analysis for the detection of Mycoplasma hominis and Ureaplasma urealyticum in women with lower urinary tract symptoms. Archives of Gynecology and Obstetrics
2012; 285(4): 1049–1053.
Xiao, L, et al.
Extensive horizontal gene transfer in ureaplasmas from humans questions the utility of serotyping for diagnostic purposes. Journal of Clinical Microbiology
2011; 49(8): 2818–2826.
Pereyre, S, et al.
Life on arginine for Mycoplasma hominis: clues from its minimal genome and comparison with other human urogenital mycoplasmas. PLoS Genetics
2009; 5(10): e1000677.
Knox, CL, et al.
Ureaplasma parvum and Ureaplasma urealyticum are detected in semen after washing before assisted reproductive technology procedures. Fertility and Sterility
2003; 80(4): 921–929.
Yoshida, T, et al.
Polymerase chain reaction-based subtyping of Ureaplasma parvum and Ureaplasma urealyticum in first-pass urine samples from men with or without urethritis. Sexually Transmitted Diseases
2005; 32(7): 454–457.
Tibaldi, C, et al.
Vaginal and endocervical microorganisms in symptomatic and asymptomatic non-pregnant females: risk factors and rates of occurrence. Clinical Microbiology and Infection
2009; 15(7): 670–679.
Jones, HP, et al.
Depletion of CD8+ T cells exacerbates CD4+ Th cell-associated inflammatory lesions during murine mycoplasma respiratory disease. Journal of Immunology
2002; 168(7): 3493–3501.
Yamazaki, T, et al.
Frequency of Chlamydia trachomatis in Ureaplasma-positive healthy women attending their first prenatal visit in a community hospital in Sapporo, Japan. BMC Infectious Diseases
Araujo, RSC, et al.
Prevalence and risk factors for Chlamydia trachomatis infection in adolescent females and young women in central Brazil. European Journal of Clinical Microbiology & Infectious Diseases
2006; 25(6): 397–400.
Guimaraes, EMB, et al.
Lack of utility of risk score and gynecological examination for screening for sexually transmitted infections in sexually active adolescents. BMC Medicine
Sutton, M, et al.
The prevalence of Trichomonas vaginalis infection among reproductive-age women in the United States, 2001–2004. Clinical Infectious Diseases
2007; 45(10): 1319–1326.
Ginocchio, CC, et al.
Prevalence of Trichomonas vaginalis and coinfection with Chlamydia trachomatis and Neisseria gonorrhoeae in the United States as determined by the Aptima Trichomonas vaginalis Nucleic Acid Amplification Assay. Journal of Clinical Microbiology
2012; 50(8): 2601–2608.
Van Der Pol, B, et al.
Prevalence, incidence, natural history, and response to treatment of Trichomonas vaginalis infection among adolescent women. Journal of Infectious Diseases
2005; 192(12): 2039–2044.
Gaydos, CA, et al.
Trichomonas vaginalis infection in women who submit self-obtained vaginal samples after internet recruitment. Sexually Transmitted Diseases
2011; 38(9): 828–832.
Chen, XS, et al.
The prevalences of Neisseria gonorrhoeae and Chlamydia trachomatis infections among female sex workers in China. BMC Public Health
Livengood, CH, Wrenn, JW. Evaluation of COBAS AMPLICOR (Roche): accuracy in detection of Chlamydia trachomatis and Neisseria gonorrhoeae by coamplification of endocervical specimens. Journal of Clinical Microbiology
2001; 39(8): 2928–2932.
Fethers, KA, et al.
Sexual risk factors and Bacterial Vaginosis: a systematic review and meta-analysis. Clinical Infectious Diseases
2008; 47(11): 1426–1435.
Nakashima, K, et al.
Prevalence of human papillomavirus infection in the oropharynx and urine among sexually active men: a comparative study of infection by papillomavirus and other organisms, including Neisseria gonorrhoeae, Chlamydia trachomatis, Mycoplasma spp., and Ureaplasma spp. BMC Infectious Diseases
Lazenby, GB, et al.
An association between Trichomonas vaginalis and high-risk human papillomavirus in rural Tanzanian women undergoing cervical cancer screening. Clinical Therapeutics
2014; 36(1): 38–45.
Guy, R, et al.
Coinfection with Chlamydia trachomatis, Neisseria gonorrhoeae and Trichomonas vaginalis: a cross-sectional analysis of positivity and risk factors in remote Australian Aboriginal communities. Sexually Transmitted Infections
2014; 3: 201–206.
Fastring, DR, et al.
Co-occurrence of Trichomonas vaginalis and bacterial vaginosis and vaginal shedding of HIV-1 RNA. Sexually Transmitted Diseases
2014; 41(3): 173–179.
Gaydos, C, et al.
Mycoplasma genitalium as a contributor to the multiple etiologies of cervicitis in women attending sexually transmitted disease clinics. Sexually Transmitted Diseases
2009; 36(10): 598–606.
Casin, I, et al.
High prevalence of Mycoplasma genitalium in the lower genitourinary tract of women attending a sexually transmitted disease clinic in Paris, France. Sexually Transmitted Diseases
2002; 29(6): 353–359.
Cauci, S, et al.
Correlation of local interleukin-1beta levels with specific IgA response against Gardnerella vaginalis cytolysin in women with bacterial vaginosis. American Journal of Reproductive Immunology
2002; 47(5): 257–264.
Cauci, S, et al.
Interrelationships of interleukin-8 with interleukin-1beta and neutrophils in vaginal fluid of healthy and bacterial vaginosis positive women. Molecular Human Reproduction
2003; 9(1): 53–58.
Weissenbacher, T, et al.
Interleukin-6, interleukin-10 and interleukin-12 in vaginal fluid from women with bacterial vaginosis. Archives of Gynecology and Obstetrics
2010; 281(1): 77–80.
Rizzo, G, et al.
Interleukin-6 concentrations in cervical secretions in the prediction of intrauterine infection in preterm premature rupture of the membranes. Gynecologic and Obstetric Investigation
1998; 46(2): 91–95.
Taylor, BD, et al.
Inflammation biomarkers in vaginal fluid and preterm delivery. Human Reproduction
2013; 28(4): 942–952.
Sturm-Ramirez, K, et al.
High levels of tumor necrosis factor-alpha and interleukin-1beta in bacterial vaginosis may increase susceptibility to human immunodeficiency virus. The Journal of Infectious Diseases
2000; 182(2): 467–473.
Fortunato, SJ, Menon, R. Distinct molecular events suggest different pathways for preterm labor and premature rupture of membranes. American Journal of Obstetrics and Gynecology
2001; 184(7): 1399–1405; discussion 1405-1396.
Patterson, AM, et al.
Ureaplasma urealyticum respiratory tract colonization is associated with an increase in interleukin 1-beta and tumor necrosis factor alpha relative to interleukin 6 in tracheal aspirates of preterm infants. The Pediatric Infectious Disease Journal
1998; 17(4): 321–328.
Perni, SC, et al.
Mycoplasma hominis and Ureaplasma urealyticum in midtrimester amniotic fluid: association with amniotic fluid cytokine levels and pregnancy outcome. American Journal of Obstetrics and Gynecology
2004; 191(4): 1382–1386.