Korean J Clin Microbiol.  2009 Dec;12(4):159-162.

Antimicrobial Susceptibilities of Ureaplasma urealyticum and Mycoplasma hominis in Pregnant Women

Affiliations
  • 1Department of Laboratory Medicine, Gyeongsang National University School of Medicine, Jinju, Korea. sjkim8239@hanmail.net
  • 2Department of Obstetrics and Gynecology, Gyeongsang National University School of Medicine, Jinju, Korea.
  • 3Institute of Health Science, Gyeongsang National University School of Medicine, Jinju, Korea.

Abstract

BACKGROUND
Ureaplasma urealyticum and Mycoplasma hominis are associated with an increased risk of pregnancy complications, such as preterm birth and premature membrane rupture. The purpose of this study was to determine the isolation rates and antimicrobial susceptibilities of genital mycoplasma in a sample of pregnant women from Jinju, Korea.
METHODS
Vaginal swabs were obtained from 258 pregnant women between 2004 and 2008 and tested for the presence of U. urealyticum and M. hominis at Gyeongsang National University Hospital. The identification and antimicrobial susceptibilities of U. urealyticum and M. hominis were determined with a commercially available kit, the Mycoplasma IST2 Kit (bioMe- rieux, Marcy-l'Etoile, France), and evaluated according to standards set by the Clinical and Laboratory Standards Institute (CLSI).
RESULTS
U. urealyticum only was detected in 105 specimens (38.6%), while M. hominis only was detected only in 2 specimens (1.8%). Seven specimens (6.7%) were positive both for U. urealyticum and M. hominis. Susceptibilities of U. urealyticum to azithromycin, erythromycin, clarithromycin, and doxycycline were 75.2%, 82.9%, 88.6%, and 88.6%, respectively, while almost all of the isolates were susceptible to josamycin (99.0%) and pristinamycin (100%). The susceptibility of U. urealyticum to ofloxacin and ciprofloxacin was 56.2% and 15.2%, respectively.
CONCLUSION
The rate of isolation of genital mycoplasma in pregnant women was 44.2% in Jinju; most of the mycoplasma were U. urealyticum. U. urealyticum and M. hominis were highly resistant to quinolones, but susceptible to josamycin. Therefore, empirical treatment without prior identification and determination of the antimicrobial susceptibility of genital mycoplasma will fail in many cases.

Keyword

Ureaplasma urealyticum; Mycoplasma hominis; Genital mycoplasma; Antimicrobial susceptibilities

MeSH Terms

Azithromycin
Ciprofloxacin
Clarithromycin
Doxycycline
Erythromycin
Female
Humans
Josamycin
Korea
Membranes
Mycoplasma
Mycoplasma hominis
Ofloxacin
Pregnancy Complications
Pregnant Women
Premature Birth
Pristinamycin
Quinolones
Rupture
Ureaplasma
Ureaplasma urealyticum
Azithromycin
Ciprofloxacin
Clarithromycin
Doxycycline
Erythromycin
Josamycin
Ofloxacin
Pristinamycin
Quinolones

Reference

1. Kilic D, Basar MM, Kaygusuz S, Yilmaz E, Basar H, Batislam E. Prevalence and treatment of Chlamydia trachomatis, Ureaplasma urealyticum, and Mycoplasma hominis in patients with non-gonococcal urethritis. Jpn J Infect Dis. 2004; 57:17–20.
2. Krohn MA, Hillier SL, Nugent RP, Cotch MF, Carey JC, Gibbs RS, et al. The genital flora of women with intraamniotic infection. Vaginal infection and prematurity study group. J Infect Dis. 1995; 171:1475–80.
3. Koch A, Bilina A, Teodorowicz L, Stary A. Mycoplasma hominis and Ureaplasma urealyticum in patients with sexually transmitted diseases. Wien Klin Wochenschr. 1997; 109:584–9.
4. McDonald HM, O'Loughlin JA, Jolley PT, Vigneswaran R, McDonald PJ. Changes in vaginal flora during pregnancy and association with preterm birth. J Infect Dis. 1994; 170:724–8.
Article
5. Waites KB, Rudd PT, Crouse DT, Canupp KC, Nelson KG, Ramsey C, et al. Chronic Ureaplasma urealyticum and Mycoplasma hominis infections of central nervous system in preterm infants. Lancet. 1988; 1:17–21.
6. Arai S, Gohara Y, Kuwano K, Kawashima T. Antimycoplasmal activities of new quinolones, tetracyclines, and macrolides against Mycoplasma pneumoniae. Antimicrob Agents Chemother. 1992; 36:1322–4.
7. Hannan PC. Comparative susceptibilities of various AIDS-associated and human urogenital tract mycoplasmas and strains of Mycoplasma pneumoniae to 10 classes of antimicrobial agent in vitro. J Med Microbiol. 1998; 47:1115–22.
8. Kenny GE, Cartwright FD. Susceptibilities of Mycoplasma hominis and Ureaplasma urealyticum to two new quinolones, sparfloxacin and WIN 57273. Antimicrob Agents Chemother. 1991; 35:1515–6.
9. Ye Y, Tu S, Li H. Clinic intervention study on urogenital mycoplasma infection of pregnant women. Zhonghua Liu Xing Bing Xue Za Zhi. 2001; 22:293–5.
10. Ullmann U, Schubert S, Krausse R. Comparative in-vitro activity of levofloxacin, other fluoroquinolones, doxycycline and erythromycin against Ureaplasma urealyticum and Mycoplasma hominis. J Antimicrob Chemother. 1999; 43(Suppl C):33–6.
11. Lister PJ, Balechandran T, Ridgway GL, Robinson AJ. Comparison of azithromycin and doxycycline in the treatment of non-gonococcal urethritis in men. J Antimicrob Chemother. 1993; 31(Suppl E):185–92.
Article
12. Romanowski B, Talbot H, Stadnyk M, Kowalchuk P, Bowie WR. Minocycline compared with doxycycline in the treatment of nongonococcal urethritis and mucopurulent cervicitis. Ann Intern Med. 1993; 119:16–22.
Article
13. Stamm WE, Hicks CB, Martin DH, Leone P, Hook EW 3rd, Cooper RH, et al. Azithromycin for empirical treatment of the nongonococcal urethritis syndrome in men. A randomized double-blind study. JAMA. 1995; 274:545–9.
Article
14. Roberts MC, Kenny GE. Dissemination of the tetM tetracycline resistance determinant to Ureaplasma urealyticum. Antimicrob Agents Chemother. 1986; 29:350–2.
15. Leng Z, Riley DE, Berger RE, Krieger JN, Roberts MC. Distribution and mobility of the tetracycline resistance determinant tetQ. J Antimicrob Chemother. 1997; 40:551–9.
Article
16. Wasiela M, Krzemiński Z, Hanke W, Kalinka J. Association between genital mycoplasmas and risk of preterm delivery. Med Wieku Rozwoj. 2003; 7(3 Suppl 1):211–6.
17. Park JK, Shin JK, Choi W, Lee SA, Lee JH, Paik WY. Mycoplasma infection of cervicovaginal fluid in women with preterm labor. Korean J Perinatol. 2005; 16:128–36.
18. Kechagia N, Bersimis S, Chatzipanagiotou S. Incidence and antimicrobial susceptibilities of genital mycoplasmas in outpatient women with clinical vaginitis in Athens, Greece. J Antimicrob Chemother. 2008; 62:122–5.
Article
19. Karabay O, Topcuoglu A, Kocoglu E, Gurel S, Gurel H, Ince NK. Prevalence and antibiotic susceptibility of genital Mycoplasma hominis and Ureaplasma urealyticum in a university hospital in Turkey. Clin Exp Obstet Gynecol. 2006; 33:36–8.
20. Bae HG, Heo WB, Lee NY, Lee WK, Koo TB. Detection of Ureaplasma urealyticum and Mycoplasma hominis in pregnant women using MYCOFAST(R) evolution 2 and PCR. Korean J Clin Microbiol. 2003; 6:74–80.
21. Kenny GE, Cartwright FD. Susceptibility of Mycoplasma pneumoniae to several new quinolones, tetracycline, and erythromycin. Antimicrob Agents Chemother. 1991; 35:587–9.
22. Kenny GE, Cartwright FD. Effect of pH, inoculum size, and incubation time on the susceptibility of Ureaplasma urealyticum to erythromycin in vitro. Clin Infect Dis. 1993; 17(Suppl 1):S215–8.
23. Renaudin H, Bébéar C. Comparative in vitro activity of azithromycin, clarithromycin, erythromycin and lomefloxacin against Mycoplasma pneumoniae, Mycoplasma hominis and Ureaplasma urealyticum. Eur J Clin Microbiol Infect Dis. 1990; 9:838–41.
24. Rylander M, Hallander HO. In vitro comparison of the activity of doxycycline, tetracycline, erythromycin and a new macrolide, CP 62993, against Mycoplasma pneumoniae, Mycoplasma hominis and Ureaplasma urealyticum. Scand J Infect Dis. 1988; 53(Suppl):12–7.
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