Group of Mycoplasmas, Laboratory of Molecular Microbiology, Vaccinology, and Biotechnology Development, Institut Pasteur de Tunis, Université de Tunis El Manar, 13, Place Pasteur-B.P 74, 1002 Tunis-Belvédère, Tunisia.
Unit of Typing & Genetics of Mycobacteria, Laboratory of Molecular Microbiology, Vaccinology, and Biotechnology Development, Institut Pasteur de Tunis, Université de Tunis El Manar, 13, Place Pasteur-B.P 74, 1002 Tunis-Belvédère, Tunisia.
Antimicrob Resist Infect Control. 2020 Jan 23;9(1):19. doi: 10.1186/s13756-020-0681-5. eCollection 2020.
spp. have been implicated in a variety of clinical conditions and certain serovars are likely to be disease-associated. Hence, the ascending trend of spp. resistance to antimicrobials should deserve more attention. Here we assessed the extent of antimicrobial resistance of serovars in Tunisia, and investigated the underlying molecular basis.
This study included 101 molecularly typed spp. clinical strains isolated over a 12-year time period (2005-2017). The antimicrobial susceptibility was tested against nine antibacterial agents using the broth microdilution method. Neighbor-joining tree was constructed to establish the phylogenetic relationships among isolates.
We found that all ureaplasma isolates were resistant to ciprofloxacin and erythromycin, intermediately resistant to azithromycin, and susceptible to doxycycline, moxifloxacin and josamycin. Ofloxacin and levofloxacin resistance was found in 73.27 and 17.82%, respectively, while 37.62% of isolates proved resistant to tetracycline. Consequently, we detected an elevated multidrug resistance rate among ureaplasma isolates (37.62%), particularly among serovars 2, 5, 8, and 9 (77.77% overall), as well as serovars 4, 10, 12, and 13 (52.63% overall). In most cases, drug resistance was found to be associated with known molecular mechanisms, yet we have identified two novel mutations in the L22 protein, which might be associated with macrolide-resistance.
To our knowledge, this is the first study that reports the widespread expansion of multidrug resistance among serovars, a finding of importance in terms of both surveillance and antimicrobial usage.
spp. 与多种临床病症有关,某些血清型可能与疾病相关。因此, spp. 对抗微生物药物的耐药性上升趋势应引起更多关注。在此,我们评估了突尼斯 spp. 血清型的抗菌药物耐药程度,并研究了其潜在的分子基础。
本研究包括 101 株在 12 年时间内(2005-2017 年)分离的分子分型 spp. 临床菌株。使用肉汤微量稀释法检测抗菌药物敏感性。构建邻接树以建立分离株之间的系统发育关系。
我们发现所有脲原体分离株均对环丙沙星和红霉素耐药,对阿奇霉素中度耐药,对多西环素、莫西沙星和交沙霉素敏感。氧氟沙星和左氧氟沙星的耐药率分别为 73.27%和 17.82%,而 37.62%的分离株对四环素耐药。因此,我们发现脲原体分离株的多药耐药率较高(37.62%),特别是血清型 2、5、8 和 9(总体 77.77%)以及血清型 4、10、12 和 13(总体 52.63%)。在大多数情况下,耐药性与已知的分子机制有关,但我们在 L22 蛋白中发现了两个新的突变,这可能与大环内酯类耐药有关。
据我们所知,这是首次报道 spp. 血清型广泛存在多药耐药的研究,这对于监测和抗菌药物的使用都很重要。