Mycoplasma Unit, Department of Avian and Fish Diseases, Kimron Veterinary Institute, Bet Dagan, Israel.
Antimicrob Agents Chemother. 2013 Jul;57(7):3072-7. doi: 10.1128/AAC.00203-13. Epub 2013 Apr 22.
The in vitro activity of enrofloxacin against 73 Mycoplasma synoviae field strains isolated in Israel and Europe was determined by broth microdilution. Decreased susceptibility to enrofloxacin was identified in 59% of strains, with the MICs ranging from 1 to >16 μg/ml. The estimated MIC50 and MIC90 values for enrofloxacin were 2 and 8 μg/ml, respectively. Moreover, this study showed that 92% of recent Israeli field isolates (2009 to 2011) of M. synoviae have MICs of ≥ 2 μg/ml to enrofloxacin. Comparison of the quinolone resistance-determining regions (QRDRs) in M. synoviae isolates revealed a clear correlation between the presence of one of the amino acid substitutions Asp79-Asn, Thr80-Ala/Ile, Ser81-Pro, and Asp84-Asn/Tyr/His of the ParC QRDR and decreased susceptibility to enrofloxacin (MIC, ≥ 1 μg/ml). Amino acid substitutions at positions GyrA 87, GyrB 401/402, and ParE 420/454 were also identified, but there was no clear-cut correlation with susceptibility to enrofloxacin. Comparison of vlhA molecular profiles revealed the presence of 9 different genotypes in the Israeli M. synoviae field isolates and 10 genotypes in the European isolates; only one vlhA genotype (type 4) was identified in both cohorts. Based on results of vlhA molecular typing, several mechanisms for emergence and dissemination of Israeli enrofloxacin-resistant M. synoviae isolates are suggested.
采用肉汤微量稀释法测定了 73 株分离自以色列和欧洲的支原体滑膜场菌株对恩诺沙星的体外活性。结果发现 59%的菌株对恩诺沙星的敏感性降低,MIC 范围为 1 至>16μg/ml。恩诺沙星的 MIC50 和 MIC90 值分别估计为 2 和 8μg/ml。此外,本研究表明,92%的最近以色列场分离株(2009 年至 2011 年)对恩诺沙星的 MIC≥2μg/ml。对支原体滑膜分离株喹诺酮耐药决定区(QRDR)的比较显示,ParC QRDR 中存在一种氨基酸取代(Asp79-Asn、Thr80-Ala/Ile、Ser81-Pro 和 Asp84-Asn/Tyr/His)与恩诺沙星(MIC≥1μg/ml)的敏感性降低之间存在明确的相关性。还发现了 GyrA 87、GyrB 401/402 和 ParE 420/454 位置的氨基酸取代,但与恩诺沙星的敏感性没有明确的相关性。vlhA 分子谱的比较表明,在以色列支原体滑膜场分离株中存在 9 种不同的基因型,在欧洲分离株中存在 10 种基因型;两种队列中均仅鉴定出一种 vlhA 基因型(类型 4)。基于 vlhA 分子分型的结果,提出了几种以色列恩诺沙星耐药支原体滑膜分离株出现和传播的机制。