Wang Rui-Ling, Liu Ping, Chen Xiao-Feng, Yao Xin, Liao Xiao-Ping, Liu Ya-Hong, Sun Jian, Zhou Yu-Feng
National Risk Assessment Laboratory for Antimicrobial Resistance of Animal Original Bacteria, College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Veterinary Pharmaceutics Development and Safety Evaluation, South China Agricultural University, Guangzhou, China.
Front Vet Sci. 2022 Jul 11;9:945632. doi: 10.3389/fvets.2022.945632. eCollection 2022.
Gamithromycin is a long-acting azalide antibiotic that has been developed recently for the treatment of swine respiratory diseases. In this study, the pharmacokinetic/pharmacodynamic (PK/PD) targets, PK/PD cutoff, and optimum dosing regimen of gamithromycin were evaluated in piglets against in China, including a subset with capsular serotype 2. Short post-antibiotic effects (PAEs) (0.5-2.6 h) and PA-SMEs (2.4-7.7 h) were observed for gamithromycin against . The serum matrix dramatically facilitated the intracellular uptake of gamithromycin by strains, thus contributing to the potentiation effect of serum on their susceptibilities, with a Mueller-Hinton broth (MHB)/serum minimum inhibitory concentration (MIC) ratio of 28.86 for . Dose-response relationship demonstrated the area under the concentration (AUC)/MIC ratio to be the predictive PK/PD index closely linked to activity ( > 0.93). For infections, the net stasis, 1-log, and 2-log kill effects were achieved at serum AUC/MIC targets of 17.9, 49.1, and 166 h, respectively. At the current clinical dose of 6.0 mg/kg, gamithromycin PK/PD cutoff value was determined to be 8 mg/L. A PK/PD-based dose assessment demonstrated that the optimum dose regimen of gamithromycin to achieve effective treatments for the observed wild-type MIC distribution of in China with a probability of target attainment (PTA) ≥ 90% was 2.53 mg/kg in this study. These results will aid in the development of clinical dose-optimization studies and the establishment of clinical breakpoints for gamithromycin in the treatment of swine respiratory infections due to .
加米霉素是一种长效氮杂内酯类抗生素,最近已被开发用于治疗猪呼吸道疾病。在本研究中,在中国针对包括2型荚膜血清型子集在内的猪肺炎支原体对加米霉素的药代动力学/药效学(PK/PD)靶点、PK/PD截止值和最佳给药方案进行了评估。观察到加米霉素对猪肺炎支原体的抗生素后效应(PAE)较短(0.5 - 2.6小时),抗生素后血清介导效应(PA - SME)为(2.4 - 7.7小时)。血清基质显著促进了加米霉素对菌株的细胞内摄取,从而有助于血清对其敏感性的增强作用,猪肺炎支原体的穆勒 - 欣顿肉汤(MHB)/血清最低抑菌浓度(MIC)比值为28.86。剂量反应关系表明浓度 - 时间曲线下面积(AUC)/MIC比值是与活性密切相关的预测性PK/PD指数(> 0.93)。对于猪肺炎支原体感染,在血清AUC/MIC靶点分别为17.9、49.1和166小时时,实现了净停滞、1对数和2对数杀灭效果。在当前6.0 mg/kg的临床剂量下,加米霉素的PK/PD截止值确定为8 mg/L。基于PK/PD的剂量评估表明,在本研究中,加米霉素实现对中国观察到的猪肺炎支原体野生型MIC分布有效治疗且目标达成概率(PTA)≥ 90%的最佳剂量方案为2.53 mg/kg。这些结果将有助于开展临床剂量优化研究,并为加米霉素治疗猪肺炎支原体引起的猪呼吸道感染建立临床断点。