Roh Kyoung Ho, Luong Nguyen Dinh, Liu Changseung, Seo Young Hee, Lee Hyukmin, Unemo Magnus, Lee Kyungwon
Department of Laboratory Medicine, National Health Insurance Ilsan Hospital, Goyang, Korea.
Pasteur Institute in Nha Trang, Nha Trang, Vietnam.
Ann Lab Med. 2025 Apr 28. doi: 10.3343/alm.2024.0522.
Novel antimicrobial agents are continually developed to address the global threat of multidrug-resistant . Promising candidates include zoliflodacin and, possibly, solithromycin. We evaluated their in-vitro activities against gonococcal isolates collected in Korea. In total, 250 isolates obtained across Korea between 2016 and 2018 were used to determine the minimum inhibitory concentrations (MICs) of 10 therapeutic agents using the CLSI agar dilution method. Most isolates (94.8%, 237/250) demonstrated non-susceptibility to penicillin G, tetracycline, and ciprofloxacin, and susceptibility to ceftriaxone and spectinomycin was substantially high. The half-maximal IC (MIC50) and 90% IC (MIC90) values for zoliflodacin were 0.03 and 0.06 μg/mL, respectively; 0.06 and 0.12 μg/mL, respectively, for solithromycin; and 0.03 and 0.12 μg/mL, respectively, for ceftriaxone. Notably, no cross-resistance was observed between zoliflodacin and ciprofloxacin, despite both targeting DNA topoisomerase II enzymes. Zoliflodacin and solithromycin demonstrated significant activity against multidrug-resistant isolates, and zoliflodacin has shown non-inferiority to ceftriaxone/azithromycin dual therapy in a clinical phase 3 trial. Collectively, our findings highlight the potential of zoliflodacin as a novel therapeutic agent for gonococcal infections, particularly in the context of rising multidrug resistance, and highlight the need for continued surveillance and development of alternative antimicrobial strategies.
新型抗菌药物不断被研发出来,以应对多重耐药这一全球威胁。有前景的候选药物包括佐利氟达辛,可能还有索利霉素。我们评估了它们对在韩国收集的淋球菌分离株的体外活性。总共使用了2016年至2018年期间在韩国各地获得的250株分离株,采用CLSI琼脂稀释法测定10种治疗药物的最低抑菌浓度(MIC)。大多数分离株(94.8%,237/250)对青霉素G、四环素和环丙沙星不敏感,对头孢曲松和壮观霉素的敏感性相当高。佐利氟达辛的半数最大抑制浓度(MIC50)和90%抑制浓度(MIC90)值分别为0.03和0.06μg/mL;索利霉素分别为0.06和0.12μg/mL;头孢曲松分别为0.03和0.12μg/mL。值得注意的是,尽管佐利氟达辛和环丙沙星都靶向DNA拓扑异构酶II酶,但未观察到它们之间的交叉耐药性。佐利氟达辛和索利霉素对多重耐药分离株显示出显著活性,并且在一项3期临床试验中,佐利氟达辛已显示出不劣于头孢曲松/阿奇霉素联合疗法。总的来说,我们的研究结果突出了佐利氟达辛作为一种治疗淋球菌感染的新型治疗药物的潜力,特别是在多重耐药性不断上升的背景下,并强调了持续监测和开发替代抗菌策略的必要性。