School of Medical and Health Sciences, Edith Cowan University, Joondalup, Western Australia.
State Key Laboratory for Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
J Antimicrob Chemother. 2021 Mar 12;76(4):967-972. doi: 10.1093/jac/dkaa522.
Clostridioides difficile is the most common cause of antimicrobial-associated diarrhoea in high-income countries. Fluoroquinolone resistance enabled the emergence and intercontinental spread of the epidemic ribotype (RT) 027 strain of C. difficile in the early 2000s. Despite frequent inappropriate antimicrobial use in Asia, RT 027 is rarely isolated in the region, but the often fluoroquinolone- and clindamycin-resistant RT 017 strain predominates.
This study evaluated the antimicrobial activity of ridinilazole, a novel antimicrobial agent with highly specific activity for C. difficile, against clinical strains of C. difficile from Asia.
C. difficile strains from Japan (n = 64), South Korea (n = 32) and China (n = 44) were tested by the agar dilution method for susceptibility to ridinilazole, metronidazole, vancomycin, clindamycin, moxifloxacin, rifaximin and fidaxomicin.
All strains were susceptible to ridinilazole, with low MICs (0.03-0.25 mg/L). Several strains showed multiresistance profiles, particularly RT 017 (100% clindamycin resistant, 91.3% moxifloxacin resistant, 82.6% rifaximin resistant) and RT 369 (94.4% clindamycin resistant, 100% moxifloxacin resistant). Rifaximin resistance was absent in all strains from Japan. Multiresistance to clindamycin, moxifloxacin and rifaximin was found in 19 RT 017 strains (from China and South Korea), 2 RT 001 strains (South Korea) and 1 RT 046 strain (South Korea).
Ridinilazole showed potent activity against a range of Asian C. difficile strains, which otherwise frequently displayed resistance to several comparator antimicrobial agents. Ongoing surveillance of antimicrobial resistance profiles is required to monitor and control the spread of resistant strains.
艰难梭菌是高收入国家最常见的抗菌药物相关性腹泻病原体。氟喹诺酮类药物耐药使艰难梭菌的流行 RT027 菌株在 21 世纪初出现并在洲际传播。尽管亚洲经常不合理地使用抗菌药物,但该地区很少分离到 RT027,而通常是氟喹诺酮类和克林霉素耐药的 RT017 菌株占优势。
本研究评估了利奈唑胺(一种新型抗菌药物,对艰难梭菌具有高度特异性)对来自亚洲的艰难梭菌临床株的抗菌活性。
采用琼脂稀释法检测来自日本(n=64)、韩国(n=32)和中国(n=44)的艰难梭菌菌株对利奈唑胺、甲硝唑、万古霉素、克林霉素、莫西沙星、利福昔明和非达霉素的敏感性。
所有菌株对利奈唑胺均敏感,MIC 值较低(0.03-0.25mg/L)。一些菌株表现出多药耐药性,特别是 RT017(100%克林霉素耐药,91.3%莫西沙星耐药,82.6%利福昔明耐药)和 RT369(94.4%克林霉素耐药,100%莫西沙星耐药)。所有来自日本的菌株均无利福昔明耐药。19 株 RT017 株(来自中国和韩国)、2 株 RT001 株(韩国)和 1 株 RT046 株(韩国)存在克林霉素、莫西沙星和利福昔明的多重耐药性。
利奈唑胺对一系列亚洲艰难梭菌菌株表现出强大的活性,而这些菌株通常对几种比较抗菌药物耐药。需要对抗菌药物耐药性进行持续监测,以监测和控制耐药菌株的传播。