Piérard D, Stone G G
Department of Microbiology and Infection Control, Universitair Ziekenhuis Brussel (UZ Brussel), Vrije Universiteit Brussel (VUB), Laarbeeklaan, 101, B-1090, Brussels, Belgium.
Pfizer Inc., Hospital Business Unit, Global Product Development, Groton Laboratories, 558 Eastern Point Rd, Groton, CT, 06340, USA.
BMC Infect Dis. 2021 Jun 23;21(1):600. doi: 10.1186/s12879-021-06153-0.
This antimicrobial surveillance study reports in vitro antimicrobial activity and susceptibility data for a panel of agents against respiratory isolates of Enterobacterales and Pseudomonas aeruginosa.
Isolates from respiratory specimens were collected in Africa/Middle East, Asia/South Pacific, Europe and Latin America between 2016 and 2018, as part of the Antimicrobial Testing Leadership and Surveillance (ATLAS) program. Broth microdilution methodology was used to quantify minimum inhibitory concentrations, from which rates of susceptibility were determined using EUCAST breakpoints (version 10). Rates of subsets with genes encoding β-lactamases (extended-spectrum β-lactamases [ESBLs], serine carbapenemases and metallo-β-lactamases [MBLs]) were also determined, as well as rates of multidrug-resistant (MDR) P. aeruginosa.
Among all respiratory Enterobacterales isolates, susceptibility to ceftazidime-avibactam, meropenem, colistin and amikacin was ≥94.4% in each region. For Enterobacterales isolates that were ESBL-positive or carbapenemase-positive/MBL-negative, ceftazidime-avibactam susceptibility was 93.6 and 98.9%, respectively. Fewer than 42.7% of MBL-positive Enterobacterales isolates were susceptible to any agents, except colistin (89.0% susceptible). Tigecycline susceptibility was ≥90.0% among Citrobacter koseri and Escherichia coli isolates, including all β-lactamase-positive subsets. ESBL-positive Enterobacterales were more commonly identified in each region than isolates that were ESBL/carbapenemase-positive; carbapenemase-positive/MBL-negative; or MBL-positive. Among all respiratory P. aeruginosa isolates, the combined susceptibility rates (susceptible at standard dosing regimen plus susceptible at increased exposure) were highest to ceftazidime-avibactam, colistin and amikacin (≥82.4% in each region). Susceptibility to colistin was ≥98.1% for all β-lactamase-positive subsets of P. aeruginosa. The lowest rates of antimicrobial susceptibility were observed among MBL-positive isolates of P. aeruginosa (≤56.6%), with the exception of colistin (100% susceptible). MDR P. aeruginosa were most frequently identified in each region (18.7-28.7%), compared with the subsets of ESBL-positive; carbapenemase-positive/MBL-negative; or MBL-positive isolates.
Rates of susceptibility among the collections of respiratory Enterobacterales and P. aeruginosa isolates were highest to ceftazidime-avibactam, colistin and amikacin in each region. Tigecycline was active against all subsets of C. koseri and E. coli, and colistin was active against all subsets of P. aeruginosa. The findings of this study indicate the need for continued antimicrobial surveillance among respiratory Gram-negative pathogens, in particular those with genes encoding MBLs.
本抗菌药物监测研究报告了一组药物对肠杆菌科细菌和铜绿假单胞菌呼吸道分离株的体外抗菌活性和药敏数据。
作为抗菌药物测试领导与监测(ATLAS)项目的一部分,2016年至2018年期间在非洲/中东、亚洲/南太平洋、欧洲和拉丁美洲收集呼吸道标本中的分离株。采用肉汤微量稀释法测定最低抑菌浓度,并根据欧洲抗菌药物敏感性试验委员会(EUCAST)标准(第10版)确定药敏率。还测定了编码β-内酰胺酶(超广谱β-内酰胺酶[ESBLs]、丝氨酸碳青霉烯酶和金属β-内酰胺酶[MBLs])的基因子集的比例,以及多重耐药(MDR)铜绿假单胞菌的比例。
在所有呼吸道肠杆菌科细菌分离株中,各地区对头孢他啶-阿维巴坦、美罗培南、黏菌素和阿米卡星的药敏率均≥94.4%。对于ESBL阳性或碳青霉烯酶阳性/MBL阴性的肠杆菌科细菌分离株,头孢他啶-阿维巴坦的药敏率分别为93.6%和98.9%。除黏菌素(药敏率89.0%)外,MBL阳性的肠杆菌科细菌分离株对任何药物的药敏率均低于42.7%。在科氏柠檬酸杆菌和大肠埃希菌分离株中,包括所有β-内酰胺酶阳性亚组,替加环素的药敏率≥90.0%。在每个地区,ESBL阳性的肠杆菌科细菌比ESBL/碳青霉烯酶阳性、碳青霉烯酶阳性/MBL阴性或MBL阳性的分离株更常见。在所有呼吸道铜绿假单胞菌分离株中,联合药敏率(标准给药方案敏感加增加暴露后敏感)对头孢他啶-阿维巴坦、黏菌素和阿米卡星最高(各地区均≥82.4%)。铜绿假单胞菌所有β-内酰胺酶阳性亚组对黏菌素的药敏率≥98.1%。在铜绿假单胞菌的MBL阳性分离株中观察到最低的抗菌药敏率(≤56.6%),黏菌素除外(100%敏感)。与ESBL阳性、碳青霉烯酶阳性/MBL阴性或MBL阳性分离株亚组相比,MDR铜绿假单胞菌在每个地区最常被鉴定到(18.7 - 28.7%)。
在每个地区,呼吸道肠杆菌科细菌和铜绿假单胞菌分离株对头孢他啶-阿维巴坦、黏菌素和阿米卡星的药敏率最高。替加环素对科氏柠檬酸杆菌和大肠埃希菌的所有亚组均有活性,黏菌素对铜绿假单胞菌的所有亚组均有活性。本研究结果表明,需要对呼吸道革兰阴性病原体,特别是那些编码MBLs基因的病原体持续进行抗菌药物监测。