Antimicrobial Resistance and Healthcare Associated Infections Reference Unit, Public Health England, London NW9 5EQ, UK.
J Antimicrob Chemother. 2014 Apr;69(4):1050-6. doi: 10.1093/jac/dkt455. Epub 2013 Nov 19.
Sulfamethoxazole/trimethoprim is standard therapy for infections caused by opportunist non-fermenters except Pseudomonas aeruginosa and Acinetobacter. Sulfametrol(e)/trimethoprim is an alternative to sulfamethoxazole/trimethoprim available in some EU countries, with possible pharmacological advantages. We compared their activities against (i) non-fermenters, (ii) multiresistant Enterobacteriaceae and (iii) reference strains with sul1 and sul2.
Test isolates were recent submissions to the reference laboratory, or were Escherichia coli previously shown to have sul1 or sul2. Identification was by MALDI-ToF, by 16S rRNA gene sequencing or with API20NE strips. MICs were determined by CLSI agar dilution. The Stenotrophomonas maltophilia and Burkholderia series were enhanced by inclusion of 25% sulfamethoxazole/trimethoprim-resistant isolates; other series were not enhanced.
MICs of sulfametrole/trimethoprim for non-fermenters tracked those of sulfamethoxazole/trimethoprim, being equal in 97/170 cases, 2-fold higher in 57/170 cases and 2-fold lower in 12/170 cases. Despite supplementing the Burkholderia and S. maltophilia collections with sulfamethoxazole/trimethoprim-resistant organisms, the antifolate combinations retained better activity against these and other non-fermenters than did piperacillin/tazobactam, moxifloxacin, ticarcillin/clavulanate, tigecycline, cefotaxime or imipenem. By contrast, few (5%-20%) of the extended-spectrum β-lactamase (ESBL)- and carbapenemase-producing Enterobacteriaceae were susceptible to the sulphonamides or their trimethoprim combinations, probably reflecting widespread co-carriage of sul1 and sul2, which both conferred resistance.
Antifolate combinations remain the most active antimicrobials against less common non-fermenters, importantly including S. maltophilia and Burkholderia spp., but resistance is prevalent among ESBL- and carbapenemase-producing Enterobacteriaceae. Sulfametrole/trimethoprim had similar activity to sulfamethoxazole/trimethoprim against non-fermenters.
磺胺甲噁唑/甲氧苄啶是除铜绿假单胞菌和不动杆菌外,治疗机会性非发酵菌感染的标准疗法。磺胺甲噁唑/甲氧苄啶在一些欧盟国家是磺胺甲噁唑/甲氧苄啶的替代药物,具有潜在的药理学优势。我们比较了它们对(i)非发酵菌、(ii)多耐药肠杆菌科和(iii)具有 sul1 和 sul2 的参考菌株的活性。
试验分离株是最近提交给参考实验室的,或先前证明具有 sul1 或 sul2 的大肠杆菌。通过基质辅助激光解吸电离飞行时间质谱、16S rRNA 基因测序或 API20NE 条带进行鉴定。采用 CLSI 琼脂稀释法测定 MICs。通过添加 25%磺胺甲噁唑/甲氧苄啶耐药分离株增强嗜麦芽窄食单胞菌和伯克霍尔德菌系列;其他系列未增强。
磺胺甲噁唑/甲氧苄啶对非发酵菌的 MIC 与磺胺甲噁唑/甲氧苄啶的 MIC 相吻合,97/170 例相等,57/170 例增加 2 倍,12/170 例减少 2 倍。尽管在伯克霍尔德菌和嗜麦芽窄食单胞菌的混合物中补充了磺胺甲噁唑/甲氧苄啶耐药菌,但这些抗叶酸组合对这些和其他非发酵菌的活性仍优于哌拉西林/他唑巴坦、莫西沙星、替卡西林/克拉维酸、替加环素、头孢噻肟或亚胺培南。相比之下,很少有(5%-20%)产超广谱β-内酰胺酶(ESBL)和碳青霉烯酶的肠杆菌科对磺胺类药物或其甲氧苄啶组合敏感,这可能反映了广泛携带 sul1 和 sul2,这两者都赋予了耐药性。
抗叶酸类药物组合仍然是针对较不常见的非发酵菌最有效的抗菌药物,重要的是包括嗜麦芽窄食单胞菌和伯克霍尔德菌属,但在产 ESBL 和碳青霉烯酶的肠杆菌科中,耐药性很普遍。磺胺甲噁唑/甲氧苄啶对非发酵菌的活性与磺胺甲噁唑/甲氧苄啶相似。