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Activity of ceftolozane/tazobactam against surveillance and ‘problem’ Enterobacteriaceae Pseudomonas aeruginosa and non-fermenters from the British Isles

机译:头孢洛赞/他唑巴坦针对不列颠群岛的监测和问题肠杆菌科铜绿假单胞菌和非发酵菌的活性

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摘要

>Background: We assessed the activity of ceftolozane/tazobactam against consecutive isolates collected in the BSAC Bacteraemia Surveillance from 2011 to 2015 and against ‘problem’ isolates sent to the UK national reference laboratory from July 2015, when routine testing began. >Methods: Susceptibility testing was by BSAC agar dilution with resistance mechanisms identified by PCR and interpretive reading. >Results: Data were reviewed for 6080 BSAC surveillance isolates and 5473 referred organisms. Ceftolozane/tazobactam had good activity against unselected ESBL producers in the BSAC series, but activity was reduced against ertapenem-resistant ESBL producers, which were numerous among reference submissions. AmpC-derepressed Enterobacter spp. were widely resistant, but Escherichia coli with raised chromosomal AmpC frequently remained susceptible, as did Klebsiella pneumoniae with acquired DHA-1-type AmpC. Carbapenemase-producing Enterobacteriaceae were mostly resistant, except for ceftazidime-susceptible isolates with OXA-48-like enzymes. Ceftolozane/tazobactam was active against 99.8% of the BSAC Pseudomonas aeruginosa isolates; against referred P. aeruginosa it was active against 99.7% with moderately raised efflux, 94.7% with strongly raised efflux and 96.6% with derepressed AmpC. Resistance in P. aeruginosa was largely confined to isolates with metallo-β-lactamases (MBLs) or ESBLs. MICs for referred Burkholderia spp. and Stenotrophomonas maltophilia were 2–4-fold lower than those of ceftazidime. >Conclusions: Ceftolozane/tazobactam is active against ESBL-producing Enterobacteriaceae; gains against other problem Enterobacteriaceae groups were limited. Against P. aeruginosa it overcame the two most prevalent mechanisms (up-regulated efflux and derepressed AmpC) and was active against 51.9% of isolates non-susceptible to all other β-lactams, rising to 80.9% if ESBL and MBL producers were excluded.
机译:>背景:我们评估了头孢洛赞/他唑巴坦对2011年至2015年BSAC细菌血症监测中收集的连续分离株以及2015年7月发送至英国国家参考实验室的“问题”分离株进行常规检测时的活性开始。 >方法:药敏试验采用BSAC琼脂稀释,并通过PCR和解释性阅读鉴定抗药性。 >结果:审查了6080个BSAC监视分离株和5473个转介生物的数据。头孢唑烷/他唑巴坦对BSAC系列中未选择的ESBL生产者具有良好的活性,但对耐ertapenem的ESBL生产者的活性却降低了,在参考文献中有很多。 AmpC抑制的肠杆菌属。它们具有广泛的抗药性,但是具有升高的染色体AmpC的大肠杆菌经常仍然易感,具有获得性DHA-1型AmpC的肺炎克雷伯菌也是如此。产生碳青霉烯酶的肠杆菌科细菌大多具有抗药性,但头孢他啶易感菌株带有OXA-48样酶。头孢唑烷/他唑巴坦对99.8%的铜绿假单胞菌铜绿假单胞菌具有活性。相对于所提到的铜绿假单胞菌,它对99.7%的适度外排有活性,对94.7%的强烈外排有活性,对AmpC抑制的有96.6%的活性。铜绿假单胞菌的抗药性主要限于金属β-内酰胺酶(MBL)或ESBLs。推荐的Burkholderia spp的MIC。和嗜麦芽窄食单胞菌比头孢他啶低2-4倍。 >结论:头孢洛赞/他唑巴坦对产生ESBL的肠杆菌科有活性;肠杆菌科人群在解决其他问题上的收益有限。针对铜绿假单胞菌,它克服了两个最普遍的机制(外排上调和AmpC抑制),对所有其他β-内酰胺类不敏感的分离株有51.9%的活性,如果排除ESBL和MBL生产者,则上升到80.9%。

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