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In vitro synergy of tigecycline against Burkholderia cepacia complex and other multi-resistant, nonfermentative, Gram negative bacteria from cystic fibrosis patients

机译:替加环素与洋葱伯克霍尔德菌复合物和其他多囊性,非发酵性革兰氏阴性细菌来自囊性纤维化患者的体外协同作用

摘要

Options for treating Burkholderia cepacia complex (Bcc) and other multi-resistant Gram negative bacilli isolated from people with cystic fibrosis (CF) are limited. We assessed the in-vitro activity of tigecycline and eleven other antimicrobial agents against a collection of these organisms. The collection comprised 128 isolates of CF-associated Gram negative bacilli (31 Burkholderia multivorans, 16 Burkholderia cenocepacia, 4 other members of the Burkholderia species, 47 Stenotrophomonas maltophilia, 20 Achromobacter xylosoxidans, and 10 other miscellaneous CF-associated Gram negative bacilli). Minimum inhibitory concentrations (MIC) of tigecycline and eleven other antimicrobials for each isolate were determined using E-test. Synergy between tigecycline and each of eight other antimicrobials was determined using an E-test overlay method. The epidemiological spread of organisms indicated that the Leeds Teaching Hospitals NHS Trust (LTHT) infection control policies have had a measure of success and our work followed the pattern of many other CF units. Tigecycline showed poor in-vitro activity versus all members of the Bcc, with only 13% and 3% of B. cenocepacia and B. multivorans susceptible, respectively. Conversely minocycline showed good activity against these species, with 94% and 91% of isolates being susceptible. Tigecycline showed good activity against A. xyloxidans and S. maltophilia with 85% and 77% of isolates being susceptible, respectively. Tigecycline in combination with other agents mostly resulted in indifference. Although the in-vitro activity of tigecycline is variable, we reviewed the potential and future clinical impact of this study and the likely issues for further study. Whilst the relationship between synergy/MIC testing and clinical success remains unclear, there are a number of promising developments and ideas that may clarify this situation – further studies are warranted.
机译:从囊性纤维化(CF)患者中分离出来的伯克霍尔德菌洋葱伯克霍尔德氏菌(Bcc)和其他多耐药革兰氏阴性杆菌的治疗方法有限。我们评估了替加环素和其他11种其他抗菌剂对这些生物的体外活性。该集合包括128株与CF相关的革兰氏阴性杆菌(31个伯克霍尔德氏菌,16个Burkholderia cenocepacia,其他4个Burkholderia物种成员,47个嗜麦芽窄食单胞菌,20种木糖氧化无色杆菌和10个其他与CF相关的革兰氏阴性细菌)。使用E检验确定每个分离株的替加环素和其他11种其他抗菌剂的最低抑菌浓度(MIC)。替加环素与其他八种抗微生物药物之间的协同作用采用E检验叠加法确定。生物的流行病学传播表明,利兹教学医院NHS信托(LTHT)感染控制政策取得了一定程度的成功,我们的工作遵循了许多其他CF部门的模式。与Bcc的所有成员相比,Tigecycline的体外活性较差,分别仅对C. cenocepacia和B. multivorans敏感,分别为13%和3%。相反,米诺环素对这些物种表现出良好的活性,其中94%和91%的分离株易感。 Tigecycline表现出良好的抗木聚糖氧化酶和嗜麦芽孢杆菌的活性,其中分离株分别有85%和77%易感。替加环素与其他药物合用时大多会引起冷漠。尽管替加环素的体外活性是可变的,但我们回顾了该研究的潜在和未来临床影响以及可能需要进一步研究的问题。尽管协同/ MIC测试与临床成功之间的关系尚不清楚,但仍有许多有希望的进展和想法可以澄清这种情况-值得进一步研究。

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    Kenning John;

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  • 年度 2012
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  • 正文语种 English
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