首页> 外文期刊>Clinical microbiology and infection: European Society of Clinical Microbiology and Infectious Diseases >Rapid detection of enterobacteriaceae producing extended spectrum beta-lactamases directly from positive blood cultures by matrix-assisted laser desorption ionization-time of flight mass spectrometry
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Rapid detection of enterobacteriaceae producing extended spectrum beta-lactamases directly from positive blood cultures by matrix-assisted laser desorption ionization-time of flight mass spectrometry

机译:基质辅助激光解吸电离-飞行时间质谱直接从阳性血液培养物中快速检测产肠杆菌科细菌产生的广谱β-内酰胺酶

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摘要

Bacteria that produce extended-spectrum -lactamases (ESBLs) are an increasing healthcare problem and their rapid detection is a challenge that must be overcome in order to optimize antimicrobial treatment and patient care. Matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry (MS) has been used to determine resistance to -lactams, including carbapenems in Enterobacteriaceae, but the methodology has not been fully validated as it remains time-consuming. We aimed to assess whether MALDI-TOF can be used to detect ESBL-producing Enterobacteriaceae from positive blood culture bottles in clinical practice. In the assay, 141 blood cultures were tested, 13 of them were real bacteraemias and 128 corresponded to blood culture bottles seeded with bacterial clinical isolates. Bacteraemias were analysed by MALDI-TOF after a positive growth result and the 128 remaining blood cultures 24h after the bacterial seeding. -lactamase activity was determined through the profile of peaks associated with the antibiotics cefotaxime and ceftazidime and its hydrolyzed forms. Clavulanic acid was added to rule out the presence of non-ESBL mechanisms. Overall data show a 99% (103 out of 104) sensitivity in detecting ESBL in positive blood cultures. Data were obtained in 90min (maximum 150min). The proposed methodology has a great impact on the early detection of ESBL-producing Enterobacteriaceae from positive blood cultures, being a rapid and efficient method and allowing early administration of an appropriate antibiotic therapy.
机译:产生广谱内酰胺酶(ESBLs)的细菌是一个日益严重的医疗保健问题,其快速检测是必须克服的挑战,以优化抗菌治疗和患者护理。基质辅助激光解吸电离飞行时间(MALDI-TOF)质谱(MS)已用于确定对内酰胺(包括肠杆菌科中的碳青霉烯)的抵抗力,但由于该方法仍然很耗时,因此尚未得到充分验证。我们旨在评估MALDI-TOF是否可用于临床实践中从阳性血液培养瓶中检测产生ESBL的肠杆菌科。在该测定中,测试了141种血液培养物,其中13种是真正的菌血症,其中128种对应于接种有细菌临床分离株的血液培养瓶。阳性生长结果后,通过MALDI-TOF分析细菌血症,细菌接种后24h,对剩余的128种血液培养物进行分析。通过与头孢噻肟和头孢他啶抗生素及其水解形式相关的峰的分布图确定β-内酰胺酶活性。加入棒酸可排除非ESBL机制的存在。总体数据显示,在阳性血液培养物中检测ESBL的灵敏度为99%(104个中的103个)。在90分钟内(最长150分钟)获得数据。所提出的方法对从阳性血液培养物中早期检测产生ESBL的肠杆菌科细菌具有重大影响,这是一种快速有效的方法,可以尽早给予适当的抗生素治疗。

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