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MALDI-TOF MS as a Tool To Detect a Nosocomial Outbreak of Extended-Spectrum-β-Lactamase- and ArmA Methyltransferase-Producing Enterobacter cloacae Clinical Isolates in Algeria

机译:MALDI-TOF MS作为一种工具用于检测阿尔及利亚产广谱β-内酰胺酶和产生ArmA甲基转移酶的阴沟肠杆菌临床分离株的医院内暴发

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摘要

Enterobacter cloacae is among the most important pathogens responsible for nosocomial infections and outbreaks. In this study, 77 Enterobacter isolates were collected: 27 isolates from Algerian hospitals (in Constantine, Annaba, and Skikda) and 50 isolates from Marseille, France. All strains were identified by matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS). Antibiotic susceptibility testing was performed by the disk diffusion method. PCR was used to detect extended-spectrum-beta-lactamase (ESBL)-encoding, fluoroquinolone resistance-encoding, and aminoglycoside-modifying enzyme (AME) genes. Epidemiological typing was performed using MALDI-TOF MS with data mining approaches, along with multilocus sequence typing (MLST). Sixty-eight isolates (27 from Algeria, 41 from Marseille) were identified by MALDI-TOF MS as E. cloacae. Resistance to antibiotics in the Algerian isolates was significantly higher than that in the strains from Marseille, especially for beta-lactams and aminoglycosides. Eighteen of the 27 Algerian isolates and 11 of the 41 Marseille isolates possessed at least one ESBL-encoding gene: blaCTX-M and/or blaTEM. AME genes were detected in 20 of the 27 Algerian isolates and 8 of the 41 Marseille isolates [ant(2″)-Ia, aac(6′)-Ib-cr, aadA1, aadA2, and armA]. Conjugation experiments showed that armA was carried on a transferable plasmid. MALDI-TOF typing showed three separate clusters according to the geographical distribution and species level. An MLST-based phylogenetic tree showed a clade of 14 E. cloacae isolates from a urology unit clustering together in the MALDI-TOF dendrogram, suggesting the occurrence of an outbreak in this unit. In conclusion, the ability of MALDI-TOF to biotype strains was confirmed, and surveillance measures should be implemented, especially for Algerian patients hospitalized in France.
机译:阴沟肠杆菌是引起医院感染和暴发的最重要的病原体之一。在这项研究中,收集了77株肠杆菌分离株:来自阿尔及利亚医院(康斯坦丁,安纳巴和斯基克达)的27株分离株和来自法国马赛的50株分离株。所有菌株均通过基质辅助激光解吸电离-飞行时间质谱(MALDI-TOF MS)进行鉴定。通过圆盘扩散法进行抗生素敏感性试验。 PCR用于检测超广谱β-内酰胺酶(ESBL)编码,氟喹诺酮耐药性编码和氨基糖苷修饰酶(AME)基因。流行病学分型使用MALDI-TOF MS和数据挖掘方法以及多基因座序列分型(MLST)进行。 MALDI-TOF MS将六十八种分离株(阿尔及利亚的27种,马赛的41种)鉴定为阴沟肠杆菌。阿尔及利亚分离株对抗生素的抵抗力明显高于马赛菌株,特别是对β-内酰胺类和氨基糖苷类。 27个阿尔及利亚分离株中的18个和41个马赛分离株中的11个具有至少一个ESBL编码基因:blaCTX-M和/或blaTEM。在27个阿尔及利亚分离株中的20个和41个马赛分离株中的8个[ant(2″)-Ia,aac(6')-Ib-cr,aadA1,aadA2和armA]中检测到AME基因。缀合实验表明,armA携带在可转移质粒上。 MALDI-TOF分型根据地理分布和物种水平显示三个单独的簇。基于MLST的系统发育树显示,一个泌尿科病房的14株阴沟肠梭菌进化枝聚集在MALDI-TOF树状图中,表明该病爆发。总之,证实了MALDI-TOF对生物型菌株的能力,并应采取监测措施,特别是对于在法国住院的阿尔及利亚患者。

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