首页> 外文期刊>Journal of Clinical Microbiology >Metallo-β-Lactamase-Producing Gram-Negative Bacilli: Laboratory-Based Surveillance in Cooperation with 13 Clinical Laboratories in the Kinki Region of Japan
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Metallo-β-Lactamase-Producing Gram-Negative Bacilli: Laboratory-Based Surveillance in Cooperation with 13 Clinical Laboratories in the Kinki Region of Japan

机译:产金属β-内酰胺酶的革兰氏阴性杆菌:与日本近畿地区的13个临床实验室合作进行实验室监测

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A total of 19,753 strains of gram-negative rods collected during two 6-month periods (October 2000 to March 2001 and November 2001 to April 2002) from 13 clinical laboratories in the Kinki region of Japan were investigated for the production of metallo-β-lactamases (MBLs). MBLs were detected in 96 (0.5%) of the 19,753 isolates by the broth microdilution method, the 2-mercaptopropionic acid inhibition test, and PCR and DNA sequencing analyses. MBL-positive isolates were detected in 9 of 13 laboratories, with the rate of detection ranging between 0 and 2.6% for each laboratory. Forty-four of 1,429 (3.1%) Serratia marcescens, 22 of 6,198 (0.4%) Pseudomonas aeruginosa, 21 of 1,108 (1.9%) Acinetobacter spp., 4 of 544 (0.7%) Citrobacter freundii, 3 of 127 (2.4%) Providencia rettgeri, 1 of 434 (0.2%) Morganella morganii, and 1 of 1,483 (0.1%) Enterobacter cloacae isolates were positive for MBLs. Of these 96 MBL-positive strains, 87 (90.6%), 7 (7.3%), and 2 (2.1%) isolates carried the genes for IMP-1-group MBLs, IMP-2-group MBLs, and VIM-2-group MBLs, respectively. The class 1 integrase gene, intI1, was detected in all MBL-positive strains, and the aac (6′)-Ib gene was detected in 37 (38.5%) isolates. Strains with identical PCR fingerprint profiles in a random amplified polymorphic DNA pattern analysis were isolated successively from five separate hospitals, suggesting the nosocomial spread of the organism in each hospital. In conclusion, many species of MBL-positive gram-negative rods are distributed widely in different hospitals in the Kinki region of Japan. The present findings should be considered during the development of policies and strategies to prevent the emergence and further spread of MBL-producing bacteria.
机译:在日本近畿地区的13个临床实验室的两个6个月期间(2000年10月至2001年3月以及2001年11月至2002年4月)共收集了19,753株革兰氏阴性杆菌,用于生产金属β-。内酰胺酶(MBL)。通过肉汤微稀释法,2-巯基丙酸抑制试验以及PCR和DNA测序分析,在19,753个分离物中的96个(0.5%)中检测到MBL。在13个实验室中的9个实验室中检测到MBL阳性分离株,每个实验室的检测率在0到2.6%之间。 1,429(3.1%)粘质沙雷氏菌中的四十四,6,198(22%)中的22(0.4%)铜绿假单胞菌,1,108(21%)(1.9%)中的不动杆菌 > spp。,弗氏柠檬酸杆菌544(4(0.7%))中的4,瑞氏省(Providencia rettgeri)127(3)(2.4%)摩根氏摩根氏菌434(1) ,而1,483(0.1%)个阴沟肠杆菌()分离株中有1例MBL阳性。在这96个MBL阳性菌株中,有87个(90.6%),7个(7.3%)和2个(2.1%)分离株带有IMP-1-group MBL,IMP-2-group MBL和VIM-2-的基因。组MBL,分别。在所有MBL阳性菌株中检测到1类整合酶基因 intI1 ,而 aac 6 ') -Ib在37个(38.5%)分离株中检测到基因。在五个独立的医院中,连续从随机扩增的多态性DNA模式分析中分离出具有相同PCR指纹图谱的菌株,这表明该生物体在医院中的传播。总之,MBK阳性革兰氏阴性杆菌的许多种类广泛分布在日本近畿地区的不同医院中。在制定政策和策略以防止产生MBL的细菌出现和进一步传播时,应考虑本研究结果。

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