Protonotariou Efthymia, Meletis Georgios, Vlachodimou Nikoletta, Malousi Andigoni, Tychala Areti, Katsanou Charikleia, Daviti Aikaterini, Mantzana Paraskevi, Skoura Lemonia
Department of Microbiology, AHEPA University Hospital, School of Medicine, Aristotle University of Thessaloniki, S. Kiriakidi Str. 1, 54636 Thessaloniki, Greece.
Laboratory of Biological Chemistry, School of Medicine, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Antibiotics (Basel). 2024 Aug 12;13(8):762. doi: 10.3390/antibiotics13080762.
Carbapenemase-producing strains present a specific geographical distribution regarding the type of carbapenemase-encoding genes that they harbor. For more than twenty years, VIM-type enzymes were the only major carbapenemases that were detected among isolates in Greece until the emergence of NDM-1-encoding in early 2023. In the present study, we present the rapid reversal of the carbapenemase-producing epidemiology from - to -harbouring isolates that occurred in our hospital since then. Between January 2023 and February 2024, 139 isolates tested positive for carbapenemase production with the NG-Test CARBA 5 immunochromatographic assay. Eight isolates were processed with the Hybrispot antimicrobial resistance direct flow chip molecular assay, and the first NDM-producing isolate was further analyzed through whole genome sequencing and bioinformatics analysis. Multiple resistance genes were detected by molecular techniques in accordance with the extensively drug-resistant phenotype. The isolate that was subjected to whole-genome sequencing belonged to the high-risk clone ST308, and the was located in the chromosome in accordance with previously reported data. During the study period, NDM-producing isolates were increasingly detected, and only five months after their emergence, they overcame VIM producers. Our results indicate the potential of this new clone to spread rapidly and predominate within healthcare institutions, further restricting the already limited treatment options.
产碳青霉烯酶菌株在其所携带的碳青霉烯酶编码基因类型方面呈现出特定的地理分布。二十多年来,VIM型酶是在希腊分离株中检测到的唯一主要碳青霉烯酶,直到2023年初出现NDM - 1编码酶。在本研究中,我们展示了自那时以来我院产碳青霉烯酶的流行病学从携带一种酶的分离株迅速转变为携带另一种酶的分离株的情况。在2023年1月至2024年2月期间,139株分离株通过NG - Test CARBA 5免疫层析法检测产碳青霉烯酶呈阳性。8株分离株采用Hybrispot抗菌药物耐药直接流式芯片分子检测法进行检测,第一株产NDM的分离株通过全基因组测序和生物信息学分析进一步分析。根据广泛耐药表型,通过分子技术检测到多个耐药基因。接受全基因组测序的分离株属于高危克隆ST308,并且[此处原文缺失部分信息]根据先前报道的数据位于染色体上。在研究期间,产NDM的分离株检测越来越多,并且在其出现仅五个月后,它们就超过了产VIM的分离株。我们的结果表明这种新克隆有在医疗机构内迅速传播并占主导地位的潜力,进一步限制了本就有限的治疗选择。