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泰国东北部产超广谱β-内酰胺酶的多重耐药菌的表型和基因型特征

Phenotypic and Genotypic Profiles of Extended-Spectrum Beta-Lactamase-Producing Multidrug-Resistant in Northeastern Thailand.

作者信息

Chaisaeng Sumontha, Phetburom Nattamol, Kasemsiri Pachara, Putthanachote Nuntiput, Wangnadee Naowarut, Boueroy Parichart, Kerdsin Anusak, Chopjitt Peechanika

机构信息

Faculty of Public Health, Kasetsart University Chalermphrakiat Sakon Nakhon Province Campus, Sakon Nakhon 47000, Thailand.

Clinical Microbiology Laboratory, Sakon Nakhon Hospital, Sakon Nakhon 47000, Thailand.

出版信息

Antibiotics (Basel). 2024 Sep 25;13(10):917. doi: 10.3390/antibiotics13100917.

Abstract

The global emergence of extended-spectrum beta-lactamase (ESBL)-producing presents a significant public health threat and complicates antibiotic treatment for infections. This study aimed to determine the prevalence of ESBL-producing in a clinical setting, analyze their antimicrobial susceptibility profiles, and characterize both phenotypic and genetic determinants. A total of 507 non-duplicate clinical isolates of were collected between 2019 and 2020, and third-generation cephalosporin resistance was screened by disk diffusion. Identification of was confirmed using biochemical tests and PCR with species-specific primers. Antimicrobial susceptibility testing was conducted using disk diffusion, and phenotypic ESBL production was confirmed using the combined disk method. Multiplex PCR detected ESBL genes (, , and ) and identified groups. The genetic relatedness of ESBL-producing strains was assessed using the ERIC-PCR approach. Fitty-four isolates were confirmed as ESBL producers, all classified as multidrug-resistant (MDR). All ESBL-producing isolates exhibited resistance to ampicillin and cefotaxime, with high resistance rates for ciprofloxacin (98.2%), azithromycin (94.4%), piperacillin-tazobactam (88.9%), and trimethoprim (83.3%). Genotypic analysis revealed was present in 94.4% of isolates, in 87%, and in 55.5%. The group was the most prevalent, accounting for 96.1% of isolates. Co-harboring of , , and occurred in 42.6% of isolates, with co-carrying of , and was observed in 23/54 isolates. The ERIC-PCR analysis revealed 15 distinct types, indicating high genetic diversity. These findings highlight the urgent need for ongoing monitoring to control the spread of ESBL among and emphasize the importance of early detection and appropriate antibiotic selection for effectively treating infection caused by these pathogens.

摘要

产超广谱β-内酰胺酶(ESBL)的[细菌名称]在全球范围内出现,对公共卫生构成重大威胁,并使感染的抗生素治疗复杂化。本研究旨在确定临床环境中产ESBL的[细菌名称]的流行率,分析其抗菌药敏谱,并鉴定表型和基因决定因素。2019年至2020年期间共收集了507株非重复的[细菌名称]临床分离株,采用纸片扩散法筛选对第三代头孢菌素的耐药性。使用生化试验和种特异性引物的PCR确认[细菌名称]的鉴定。采用纸片扩散法进行抗菌药敏试验,并使用联合纸片法确认表型ESBL的产生。多重PCR检测ESBL基因([基因名称1]、[基因名称2]和[基因名称3])并鉴定[细菌名称]组。使用ERIC-PCR方法评估产ESBL菌株的遗传相关性。54株分离株被确认为ESBL生产者,均被分类为多重耐药(MDR)。所有产ESBL的[细菌名称]分离株均对氨苄西林和头孢噻肟耐药,对环丙沙星(98.2%)、阿奇霉素(94.4%)、哌拉西林-他唑巴坦(88.9%)和甲氧苄啶(83.3%)的耐药率较高。基因型分析显示,94.4%的分离株中存在[基因名称1],87%存在[基因名称2],55.5%存在[基因名称3]。[细菌名称]组最为常见,占分离株的96.1%。42.6%的分离株中同时存在[基因名称1]、[基因名称2]和[基因名称3],23/54株分离株中观察到[基因名称1]和[基因名称2]的共同携带。ERIC-PCR分析显示有15种不同类型,表明遗传多样性高。这些发现突出了持续监测以控制ESBL在[细菌名称]中传播的迫切需要,并强调了早期检测和适当选择抗生素以有效治疗这些病原体引起的感染的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/282e/11505529/51901cabd5ba/antibiotics-13-00917-g001.jpg

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