尼泊尔加德满都临床、河水和家禽样本中分离细菌的抗生素耐药性和β-内酰胺耐药基因

IF 3.3 Q2 INFECTIOUS DISEASES
JAC-Antimicrobial Resistance Pub Date : 2025-10-17 eCollection Date: 2025-10-01 DOI:10.1093/jacamr/dlaf186
Upendra Thapa Shrestha, Manash Shrestha, Nabaraj Shrestha, Komal Raj Rijal, Megha Raj Banjara
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引用次数: 0

摘要

目的:评价临床、河水和家禽分离的细菌对抗生素的耐药性和对β -内酰胺的耐药基因。方法:从2020- 2022年采集的临床、家禽和河流水样中分离金黄色葡萄球菌、大肠杆菌和铜绿假单胞菌。他们按照CLSI指南进行了抗菌药物敏感性试验。筛选β-内酰胺耐药基因bla TEM、mcr-1、mecA和blaNDM-1。结果:2835份临床样本中,大肠杆菌的分离率最高(10.3%,292份),其次是金黄色葡萄球菌(6.0%,169份)和铜绿假单胞菌(4.0%,143份)。64.4%的菌株具有多药耐药(MDR), 43.8%的菌株具有广谱β-内酰胺酶(ESBL)产生菌,其中44.5%的菌株携带blaTEM基因,16.4%的菌株携带mcr-1基因。在金黄色葡萄球菌分离株中,80.9%的耐甲氧西林菌株(MRSA)携带mecA基因,30.1%的产金属β-内酰胺酶(MBL) P. aeruginosa携带blaNDM-1基因。在家禽样本中,在128个ESBL生产者中,30.4%的大肠杆菌分离株携带blaTEM基因,携带mcr-1的耐粘菌素分离株的患病率高于临床样本。相比之下,水样中产生esbl的大肠杆菌和MRSA及其相关耐药基因的发生率较低。结论:该研究表明加德满都山谷的临床、家禽和河水分离细菌中广泛存在多药耐药(MDR)和ESBL产生。携带mcr-1基因的耐粘菌素大肠杆菌,携带mecA的耐甲氧西林金黄色葡萄球菌(MRSA)和携带blaNDM-1基因的产生金属β-内酰胺酶(MBL)的铜绿假单胞菌(P. aeruginosa)在不同来源均被检测到。这些发现强调,迫切需要采取“同一个健康”方针来遏制该地区日益严重的抗菌素耐药性威胁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antibiotic resistance and β-lactam resistant genes among bacterial isolates from clinical, river water and poultry samples from Kathmandu, Nepal.

Antibiotic resistance and β-lactam resistant genes among bacterial isolates from clinical, river water and poultry samples from Kathmandu, Nepal.

Objective: To assess the antibiotic resistance and beta-lactam resistance genes among bacterial isolates from clinical, river water and poultry samples.

Methods: Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa were isolated from clinical, poultry and river water samples collected during 2020-22. They were subjected to antimicrobial susceptibility tests following the CLSI guidelines. The bacteria were screened for β-lactam resistance genes bla TEM, mcr-1, mecA and blaNDM-1 .

Results: Among 2835 clinical samples, E. coli was the most frequently isolated bacterium (10.3%, 292), followed by S. aureus (6.0%, 169) and P. aeruginosa (4.0%, 143). Of the E. coli isolates, 64.4% exhibited multidrug resistance (MDR) and 43.8% were extended-spectrum β-lactamase (ESBL) producers, with 44.5% and 16.4% harbouring the blaTEM and mcr-1 genes, respectively. Among S. aureus isolates, 80.9% of methicillin-resistant strains (MRSA) carried the mecA gene, while 30.1% of metallo-β-lactamase (MBL)-producing P. aeruginosa were positive for the blaNDM-1 gene. In poultry samples, 30.4% of E. coli isolates harboured the blaTEM gene among 128 ESBL producers, and the prevalence of colistin-resistant isolates carrying mcr-1 was higher than in clinical samples. In contrast, the occurrence of ESBL-producing E. coli and MRSA, along with their associated resistance genes, was lower in water samples.

Conclusions: This study demonstrated widespread multidrug resistance (MDR) and ESBL production among clinical, poultry and river water bacterial isolates in the Kathmandu valley. Colistin-resistant E. coli carrying the mcr-1 gene, methicillin-resistant S. aureus (MRSA) with mecA and metallo-β-lactamase (MBL)-producing P. aeruginosa harboring blaNDM-1 were detected across sources. These findings emphasize an urgent One Health approach to curb the growing threat of antimicrobial resistance in the region.

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