印度东北部耐碳青霉烯类鲍曼不动杆菌临床分离株中金属-β-内酰胺酶和 OXA 型 β-内酰胺酶的共同产生

Shyamalima Saikia, Indrani Gogoi, Amos Oloo, Mohan Sharma, Minakshi Puzari, Pankaj Chetia
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引用次数: 0

摘要

耐碳青霉烯类鲍曼不动杆菌对全球公共卫生构成重大威胁,特别是由于它能够产生多种碳青霉烯酶,从而导致治疗难题。本研究旨在调查从印度东北部不同临床环境中收集到的耐碳青霉烯鲍曼不动杆菌分离株的抗生素耐药性模式,重点研究其基因型和表型耐药性特征。共收集了 172 个耐多药鲍曼尼氏菌分离株,并使用柯比鲍尔盘扩散法对其进行了抗生素药敏试验。对分离株进行了各种表型测试,以检测扩谱β-内酰胺酶(ESBL)、金属-β-内酰胺酶(MBL)、C类AmpC β-内酰胺酶(AmpC)和碳青霉烯水解D类β-内酰胺酶(CHDL)的产生情况。通过表型和基因型调查,在分离物中检测到碳青霉烯酶和头孢菌素酶基因的过度表达。分离菌株的抗生素耐药性特征显示,所有分离菌株都具有多重耐药性;25%具有广泛耐药性,9.30%具有泛耐药性,而91.27%对碳青霉烯类具有耐药性。在基因型调查中,80.81%的分离物至少含有一种金属-β-内酰胺酶编码基因,其中以 blaNDM 最为普遍,占 70.34%,其次是 blaIMP,占 51.16%。在 D 类碳青霉烯酶方面,在所有检测到的分离物中都检测到了 blaOXA-51 和 blaOXA-23 基因,而在 15.11%、6.97% 和 1.74% 的分离物中分别发现了 blaOXA-24、blaOXA-48 和 blaOXA-58。进一步的分析表明,31.97%的分离株同时具有ESBL、MBL、AmpC和CHDL基因,而31.39%的分离株同时具有ESBL、MBL和CHDL基因以及或不具有ISAba1基因,从而导致广泛耐药或泛耐药表型。这项研究突显了印度东北部流行的分离株复杂的遗传特征和抗菌模式,强调了采取有效的感染控制措施和开发替代治疗策略来对抗这些具有挑战性的病原体的迫切需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Co-production of metallo-β-lactamase and OXA-type β-lactamases in carbapenem-resistant Acinetobacter baumannii clinical isolates in North East India

Co-production of metallo-β-lactamase and OXA-type β-lactamases in carbapenem-resistant Acinetobacter baumannii clinical isolates in North East India

Carbapenem-resistant Acinetobacter baumannii poses a significant threat to public health globally, especially due to its ability to produce multiple carbapenemases, leading to treatment challenges. This study aimed to investigate the antibiotic resistance pattern of carbapenem-resistant A. baumannii isolates collected from different clinical settings in North East India, focusing on their genotypic and phenotypic resistance profiles. A total of 172 multidrug-resistant A. baumannii isolates were collected and subjected to antibiotic susceptibility test using the Kirby–Bauer disk diffusion method. Various phenotypic tests were performed to detect extended-spectrum β-lactamase (ESBL), metallo-β-lactamase (MBL), class C AmpC β-lactamase (AmpC), and carbapenem hydrolyzing class D β-lactamase (CHDL) production among the isolates. Overexpression of carbapenemase and cephalosporinase genes was detected among the isolates through both phenotypic and genotypic investigation. The antibiotic resistance profile of the isolates revealed that all were multidrug-resistant; 25% were extensively drug-resistant, 9.30% were pan-drug-resistant, whereas 91.27% were resistant to carbapenems. In the genotypic investigation, 80.81% of isolates were reported harbouring at least one metallo-β-lactamase encoding gene, with blaNDM being the most prevalent at 70.34%, followed by blaIMP at 51.16% of isolates. Regarding class D carbapenemases, blaOXA-51 and blaOXA-23 genes were detected in all the tested isolates, while blaOXA-24, blaOXA-48, and blaOXA-58 were found in 15.11%, 6.97%, and 1.74% isolates respectively. Further analysis showed that 31.97% of isolates co-harboured ESBL, MBL, AmpC, and CHDL genes, while 31.39% of isolates co-harboured ESBL, MBL, and CHDL genes with or without ISAba1 leading to extensively drug-resistant or pan drug-resistant phenotypes. This study highlights the complex genetic profile and antimicrobial-resistant pattern of the isolates circulating in North East India, emphasizing the urgent need for effective infection control measures and the development of alternative treatment strategies to combat these challenging pathogens.

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