Isothermal recombinase polymerase amplification and silver nanoparticle assay: a sustainable approach for ultrasensitive detection of Klebsiella pneumoniae†

IF 2.6 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Naresh Patnaik, Nidhi Orekonday and Ruchi Jain Dey
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Abstract

Our study addresses the urgent need for effective detection of Klebsiella pneumoniae, a recognized threat by the World Health Organization (WHO). Current challenges in managing K. pneumoniae infections include the lack of rapid and affordable detection tools, particularly in resource-limited point-of-care (POC) settings. To tackle this, we developed an innovative molecular detection pipeline combining three POC-compatible methods. Firstly, we employed Insta DNA™ card-based sample collection and DNA extraction for simplicity and ease of use. Next, we utilized recombinase polymerase amplification (RPA) targeting the Klebsiella hemolysin gene, khe, specific to the K. pneumoniae species complex (KpSC). Finally, we integrated a silver nanoparticle (AgNP) aggregation assay for visual detection, offering a rapid, sensitive, and specific method capable of detecting as few as ∼3 bacteria of K. pneumoniae within ∼45 minutes. This approach eliminates the need for complex equipment, making it highly suitable for field and resource-limited POC applications. Moreover, our method introduces an environmentally significant detection strategy. The method developed minimizes chemical reagent usage and reduces the carbon footprint associated with sample transportation. Furthermore, our method reduces waste compared to the traditional detection techniques, offering a safer alternative to ethidium bromide or other DNA dyes which are often genotoxic and mutagenic in nature. Silver nanoparticles, being environmentally safer, can also be recycled from the waste, contributing to sustainability in nanoparticle production and disposal. Overall, our technique presents a promising solution for detecting K. pneumoniae in various settings, including environmental, water, and food samples, as well as industrial or hospital effluents. By aligning with global efforts to improve public health and environmental sustainability, our approach holds significant potential for enhancing disease management and reducing environmental impact.

Abstract Image

等温重组聚合酶扩增和银纳米粒子检测:超灵敏检测肺炎克雷伯氏菌的可持续方法。
肺炎克雷伯氏菌是世界卫生组织(WHO)公认的威胁,我们的研究满足了有效检测肺炎克雷伯氏菌的迫切需求。目前,肺炎克雷伯菌感染管理面临的挑战包括缺乏快速、经济的检测工具,尤其是在资源有限的护理点(POC)环境中。为了解决这个问题,我们开发了一种创新的分子检测管道,结合了三种与 POC 兼容的方法。首先,我们采用了基于 Insta DNA™ 卡的样本采集和 DNA 提取方法,简单易用。接着,我们利用重组酶聚合酶扩增(RPA)技术,针对肺炎克雷伯菌种群(KpSC)的特异性溶血素基因 khe 进行扩增。最后,我们整合了银纳米粒子(AgNP)聚集检测法进行肉眼检测,提供了一种快速、灵敏、特异的方法,能够在 45 分钟内检测出 3 个肺炎克雷伯菌。这种方法无需复杂的设备,因此非常适合现场和资源有限的 POC 应用。此外,我们的方法还引入了一种环保的检测策略。所开发的方法最大限度地减少了化学试剂的使用,降低了与样本运输相关的碳足迹。此外,与传统检测技术相比,我们的方法减少了浪费,为溴化乙锭或其他 DNA 染料提供了更安全的替代品,因为它们通常具有遗传毒性和致突变性。银纳米粒子对环境更安全,还可以从废物中回收利用,有助于纳米粒子生产和处理的可持续性。总之,我们的技术为检测各种环境(包括环境、水和食品样本以及工业或医院污水)中的肺炎克氏菌提供了一种前景广阔的解决方案。通过与全球改善公共卫生和环境可持续性的努力保持一致,我们的方法在加强疾病管理和减少环境影响方面具有巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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