Proposition of a phagosensor with a unique Teseptimavirus SAL_R1S on a carbon nanotube platform for efficient detection of typhoid pathogen

IF 6.5 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Md Hasibul Hassan , Md. Romzan Ali , Md. Arifur Rahman , Anamica Hossain , Sunjida Afrin , Md. Abdul Khaleque , Md. Anwar Hossain , Md. Zaved Hossain Khan , Munawar Sultana
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引用次数: 0

Abstract

The detection of the typhoid pathogen, Salmonella enterica serotype Typhi (S. Typhi), holds massive clinical, public health, and epidemiological significance around the globe. Conventional diagnosis relies on bacterial isolation having a set of challenges when it comes to accurate detection, therapeutic intervention and disease management. Substantial reviews and reports exist on the advantages of bacteriophage-based biosensors (phagosensors) concerning Salmonella. However, phagosensor for Salmonella Typhi point of care detection at a lower limit of detection (LOD) has yet to be reported. This study is the earliest endeavor to develop a multi-wall carbon nanotubes (MWCNTs) based electrochemical phagosensor utilizing a unique bacteriophage SAL_R1S as a biomolecular recognition element, selectively binding S. Typhi DMS_A1 at LOD of 1 CFU/ml. S. Typhi DMS_A1, retrieved from patient's blood, consists of 10 pathogenicity islands and a wide range of efflux pump genes in its whole genome, which has not yet been documented for Salmonella. Subsequent screening for its specific bacteriophage from a sewage sample pinpointed the phage SAL_R1S of class Caudoviricetes, family Autographiviridae and genus Teseptimavirus. The whole genome- and tail-fiber protein- based alignment was close to Salmonella phage Vi06 covering 88.8 % and 90 % similarity, respectively. SAL_R1S exclusively binds S. Typhi in a specific manner and also possess excellent genetic feature as a candidate for developing a highly sensitive electrochemical phagosensor. Therefore, it was covalently immobilized onto a modified SPE/MWCNT/PANI-based electrode surface, allowing charge-directed, oriented immobilization which then confirmed through scanning electron microscopy. The electrode surface was featured via field emission scanning electron microscopy, electrochemical impedance spectroscopy, and cyclic voltammetry. The pathogen detection process of the phagosensor is quick (∼ 20 min). It has exceptional selectivity for typhoid pathogens from blood, wastewater or within mixed populations, indicating the application of this proposed phagosensor in clinical settings as a rapid, alternative to available conventional detection techniques, and low-cost surveillance tool.

Abstract Image

提出一种在碳纳米管平台上使用独特的 Teseptimavirus SAL_R1S 的吞噬传感器,用于高效检测伤寒病原体
伤寒病原体肠炎沙门氏菌血清型 Typhi(S. Typhi)的检测在全球范围内具有重要的临床、公共卫生和流行病学意义。传统诊断依赖细菌分离,在准确检测、治疗干预和疾病管理方面存在一系列挑战。关于噬菌体生物传感器(噬菌体传感器)在沙门氏菌方面的优势,已有大量评论和报告。然而,以较低的检测限(LOD)进行伤寒沙门氏菌护理点检测的噬菌体传感器尚未见报道。本研究首次尝试开发基于多壁碳纳米管(MWCNTs)的电化学吞噬传感器,利用独特的噬菌体 SAL_R1S 作为生物分子识别元件,选择性结合伤寒杆菌 DMS_A1,检测限为 1 CFU/ml。从患者血液中提取的伤寒杆菌 DMS_A1 在其全基因组中包含 10 个致病性岛和多种外排泵基因,这在沙门氏菌中尚无记录。随后从污水样本中筛选出了其特异性噬菌体,最终确定了噬菌体 SAL_R1S,属于 Caudoviricetes 类、Autographiviridae 科和 Teseptimavirus 属。基于全基因组和尾纤蛋白的比对结果与沙门氏菌噬菌体 Vi06 非常接近,相似度分别为 88.8 % 和 90 %。SAL_R1S 能以特异的方式与 Typhi 沙门氏菌独家结合,并具有优良的遗传特性,可作为开发高灵敏度电化学吞噬传感器的候选基因。因此,SAL_R1S 被共价固定在基于 SPE/MWCNT/PANI 的修饰电极表面上,实现了电荷定向、定向固定,并通过扫描电子显微镜进行了确认。通过场发射扫描电子显微镜、电化学阻抗光谱和循环伏安法对电极表面进行了鉴定。噬菌体传感器的病原体检测过程非常迅速(20 分钟以内)。它对血液、废水或混合人群中的伤寒病原体具有极高的选择性,这表明这种拟议的噬菌体传感器可应用于临床环境,成为现有传统检测技术的快速替代品和低成本监测工具。
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来源期刊
CiteScore
9.60
自引率
0.00%
发文量
60
审稿时长
49 days
期刊介绍: Sensors and Actuators Reports is a peer-reviewed open access journal launched out from the Sensors and Actuators journal family. Sensors and Actuators Reports is dedicated to publishing new and original works in the field of all type of sensors and actuators, including bio-, chemical-, physical-, and nano- sensors and actuators, which demonstrates significant progress beyond the current state of the art. The journal regularly publishes original research papers, reviews, and short communications. For research papers and short communications, the journal aims to publish the new and original work supported by experimental results and as such purely theoretical works are not accepted.
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