Development of a novel immunoFET technology-based POC assay for detection of Leishmania donovani and Leishmania major.

IF 1.4 4区 医学 Q4 IMMUNOLOGY Parasite Immunology Pub Date : 2023-07-01 DOI:10.1111/pim.12984
Nebiye Yentur Doni, Paul J Bertani, Greta Volpedo, Noushin Saljoughian, Sanjay Varikuti, Greg Matlashewski, Wu Lu, Abhay R Satoskar
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Abstract

Leishmaniasis is considered as one of the 20 neglected tropical diseases. Current methods of leishmanial diagnosis depend on conventional laboratory-based techniques, which are time-consuming, costly and require special equipment and trained personnel. In this context, we aimed to provide an immuno field effect transistors (ImmunoFET) biosensor that matches the conventional standards for point-of-care (POC) monitoring and detection of Leishmania (L.) donovani/Leishmania major. Crude antigens prepared by repeated freeze thawing of L. donovani/L. major stationary phase promastigotes were used for ELISA and ImmunoFETs. Lesishmania-specific antigens were serially diluted in 1× PBS from a concentration of 106 -102 parasites/mL. A specific polyclonal antibody-based sandwich ELISA was established for the detection of Leishmania antigens. An immunoFET technology-based POC novel assay was constructed for the detection of Leishmania antigens. Interactions between antigen-antibody at the gate surface generate an electrical signal that can be measured by semiconductor field-effect principles. Sensitivity was considered and measured as the change in current divided by the initial current. The final L. donovani/L. major crude antigen protein concentrations were measured as 1.50 mg/mL. Sandwich ELISA against the Leishmania 40S ribosomal protein detected Leishmania antigens could detect as few as 100 L. donovani/L. major parasites. An immunoFET biosensor was constructed based on the optimization of aluminium gallium nitride/gallium nitride (AlGaN/GaN) surface oxidation methods. The device surface was composed by an AlGaN/GaN wafer with a 23 nm AlGaN barrier layer, a 2 μm GaN layer on the silicon carbide (SiC) substrate for Leishmania binding, and coated with a specific antibody against the Leishmania 40S ribosomal protein, which was successfully detected at concentrations from 106 to 102 parasites/mL in 1× PBS. At the concentration of 104 parasites, the immunoFETs device sensitivities were 13% and 0.052% in the sub-threshold regime and the saturation regime, respectively. Leishmania parasites were successfully detected by the ImmunoFET biosensor at a diluted concentration as low as 150 ng/mL. In this study, the developed ImmunoFET biosensor performed well. ImmunoFET biosensors can be used as an alternative diagnostic method to ELISA. Increasing the sensitivity and optimization of immuno-FET biosensors might allow earlier and faster detection of leishmaniasis.

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基于免疫场效应晶体管技术的新型多诺瓦利什曼原虫和大利什曼原虫POC检测方法的开发。
利什曼病被认为是20种被忽视的热带病之一。目前的利什曼病诊断方法依赖于传统的基于实验室的技术,这些技术耗时、昂贵并且需要特殊设备和训练有素的人员。在这种情况下,我们的目标是提供一种免疫场效应晶体管(ImmunoFET)生物传感器,它符合传统的护理点(POC)监测和检测利什曼原虫(L.) donovani/ major利什曼原虫的标准。利用反复冻融法制备多诺瓦氏乳杆菌原抗原。主要固定相原毛菌用于ELISA和免疫场效应体。利什曼原虫特异性抗原在1倍PBS中连续稀释,浓度为106 -102只/mL。建立了一种特异的多克隆抗体夹心ELISA检测利什曼原虫抗原。建立了一种基于免疫场效应晶体管技术的新方法检测利什曼原虫抗原。抗原-抗体在栅极表面的相互作用产生电信号,可以通过半导体场效应原理来测量。灵敏度被认为和测量为电流的变化除以初始电流。最终L. donovani/L。测定主要粗抗原蛋白浓度为1.50 mg/mL。夹心ELISA法对利什曼原虫40S核糖体蛋白检测利什曼原虫抗原可检出少至100 L。donovani / L。主要的寄生虫。在优化氮化镓铝/氮化镓(AlGaN/GaN)表面氧化方法的基础上,构建了免疫场效应晶体管生物传感器。该器件表面由具有23 nm AlGaN阻挡层的AlGaN/GaN晶片组成,在碳化硅(SiC)底物上有2 μm GaN层用于利什曼原虫结合,并包被针对利什曼原虫40S核糖体蛋白的特异性抗体,该抗体在1× PBS浓度为106 ~ 102寄生虫/mL时成功检测到。在104种寄生虫浓度下,免疫fet器件在亚阈值和饱和状态下的灵敏度分别为13%和0.052%。免疫场效应晶体管生物传感器在低至150 ng/mL的稀释浓度下成功检测利什曼原虫。在本研究中,所研制的免疫场效应晶体管生物传感器表现良好。免疫场效应晶体管生物传感器可作为ELISA的替代诊断方法。提高免疫场效应晶体管生物传感器的灵敏度和优化可能使利什曼病的检测更早和更快。
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来源期刊
Parasite Immunology
Parasite Immunology 医学-寄生虫学
CiteScore
4.70
自引率
4.50%
发文量
61
审稿时长
6-12 weeks
期刊介绍: Parasite Immunology is an international journal devoted to research on all aspects of parasite immunology in human and animal hosts. Emphasis has been placed on how hosts control parasites, and the immunopathological reactions which take place in the course of parasitic infections. The Journal welcomes original work on all parasites, particularly human parasitology, helminths, protozoa and ectoparasites.
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