The efficacy of AuNP-probe conjugate nanobiosensor in non-amplification and amplification forms for the diagnosis of leishmaniasis

被引:7
作者
Deris, Someye [1 ]
Osanloo, Mahmoud [2 ]
Ghasemian, Abdolmajid [3 ]
Ataei, Saeed [4 ]
Kohansal, Maryam [3 ]
Samsami, Sahar [1 ]
Yazdanpanah, Ava [1 ]
Ebrahimnezhad, Alireza [4 ,6 ]
Ghanbariasad, Ali [3 ,5 ]
机构
[1] Fasa Univ Med Sci, Student Res Comm, Fasa, Iran
[2] Fasa Univ Med Sci, Sch Adv Technol Med, Dept Med Nanotechnol, Fasa, Iran
[3] Fasa Univ Med Sci, Noncommunicable Dis Res Ctr, Fasa, Iran
[4] Shiraz Univ Med Sci, Biotechnol Res Ctr, Shiraz, Iran
[5] Fasa Univ Med Sci, Sch Adv Technol Med, Dept Med Biotechnol, Fasa, Iran
[6] Shiraz Univ Med Sci, Sch Adv Med Sci & Technol, Dept Med Nanotechnol, Unit 23, 2nd Floor,Almass Bldg,Alley 29, Shiraz, Iran
关键词
Gold nanoparticles; Leishmania spp; Diagnosis; Biosensor; Hybridization; DNA;
D O I
10.1186/s12879-022-07835-z
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Nanobiosensor platforms have emerged as convenient and promising approaches with remarkable efficacy for the diagnosis of infectious diseases. Gold nanoparticles (AuNPs) have been widely used due to numerous advantageous properties such as optical, electrical, physicochemical and great biomolecules binding capabilities. This study aimed to apply AuNP-Probe Conjugate for the detection of Leishmania spp., using colorimetric and amplification methods targeting parasitic ITS2 fragment. The first method was carried out by hybridization of 10 mu L of DNA with 4 mu L of probe and addition of 5 mu L of 0.2 N HCl (non-amplification method). Second method was followed by polymerase chain reaction (PCR) amplification using thiolated primer, 5 mu L of AuNP and 5 mu L of 0.2 N HCl. The appearance of red and purple colors indicated positive and negative results, respectively. The minimum of detection for non-amplification and amplification methods for three strains of Leishmania namely L. major, L. tropica and L. infantum were determined to be 32 fg/mu L and 16 fg/mu L, respectively. Sensitivity for detection of visceral leishmaniasis (VL) for non-amplification and amplification methods included 96% and 100%, respectively and for cutaneous leishmaniasis (CL) included 98% and 100%, respectively. The results of this investigation revealed that sensitivity of amplification method was the same as RT-qPCR, while that of non-amplification method was lower. However, this method was promising because of no need for any equipment, high specificity, enough sensitivity, low cost and rapidity (less than 30 min) to complete after genomic DNA extraction.
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页数:10
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