Triple lines gold nanoparticle-based lateral flow assay for enhanced and simultaneous detection of Leishmania DNA and endogenous control

被引:63
作者
Rivas, Lourdes [1 ,2 ]
de la Escosura-Muniz, Alfredo [1 ]
Serrano, Lorena [3 ]
Altet, Laura [3 ]
Francino, Olga [2 ,3 ]
Sanchez, Armand [2 ,4 ]
Merkoci, Arben [1 ,5 ]
机构
[1] Inst Catala Nanociencia & Nanotecnol, Nanobioelect & Biosensors Grp ICN2, Campus UAB, Bellaterra 08193, Barcelona, Spain
[2] Autonomous Univ Barcelona, Bellaterra 08193, Barcelona, Spain
[3] Vetgenomics, Bellaterra 08193, Barcelona, Spain
[4] CSIC IRTA UAB UB, Ctr Res Agr Genom, Cerdanyola Del Valles 08193, Catalonia, Spain
[5] Inst Catalana Recerca & Estudis Avancats, Barcelona 08010, Spain
关键词
lateral-flow assay; gold nanoparticles; secondary antibodies; Leishmania DNA; endogenous control; REAL-TIME PCR; PROSTATE-SPECIFIC ANTIGEN; VISCERAL LEISHMANIASIS; CANINE LEISHMANIASIS; SEROLOGICAL DIAGNOSIS; STRIP TESTS; SENSITIVITY; PAPER; IMMUNOASSAY; DIPSTICK;
D O I
10.1007/s12274-015-0870-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A novel triple lines lateral-flow assay (LFA) with enhanced sensitivity for the detection of Leishmania infantum DNA in dog blood samples was designed and successfully applied. The enhanced LFA methodology takes advantage of the gold nanoparticle tags (AuNPs) conjugated to polyclonal secondary antibodies, which recognize anti-FITC antibodies. The polyclonal nature of the secondary antibodies allows for multiple binding to primary antibodies, leading to enhanced AuNP plasmonics signal. Furthermore, endogenous control consisting of the amplified dog 18S rRNA gene was introduced to avoid false negatives. Using this strategy, 0.038 spiked Leishmania parasites per DNA amplification reaction (1 parasite/100 mu L of DNA sample) were detected. Detection limit of LFA was found to be lower than that of the conventional techniques. In summary, our novel LFA design is a universal and simple sensing alternative that can be extended to several other biosensing scenarios.
引用
收藏
页码:3704 / 3714
页数:11
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