Sandwich enzyme-linked aptamer-based assay for the detection of Trichomonas vaginalis

Trichomoniasis is the most prevalent curable, non-viral sexually transmitted infection (STI), with an estimated 156 million new infections in 2020. It can potentially result in adverse birth outcomes as well as infertility in men, whilst it also increases the risk of acquiring HIV and contracting ot...

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Detalles Bibliográficos
Autores: Justo, Christine Aubrey C., Jauset-Rubio, Miriam, Svobodova, Marketa, Skouridou, Vasso, Cools, Piet, Mulinganya, Guy, Ibáñez Escribano, Alexandra, Rivera, Windell L., O'Sullivan, Ciara K.
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/108047
Acceso en línea:https://hdl.handle.net/20.500.14352/108047
Access Level:acceso abierto
Palabra clave:579.6
615.28
576.8
Adhesion protein 65
Hydrogenosomal malic enzyme
Enzyme-linked aptamer assay (ELAA)
Sandwich aptamer assay
Dual aptamers
Trichomonas vaginalis
Trichomoniasis
Ciencias Biomédicas
Microbiología (Farmacia)
Parasitología (Farmacia)
3207.12 Parasitología
Descripción
Sumario:Trichomoniasis is the most prevalent curable, non-viral sexually transmitted infection (STI), with an estimated 156 million new infections in 2020. It can potentially result in adverse birth outcomes as well as infertility in men, whilst it also increases the risk of acquiring HIV and contracting other vaginal infections. It is mostly prevalent among women in low-income countries and especially in Africa and the Americas. This STI is caused by Trichomonas vaginalis (TV) and a robust, cost-effective, sensitive, specific and rapid diagnostic test is urgently required. We report the screening of 6 full-length and 4 truncated aptamers previously selected in our group for use in a microplate-based sandwich assay. The combination of dual aptamers comprising a short 14-mer truncated capture aptamer (termed A1_14mer) and a full-length non-truncated reporter aptamer (A6) was elucidated to be the optimum pair for a sensitive sandwich enzyme-linked aptamer assay (ELAA) for the detection of TV achieving a detection limit of 3.02 × 104 TV cells/mL. The results obtained with the A1_14mer-A6 ELAA correlate excellently with wet-mount microscopy for the detection of TV in clinical specimens, cervicovaginal lavages and vaginal swabs, highlighting the potential clinical application of this assay for cost-effective population screening and subsequent prevention of the onset of complications associated with undiagnosed and untreated TV.