| Literature DB >> 28390319 |
Seon-Ju Yeo1, Bui Thi Cuc1, Soon-Ai Kim2, Do Thi Hoang Kim1, Duong Tuan Bao1, Trinh Thi Thuy Tien1, Nguyen Thi Viet Anh1, Do-Young Choi3, Chom-Kyu Chong4, Hak Sung Kim5, Hyun Park6.
Abstract
Sensitive and rapid diagnostic systems for avian influenza (AI) virus are required to screen large numbers of samples during a disease outbreak and to prevent the spread of infection. In this study, we employed a novel fluorescent dye for the rapid and sensitive recognition of AI virus. The styrylpyridine phosphor derivative was synthesized by adding allyl bromide as a stable linker and covalently immobilizing it on latex beads with antibodies generating the unique Red dye 53-based fluorescent probe. The performance of the innovative rapid fluorescent immnunochromatographic test (FICT) employing Red dye 53 in detecting the AI virus (A/H5N3) was 4-fold and 16-fold higher than that of Europium-based FICT and the rapid diagnostic test (RDT), respectively. In clinical studies, the presence of human nasopharyngeal specimens did not alter the performance of Red dye 53-linked FICT for the detection of H7N1 virus. Furthermore, in influenza A virus-infected human nasopharyngeal specimens, the sensitivity of the Red dye 53-based assay and RDT was 88.89% (8/9) and 55.56% (5/9) relative to rRT-PCR, respectively. The photostability of Red dye 53 was higher than that of fluorescein isothiocyanate (FITC), showing a stronger fluorescent signal persisting up to 8min under UV. The Red dye 53 could therefore be a potential probe for rapid fluorescent diagnostic systems that can recognize AI virus in clinical specimens.Entities:
Keywords: Avian influenza A virus; Novel pyridine-styrylpyridine fluorescent dye; Photostability; Rapid fluorescent immunochromatographic test
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Year: 2017 PMID: 28390319 DOI: 10.1016/j.bios.2017.03.068
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618