Rapid and sensitive detection of Pseudomonas aeruginosa using multiple cross displacement amplification and gold nanoparticle-based lateral flow biosensor visualization
Author(s) -
Fan Zhao,
Liiu,
Jinqing g,
Chunmei Wang,
Jing Wang,
Yan Liu,
Naishu Gao,
Xiaoxue Zhu,
Lei Wu,
Shoukui Hu
Publication year - 2018
Publication title -
fems microbiology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1093/femsle/fny147
Subject(s) - pseudomonas aeruginosa , multiple displacement amplification , gold standard (test) , colloidal gold , sputum , biosensor , microbiology and biotechnology , chromatography , chemistry , nanoparticle , biology , bacteria , materials science , polymerase chain reaction , nanotechnology , dna extraction , medicine , gene , biochemistry , genetics , pathology , tuberculosis
Pseudomonas aeruginosa causes nosocomial infections of burn patients and other immunocompromised individuals, but the conventional diagnosis of P. aeruginosa infection depends on time-consuming culture-based methods. Hence, a simple, fast, sensitive technique for detection of P. aeruginosa using multiple cross displacement amplification (MCDA) and gold nanoparticle-based lateral flow biosensors (LFB) was developed. By using this technique, the reaction could be completed at an optimized constant temperature (67°C) within only 40 min. The reaction product could be detected visually using an LFB, eliminating the need for special equipment. The P. aeruginosa-MCDA-LFB method was highly specific, and accurately distinguished P. aeruginosa from other pathogens. Just 10 fg of genomic DNA template (from pure culture) could be detected. The assay could also detect P. aeruginosa in clinical sputum samples and showed the same sensitivity and specificity as the reference (culture-biochemical) method. In the future, this rapid, simple and accurate P. aeruginosa-MCDA-LFB technique might be applied in clinical practice.
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