Immunomagnetic nanoparticle based quantitative PCR for rapid detection of Salmonella

被引:23
作者
Bakthavathsalam, Padmavathy [1 ]
Rajendran, Vinoth Kumar [1 ]
Saran, Uttara [1 ]
Chatterjee, Suvro [1 ]
Ali, Baquir Mohammed Jaffar [2 ]
机构
[1] Anna Univ, AU KBC Res Ctr, Madras 600044, Tamil Nadu, India
[2] Pondicherry Univ, Ctr Green Energy Technol, Pondicherry 605014, India
关键词
Immunomagnetic separation; Salmonella; PCR; Multiplex detection; Biofunctionalized nanoparticles; REAL-TIME PCR; FUNCTIONALIZED MAGNETIC NANOPARTICLES; POLYMERASE-CHAIN-REACTION; LISTERIA-MONOCYTOGENES; GROUND-BEEF; SEPARATION; FOOD; ASSAY; PREENRICHMENT; TYPHIMURIUM;
D O I
10.1007/s00604-013-1052-1
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have developed a rapid and sensitive method for immunomagnetic separation (IMS) of Salmonella along with their real time detection via PCR. Silica-coated magnetic nanoparticles were functionalized with carboxy groups to which anti-Salmonella antibody raised against heat-inactivated whole cells of Salmonella were covalently attached. The immuno-captured target cells were detected in beverages like milk and lemon juice by multiplex PCR and real time PCR with a detection limit of 10(4) cfu.mL(-1) and 10(3) cfu.mL(-1), respectively. We demonstrate that IMS can be used for selective concentration of target bacteria from beverages for subsequent use in PCR detection. PCR also enables differentiation of Salmonella typhi and Salmonella paratyphi A using a set of four specific primers. In addition, IMS-PCR can be used as a screening tool in the food and beverage industry for the detection of Salmonella within 3-4 h which compares favorably to the time of several days that is needed in case of conventional detection based on culture and biochemical methods.
引用
收藏
页码:1241 / 1248
页数:8
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