Author: Kim, Yong Kwan; Lim, Seong-In; Cho, In-Soo; Cheong, Kwang-Myun; Lee, Eun-Jeong; Lee, Sang-Oh; Kim, Joon-Bae; Kim, Jung-Hwa; Jeong, Dong-Soo; An, Byung-Hyun; An, Dong-Jun
                    Title: A novel diagnostic approach to detecting porcine epidemic diarrhea virus: The lateral immunochromatography assay  Cord-id: in5n7sed  Document date: 2015_12_1
                    ID: in5n7sed
                    
                    Snippet: Porcine epidemic diarrhea virus (PEDV) causes acute diarrhea and dehydration in sucking piglets and has a high mortality rate. An immunochromatography (IC) assay, known as a lateral flow test, is a simple device intended to detect the presence of target pathogens. Here, we developed an IC assay that detected PEDV antigens with 96.0% (218/227) sensitivity and 98.5% (262/266) specificity when compared with real-time reverse transcriptase (RT)-PCR using FAM-labeled probes based on sequences from nu
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Porcine epidemic diarrhea virus (PEDV) causes acute diarrhea and dehydration in sucking piglets and has a high mortality rate. An immunochromatography (IC) assay, known as a lateral flow test, is a simple device intended to detect the presence of target pathogens. Here, we developed an IC assay that detected PEDV antigens with 96.0% (218/227) sensitivity and 98.5% (262/266) specificity when compared with real-time reverse transcriptase (RT)-PCR using FAM-labeled probes based on sequences from nucleocapsid genes. The detection limits of the real-time RT-PCR and IC assays were 1 × 10(2) and 1 × 10(3) copies, respectively. The IC assay developed herein did not detect non-specific reactions with other viral or bacterial pathogens, and the assay could be stored at 4 °C or room temperature for 15 months without affecting its efficacy. Thus, the IC assay may result in improved PED detection and control on farms, and is a viable alternative to current diagnostic tools for PEDV.
 
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