Monoclonal antibody-based triple antibody sandwich-enzyme-linked immunosorbent assay and immunocapture reverse transcription-polymerase chain reaction for Odontoglossum ringspot virus detection

2011 ◽  
Vol 171 (1) ◽  
pp. 40-45 ◽  
Author(s):  
Jianxiang Wu ◽  
Chunmei Meng ◽  
Haili Shang ◽  
Song Rong ◽  
Chao Zhang ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Polymerase Chain Reaction ◽  
Immunosorbent Assay ◽  
Reverse Transcription ◽  
Virus Detection ◽  
Ringspot Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Chain Reaction ◽  
Odontoglossum Ringspot Virus ◽  
Polymerase Chain

Detection and differentiation of Norwalk virus by reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay

2002 ◽  
Vol 68 (2) ◽  
pp. 285-290 ◽  
Author(s):  
Masatoshi Tatsumi ◽  
Shuji Nakata ◽  
Yoshiyuki Sakai ◽  
Shinjiro Honma ◽  
Kazuko Numata-Kinoshita ◽  
...  
Keyword(s):  
Polymerase Chain Reaction ◽  
Immunosorbent Assay ◽  
Reverse Transcription ◽  
Enzyme Linked Immunosorbent Assay ◽  
Norwalk Virus ◽  
Chain Reaction ◽  
Polymerase Chain

scholarly journals Enzyme-Linked Immunosorbent Assay Testing of Shoots Grown In Vitro and the Use of Immunocapture-Reverse Transcription-Polymerase Chain Reaction Improve the Detection of Prunus necrotic ringspot virus in Rose

2000 ◽  
Vol 90 (5) ◽  
pp. 522-528 ◽  
Author(s):  
Benoît Moury ◽  
Loïc Cardin ◽  
Jean-Paul Onesto ◽  
Thierry Candresse ◽  
Alain Poupet
Keyword(s):  
Polymerase Chain Reaction ◽  
Immunosorbent Assay ◽  
Reverse Transcription ◽  
Shoot Tips ◽  
Enzyme Linked Immunosorbent Assay ◽  
Chain Reaction ◽  
Simple Method ◽  
Mother Plants ◽  
Polymerase Chain

We developed and evaluated two different methods to improve the detection of the most prevalent virus of rose in Europe, Prunus necrotic ring-spot virus (PNRSV). Immunocapture-reverse transcription-polymerase chain reaction was estimated to be about 100 times more sensitive than double-antibody sandwich-enzyme-linked immunosorbent assay (DAS-ELISA) and showed an equivalent specificity. Based on the observation that PNRSV multiplies actively in young growing tissues (axillary shoots and cuttings), an in vitro culture method allowing rapid (about 15 days) and homogeneous development of dormant axillary buds with high virus titers was standardized. ELISA tests of these young shoots showed, in some cases, a 104 to 105 increase in sensitivity in comparison to adjacent leaf tissues from the rose mother plants. Between 21 and 98% (depending on the season) more samples were identified as positive by using ELISA on samples from shoot tips grown in vitro rather than on leaves collected directly from the PNRSV-infected mother plants. This simple method of growing shoot tips in vitro improved the confidence in the detection of PNRSV and eliminated problems in sampling appropriate tissues.

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