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Immuno-capture PCR method for detecting Acidovorax avenae subsp. citrulli from watermelon

Published online by Cambridge University Press:  02 August 2007

Wang Xiao
Affiliation:
Institute of Biotechnology, Zhejiang University, Hangzhou 310029, China
Zhang Le
Affiliation:
Chinese Academy of Inspection and Quarantine, Beijing 200025, China
Xu Fu-Shou
Affiliation:
Hangzhou Plant Protection Station, Hangzhou 310020, China
Zhao Li-Han
Affiliation:
Institute of Biotechnology, Zhejiang University, Hangzhou 310029, China
Xie Guan-Lin*
Affiliation:
Institute of Biotechnology, Zhejiang University, Hangzhou 310029, China
*
*Corresponding author. E-mail: [email protected]

Abstract

An immuno-capture polymerase chain reaction (IC-PCR) method for detection of Acidovorax avenae subsp. citrulli (AAC), the causal organism of bacterial fruit blotch (BFB) of watermelon, was developed by combining the immunosorbent enrichment (ISE) method with classical PCR and comparing with the direct PCR and growth check methods. The results showed that all A. avenae subsp. citrulli strains tested have produced 360 bp specific fragments using IC-PCR and direct PCR methods, while other strains from 10 different genera showed negative PCR results. The minimum detection concentration was about 50–100 cfu/ml and 104 cfu/ml, respectively. The IC-PCR sensitivity was 100 times higher than that of direct PCR. The examination of seven batches of different melon seeds from the markets by IC-PCR showed that one cantaloupe, two honeydew melon and two watermelon seed varieties carried the pathogen, indicating that the IC-PCR is an accurate, sensitive, rapid and low-cost technique.

Type
Research Article
Copyright
Copyright © China Agricultural University and Cambridge University Press 2007

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Footnotes

First published in Journal of Agricultural Biotechnology 2006, 14(6): 946–951

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