Quantitative loop-mediated isothermal amplification method for the detection of Vibrio nigripulchritudo in shrimp |
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Authors: | Jean Fall Gunimala Chakraborty Tomoya Kono Minoru Maeda Yoshihiro Suzuki Toshiaki Itami Masahiro Sakai |
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Affiliation: | (1) Faculty of Agriculture, University of Miyazaki, Gakuen Kibanadai Nishi 1-1, Miyazaki 889-2192, Japan;(2) Interdisciplinary Research Organization, University of Miyazaki, Gakuen Kibanadai Nishi 1-1, Miyazaki 889-2192, Japan;(3) Kyushu Medical Co., Ltd., 13-4 Ohte-machi, Kokurakita-ku, Kitakyushu Fukuoka, 803-0814, Japan;(4) Faculty of Engineering, University of Miyazaki, Gakuen Kibanadai Nishi 1-1, Miyazaki 889-2192, Japan; |
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Abstract: | Vibrio nigripulchritudo is considered one of the major pathogens threatening shrimp aquaculture. In this study, we developed a novel and highly specific quantitative loop-mediated isothermal amplification (Q-LAMP) assay. A set of four specific primers were designed targeting the V. nigripulchritudo intergenic spacer region. The reaction time and temperature were optimized for 60 min at 63°C. Quantitative analysis was then performed by measuring the turbidity of the reaction solution using a real-time turbidimeter, allowing for quantification of the initial DNA concentration with a sensitivity of 102 copy numbers equivalent to 2.3 colony forming units/ml or 0.3 fg/μl. The LAMP assay was able to specifically detect two representative strains of V. nigripulchritudo, whereas other Vibrio and non-Vibrio species were not amplified. A standard curve was generated for V. nigripulchritudo by plotting the threshold time (T t) versus the log of bacterial number. A high correlation coefficient (R 2 = 0.9749) was observed for the Q-LAMP reaction. In conclusion, Q-LAMP assay is a sensitive, rapid, and simple tool that can be used for the detection and quantification of V. nigripulchritudo in shrimp, thereby facilitating surveillance of vibriosis infection. |
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