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DC Field | Value | Language |
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dc.contributor.author | Wangman P. | |
dc.contributor.author | Chaivisuthangkura P. | |
dc.contributor.author | Sritunyalucksana K. | |
dc.contributor.author | Taengchaiyaphum S. | |
dc.contributor.author | Senapin S. | |
dc.contributor.author | Pengsuk C. | |
dc.contributor.author | Sithigorngul P. | |
dc.contributor.author | Longyant S. | |
dc.date.accessioned | 2021-04-05T03:22:18Z | - |
dc.date.available | 2021-04-05T03:22:18Z | - |
dc.date.issued | 2017 | |
dc.identifier.issn | 448486 | |
dc.identifier.other | 2-s2.0-85016138657 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/13092 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016138657&doi=10.1016%2fj.aquaculture.2017.03.039&partnerID=40&md5=c36e86c438114d0d9683bdf516440c8d | |
dc.description.abstract | Toxin A (ToxA) and toxin B (ToxB) of Vibrio parahaemolyticus, which cause acute hepatopancreatic necrosis disease (AHPND), were prepared in a bacterial supernatant from Chinese isolates (CN-VPAHPND) by washing bacterial colonies off of TSA cultures. The supernatant was subsequently used in mouse immunization to produce monoclonal antibodies (MAbs). Three groups of MAbs were selected: one MAb specific to ToxA, two MAbs specific to ToxB and one MAb specific to V. parahaemolyticus (CN-VPAHPND). The MAbs specific to ToxA and ToxB recognized all 10 VPAHPND isolates from China, Vietnam, Malaysia and Thailand, but did not bind to the 20 non-VPAHPND isolates from various other sources, including Vibrio spp. and other bacteria. The MAbs specific to toxins were used to detect the recombinant proteins of His-tagged ToxA and GST-ToxB with sensitivities of 200fmolspot−1 and 10fmolspot−1, respectively, as determined by dot-ELISA. The MAbs were used to detect the toxins produced by bacteria or shrimp tissue lysate spiked with bacteria in a complex tissue sample at concentrations as low as 1CFUml−1 after pre-enrichment of the bacteria for 6h. The third group of MAb was specific to CN-VPAHPND isolate but did not recognize the other 9 out of 10 VPAHPND isolates from Vietnam, Malaysia and Thailand. However, this MAb demonstrated cross-reactivity to 1 out of 20 of the non-VPAHPND isolates and 3 out of 9 of the V. alginolyticus isolates. These findings indicate that the AHPND epidemic in Southeast Asia was not caused by the CN-VPAHPND isolate. The MAbs specific to ToxA and ToxB produced in this study could be used to detect both toxins directly by dot blotting. © 2017 Elsevier B.V. | |
dc.subject | antibody | |
dc.subject | bacterial disease | |
dc.subject | bacterium | |
dc.subject | epidemic | |
dc.subject | immunization | |
dc.subject | molecular analysis | |
dc.subject | rodent | |
dc.subject | symptom | |
dc.subject | toxin | |
dc.subject | China | |
dc.subject | Malaysia | |
dc.subject | Thailand | |
dc.subject | Viet Nam | |
dc.subject | Bacteria (microorganisms) | |
dc.subject | Decapoda (Crustacea) | |
dc.subject | Vibrio | |
dc.subject | Vibrio alginolyticus | |
dc.subject | Vibrio parahaemolyticus | |
dc.title | Development of monoclonal antibodies specific to ToxA and ToxB of Vibrio parahaemolyticus that cause acute hepatopancreatic necrosis disease (AHPND) | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Aquaculture. Vol 474, (2017), p.75-81 | |
dc.identifier.doi | 10.1016/j.aquaculture.2017.03.039 | |
Appears in Collections: | Scopus 1983-2021 |
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