Abstract
A loop-mediated isothermal amplification assay was developed. It was designed for recognizing Vibrio cholerae O1/O139, where atpA, rfbN, and wfbR genes were adopted. The assay specifically detected the target with sensitivities of 5-67 copies per reaction in 1 h. The assay will aid rapid detection of the cholera bacterium.
Keywords:
Cholera; LAMP; O1/O139.
Copyright © 2019 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Bacterial Proteins / genetics*
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Cholera / diagnosis
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Environmental Monitoring
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Humans
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Limit of Detection
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Molecular Diagnostic Techniques / methods*
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Nucleic Acid Amplification Techniques / methods*
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Vibrio cholerae O1 / genetics
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Vibrio cholerae O1 / isolation & purification*
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Vibrio cholerae O139 / genetics
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Vibrio cholerae O139 / isolation & purification*
Substances
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Bacterial Proteins
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RfbN protein, Vibrio cholerae