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Use of a high resolution melt real-time polymerase chain reaction (PCR) assay for the environmental monitoring of Vibrio cholerae

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dc.contributor.author Le Roux, Wouter J
dc.contributor.author Van Blerk, GN
dc.date.accessioned 2012-01-20T08:41:07Z
dc.date.available 2012-01-20T08:41:07Z
dc.date.issued 2011-10
dc.identifier.citation Le Roux, WJ and Van Blerk, GN. 2011. Use of a high resolution melt real-time polymerase chain reaction (PCR) assay for the environmental monitoring of Vibrio cholerae. African Journal of Microbiology Research, Vol 5(21), pp 3520-3526 en_US
dc.identifier.issn 1996-0808
dc.identifier.uri http://www.academicjournals.org/ajmr/PDF/pdf2011/9Oct/Roux%20and%20Blerk.pdf
dc.identifier.uri http://hdl.handle.net/10204/5520
dc.description Copyright: Academic Journals en_US
dc.description.abstract A real-time polymerase chain reaction (PCR) assay utilizing high resolution melt (HRM) curve analysis was developed and tested for the monitoring of Vibrio cholerae in water samples. The assay utilized previously published primers that are specific to regions of the V. cholerae ompW and ctxAB genes, allowing it to differentiate between toxigenic and non-toxigenic strains. The ompW and ctxAB primers amplify target regions of 588 and 564 bp in length (respectively) and the amplicons could be accurately identified using HRM curve analysis. High resolution melt curve analysis provided additional accuracy for the determination of amplicon melting temperatures, and allowed amplification of the two targets in a multiplex reaction. Two laboratories employed the assay to analyse 178 water samples obtained from diverse environmental water sources, for the presence of V. cholerae. The assay was found to be a rapid, highly accurate, sensitive and cost effective method for the detection and distinction between toxigenic and non-toxigenic V. cholerae strains in water. en_US
dc.language.iso en en_US
dc.publisher Academic Journals en_US
dc.relation.ispartofseries Workflow request;7957
dc.subject Vibrio cholerae en_US
dc.subject High resolution melt en_US
dc.subject Real-time polymerase chain reaction en_US
dc.subject Microbiology en_US
dc.subject Biological sciences en_US
dc.title Use of a high resolution melt real-time polymerase chain reaction (PCR) assay for the environmental monitoring of Vibrio cholerae en_US
dc.type Article en_US
dc.identifier.apacitation Le Roux, W. J., & Van Blerk, G. (2011). Use of a high resolution melt real-time polymerase chain reaction (PCR) assay for the environmental monitoring of Vibrio cholerae. http://hdl.handle.net/10204/5520 en_ZA
dc.identifier.chicagocitation Le Roux, Wouter J, and GN Van Blerk "Use of a high resolution melt real-time polymerase chain reaction (PCR) assay for the environmental monitoring of Vibrio cholerae." (2011) http://hdl.handle.net/10204/5520 en_ZA
dc.identifier.vancouvercitation Le Roux WJ, Van Blerk G. Use of a high resolution melt real-time polymerase chain reaction (PCR) assay for the environmental monitoring of Vibrio cholerae. 2011; http://hdl.handle.net/10204/5520. en_ZA
dc.identifier.ris TY - Article AU - Le Roux, Wouter J AU - Van Blerk, GN AB - A real-time polymerase chain reaction (PCR) assay utilizing high resolution melt (HRM) curve analysis was developed and tested for the monitoring of Vibrio cholerae in water samples. The assay utilized previously published primers that are specific to regions of the V. cholerae ompW and ctxAB genes, allowing it to differentiate between toxigenic and non-toxigenic strains. The ompW and ctxAB primers amplify target regions of 588 and 564 bp in length (respectively) and the amplicons could be accurately identified using HRM curve analysis. High resolution melt curve analysis provided additional accuracy for the determination of amplicon melting temperatures, and allowed amplification of the two targets in a multiplex reaction. Two laboratories employed the assay to analyse 178 water samples obtained from diverse environmental water sources, for the presence of V. cholerae. The assay was found to be a rapid, highly accurate, sensitive and cost effective method for the detection and distinction between toxigenic and non-toxigenic V. cholerae strains in water. DA - 2011-10 DB - ResearchSpace DP - CSIR KW - Vibrio cholerae KW - High resolution melt KW - Real-time polymerase chain reaction KW - Microbiology KW - Biological sciences LK - https://researchspace.csir.co.za PY - 2011 SM - 1996-0808 T1 - Use of a high resolution melt real-time polymerase chain reaction (PCR) assay for the environmental monitoring of Vibrio cholerae TI - Use of a high resolution melt real-time polymerase chain reaction (PCR) assay for the environmental monitoring of Vibrio cholerae UR - http://hdl.handle.net/10204/5520 ER - en_ZA


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