Simultaneous detection of Photobacteriumdamselae, Vibrio alginolyticus, Vibrio harveyi and Vibrio parahaemolyticus using multiplex PCR amplification method

The aim of this study was to develop a multiplex PCR amplification method that simultaneously detects the presence of four bacterial pathogens(Photobacteriumdamselae, V. alginolyticus, V. harveyi and V. parahaemolyticus), which are often synergistically caused disease to culture fish throughout the...

Full description

Saved in:
Bibliographic Details
Main Authors: Julian Ransangan, Mohammad Tamrin Mohammad Lal
Format: Article
Language:English
Published: 2013
Subjects:
Online Access:https://eprints.ums.edu.my/id/eprint/18988/1/Simultaneous%20detection%20of%20Photobacteriumdamselae.pdf
https://eprints.ums.edu.my/id/eprint/18988/
Tags: Add Tag
No Tags, Be the first to tag this record!
id my.ums.eprints.18988
record_format eprints
spelling my.ums.eprints.189882018-03-01T02:24:34Z https://eprints.ums.edu.my/id/eprint/18988/ Simultaneous detection of Photobacteriumdamselae, Vibrio alginolyticus, Vibrio harveyi and Vibrio parahaemolyticus using multiplex PCR amplification method Julian Ransangan Mohammad Tamrin Mohammad Lal SH Aquaculture. Fisheries. Angling The aim of this study was to develop a multiplex PCR amplification method that simultaneously detects the presence of four bacterial pathogens(Photobacteriumdamselae, V. alginolyticus, V. harveyi and V. parahaemolyticus), which are often synergistically caused disease to culture fish throughout the tropical waters, and occasionally cause food poisoning and wound infection to human. Specific multiplex PCR primers targeting conserve regions of virulence genes of the pathogens were designed and tested against different concentrations of MgCl and annealing temperatures. In addition to specificity against different bacterial species, the multiplex PCR was also tested against tissue and environmental samples known to harbor the pathogens. The result showed that the multiplex PCR was highly specific to the target pathogens. The optimum MgCl2 concentration and annealing temperature for successful multiplex PCR amplification of the pathogens were at5.0 mM and 56 °C, respectively. The detection limit of the multiplex PCR was at 10 pg of DNA template. Although the concentration of the pathogens in the environment is often lower, enrichment with tryptic soy broth supplemented with 2% NaCl (w/v) has shown to enhance the growth of the bacterial pathogens and hence improved detection. The rapidity, simplicity and cost-effectiveness of the multiplex PCR amplification method described in this paper provide a useful biosecurity tool for the determination of the pathogens in aquaculture farms and seafood processing industries throughout the tropical countries. 2013 Article PeerReviewed text en https://eprints.ums.edu.my/id/eprint/18988/1/Simultaneous%20detection%20of%20Photobacteriumdamselae.pdf Julian Ransangan and Mohammad Tamrin Mohammad Lal (2013) Simultaneous detection of Photobacteriumdamselae, Vibrio alginolyticus, Vibrio harveyi and Vibrio parahaemolyticus using multiplex PCR amplification method. International Research Journal of Biological Sciences, 2 (12). pp. 79-84. ISSN 2278-3202
institution Universiti Malaysia Sabah
building UMS Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sabah
content_source UMS Institutional Repository
url_provider http://eprints.ums.edu.my/
language English
topic SH Aquaculture. Fisheries. Angling
spellingShingle SH Aquaculture. Fisheries. Angling
Julian Ransangan
Mohammad Tamrin Mohammad Lal
Simultaneous detection of Photobacteriumdamselae, Vibrio alginolyticus, Vibrio harveyi and Vibrio parahaemolyticus using multiplex PCR amplification method
description The aim of this study was to develop a multiplex PCR amplification method that simultaneously detects the presence of four bacterial pathogens(Photobacteriumdamselae, V. alginolyticus, V. harveyi and V. parahaemolyticus), which are often synergistically caused disease to culture fish throughout the tropical waters, and occasionally cause food poisoning and wound infection to human. Specific multiplex PCR primers targeting conserve regions of virulence genes of the pathogens were designed and tested against different concentrations of MgCl and annealing temperatures. In addition to specificity against different bacterial species, the multiplex PCR was also tested against tissue and environmental samples known to harbor the pathogens. The result showed that the multiplex PCR was highly specific to the target pathogens. The optimum MgCl2 concentration and annealing temperature for successful multiplex PCR amplification of the pathogens were at5.0 mM and 56 °C, respectively. The detection limit of the multiplex PCR was at 10 pg of DNA template. Although the concentration of the pathogens in the environment is often lower, enrichment with tryptic soy broth supplemented with 2% NaCl (w/v) has shown to enhance the growth of the bacterial pathogens and hence improved detection. The rapidity, simplicity and cost-effectiveness of the multiplex PCR amplification method described in this paper provide a useful biosecurity tool for the determination of the pathogens in aquaculture farms and seafood processing industries throughout the tropical countries.
format Article
author Julian Ransangan
Mohammad Tamrin Mohammad Lal
author_facet Julian Ransangan
Mohammad Tamrin Mohammad Lal
author_sort Julian Ransangan
title Simultaneous detection of Photobacteriumdamselae, Vibrio alginolyticus, Vibrio harveyi and Vibrio parahaemolyticus using multiplex PCR amplification method
title_short Simultaneous detection of Photobacteriumdamselae, Vibrio alginolyticus, Vibrio harveyi and Vibrio parahaemolyticus using multiplex PCR amplification method
title_full Simultaneous detection of Photobacteriumdamselae, Vibrio alginolyticus, Vibrio harveyi and Vibrio parahaemolyticus using multiplex PCR amplification method
title_fullStr Simultaneous detection of Photobacteriumdamselae, Vibrio alginolyticus, Vibrio harveyi and Vibrio parahaemolyticus using multiplex PCR amplification method
title_full_unstemmed Simultaneous detection of Photobacteriumdamselae, Vibrio alginolyticus, Vibrio harveyi and Vibrio parahaemolyticus using multiplex PCR amplification method
title_sort simultaneous detection of photobacteriumdamselae, vibrio alginolyticus, vibrio harveyi and vibrio parahaemolyticus using multiplex pcr amplification method
publishDate 2013
url https://eprints.ums.edu.my/id/eprint/18988/1/Simultaneous%20detection%20of%20Photobacteriumdamselae.pdf
https://eprints.ums.edu.my/id/eprint/18988/
_version_ 1760229520459169792
score 13.18916