|Appears in Collections:||Aquaculture Journal Articles|
|Peer Review Status:||Refereed|
|Title:||Identification of Vibrio harveyi using PCR amplification of the toxR gene|
polymerase chain reaction
|Citation:||Pang L, Zhang X, Zhong Y, Chen J, Li Y & Austin B (2006) Identification of Vibrio harveyi using PCR amplification of the toxR gene. Letters in Applied Microbiology, 43 (3), pp. 249-255. https://doi.org/10.1111/j.1472-765X.2006.01962.x|
|Abstract:||Aims: The aim of this study was to develop an effective method for the identification of Vibrio harveyi based on using the toxR gene as a taxonomic marker. Methods and Results: Primers for the toxR gene were designed for specificity to V. harveyi, and incorporated in a polymerase chain reaction (PCR). The results of the PCR, which took <5 h from DNA extraction to amplification, revealed positive amplification of the toxR gene fragment in 20 V. harveyi isolates including type strains, whereas DNA from 23 other Vibrionaceae type strains and 13 Vibrio parahaemolyticus strains were negative. The detection limit of the PCR was 4.0 × 103 cells ml−1. In addition, the technique enabled the recognition of V. harveyi from diseased fish. Conclusions: The PCR was specific and sensitive, enabling the identification of V. harveyi within 5 h. Significance and Impact of the Study: The PCR allowed the rapid and sensitive detection of V. harveyi.|
|Rights:||The publisher does not allow this work to be made publicly available in this Repository. Please use the Request a Copy feature at the foot of the Repository record to request a copy directly from the author. You can only request a copy if you wish to use this work for your own research or private study.|
|austin_identificationofvibrioharveyi_2006.pdf||Fulltext - Published Version||578.21 kB||Adobe PDF||Under Permanent Embargo Request a copy|
Note: If any of the files in this item are currently embargoed, you can request a copy directly from the author by clicking the padlock icon above. However, this facility is dependent on the depositor still being contactable at their original email address.
This item is protected by original copyright
Items in the Repository are protected by copyright, with all rights reserved, unless otherwise indicated.
The metadata of the records in the Repository are available under the CC0 public domain dedication: No Rights Reserved https://creativecommons.org/publicdomain/zero/1.0/
If you believe that any material held in STORRE infringes copyright, please contact firstname.lastname@example.org providing details and we will remove the Work from public display in STORRE and investigate your claim.