Design and evaluation of a unique RT-qPCR assay for diagnostic quality control assessment that is applicable to pathogen detection in three species of salmonid fish

Art. 183, 8 S. Background: The detection of pathogens at early stages of infection is a key point for disease control in aquaculture. Therefore, accurate diagnostic procedures are a must. Real-time PCR has been a mainstay in diagnostics over the years due to its speed, specificity, sensitivity, repr...

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Published in:BMC Veterinary Research
Main Authors: Sepúlveda, D., Bohle, H., Labra, T., Grothusen, H., Marshall, S.H.
Format: Article in Journal/Newspaper
Language:English
Published: 2013
Subjects:
Online Access:https://publica.fraunhofer.de/handle/publica/233475
https://doi.org/10.1186/1746-6148-9-183
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spelling ftfrauneprints:oai:publica.fraunhofer.de:publica/233475 2024-05-19T07:47:56+00:00 Design and evaluation of a unique RT-qPCR assay for diagnostic quality control assessment that is applicable to pathogen detection in three species of salmonid fish Sepúlveda, D. Bohle, H. Labra, T. Grothusen, H. Marshall, S.H. 2013 https://publica.fraunhofer.de/handle/publica/233475 https://doi.org/10.1186/1746-6148-9-183 en eng BMC veterinary research doi:10.1186/1746-6148-9-183 https://publica.fraunhofer.de/handle/publica/233475 journal article 2013 ftfrauneprints https://doi.org/10.1186/1746-6148-9-183 2024-04-24T00:41:35Z Art. 183, 8 S. Background: The detection of pathogens at early stages of infection is a key point for disease control in aquaculture. Therefore, accurate diagnostic procedures are a must. Real-time PCR has been a mainstay in diagnostics over the years due to its speed, specificity, sensitivity, reproducibility and throughput; as such, real-time PCR is a target for improvement. Nevertheless, to validate a novel diagnostic tool, correct setup of the assay, including proper endogenous controls to evaluate the quantity and quality of the samples and to detect possible sample degradation, is compulsory. This work aims to design a unique RT-qPCR assay for pathogen detection in the three salmonid species reared in Chile. The assay uses elongation factor 1 alpha as the single endogenous control, thus avoiding the need for multiple endogenous controls, as well as multiple validations and non-comparable quality control parameters. Results: The in vivo and in vitro analyses of samples from Salmo salar, Oncorhynchus mykiss and Oncorhynchus kisutch showed that when primers were accurately selected to target conserved regions of the elongation factor 1 alpha (ELF1) gene, a single novel RT-qPCR assay yielding similar and reproducible Ct values between the three species could be designed. The opposite occurred when an assay originally designed for Salmo salar was tested in samples from the two species of the genus Oncorhynchus. Conclusions: Here, we report the design and evaluation of an accurate trans-species RT-qPCR assay that uses the elongation factor 1 alpha (ELF1) gene as an endogenous control and is applicable for diagnostic purposes in samples obtained from the three salmonid species reared in Chile. 9 Article in Journal/Newspaper Salmo salar Publikationsdatenbank der Fraunhofer-Gesellschaft BMC Veterinary Research 9 1
institution Open Polar
collection Publikationsdatenbank der Fraunhofer-Gesellschaft
op_collection_id ftfrauneprints
language English
description Art. 183, 8 S. Background: The detection of pathogens at early stages of infection is a key point for disease control in aquaculture. Therefore, accurate diagnostic procedures are a must. Real-time PCR has been a mainstay in diagnostics over the years due to its speed, specificity, sensitivity, reproducibility and throughput; as such, real-time PCR is a target for improvement. Nevertheless, to validate a novel diagnostic tool, correct setup of the assay, including proper endogenous controls to evaluate the quantity and quality of the samples and to detect possible sample degradation, is compulsory. This work aims to design a unique RT-qPCR assay for pathogen detection in the three salmonid species reared in Chile. The assay uses elongation factor 1 alpha as the single endogenous control, thus avoiding the need for multiple endogenous controls, as well as multiple validations and non-comparable quality control parameters. Results: The in vivo and in vitro analyses of samples from Salmo salar, Oncorhynchus mykiss and Oncorhynchus kisutch showed that when primers were accurately selected to target conserved regions of the elongation factor 1 alpha (ELF1) gene, a single novel RT-qPCR assay yielding similar and reproducible Ct values between the three species could be designed. The opposite occurred when an assay originally designed for Salmo salar was tested in samples from the two species of the genus Oncorhynchus. Conclusions: Here, we report the design and evaluation of an accurate trans-species RT-qPCR assay that uses the elongation factor 1 alpha (ELF1) gene as an endogenous control and is applicable for diagnostic purposes in samples obtained from the three salmonid species reared in Chile. 9
format Article in Journal/Newspaper
author Sepúlveda, D.
Bohle, H.
Labra, T.
Grothusen, H.
Marshall, S.H.
spellingShingle Sepúlveda, D.
Bohle, H.
Labra, T.
Grothusen, H.
Marshall, S.H.
Design and evaluation of a unique RT-qPCR assay for diagnostic quality control assessment that is applicable to pathogen detection in three species of salmonid fish
author_facet Sepúlveda, D.
Bohle, H.
Labra, T.
Grothusen, H.
Marshall, S.H.
author_sort Sepúlveda, D.
title Design and evaluation of a unique RT-qPCR assay for diagnostic quality control assessment that is applicable to pathogen detection in three species of salmonid fish
title_short Design and evaluation of a unique RT-qPCR assay for diagnostic quality control assessment that is applicable to pathogen detection in three species of salmonid fish
title_full Design and evaluation of a unique RT-qPCR assay for diagnostic quality control assessment that is applicable to pathogen detection in three species of salmonid fish
title_fullStr Design and evaluation of a unique RT-qPCR assay for diagnostic quality control assessment that is applicable to pathogen detection in three species of salmonid fish
title_full_unstemmed Design and evaluation of a unique RT-qPCR assay for diagnostic quality control assessment that is applicable to pathogen detection in three species of salmonid fish
title_sort design and evaluation of a unique rt-qpcr assay for diagnostic quality control assessment that is applicable to pathogen detection in three species of salmonid fish
publishDate 2013
url https://publica.fraunhofer.de/handle/publica/233475
https://doi.org/10.1186/1746-6148-9-183
genre Salmo salar
genre_facet Salmo salar
op_relation BMC veterinary research
doi:10.1186/1746-6148-9-183
https://publica.fraunhofer.de/handle/publica/233475
op_doi https://doi.org/10.1186/1746-6148-9-183
container_title BMC Veterinary Research
container_volume 9
container_issue 1
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