Over het archief
Het OWA, het open archief van het Waterbouwkundig Laboratorium heeft tot doel alle vrij toegankelijke onderzoeksresultaten van dit instituut in digitale vorm aan te bieden. Op die manier wil het de zichtbaarheid, verspreiding en gebruik van deze onderzoeksresultaten, alsook de wetenschappelijke communicatie maximaal bevorderen.
Dit archief wordt uitgebouwd en beheerd volgens de principes van de Open Access Movement, en het daaruit ontstane Open Archives Initiative.
Basisinformatie over ‘Open Access to scholarly information'.
| one publication added to basket [301304] |
Rapid detection and identification of viral and bacterial fish pathogens using a DNA array-based multiplex assay
Lievens, B.; Frans, I.; Heusdens, C.; Justé, A.; Jonstrup, S.P.; Lieffrig, F.; Willems, K.A. (2011). Rapid detection and identification of viral and bacterial fish pathogens using a DNA array-based multiplex assay. J. Fish Dis. 34(11): 861-875. https://dx.doi.org/10.1111/j.1365-2761.2011.01304.x
In: Journal of Fish Diseases. Blackwell Science: Oxford; London; Edinburgh; Boston; Melbourne. ISSN 0140-7775; e-ISSN 1365-2761, meer
|  |
| Trefwoord |
Flavobacterium Bergey, Harrison, Breed, Hammer & Huntoon, 1923 [WoRMS]
|
| Author keywords |
diagnosis; Flavobacterium; herpesvirus; koi herpesvirus (KHV); multiplex |
| Auteurs | | Top |
- Lievens, B., meer
- Frans, I., meer
- Heusdens, C.
- Justé, A.
|
- Jonstrup, S.P.
- Lieffrig, F.
- Willems, K.A., meer
|
|
| Abstract |
Fish diseases can be caused by a variety of diverse organisms, including bacteria, fungi, viruses and protozoa, and pose a universal threat to the ornamental fish industry and aquaculture. The lack of rapid, accurate and reliable means by which fish pathogens can be detected and identified has been one of the main limitations in fish pathogen diagnosis and fish disease management and has consequently stimulated the search for alternative diagnostic techniques. Here, we describe a method based on multiplex and broad‐range PCR amplification combined with DNA array hybridization for the simultaneous detection and identification of all cyprinid herpesviruses (CyHV‐1, CyHV‐2 and CyHV‐3) and some of the most important fish pathogenic Flavobacterium species, including F. branchiophilum, F. columnare and F. psychrophilum. For virus identification, the DNA polymerase and helicase genes were targeted. For bacterial identification, the ribosomal RNA gene was used. The developed methodology permitted 100% specificity for the identification of the target species. Detection sensitivity was equivalent to 10 viral genomes or less than a picogram of bacterial DNA. The utility and power of the array for sensitive pathogen detection and identification in complex samples such as infected tissue is demonstrated in this study. |
IMIS is ontwikkeld en wordt gehost door het VLIZ.
