A longitudinal study of amoebic gill disease on a marine atlantic salmon farm utilising a real-time pcr assay for the detection of neoparamoeba perurans

Amoebic gill disease (AGD) is a proliferative gill disease of marine cultured Atlantic salmon Salmo salar, with the free-living protozoan Neoparamoeba perurans being the primary aetiological agent. The increased incidence of AGD in recent years presents a significant challenge to the Atlantic salmon...

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Bibliographic Details
Main Authors: Downes, JK, Henshilwood, K, Collins, EM, Ryan, A, O’Connor, I, Rodger, HD, MacCarthy, E, Ruane, NM
Format: Article in Journal/Newspaper
Language:unknown
Published: Inter-Research Science Center 2015
Subjects:
amoebic gill disease
neoparamoeba perurans
diagnostics
atlantic salmon
salar l
agd
ireland
water
infections
pathology
agent
environment
challenge
sequences
Atlantic salmon
Salmo salar
Online Access:http://hdl.handle.net/10379/11247
https://doi.org/10.13025/26690
https://doi.org/10.3354/aei00150
Description
Summary:Amoebic gill disease (AGD) is a proliferative gill disease of marine cultured Atlantic salmon Salmo salar, with the free-living protozoan Neoparamoeba perurans being the primary aetiological agent. The increased incidence of AGD in recent years presents a significant challenge to the Atlantic salmon farming industry in Europe. In this study, a real-time TaqMan (R) PCR assay was developed and validated to detect Neoparamoeba perurans on Atlantic salmon gills and further used to monitor disease progression on a marine Atlantic salmon farm in Ireland in conjunction with gross gill pathology and histopathology. The assay proved specific for N. perurans, with no cross-reactivity with the related species N. pemaquidensis, N. branchiphila or N. aestuarina, and was capable of detecting 2.68 copies of N. perurans DNA mu l(-1). Although the parasite was detected throughout the 18 mo period of this study, mortality peaks associated with clinical AGD were only recorded during the first 12 mo of the marine phase of the production cycle. The initial AGD outbreak resulted in peak mortality in Week 17, which was preceded by PCR detections from Week 13 onwards. Freshwater treatments were an effective method for controlling the disease, resulting in a reduction in the weekly mortality levels and also a reduction in the number of PCR-positive fish. In comparison to traditional diagnostic methods, our PCR assay proved to be highly sensitive and a valuable tool to monitor disease progression and, therefore, has the potential to provide information on the timing and effectiveness of treatments.

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