Factors influencing transmission, onset and severity of outbreaks due to white sturgeon iridovirus in a commercial hatchery

Aquaculture ◽  
2001 ◽  
Vol 194 (1-2) ◽  
pp. 21-35 ◽  
Author(s):  
M.P. Georgiadis ◽  
R.P. Hedrick ◽  
T.E. Carpenter ◽  
I.A. Gardner
2005 ◽  
Vol 36 (8) ◽  
pp. 824-827 ◽  
Author(s):  
John D Drennan ◽  
Sue Ireland ◽  
Scott E LaPatra ◽  
Leslie Grabowski ◽  
Tarita K. Carrothers ◽  
...  

2006 ◽  
Vol 70 ◽  
pp. 37-45 ◽  
Author(s):  
JD Drennan ◽  
SE LaPatra ◽  
JT Siple ◽  
S Ireland ◽  
KD Cain

2020 ◽  
Vol 64 (3) ◽  
pp. 363-368
Author(s):  
Paulina Hofsoe-Oppermann ◽  
Jolanta Kiełpińska ◽  
Remigiusz Panicz ◽  
Sven M. Bergmann

AbstractIntroductionWhite sturgeon iridovirus (WSIV) disease is caused by a virus of the eponymous family and is mostly triggered by stressful environmental conditions, i.e. high rearing density, excessive handling, or temporary loss of water. The aim of this study was to develop the most effective diagnostic method for quick and efficient confirmation or exclusion of the presence of WSIV.Material and MethodsA total of 42 samples (spleen, gills, intestine, skin, kidney, and brain) were collected from eight sturgeon (Acipenser gueldenstaedtii and A. oxyrinchus) aged ≤5+ farmed or caught between 2010 and 2014 in open waters (Dąbie Lake and Szczecin Lagoon). They were tested for WSIV presence using conventional PCR, qPCR, and in situ hybridisation (ISH).ResultsIn gross examination, all fish appeared to be healthy. Neither species showed clinical signs typical of WSIV infection. In the majority of cases, fragments of iridoviral DNA were found using molecular methods in the kidneys, and also in the liver, gills, and skin. The detection rate using ISH was 47.37% and most commonly the brain and kidney tissues were positive. The most efficient of the methods used was real-time PCR, with 100% effectiveness in detection of WSIV DNA.ConclusionThe study demonstrates the capabilities for WSIV diagnosis available to sturgeon farmers and water administrators, indicating useful methods of adequate sensitivity as well as organs to sample in order to achieve the highest probability of viral detection.


1996 ◽  
Vol 6 (3) ◽  
pp. 51-58 ◽  
Author(s):  
S. E. LaPatra ◽  
J. M. Groff ◽  
T. L. Patterson ◽  
W. D. Shewmaker ◽  
M. Casten ◽  
...  

2000 ◽  
Vol 61 (10) ◽  
pp. 1232-1240 ◽  
Author(s):  
Marios P. Georgiadis ◽  
Ronald P. Hedrick ◽  
Wesley O. Johnson ◽  
Susan Yun ◽  
Ian A. Gardner

Author(s):  
Y. Kawato ◽  
S Kuttichantran ◽  
K. Nakajima ◽  
T. Waltzek ◽  
R. Whittington

Aquaculture ◽  
2006 ◽  
Vol 254 (1-4) ◽  
pp. 92-101 ◽  
Author(s):  
Kevin T. Kwak ◽  
Ian A. Gardner ◽  
Thomas B. Farver ◽  
Ronald P. Hedrick

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