scholarly journals Real-time quantitative polymerase chain reaction (QPCR) to identify Myxobolus cerebralis in rainbow trout Oncorhynchus mykiss

2004 ◽  
Vol 60 ◽  
pp. 205-213 ◽  
Author(s):  
WP Cavender ◽  
JS Wood ◽  
MS Powell ◽  
K Overturf ◽  
KD Cain
2013 ◽  
Vol 634-638 ◽  
pp. 934-938 ◽  
Author(s):  
Ying Han ◽  
Kun Wang ◽  
Hai Long Li ◽  
Dana X Gao

Reverse transcription real-time quantitative polymerase chain reaction (RT-qPCR) was used to determine the differential expression of the Dmrt1 gene in ovaries of diploid and triploid rainbow trout (Oncorhynchus mykiss) 10 and 20 months post-hatch. At 10 months post-hatch there was little relative difference in the expression of the Dmrt1 gene between triploid and diploid trout. However, at 20 months the expression of the Dmrt1 gene in triploids was more than 14 times higher than in diploids. Dmrt1 expression from 10 to 20 months suggests masculinization of the ovaries, which may be virilescent in triploid females at the later development phase (20 months). This study provides molecular evidence supporting the general claims that ovaries of female triploid rainbow trout do not develop normally resulting in sterility.


1998 ◽  
Vol 61 (4) ◽  
pp. 482-486 ◽  
Author(s):  
ESTHER CARRERA ◽  
TERESA GARCÍA ◽  
ANA CÉSPEDES ◽  
ISABEL GONZÁLEZ ◽  
BERNABÉ SANZ ◽  
...  

Restriction site analysis of polymerase chain reaction (PCR) products from a conserved region of the cytochrome b gene has been used for the identification of fresh and smoked samples of Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss). Digestion of the 359-bp PCR product with the endonucleases EcoRV and TaqI yielded specific banding patterns for salmon and trout. This genetic marker can be very useful for detecting fraudulent substitution of the cheaper smoked trout for the more expensive smoked salmon.


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