A kind of attenuated strain of carp herpesvirus type II and its application
A carp herpes virus and attenuated strain technology, applied in the direction of viruses, antiviral agents, viruses/bacteriophages, etc., can solve the problems of high lethality, strong infectivity, and economic losses in crucian carp breeding, so as to improve the survival rate and reduce the incidence of disease rate effect
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Embodiment 1
[0019] Isolation and identification of carp herpesvirus type II CyHV-2DX2019
[0020] (1) Detection of carp herpesvirus type II
[0021] The carp herpes virus type II CyHV-2DX2019 attenuated strain of the present invention is taken from silver carp in a crucian carp-silver carp polyculture pond in Jingzhou, Hubei. The silver carp kidney tissue is placed in a sterile culture dish and cut with sterile ophthalmic scissors Add 10 times the volume (V / W) of phosphate buffered solution (PBS), transfer to a glass homogenizer, and grind into a tissue homogenate under ice-bath conditions. The DNA of tissue homogenate was extracted and amplified with primers CyHV2Hel-F: 5’-GGACTTGCGAAGAGTTTGATTTCTTAC-3’ and CyHV2Hel-R: 5’-CCATAGTCACCATCGTCTCATC-3’. The gel running results of the amplified product showed that the test sample had a specific band at 360 bp, which was consistent with the band size of the positive result of carp herpesvirus type II. After the amplified product was sequenced...
Embodiment 2
[0030] Pathogenicity experiment of CyHV-2DX2019 strain of carp herpesvirus type II to crucian carp
[0031] Take 180 crucian carp, with an average body weight of (150.0±4.0) g and an average body length of (25.0±2.5) cm. Before the experiment, crucian carp needs to be tested for viral nucleic acid to confirm that the carp herpesvirus type II is negative before it can be used in the experiment. Crucian carp is randomly divided into 6 groups according to the test strain, with 30 tails in each group, and the fresh culture of the 6th-10th generation test strain (CyHV-2DX2019 strain) is inoculated respectively by intraperitoneal injection method, 0.2ml / tail, the virus concentration of the virus liquid ≥5×10 5 copies / ml, the control group was inoculated with PBS in the same way, and observed continuously for 14 days.
[0032]The results showed that the behavior, appetite and other physiological indicators of the crucian carp inoculated with different generations of viruses were no...
Embodiment 3
[0034] Preparation of live vaccine against hematopoietic organ necrosis of crucian carp
[0035] In Example 1, the 10th and subsequent generations of inoculated cells blindly passed were observed continuously for 14 days, and then the cell cultures were harvested. After being frozen at -80°C, it was thawed at room temperature, repeated freezing and thawing three times, and then centrifuged at 4000r / min for 30min at 4°C. The supernatant was taken to extract virus DNA, and the virus content was detected by digital PCR. The virus concentration ≥ 5 × 10 5 The supernatant of copies / ml was diluted 100 times with PBS to prepare a live vaccine for crucian carp hematopoietic organ necrosis. 3 copies / ml.
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