Technique for allowing aquatic invertebrate larvae and parents to harmlessly carry Vibrio phages
A technology of invertebrates and phages, applied in the direction of microorganism-based methods, viruses/phages, biochemical equipment and methods, etc., can solve problems such as inapplicability, and achieve the effect of meeting production needs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0033] Embodiment 1 Taking the newly hatched larvae of Litopenaeus vannamei (hereinafter referred to as "prawn larvae") as an example, the technology of the present invention is implemented according to the following steps.
[0034] 1. Isolate Vibrio strains and their phages routinely from the aquaculture water body to obtain a phage lysate.
[0035] 2. The phage lysate obtained in step 1 was recovered by centrifugation, filtered through a 0.22 μm filter membrane, and the titer was measured by the double-plate method, and the obtained concentration was 1.1×10 11 pfu / ml phage solution, stored at 4°C, as a storage solution, for later use; specific method: add freshly prepared phage stock solution from a single phage spot to the logarithmic growth phase bacterial solution cultured by a single colony, and put it into a shaker for vigorous shaking After shaking, the obtained lysate was centrifuged to remove bacterial fragments, and trypanase DNAI and trypsinase were added to remove...
Embodiment 2
[0049] Example 2 Taking the parent Litopenaeus vannamei (hereinafter referred to as "parent prawn") with a body length of 16-18 cm as an example, implement the technology of the present invention according to the following steps.
[0050] 1. Isolate Vibrio strains and their phages routinely from the aquaculture water body to obtain a phage lysate.
[0051] 2. The phage lysate obtained in step 1 was recovered by centrifugation, filtered through a 0.22 μm filter membrane, and the titer was measured by the double-plate method to obtain a concentration of 8.5×10 10 pfu / ml phage solution, stored at 4°C, as a storage solution, for later use; specific method: add freshly prepared phage stock solution from a single phage spot to the logarithmic growth phase bacterial solution cultured by a single colony, and put it into a shaker for vigorous shaking After shaking, the obtained lysate was centrifuged to remove bacterial fragments, and trypanase DNAI and trypsinase were added to remove ...
Embodiment 3
[0065] Example 3 Vibrio parahaemolyticus and its bacteriophage were obtained from a local farm on Donghai Island, Zhanjiang. In clean seawater, the final concentration was 4×10 6 pfu / mL selected Vibrio parahaemolyticus phage, soak the newly hatched Litopenaeus vannamei larvae in it for 1.0h, and continue to cultivate them for 20 days according to the conventional seedling method. No host bacteria were found in the larvae, and the survival rate was 65%. The host bacteria in the larvae of the control group were as high as 4×10 4 cfu / mL, the survival rate is 5%.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com