Vibrio harveyi secretory type vaccine and structure and application thereof

A technology of Vibrio harveta and secretory type, which is applied in the fields of molecular biology and immunology, can solve the problems of limited use, the application of secretory vaccines has not been reported yet, and the harm of antibiotics, etc., and achieves high protection rate, low cost, and immune effect. strong effect

Inactive Publication Date: 2010-07-21
INST OF OCEANOLOGY - CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The use of antibiotics has gradually been restricted internationally due to their potential hazards to the environment and human heal...

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] The vibrio harveyi secreted vaccine is shown in the base sequence of SEQ ID No.1 in the sequence table. Sequence listing SEQ ID No1

[0025] ATGTTAAAAGAAACTACTAAGTTGTTGTATCACCTCGGCACTCTGTTTCCATTCTTCTCTCGCTTTTTCGCAATCGACAGA

[0026] ACTCCCAAATGATGCGGATTTAGCGCAGACACCTGCGTCACTGATGCTTGCGCCTGAAGACGTCGCCATCGCTGATCGTT

[0027] ATATCGTTGTATTTCATCAACTCAAATGATGATGAATAATTCACTTGAATTACAGCAGTTCACACAACAATCTGTGGAC

[0028] CGAATGTCTGGTTTGTACTCAATAGAAGTGGAATCAGTATTCGACAATTCGATCAGCGGTTTCGTTGCGACGTTAGCTCC

[0029] TGAACAGCTGAAAGCGTTACGTGCTGATCCACGTGTTGAATACATCGAGCAAGACAGAATTCTTACACTAGACCCAATAG

[0030] TCTCGGCAGAAGTAAACCAAAGTAATGCAATTTGGGGGCTAGACCGAATTGATCAACGTAGTCTGCCTCTCAATAACAAT

[0031] TACAGCGCCAACTTTGATGGAACGGGCGTCACGGCTTACGTTATCGATACGGGTGTGAACAACTCGCACGTTGAATTTGC

[0032] CGGACGCTCCATTTCGGGATATGACTTTGTCGACAATGATGCGGATGCCAGTGACTGTAATGGACACGGCACACACGTAG

[0033] CGGGCACGATCGGCGGATCTTTGTATGGCGTGGCAAAGAACGTGAGCATTGTTGGTGTCAGAGTGCTTAGCTGTTCTGGC

[0034] TCAGGTTCAACGTCCGGCGTTATTGC...

Embodiment 2

[0061] Vaccine bacterial suspension: culture the Vibrio harveyi secretory vaccine strain DH5α / pTVP1M containing the nucleotide sequence in the sequence table SEQ ID No.1 obtained above in LB liquid medium containing 50ug / ml Ap overnight; Add 0.1ml of the overnight culture solution into 10ml of fresh LB liquid medium containing Ap (50ug / ml), and culture at 28°C with shaking at 160rpm until OD 600 0.8-1, then the bacterial culture solution was centrifuged (5000g, 4°C, 10min), and the bacterial cells were collected and suspended in PBS to a final concentration of 4×10 8 cfu / ml is the vaccine preparation solution.

[0062] Vaccine control solution: The plasmid pBT3 was transformed into DH5α by the Hanahan method to obtain the transformant DH5α / pBT3. Cultivate DH5α / pBT3 overnight in LB liquid medium containing 50ug / ml Ap; take 0.1ml of overnight culture solution, add it to 10ml of fresh LB liquid medium containing Ap (50ug / ml), at 28 Shake culture at 160rpm at ℃ to OD 600 0.8-1,...

Embodiment 3

[0065] Immunization injection of the above-mentioned vaccine bacteria suspension: 80 flounder (each weighing about 10 g) were randomly divided into 2 groups, 40 in each group. These two groups are named A and B respectively. Each fish in Group A was injected intraperitoneally with 100ul of the vaccine bacteria suspension, and each fish in Group B was injected intraperitoneally with 100ul vaccine control solution. After 20 days, each fish in group A was injected intraperitoneally with 100ul of the vaccine bacteria suspension again, and each fish in group B was injected with 100ul vaccine control solution intraperitoneally.

[0066] Preparation of Vibrio harveyi suspension: culture Vibrio harveyi from T4 to OD in LB medium 600 0.6, and then centrifuged (5000g, 4°C, 10min). Collect the cells and suspend them in PBS to a final concentration of 8×10 7 cfu / ml is Vibrio harveyi suspension.

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Abstract

The invention relates to the fields of molecular biology and immunology, in particular to a vibrio harveyi secretory type vaccine and a structure and application thereof. Particularly, the secretory type vaccine is a base sequence in a sequence table SEQ ID No.1, and the construction process thereof is as follows: utilizing vibrio harveyi T4 as a template and F11 and R8 as primers for PCR amplification, connecting the product with pBS-T at room temperature, utilizing NdeI/XhoI double-enzyme cleavage to recover 1.2kb segment from plasmids pBSVhP1, simultaneously utilizing NdeI/XhoI double-enzyme cleavage to recover 4.3kb segment of plasmids pBT3, connecting the two segments at room temperature by ligase T4DNA for 2-4h, transforming connection liquid into colon bacillus DH5 alpha, culturing on an LB solid medium containing Ap for 24h to screen out white transformant, i.e. the Vibrio harveyi secretory type vaccine of base sequence in the expression sequence table SEQ ID No.1. The obtained vaccine has immune and protective functions on Vibrio harveyi. The obtained vaccine has the immune and protective effects on the Vibrio harbeyi, and the immune and protective efficiency of the vaccine of the invention on the Vibrio harveyi can reach to 90%. The preparation process is simple, devitalization and other steps do not needed, and no adjuvant is needed.

Description

technical field [0001] The invention relates to the fields of molecular biology and immunology, in particular to a vibrio harveyi secreted vaccine and its construction and application. Background technique [0002] Vibrio harveyi (Vibrio harveyi) is an important pathogenic bacteria in aquaculture, which can infect a variety of aquaculture animals, including fish, shrimp, and shellfish. The current prevention and control of Vibrio harveyi relies on antibiotics and immune control. Due to the potential hazards of antibiotics to the environment and human health, their use has gradually been restricted internationally. Vaccines against Vibrio harveyi are mainly simple inactivated vaccines, and the application of secreted vaccines has not been reported. Contents of the invention [0003] The purpose of the present invention is to provide a vibrio harveyi secretory vaccine and its construction and application. [0004] To achieve the above object, the technical solution adopte...

Claims

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Application Information

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IPC IPC(8): A61K39/108A61P31/04C12N15/31C12N1/21
Inventor 孙黎程爽张卫卫
Owner INST OF OCEANOLOGY - CHINESE ACAD OF SCI
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