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Clostridium welchii disease resistant transgenic plant vaccine and preparation method thereof

A technology for transgenic plants, Clostridium wilfordii disease, applied in the fields of botanical equipment and methods, biochemical equipment and methods, antibacterial drugs, etc. Bacteria environmental pollution and other problems, to achieve the effect of improving effectiveness, improving immunity, and enriching nutrients

Inactive Publication Date: 2011-04-13
NORTHEAST AGRICULTURAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] At present, formaldehyde is still the most commonly used chemical substance for exotoxin inactivation. Its inactivation effect is mainly related to the concentration, temperature, action time and pH of formaldehyde. High concentration formaldehyde and high temperature are used for inactivation. Although the inactivation time can be shortened, the effect on the antigen The loss of formaldehyde solution is also very large. Formaldehyde solution has a reducing effect and can inhibit protein activity. It also involves the issue of retaining the antigenicity of the toxin and eliminating its toxicity to the greatest extent. Due to many factors affecting inactivation, it is difficult to achieve an ideal inactivation. condition
The formaldehyde-detoxified Clostridium welchii α-toxin toxoid has a protective effect after immunizing sheep, but the toxoid may also contain other antigenic components of Clostridium welchii, which requires multiple intraperitoneal injections for immunization, and the inactivation of formaldehyde is not complete Clostridium welchii causes environmental pollution. The biggest problem is that the time required for toxoid-induced antibody production often exceeds the time for gas gangrene symptoms to appear
At the same time, inactivated vaccines are not easy to stimulate the body to produce local mucosal immunity, and the ability to mediate cellular immunity is weak, which reduces the immune efficacy of inactivated vaccines. Moreover, the manufacturing process is cumbersome, and it must be inoculated through non-oral routes to induce the body to produce circulating antibodies. Difficulty producing secreted local antibodies and therefore not blocking absorption of toxins from mucous membranes into the body

Method used

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  • Clostridium welchii disease resistant transgenic plant vaccine and preparation method thereof
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  • Clostridium welchii disease resistant transgenic plant vaccine and preparation method thereof

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Embodiment 1

[0047] A method for making a transgenic plant vaccine against Clostridium welchiiosis, the method comprising:

[0048] (1) Using a plasmid or disease material encoding Clostridium welchii α toxin as a template, PCR or RT-PCR is used to amplify the Clostridium welchii α toxin gene, and the obtained Clostridium welchii α toxin gene and Ti plasmid Carry out enzyme digestion respectively, recover the target gene and plant expression vector fragments, connect and transform Escherichia coli, carry out enzyme digestion, PCR and sequencing identification on the recombinant Ti, transform Agrobacterium tumefaciens with the recombinant plasmid, and obtain positive recombinant Agrobacterium tumefaciens through screening and PCR identification pA: It was deposited in the China Center for Type Culture Collection on June 2, 2010, and the preservation number is: CCTCC NO: M 2010130.

[0049] (2) Plant seeds undergo vernalization, germination, and splicing to obtain explants, respectively infe...

Embodiment 2

[0054] A preparation method of an anti-clostridium welchiiosis transgenic plant vaccine, the method comprising:

[0055] (1) Using the plasmid or disease material containing the mucosal adjuvant Escherichia coli heat labile enterotoxin B subunit (LT-B) as a template, use PCR or RT-PCR to amplify the mucosal adjuvant LT-B gene to contain The plasmid or disease material encoding Clostridium welchii α-toxin is used as a template, and PCR or RT-PCR is used to amplify the α-toxin gene of Clostridium welchii, and the mucosal adjuvant LT-B gene and the Clostridium welchii Bacterial α-toxin gene fusion to obtain the fusion gene, the obtained fusion gene and Ti plasmid were digested separately, the target gene and plant expression vector fragments were recovered, ligated and transformed into Escherichia coli, and the recombinant Ti plasmid was identified by enzyme digestion, PCR and sequencing. The recombinant plasmid was transformed into Agrobacterium tumefaciens, and positive recombi...

Embodiment 3

[0062] 1 test material

[0063] 1.1 Plasmids and strains

[0064] Plasmid pET-30b-a contains the α-toxin gene sequence of Clostridium welchii and was constructed by our laboratory; plasmid pLT-b contains the gene sequence of Escherichia coli heat-labile enterotoxin B subunit (LT-B) and was constructed by Mr. Ge Junwei of our laboratory ; The plant expression vector p33EG contains the E12 promoter sequence, the Ω sequence that enhances translation, the Bar gene of resistance to PPT (Phosphinothricin) herbicide, the prokaryotic expression of NptⅡ (Km resistance) gene and Agrobacterium tumefaciens LBA 4404. Gifted by Professor Zhu Yanming of the college; Clostridium welchii type A (C57-1) was purchased from China Veterinary Drug Control Institute.

[0065] 1.2 Antibody preparations

[0066] Anti-clostridium welchii alpha toxin rabbit serum, mouse serum and anti-Escherichia coli heat-labile enterotoxin B subunit (LT-B) mouse serum were prepared by our laboratory; Anti-mouse IgA...

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Abstract

The invention discloses a clostridium welchii disease resistant transgenic plant vaccine and a preparation method thereof. At present, the protective ratio on immunization of clostridium welchii disease resistant vaccines is lower. The preparation method of the clostridium welchii disease resistant transgenic plant vaccine comprises the steps of: (1) with a plasmid or disease sample containing coded clostridium welchii toxin as a template, carrying out PCR (Polymerase Chain Reaction) or RT-PCR (Reverse Transcription-Polymerase Chain Reaction) amplification to obtain a clostridium welchii toxin gene, carrying out enzyme cutting on the obtained clostridium welchii toxin gene or the Ti or Ri plasmid respectively, recycling a target gene and a plant expression vector segment, connecting with and converting escherichia coli, carrying out enzyme cutting, PCR and sequencing identification on the recombinant Ti or Ri plasmid, converting agrobacterium tume faciens or agrobacterium rhizogene with the recombinant plasmid, and screening and identifying positive recombinant agrobacterium; and (2) carrying out vernalization, germination and splicing on plant seeds to obtain explants, infecting the explants respectively with the recombinant agrobacterium in the step (1), carrying out screening, subculturing, rooting and transplanting on the infected explants to obtain transformed plants, and screening and identifying positive transgenic plants.

Description

Technical field: [0001] The invention relates to a transgenic plant vaccine against Clostridium welchii disease and a preparation method thereof. Background technique: [0002] Clostridium welchii (Clostridium welchii), also known as Clostridium perfringens (Clostridium perfringens) is one of the normal flora in the intestinal tract of animals, and it is also the original culprit that causes Clostridium welchii disease. The pathogenesis is that Clostridium welchii multiplies in large numbers in the intestines due to sudden changes in the feeding environment and feed, and the toxins produced are absorbed through the digestive tract, leading to enterotoxemia, necrotic enteritis, soft kidney disease in sheep, and red piglets. Dysentery, lamb dysentery, rabbit hemorrhagic diarrhea, traumatic gas gangrene, animal sudden death syndrome, etc. According to the different exotoxins secreted by the bacteria, Clostridium welchii can be divided into five serotypes, namely A, B, C, D, an...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K39/08C12N15/31C12N15/82A61P31/04
Inventor 刘松梅李一经葛俊伟朱延明
Owner NORTHEAST AGRICULTURAL UNIVERSITY
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