Pig erysipelothrix rhusiopathiae antigen and vaccine composition thereof
A technology of Erysipelothrix rhusiopathiae and vaccine composition, which is applied in the direction of viral antigen components, bacterial antigen components, drug combinations, etc., and can solve the problems of lack of immunity and persistence
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Embodiment 1
[0043] The invention is described in the following illustrative but non-limiting examples. Embodiment 1. Erysipelas rhusiopathiae culture
[0044] Rhusiopathiae strain CN 3342 containing Difco Peptone (concentration is 2.75%), Difco yeast extract (0.55%), Tween 80 (0.2%), K 2 HPO 4 (0.217%) and KH 3 PO 4 (0.061%) (in deionized water) medium. The pH of the medium was adjusted to 7.2 with 5N NaOH. The medium was steam sterilized at a temperature of at least 122°C for 30-90 minutes. After autoclaving, 50% sterile glucose solution was added to a final concentration of 3% (w / v).
[0045] To prepare the working seed culture, first transfer the strain in a cryogenic tube from the frozen storage place (-70°C), thaw it quickly, and transfer it aseptically to the Erlenmeyer flask containing the culture medium. Incubate flasks at 37°C for 12 to 36 hours with constant shaking and check for purity by Gram stain. When a pure culture was found, the culture was mixed with sterile gl...
Embodiment 2
[0048] Prior to harvesting, cultures were checked microscopically for purity, cell morphology, and Gram response. Bacterial growth was monitored by measuring the optical density of the culture at 625 nm. Cultures were harvested when their optical density at 625 nm was 4.0 or greater. Embodiment 2. Preparation of Erysipelothrix rhusiopathiae vaccine
[0049] Formalin solution was added to the cultures at a final concentration of 0.5% (v / v) to inactivate the cultures. Cultures were transferred to sterile tanks and placed in an incubator at 37±2°C for at least 24 hours (up to 60 hours) with constant agitation. Cultures that were not processed immediately were stored at 2-8°C for up to 7 days. Inactivated cultures were clarified by a continuous flow centrifuge. The liquid fraction was retained for further processing and bacteria were discarded.
[0050] In the experiments, a 10-fold concentrate of the culture filtrate of Erysipelothrix rhusiopathiae was made, and the culture ...
Embodiment 3
10
[0056] Satisfactory results in the control group, in which the infection was characterized by hyperthermia (40.9°C [105.6°F] or higher on at least two consecutive days), cultures at necropsy, and / or characteristic after infection with Erysipelothrix rhusiopathiae Clinical symptoms are clearly visible. Clinical features considered characteristic of this disease include sudden death, depression, abdominal and ear congestion, metastatic skin lesions, or joint stiffness and joint-related disorders. Pigs with clinical symptoms but not hyperthermic body temperature were sacrificed and their blood, spleen, and liver were cultured in an attempt to isolate Erysipelothrix rhusiopathiae from them.
[0057] According to Fisher's exact assay, the proportion of pigs determined to be protected or not differed with different vaccines (P<0.05). An optimization control experiment was constructed comparing each dosage group to the control group and comparing each group to ...
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