Vaccine composition for resisting pig mycoplasma pneumonia and infectious pleuropneumonia and preparation method
A technology of mycoplasma pneumonia and vaccine composition, which is applied in the direction of bacterial antigen components, antibody medical components, antibacterial drugs, etc., can solve the problem that there is no dual combination vaccine that can prevent and treat mycoplasma pneumonia and porcine infectious pleuropneumonia at the same time, and achieve Immunization is cheap, labor-intensive, and practical
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Embodiment 1
[0047] Example 1: Isolation and identification of Mycoplasma hyopneumoniae HN0613
[0048] 1. Materials and methods
[0049] (1) Material
[0050] ① source of disease material
[0051] In 2006, 16 suspected lungs with mycoplasma swine pneumonia were collected from various places in Henan Province.
[0052] ② Culture medium
[0053] Mycoplasma hyopneumoniae Friis medium was purchased from BD Company; pig serum was purchased from GIBCO Company; phenol red indicator was purchased from American AMRESCO Company.
[0054] ③ Reagent
[0055] Biochemical reagents and chemical reagents were purchased from Sinopharm Chemical Reagent Co., Ltd.
[0056] Bacterial Genomic DNA Extraction Kit was purchased from TIANGEN Company, and Dieter's Staining Kit was purchased from Chongqing Pangtong Medical Instrument Co., Ltd. Biochemical identification reagents were purchased from Hangzhou Tianhe Microbiological Reagent Co., Ltd.
[0057] ④ Negative and positive serum
[0058] Rabbit anti-M...
Embodiment 2
[0094] Embodiment 2: Identification of the isolation of serum type 1 LC strain, type 5 YC strain, and type 7 YS strain
[0095] 1. Materials and Methods
[0096] (1) Disease materials to be tested
[0097] The disease materials of pigs with suspected pleuropneumonia were collected from 10 pig farms in Henan, Hubei and other provinces and cities.
[0098] (2) PCR primer sequence
[0099] PF-5'CCGACTTTTAAATCCGT3', PR-5'GAACAGTTGTTCGCTAA3'
[0100] (3) mice
[0101] Bought from Animal Experiment Center of Henan Province.
[0102] (4) Isolation and purification of pathogenic bacteria and liquid culture
[0103] Aseptically take dying pig lungs, throat tonsils and other tissues, inoculate them on TSA (containing 1wt% NAD) agar medium, place in 10% CO 2 After culturing at 37°C for 24-36 hours, select a typical single colony for purification and culture. The purified single colonies were selected and inoculated in TSB (containing 1 wt% NAD) liquid culture medium, and cultured ...
Embodiment 3
[0129] Example 3: Preparation of Mycoplasma hyopneumoniae antigen and Actinobacillus pleuropneumoniae antigen
[0130] 1. The source of bacteria (virus) strains
[0131] The selected Actinobacillus pleuropneumoniae strains are: the preservation number of the serum type 1 LC strain is CCTCC M2011458; the preservation number of the serum type 5 YC strain is CCTCC M2011459; the preservation number of the serum type 7 YS strain is CCTCC M2011460. The date of deposit is December 9, 2011.
[0132] The selected Mycoplasma hyopneumoniae is HN0613, and the preservation number is CCTCC No. M2012230. The date of deposit is June 13, 2012.
[0133] 2. Preparation and inspection of vaccine semi-finished products
[0134] (1) Preparation of seeds for production
[0135] ① Actinobacillus pleuropneumoniae:
[0136] Propagation of primary seeds
[0137] Streak and inoculate the LC, YC, and YS strains of freeze-dried strains on TSA (soybean casein agar) plates respectively, and inoculate t...
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