Isolated culture method of Mycoplasma capricolum subsp.Capripneumoniae (Mccp)
A technology for separating and culturing mycoplasma, which is applied in the field of separating and culturing Mycoplasma capricolum subsp. capricolum, can solve the problems that have not yet been seen, and achieves the effects of avoiding unstable differences between batches, high separation success rate, and high titer of viable bacteria.
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Embodiment 1
[0027] The method for isolating Mycoplasma capricoides goat pneumonia subspecies in pleural effusion samples is as follows:
[0028] (1) Treatment of disease samples: aseptically collect pleural effusion of fresh disease materials from goats with Mycoplasma goati subsp. Draw 1.0ml of the filtered sample solution into a sterile EP tube, add 200μl of 200,000 IU penicillin, mix well, place at 4°C for 24 hours, and store for later use.
[0029] (2) Sample inoculation: Dilute the processed sample solution 10 times with sterile 0.01M pH7.2 PBS to prepare 10- 1 Diluted sample solution, the sample treatment solution, 10 -1 The yolk sac of the diluted sample solution was inoculated with 7-day-old healthy SPF chicken embryos (with clear blood vessels and vigorous vitality), and each chicken embryo was inoculated with 0.2ml, and the sample processing stock solution, 10 -1 Two 7-day-old healthy SPF chicken embryos were inoculated with each dilution sample treatment solution. After the ...
Embodiment 2
[0034] The method for isolating Mycoplasma capricosum subsp. goat pneumonia in alveolar lavage fluid samples is as follows:
[0035] (1) Treatment of disease samples: aseptically collect alveolar lavage fluid from dead goats with Mycoplasma capricoides subsp. Draw 1.0ml of the filtered sample solution into a sterile EP tube, add 200μl of 200,000 IU penicillin, mix well, place at 4°C for 24 hours, and store for later use.
[0036] (2) Sample inoculation: Dilute the processed sample solution 10 times with sterile 0.01M pH7.2 PBS to prepare 10 -1 Diluted sample solution, the sample treatment solution, 10 -1 The yolk sac of the diluted sample solution was inoculated with 7-day-old healthy SPF chicken embryos (with clear blood vessels and vigorous vitality), and each chicken embryo was inoculated with 0.2ml, and the sample processing stock solution, 10 -1 Two 7-day-old healthy SPF chicken embryos were inoculated with each dilution sample treatment solution. After the sample inoc...
Embodiment 3
[0042] The method of the present invention is compared with the culture medium of the prior art on the separation of Mycoplasma capricoides goat pneumonia subspecies.
[0043] Under the same conditions, use the method of the present invention and the prior art (improved Thiaucourt's culture medium) to separate the disease material (Mycoplasma capricosum subspecies capricornus pneumonia PCR positive). The specific method is as follows: Aseptically collect and process 4 parts of pleural effusion or alveolar lavage fluid of goats that died of the disease, filter them with a sterile filter with a filter membrane of 0.45 μm, and store the filtrate for future use. Draw 1.0ml filter sample liquid and carry out separation and cultivation according to the method of the present invention; Get 0.5ml and inoculate into 4.5ml improved Thiaucourt's substratum in addition, cultivate in 37 ℃ of incubators, judge according to substratum color change and PCR identification result Mycoplasma goat...
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