Construction method of mice infection model of Suis Eperythrozoonsis
A porcine eperythrozoon and porcine eperythrocytic technology, applied in the field of bioengineering, can solve the problems of affecting test results, one-sidedness, and not a single source of infection
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Embodiment 1
[0022] Example 1 Construction of Eperythrozoon porcine SPF Kunming mouse infection model
[0023] (1) Separation and purification of porcine Eperythrozoon
[0024] First, 200 ml of pig blood suffering from porcine eperythrozoonosis was aseptically collected, centrifuged at 2000 r / min for 10 min, and the supernatant was removed. Add the precipitated erythrocyte sludge to an equal volume of normal saline to resuspend the erythrocyte suspension. Add an equal volume of lymphocyte separation medium and red blood cell suspension into a new centrifuge tube, centrifuge at 2500r / min for 20min, remove the uppermost and middle white blood cell layers, and remove the lower red blood cell layer. Resuspend the erythrocyte layer with an equal volume of normal saline, and after bathing in 50°C water for 15 minutes, the separation of Eperythrozoon and erythrocytes can be observed under an oil microscope. At this time, centrifuge at 2000r / min for 10min, and take the supernatant into a centrifu...
Embodiment 2
[0039] Example 2 Construction of Eperythrozoon porcine SPF BALB / c mouse infection model
[0040] (1) Separation and purification of porcine Eperythrozoon
[0041] First, 200 ml of pig blood suffering from porcine eperythrozoonosis was aseptically collected, centrifuged at 2000 r / min for 10 min, and the supernatant was removed. Add the precipitated erythrocyte sludge to an equal volume of normal saline to resuspend the erythrocyte suspension. Add an equal volume of lymphocyte separation medium and red blood cell suspension into a new centrifuge tube, centrifuge at 2500r / min for 20min, remove the uppermost and middle white blood cell layers, and remove the lower red blood cell layer. Resuspend the erythrocyte layer with an equal volume of normal saline, and after bathing in 50°C water for 15 minutes, the separation of Eperythrozoon and erythrocytes can be observed under an oil microscope. At this time, centrifuge at 2000r / min for 10min, and take the supernatant into a centrifug...
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