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Babesia bigemina: Advances in continuous in vitro culture using serum-free medium supplemented with insulin, transferrin, selenite, and putrescine

机译:Babesia Bigemina:使用含有胰岛素,转铁蛋白,硒矿和Putrescine的无血清培养基进行血清培养基

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This study reported that Babesia bigemina (Bbig-SF) was continuously cultured in vitro in a serum-free medium supplemented with a mixture of insulin-transferrin-selenite (M-ITS) and putrescine (Pu). Firstly, the effect of five different types of basal culture media supplemented with 40% bovine serum was evaluated regarding the proliferation of the protozoan parasite. Cultures with the advanced DMEM/F12 medium (A-DMEM/F12) showed the highest percentage of parasitized erythrocytes (PPE) at 8.37%. Using A-DMEM/F12, a strain of B. bigemina (Bbig-SF) was adapted for growth in bovine serum-free medium by a sequential reduction of serum and demonstrated a maximum PPE of 7.18% in the absence of serum. The next study was the evaluation of the effect of adding four different concentrations of M-ITS to the serum-free A-DMEM/F12 medium on Bbig-SF; the optimal concentrations of M-ITS were 2000, 1100, and 1.34 mg/L, which yielded a PPE of 7.23%. Next, eight levels of Pu were evaluated on Bbig-SF cultured in serum-free A-DMEM/F12. After the addition of 0.1012 mg/L of Pu, the maximum PPE was 7.61%. When the combination of serum-free A-DMEM/F12 + M-ITS (2000, 1100, and 1.34 mg/L) + Pu (0.1012 mg/L) was evaluated, it yielded a maximum PPE of 14.80%. Finally, the combination of M-ITS + Pu in A-DMEM/F12 without serum and incorporation of a perfusion bioreactor yielded a maximum PPE of 33.45%. We concluded these culturing innovations for B. bigemina in vitro allow the optimization of small- and large-scale proliferation as a source of this protozoan parasite for future studies.
机译:本研究报告说,Babesia Bigemina(Bbig-SF)在补充有胰岛素 - 转铁蛋白 - 硒沸石(M-ITS)和Putrescine(PU)的混合物中在血清培养基中在体外培养。首先,对化学原生动物寄生虫的增殖评估了补充有40%牛血清的五种不同类型的基础培养基的效果。具有晚期DMEM / F12培养基(A-DMEM / F12)的培养物显示出寄生红细胞(PPE)的最高百分比为8.37%。使用A-DMEM / F12,B.Bigemina(Bbig-Sf)的菌株适于通过血清顺序减少血清无血清培养基的生长,并在没有血清的情况下证明了7.18%的最大PPE。下一步研究是评估在BBIG-SF上添加四种不同浓度的M-ITS与无血清A-DMEM / F12培养基的效果; M-ITS的最佳浓度为2000,1100和1.34mg / L,其PPE为7.23%。接下来,在无血清A-DMEM / F12中培养的BBIG-SF评估八种PU。添加0.1012mg / L的PU后,最大PPE为7.61%。当评估无血清A-DMEM / F12 + M-ITS(2000,1100和1.34mg / L)+ PU(0.1012mg / L)的组合时,它产生的最大PPE为14.80%。最后,在没有血清的A-DMEM / F12中的M-ITS + PU的组合并掺入灌注生物反应器,产生33.45%的最大PPE。我们总结了B. Bigemina体外的培养创新,允许优化小型和大规​​模扩散作为这种原生动物寄生虫的来源,以便进行未来的研究。

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