Vega C A, Buening G M, Rodriguez S D, Carson C A, McLaughlin K
Am J Vet Res. 1985 Feb;46(2):421-3.
Babesia bigemina-infected RBC and merozoites were cryopreserved and used to initiate in vitro cultures in normal bovine RBC; the cryoprotectant was a final 10% polyvinylpyrrolidone in Vega y Martinez solution. A cooling rate of 20 C/min until -80 C and then rapid transfer to liquid N2 storage was satisfactory. Samples for culture initiation were rapidly thawed at 37 C, washed in Vega y Martinez solution and resuspended in complete culture media containing 10% normal bovine RBC. The optimum culture conditions to reestablish cultures were a 24-well plate (16 mm ID), 5 mm in depth, and an atmosphere of 2% to 5% O2, 5% CO2, and 93% to 90% N2.
将感染双芽巴贝斯虫的红细胞和裂殖子进行冷冻保存,并用于在正常牛红细胞中启动体外培养;冷冻保护剂是在维加·马丁内斯溶液中最终浓度为10%的聚乙烯吡咯烷酮。以20℃/分钟的降温速率降至-80℃,然后迅速转移至液氮储存,效果良好。用于启动培养的样本在37℃迅速解冻,用维加·马丁内斯溶液洗涤,并重悬于含有10%正常牛红细胞的完全培养基中。重新建立培养的最佳培养条件是使用24孔板(内径16毫米),深度为5毫米,以及2%至5%氧气、5%二氧化碳和93%至90%氮气的气氛。