肯尼亚Thika地区部分家庭猫和鸡中刚地弓形虫的分离和低温保存

A. Njuguna, N. Maina, J. Kagira, S. Karanja, D. Kamau, M. Ngotho, J. Mose, L. Mutharia
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摘要

在非洲,关于刚地弓形虫在家猫(Felis catus)和中间宿主(如鸡)中传播的基因型和表型特征的信息缺乏。由于没有收集到保存良好的分离株,情况更加复杂。本研究旨在建立弓形虫慢殖子、速殖子和卵囊的冷冻库。这些寄生虫是从肯尼亚Thika地区家庭饲养的猫和鸡中分离出来的。获得8份刚地弓形虫卵囊阳性的猫粪便样本和38份鸡脑组织囊(慢殖子)样本,在小鼠体内进行繁殖并冷冻保存。对于猫的每个样本,(两个供体)BALB/c小鼠口服感染1 × 104/ml卵囊。从每个鸡样本中,(两个供体)腹腔内感染20-30个组织囊肿BALB/c小鼠。在感染后第三天,从一只供体小鼠的腹腔中收获速殖子。对另外两只感染小鼠进行了8周的进一步监测,对其实施安乐死,并采集脑组织进行弓形虫囊肿的纯化和冷冻保存。从感染猫卵囊样本的小鼠中,分离出2个(25%)速殖子,但从脑组织囊肿中分离出8个(100%)速殖子。鸡样品中产生速殖子18个(47.3%),组织囊肿38个(100%)。将分离的卵囊(来自猫)、速殖子和组织囊(来自小鼠)用15%甘油作为冷冻保护剂冷冻保存,并保存在液氮(-196℃)中。冷冻保存6个月后,在手工血细胞计上用台盼蓝染料排除法检测分离株的活力。弓形虫冻存前后的存活率无显著变化(p>0.05),冻存前后的存活率均保持在99.5% ~ 96%之间。该冷冻库将作为后续研究肯尼亚刚地弓形虫分离株分子和表型特征的储存库。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation and Cryopreservation of Toxoplasma gondii Isolates from Cats and Chickens from Selected Households in the Thika Region, Kenya
There is a shortage of information in Africa regarding the genotypic and phenotypic characteristics of the Toxoplasma gondii circulating in domestic cats (Felis catus) and the intermediate hosts such as chicken. The situation is compounded by a lack of collection of well-stored isolates. The present study was aimed at creating a cryobank of T. gondii bradyzoites, tachyzoites, and oocysts. The parasites were isolated from cats and chickens kept in households in the Thika region, Kenya. Eight (8) cat fecal samples positive for T. gondii oocysts and 38 chicken brain tissue cysts (bradyzoites) were obtained and used for propagation in mice before cryopreservation. For each sample from the cats, (two donors) BALB/c mice were infected orally with 1 x 104/ml of oocysts. From each chicken sample, (two donors) BALB/c mice were infected intraperitoneally with 20-30 tissue cysts. On the third day after infection, tachyzoites were harvested from the peritoneal cavity of one donor mouse. The other two infected mice were further monitored for eight weeks, euthanized and the brain tissue harvested for toxoplasma cysts which were purified and cryopreserved. From the mice infected with oocysts from the cats’ samples, 2 (25%) tachyzoites but a higher 8 (100%) isolation was obtained from brain tissue cysts. On the other hand, from chicken samples generated 18 (47.3%) tachyzoites and 38 (100%), tissue cysts were obtained. The isolated oocysts (from cats), tachyzoites, and tissue cysts (from mice) were cryopreserved using 15% glycerol as cryoprotectant and stored in liquid nitrogen (-196oC). After 6 months of cryopreservation, the viability of the isolates was tested using Trypan blue dye exclusion on a manual hemocytometer. Viability (99.5% - 96%) of the cryopreserved samples was maintained for the three toxoplasma stages and there was no significant change (p>0.05) in the viability of the parasites before and after cryopreservation. The cryobank will serve as a repository for subsequent studies on molecular and phenotypic characterization of T. gondii isolates from Kenya. 
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