Carter R, Miller L H
Bull World Health Organ. 1979;57 Suppl 1(Suppl):37-52.
With the introduction of continuous culture of Plasmodium falciparum it has become possible to study the factors involved in gametocyte production in vitro and thus eliminate the uncontrollable in vivo variables of the host. The authors have developed a method for measuring quantitatively the rate of production of gametocytes at any time in such cultures. The method is based on an estimation of the percentage of ring forms that develop into stage II gametocytes.Using this approach, it was found that dilution of cultures with fresh red blood cells so as to lower the parasitaemia led to rapid fall in the rate of conversion to gametocytes. The conversion rates subsequently rose again to levels typically in the order of 10% after several days of growth in the new culture. In the parental cultures from which the dilutions were made, conversion rates remained high at all times. This pattern was consistently observed in three different isolates of P. falciparum from Africa and the results indicate that the reduction of parasitaemia by addition of fresh cells was responsible for reducing production of gametocytes and that conditions associated with a period of growth in culture induced renewed gametocytogenesis. The authors conclude, therefore, that environmental conditions directly modulate the rate of gametocyte production by P. falciparum in culture.After 1(1/2) years in culture, parasites have retained their ability to produce gametocytes and the gametocytes to undergo exflagellation.
随着恶性疟原虫连续培养技术的引入,在体外研究配子体产生所涉及的因素成为可能,从而消除了宿主体内不可控的变量。作者开发了一种方法,用于定量测量此类培养物中任何时候配子体的产生速率。该方法基于对发育成II期配子体的环状体百分比的估计。使用这种方法发现,用新鲜红细胞稀释培养物以降低疟原虫血症会导致向配子体转化的速率迅速下降。在新培养物中生长几天后,转化率随后再次上升至通常约为10%的水平。在进行稀释的亲代培养物中,转化率始终保持较高水平。在来自非洲的三种不同恶性疟原虫分离株中均一致观察到这种模式,结果表明添加新鲜细胞降低疟原虫血症是导致配子体产生减少的原因,并且与培养一段时间相关的条件诱导了新的配子体生成。因此,作者得出结论,环境条件直接调节体外培养的恶性疟原虫配子体的产生速率。培养1.5年后,疟原虫仍保留产生配子体的能力,并且配子体仍能进行配子出丝。