Garg Swati, Agarwal Shalini, Dabral Surbhi, Kumar Naveen, Sehrawat Seema, Singh Shailja
Malaria Group, International Centre for Genetic Engineering and Biotechnology (ICGEB), New Delhi, 110067 India.
Department of Life Sciences, Shiv Nadar University, Gautam Budha Nagar, 203207 UP India.
Syst Synth Biol. 2015 Dec;9(Suppl 1):23-6. doi: 10.1007/s11693-015-9167-9. Epub 2015 Apr 5.
Malaria, a leading parasitic killer, is caused by Plasmodium spp. The pathology of the disease starts when Plasmodium merozoites infect erythrocytes to form rings, that matures through a large trophozoite form and develop into schizonts containing multiple merozoites. The number of intra-erythrocytic merozoites is a key-determining factor for multiplication rate of the parasite. Counting of intraerythrocytic merozoites by classical 2-D microscopy method is error prone due to insufficient representation of merozoite in one optical plane of a schizont. Here, we report an alternative 3-D microscopy based automated method for counting of intraerythrocytic merozoites in entire volume of schizont. This method offers a considerable amount of advantages in terms of both, ease and accuracy.
疟疾是主要的寄生虫杀手,由疟原虫属引起。当疟原虫裂殖子感染红细胞形成环状体时,疾病的病理过程开始,环状体通过大型滋养体形式成熟并发育成含有多个裂殖子的裂殖体。红细胞内裂殖子的数量是寄生虫繁殖率的关键决定因素。由于裂殖体的一个光学平面中裂殖子的显示不足,通过经典的二维显微镜方法对红细胞内裂殖子进行计数容易出错。在此,我们报告了一种基于三维显微镜的替代自动化方法,用于对裂殖体的整个体积中的红细胞内裂殖子进行计数。该方法在简便性和准确性方面都具有相当多的优势。