遗传多样性恶性疟原虫分离株的寄生虫生长动态

IF 1.4 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular and biochemical parasitology Pub Date : 2023-06-01 DOI:10.1016/j.molbiopara.2023.111552
Standwell C. Nkhoma, Amel O.A. Ahmed, Danielle Porier , Sujatha Rashid, Rebecca Bradford, Robert E. Molestina, Timothy T. Stedman
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引用次数: 2

摘要

具有不同增殖率或适应度的多种寄生虫谱系可能共存于临床疟疾分离株中,导致复杂的生长相互作用和表型变化。为了阐明多克隆分离株中寄生虫生长的动力学,我们测量了三种恶性疟原虫柬埔寨分离株的生长率(GRs),包括IPC_3445(MRA-1236)、IPC_5202(MRA-1240)、IPC_6403(MRA-1285),以及之前通过限制稀释从这些分离株中克隆的寄生虫谱系。同步后,每个寄生虫系的体外培养在四个连续的无性周期(192小时)内保持,在每个48小时的周期制备薄涂片,以估计GR和寄生虫血症(FCP)的倍数变化。细胞周期时间(CCT)是指环期寄生虫发育成成熟分裂体所需的时间,通过监测入侵后0–3小时环的发育,在孵化后52小时内进行测量。使用实验室品系3D7(MRA-102)和Dd2(MRA-150)作为对照。在寄生虫分离株和每个分离株的克隆谱系之间观察到GR、FCP和CCT的显著差异。这里研究的寄生虫系具有明确的生长表型,将有助于基础疟疾研究和新型疟疾干预措施的开发。通过NIAID的BEI资源计划的MR4集合,疟疾研究人员可以获得这些线路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Dynamics of parasite growth in genetically diverse Plasmodium falciparum isolates

Multiple parasite lineages with different proliferation rates or fitness may coexist within a clinical malaria isolate, resulting in complex growth interactions and variations in phenotype. To elucidate the dynamics of parasite growth in multiclonal isolates, we measured growth rates (GRs) of three Plasmodium falciparum Cambodian isolates, including IPC_3445 (MRA-1236), IPC_5202 (MRA-1240), IPC_6403 (MRA-1285), and parasite lineages previously cloned from each of these isolates by limiting dilution. Following synchronization, in vitro cultures of each parasite line were maintained over four consecutive asexual cycles (192 h), with thin smears prepared at each 48-h cycle to estimate GR and fold change in parasitemia (FCP). Cell cycle time (CCT), the duration it takes for ring-stage parasites to develop into mature schizonts, was measured by monitoring the development of 0–3-h post-invasion rings for up to 52 h post-incubation. Laboratory lines 3D7 (MRA-102) and Dd2 (MRA-150) were used as controls. Significant differences in GR, FCP, and CCT were observed between parasite isolates and clonal lineages from each isolate. The parasite lines studied here have well-defined growth phenotypes and will facilitate basic malaria research and development of novel malaria interventions. These lines are available to malaria researchers through the MR4 collection of NIAID’s BEI Resources Program.

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来源期刊
CiteScore
2.90
自引率
0.00%
发文量
51
审稿时长
63 days
期刊介绍: The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are: • the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances • intermediary metabolism and bioenergetics • drug target characterization and the mode of action of antiparasitic drugs • molecular and biochemical aspects of membrane structure and function • host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules. • analysis of genes and genome structure, function and expression • analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance. • parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules • parasite programmed cell death, development, and cell division at the molecular level.
期刊最新文献
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