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Use of fluorescent nanoparticles to investigate nutrient acquisition by developing Eimeria maxima macrogametocytes

机译:利用荧光纳米颗粒研究最大艾美球虫大配子细胞的养分吸收

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摘要

The enteric disease coccidiosis, caused by the unicellular parasite Eimeria, is a major and reoccurring problem for the poultry industry. While the molecular machinery driving host cell invasion and oocyst wall formation has been well documented in Eimeria, relatively little is known about the host cell modifications which lead to acquisition of nutrients and parasite growth. In order to understand the mechanism(s) by which nutrients are acquired by developing intracellular gametocytes and oocysts, we have performed uptake experiments using polystyrene nanoparticles (NPs) of 40 nm and 100 nm in size, as model NPs typical of organic macromolecules. Cytochalasin D and nocodazole were used to inhibit, respectively, the polymerization of the actin and microtubules. The results indicated that NPs entered the parasite at all stages of macrogametocyte development and early oocyst maturation via an active energy dependent process. Interestingly, the smaller NPs were found throughout the parasite cytoplasm, while the larger NPs were mainly localised to the lumen of large type 1 wall forming body organelles. NP uptake was reduced after microfilament disruption and treatment with nocodazole. These observations suggest that E. maxima parasites utilize at least 2 or more uptake pathways to internalize exogenous material during the sexual stages of development.
机译:由单细胞寄生虫艾美球虫引起的肠球虫病是家禽业的一个主要且反复出现的问题。虽然在艾美尔球虫中已充分证明了驱动宿主细胞入侵和卵囊壁形成的分子机制,但对导致获取养分和寄生虫生长的宿主细胞修饰的了解相对较少。为了了解通过发展细胞内配子细胞和卵囊获取营养的机制,我们使用大小为40 nm和100 nm的聚苯乙烯纳米颗粒(NP)作为有机大分子的典型NPs进行了吸收实验。细胞松弛素D和诺考达唑分别用于抑制肌动蛋白和微管的聚合。结果表明,NPs通过活跃的能量依赖过程进入巨配子细胞发育和卵囊早期成熟的所有阶段。有趣的是,在整个寄生虫细胞质中都发现了较小的NP,而较大的NP主要定位在形成体细胞器的1型大壁腔中。微丝破坏和诺考达唑处理后,NP吸收减少。这些观察结果表明,在发育的性阶段,最大的大肠杆菌寄生虫利用至少2种或更多的吸收途径内化外源物质。

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