Redistribution of FLAgellar Member 8 during the trypanosome life cycle: Consequences for cell fate prediction

IF 2.6 2区 生物学 Q3 CELL BIOLOGY
Estefanía Calvo-Álvarez, Serge Bonnefoy, Audrey Salles, Fiona E. Benson, Paul G. McKean, Philippe Bastin, Brice Rotureau
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引用次数: 9

Abstract

The single flagellum of African trypanosomes is essential in multiple aspects of the parasites' development. The FLAgellar Member 8 protein (FLAM8), localised to the tip of the flagellum in cultured insect forms of Trypanosoma brucei, was identified as a marker of the locking event that controls flagellum length. Here, we investigated whether FLAM8 could also reflect the flagellum maturation state in other parasite cycle stages. We observed that FLAM8 distribution extended along the entire flagellar cytoskeleton in mammalian-infective forms. Then, a rapid FLAM8 concentration to the distal tip occurs during differentiation into early insect forms, illustrating the remodelling of an existing flagellum. In the tsetse cardia, FLAM8 further localises to the entire length of the new flagellum during an asymmetric division. Strikingly, in parasites dividing in the tsetse midgut and in the salivary glands, the amount and distribution of FLAM8 in the new flagellum were seen to predict the daughter cell fate. We propose and discuss how FLAM8 could be considered a meta-marker of the flagellum stage and maturation state in trypanosomes.

Abstract Image

鞭毛成员8在锥虫生命周期中的再分配:对细胞命运预测的影响
非洲锥虫的单鞭毛在寄生虫发育的多个方面都是必不可少的。鞭毛成员8蛋白(FLAM8),定位于培养的布氏锥虫的鞭毛顶端,被确定为控制鞭毛长度的锁定事件的标记。在这里,我们研究了FLAM8是否也能反映其他寄生虫周期阶段的鞭毛成熟状态。我们观察到,在哺乳动物感染形式中,FLAM8分布沿着整个鞭毛细胞骨架延伸。然后,在分化成早期昆虫形态的过程中,FLAM8迅速集中到远端,说明了现有鞭毛的重塑。在采采心中,在不对称分裂过程中,FLAM8进一步定位于新鞭毛的整个长度。引人注目的是,在采采中肠和唾液腺中分裂的寄生虫中,新鞭毛中FLAM8的数量和分布可以预测子细胞的命运。我们提出并讨论了FLAM8如何被认为是锥虫鞭毛阶段和成熟状态的元标记。
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来源期刊
Cellular Microbiology
Cellular Microbiology 生物-微生物学
CiteScore
9.70
自引率
0.00%
发文量
26
审稿时长
3 months
期刊介绍: Cellular Microbiology aims to publish outstanding contributions to the understanding of interactions between microbes, prokaryotes and eukaryotes, and their host in the context of pathogenic or mutualistic relationships, including co-infections and microbiota. We welcome studies on single cells, animals and plants, and encourage the use of model hosts and organoid cultures. Submission on cell and molecular biological aspects of microbes, such as their intracellular organization or the establishment and maintenance of their architecture in relation to virulence and pathogenicity are also encouraged. Contributions must provide mechanistic insights supported by quantitative data obtained through imaging, cellular, biochemical, structural or genetic approaches.
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