期刊
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY
卷 12, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2022.945750
关键词
kinetoplastid; Crithidia; lipids; fatty acids; plasticity; oils; sugars
资金
- Engineering and Physical Sciences Research Council
- EPSRC Centre for Doctoral Training in Critical Resource Catalysis (CRITICAT) [EP/L016419/1]
- University of St. Andrews
Crithidia fasiculata is a parasitic protozoan closely related to other kinetoplastid parasites. Studying kinetoplastid parasites provides unique insights into alternative mechanisms to traditional eukaryotic metabolic pathways. Crithidia is a monogenetic parasite and can be used as a model organism for kinetoplastid research. Little is known about Crithidia, but similarities to other kinetoplast species have been shown in terms of energy metabolism and genetics. Additionally, Crithidia can be used as a eukaryotic expression system for expressing proteins from other kinetoplastids and other eukaryotes.
Crithidia fasiculata belongs to the trypanosomatidae order of protozoan parasites, bearing close relation to other kinetoplastid parasites such as Trypanosoma brucei and Leishmania spp. As an early diverging lineage of eukaryotes, the study of kinetoplastid parasites has provided unique insights into alternative mechanisms to traditional eukaryotic metabolic pathways. Crithidia are a monogenetic parasite for mosquito species and have two distinct lifecycle stages both taking place in the mosquito gut. These consist of a motile choanomastigote form and an immotile amastigote form morphologically similar to amastigotes in Leishmania. Owing to their close relation to Leishmania, Crithidia are a growing research tool, with continuing interest in its use as a model organism for kinetoplastid research with the added benefit that they are non-pathogenic to humans and can be grown with no special equipment or requirements for biological containment. Although comparatively little research has taken place on Crithidia, similarities to other kinetoplast species has been shown in terms of energy metabolism and genetics. Crithidia also show similarities to kinetoplastids in their production of the monosaccharide D-arabinopyranose similar to Leishmania, which is incorporated into a lipoarabinogalactan a major cell surface GPI-anchored molecule. Additionally, Crithidia have been used as a eukaryotic expression system to express proteins from other kinetoplastids and potentially other eukaryotes including human proteins allowing various co- and post-translational protein modifications to the recombinant proteins. Despite the obvious usefulness and potential of this organism very little is known about its lipid metabolism. Here we describe a detailed lipidomic analyses and demonstrate the possible placidity of Crithidia's lipid metabolis. This could have important implications for biotechnology approaches and how other kinetoplastids interact with, and scavenge nutrients from their hosts.
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