Unique features of Entamoeba histolytica glycerophospholipid metabolism; has the E. histolytica lipid metabolism network evolved through gene loss and gain to enable parasitic life cycle adaptation?

被引:2
|
作者
Mi-ichi, Fumika [1 ,2 ]
Tsugawa, Hiroshi [3 ,4 ,5 ]
Yoshida, Hiroki [2 ]
Arita, Makoto [4 ,5 ,6 ,7 ]
机构
[1] Nagasaki Univ, Inst Trop Med NEKKEN, Cent Lab, Nagasaki, Japan
[2] Saga Univ, Fac Med, Dept Biomol Sci, Div Mol & Cellular Immunosci, Saga, Japan
[3] Tokyo Univ Agr & Technol, Dept Biotechnol & Life Sci, Tokyo, Japan
[4] RIKEN Ctr Integrat Med Sci, Lab Metabol, Yokohama, Japan
[5] Yokohama City Univ, Grad Sch Med Life Sci, Yokohama, Japan
[6] Keio Univ, Grad Sch Pharmaceut Sci, Div Physiol Chem & Metab, Tokyo, Japan
[7] Keio Univ, Human Biol Microbiome Quantum Res Ctr WPI Bio2Q, Tokyo, Japan
关键词
lipid metabolism; Entamoeba; lateral gene transfer; MITOSOMES; BIOLOGY;
D O I
10.1128/msphere.00174-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Entamoeba histolytica, a protozoan parasite, causes amoebiasis, which is a global public health problem. During the life cycle of this parasite, the properties of the cell membrane are changed markedly. To clarify the mechanism of membrane lipid changes, we exploited state-of-the-art untargeted lipidomic analysis, and atypical features of glycerophospholipids, lysoglycerophospholipids, and sphingolipids were observed compared with human equivalents. Here, we overview an entire E. histolytica glycerophospholipid metabolic pathway based on re-evaluated whole lipidome and genome along with the results of metabolic labeling experiments. We also discuss whether the E. histolytica lipid metabolism network, including the glycerophospholipid metabolic pathway, has unique features necessary for parasitic life cycle adaptation through gene loss and/or gain, and raise important questions involving biochemistry, molecular cell biology, and physiology underlying this network. Answering these questions will advance the understanding of Entamoeba physiology and will provide potential targets to develop new anti-amoebiasis drugs.
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页数:9
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