期刊文献+

弓形虫能量代谢及营养物质的来源概述

Energy Metabolism and Nutrients Sources of Toxoplasma gondii
下载PDF
导出
摘要 弓形虫病是由弓形虫感染引起的严重人兽共患寄生虫病,对人类健康及畜牧业发展造成巨大威胁。弓形虫通过独特的代谢途径从宿主细胞获得营养物质进而满足其在细胞内增殖及存活。虫体自身的糖酵解及三羧酸循环途径对于其正常生长至关重要,糖酵解关键酶被抑制可促进缓殖子的形成,明确糖酵解及营养物质存储在缓殖子阶段的作用,将有助于揭示包囊形成过程中的营养需求。弓形虫嘧啶从头合成途径及生物素合成途径对于虫体存活同样不可或缺,可作为抗弓形虫药物研发的重要靶标。认识并了解弓形虫的能量代谢及营养物质的摄取方式对弓形虫病的预防和治疗发挥重要作用。 Toxoplasmosis is a severe zoonotic parasitic disease caused by Toxoplasma gondii,which has led a huge threat to human health and the development of animal husbandry.Toxoplasma gondii obtains nutrients from host cells through unique metabolic pathways to satisfy their intracellular proliferation and survival.The glycolysis and tricarboxylic acid cycle pathway are essential for its normal growth,the formation of bradyzoites will be promoted by inhibiting the key enzymes of glycolysis,it will be helpful to reveal the nutritional requirements during the formation of cysts if the role of glycolysis and nutrient storage in the bradyzoite stage were clarified.The de novo synthesis of pyrimidine and the biotin synthesis pathway are also indispensable for the survival of Toxoplasma gondii,which could be used as important targets for the development of anti-toxoplasmosis drugs.It plays an important role to know and understand the energy metabolism and nutrient ingestion of Toxoplasma gondii,which is beneficial to explore the new anti-toxoplasmosis drug targets.
作者 孙洪超 付媛 黄靖 张红丽 石团员 SUN Hong-chao;FU Yuan;HUANG Jing;ZHANG Hong-li;SHI Tuan-yuan(Department of Animal Parasitology,Institute of Animal Husbandry and Veterinary Medicine,Zhejiang Academy of Agricultural Science,Hangzhou,Zhejiang,310021,China;Zhejiang Center for Animal Disease Control and Prevention,Hangzhou,Zhejiang,310000,China.)
出处 《动物医学进展》 北大核心 2021年第1期120-124,共5页 Progress In Veterinary Medicine
基金 国家自然科学基金青年基金项目(31802183)。
关键词 弓形虫 能量代谢 营养物质摄取 Toxoplasma energy metabolism nutrient ingestion
  • 相关文献

参考文献1

二级参考文献33

  • 1Hannaert V, Bringaud F, Opperdoes F R, et al. Evolution of energy metabolism and its compartmentation in Kinetoplastida [ J]. Kineto- plastid Biol Dis, 2003, 2( 11 ) : 1-30.
  • 2Ambrahamsen M S, Templeton T J, Enomoto S, et al. Complete ge- nome sequence of the apicomplexan, Cryptosporidium parvum [ J ]. Science, 2004; 304(5669): 441-445.
  • 3Bringaud F, Rivi'ere L, Coustou V. Energy metabolism of trypanoso- matids: Adaptation to available carbon sources [ J ]. Mol BiochemParasitol, 2006, 149(1) : 1-9.
  • 4Bhowmick I P, Kumar N, Sharm S, et al. Plasmodium falciparum enolase: stage-specific expression and sub-cellar localization [ J ]. Malaria J, 2009, 8(179) : 1-16.
  • 5Ginger M L, McFadden G I, Michels P A M. Rewiring and regula- tion of cross-compartmentalized metabolism in protists [ J 1. Philos Trans R Soc Lond B Biol Sci, 2010, 365( 1541 ) : 831-845.
  • 6Rider S D Jr, Zhu G. Cryptosporidium: genomic and biochemical features [J]. ExpParasitol, 2010, 124(1):2-9.
  • 7Saito T, Maeda T, Nakazawa M, et al. Characterisation of hexoki- nase in Toxoplasma gondii tachyzoites [ J 1. Int J Parasitol, 2002, 32(8) : 961-967.
  • 8Coombs G H, Muller S. Recent advances in the search for new anti- coccidal drugs [J]. Int J Parasitol, 2002, 32(5) : 497-508.
  • 9Sanz-Rodfiguez C E, Concepci6n J L, Pekerar S, etal. Bisphospho- nates as Inhibitors of Trypanosoma cruzi Hexokinase [ J]. J Biol Chem, 2007, 282(17): 12377-12387.
  • 10Vermeulen A N, Kok J J, van den Boogaart P, et al. Eimeria refrac- tile body proteins contain two potentially functional characteristics: transhydrogenase and carbohydrate transport [ J ~. FEMS Microbiol Lett, 1993, 110(2) : 223-229.

共引文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部