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Multiple pathways for glucose phosphate transport and utilization support growth of Cryptosporidium parvum.
Xu, Rui; Beatty, Wandy L; Greigert, Valentin; Witola, William H; Sibley, L David.
Afiliação
  • Xu R; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63130, USA.
  • Beatty WL; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63130, USA.
  • Greigert V; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63130, USA.
  • Witola WH; Department of Pathobiology, University of Illinois Urbana-Champaign, Urbana, IL 61802, USA.
  • Sibley LD; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63130, USA.
bioRxiv ; 2023 Jun 27.
Article em En | MEDLINE | ID: mdl-37425855
ABSTRACT
Cryptosporidium parvum is an obligate intracellular parasite with a highly reduced mitochondrion that lacks the TCA cycle and the ability to generate ATP, making the parasite reliant on glycolysis. Genetic ablation experiments demonstrated that neither of the two putative glucose transporters CpGT1 and CpGT2 were essential for growth. Surprisingly, hexokinase was also dispensable for parasite growth while the downstream enzyme aldolase was required, suggesting the parasite has an alternative way of obtaining phosphorylated hexose. Complementation studies in E. coli support a role for direct transport of glucose-6-phosphate from the host cell by the parasite transporters CpGT1 and CpGT2, thus bypassing a requirement for hexokinase. Additionally, the parasite obtains phosphorylated glucose from amylopectin stores that are released by the action of the essential enzyme glycogen phosphorylase. Collectively, these findings reveal that C. parvum relies on multiple pathways to obtain phosphorylated glucose both for glycolysis and to restore carbohydrate reserves.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article