Leishmania carbon metabolism in the macrophage phagolysosome- feast or famine? [version 1; referees: 3 approved]

F1000Research

Michael J. Dagley¹  Eleanor C. Saunders¹  Joachim Kloehn¹  Malcolm J. McConville¹ 

[1] Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Flemington Rd, Parkville, 3010, Australia;

关键词: Antimicrobials & Drug Resistance;    Biocatalysis;    Cellular Microbiology & Pathogenesis;    Chemical Biology of the Cell;    Control of Gene Expression;    Immunity to Infections;    Innate Immunity;    Medical Microbiology;    Membranes & Sorting;    Microbial Growth & Development;    Microbial Physiology & Metabolism;    Parasitology;   

DOI  :  10.12688/f1000research.6724.1

来源: DOAJ

【 摘 要 】

A number of medically important microbial pathogens target and proliferate within macrophages and other phagocytic cells in their mammalian hosts. While the majority of these pathogens replicate within the host cell cytosol or non-hydrolytic vacuolar compartments, a few, including protists belonging to the genus Leishmania, proliferate long-term within mature lysosome compartments.  How these parasites achieve this feat remains poorly defined. In this review, we highlight recent studies that suggest that Leishmania virulence is intimately linked to programmed changes in the growth rate and carbon metabolism of the obligate intra-macrophage stages. We propose that activation of a slow growth and a stringent metabolic response confers resistance to multiple stresses (oxidative, temperature, pH), as well as both nutrient limitation and nutrient excess within this niche. These studies highlight the importance of metabolic processes as key virulence determinants in Leishmania.

【 授权许可】

Unknown