Modulation of mitochondrial metabolism as a biochemical trait in blood feeding organisms: the redox vampire hypothesis redux

Cell Biol Int. 2018 Jun;42(6):683-700. doi: 10.1002/cbin.10945. Epub 2018 Feb 23.

Abstract

Hematophagous organisms undergo remarkable metabolic changes during the blood digestion process, increasing fermentative glucose metabolism, and reducing respiratory rates, both consequence of functional mitochondrial remodeling. Here, we review the pathways involved in energy metabolism and mitochondrial functionality in a comparative framework across different hematophagous species, and consider how these processes regulate redox homeostasis during blood digestion. The trend across distinct species indicate that a switch in energy metabolism might represent an important defensive mechanism to avoid the potential harmful interaction of oxidants generated from aerobic energy metabolism with products derived from blood digestion. Indeed, in insect vectors, blood feeding transiently reduces respiratory rates and oxidant production, irrespective of tissue and insect model. On the other hand, a different scenario is observed in several unrelated parasite species when exposed to blood digestion products, as respiratory rates reduce and mitochondrial oxidant production increase. The emerging picture indicates that re-wiring of energy metabolism, through reduced mitochondrial function, culminates in improved tolerance to redox insults and seems to represent a key step for hematophagous organisms to cope with the overwhelming and potentially toxic blood meal.

Keywords: ATP; energy; heme; hemoglobin; insect vector; iron; oxygen; parasite.

Publication types

  • Review

MeSH terms

  • Animals
  • Electron Transport Chain Complex Proteins / metabolism
  • Energy Metabolism*
  • Hemeproteins / metabolism
  • Humans
  • Insect Vectors
  • Mitochondria / metabolism*
  • Oxidation-Reduction
  • Protozoan Proteins / metabolism
  • Reactive Oxygen Species / metabolism

Substances

  • Electron Transport Chain Complex Proteins
  • Hemeproteins
  • Protozoan Proteins
  • Reactive Oxygen Species