Glutathione-deficient Plasmodium berghei parasites exhibit growth delay and nuclear DNA damage

Abstract

Plasmodium parasites are exposed to endogenous and exogenous oxidative stress during their complex life cycle. To minimize oxidative damage, the parasites use glutathione (GSH) and thioredoxin (Trx) as primary antioxidants. We previously showed that disruption of the Plasmodium berghei gamma-glutamylcysteine synthetase (pbggcs-ko) or the glutathione reductase (pbgr-ko) genes resulted in a significant reduction of GSH in intraerythrocytic stages, and a defect in growth in the pbggcs-ko parasites. In this report, time course experiments of parasite intraerythrocytic development and morphological studies showed a growth delay during the ring to schizont progression. Morphological analysis shows a significant reduction in size (diameter) of trophozoites and schizonts with increased number of cytoplasmic vacuoles in the pbggcs-ko parasites in comparison to the wild type (WT). Furthermore, the pbggcs-ko mutants exhibited an impaired response to oxidative stress and increased levels of nuclear DNA (nDNA) damage. Reduced GSH levels did not result in mitochondrial DNA (mtDNA) damage or protein carbonylations in neither pbggcs-ko nor pbgr-ko parasites. In addition, the pbggcs-ko mutant parasites showed an increase in mRNA expression of genes involved in oxidative stress detoxification and DNA synthesis, suggesting a potential compensatory mechanism to allow for parasite proliferation. These results reveal that low GSH levels affect parasite development through the impairment of oxidative stress reduction systems and damage to the nDNA. Our studies provide new insights into the role of the GSH antioxidant system in the intraerythrocytic development of Plasmodium parasites, with potential translation into novel pharmacological interventions.

Differential Effect of Antioxidants Glutathione and Vitamin C on the Hepatic Injuries Induced by Plasmodium berghei ANKA Infection

“…Data presented in our study have demonstrated that GSH treatment has favored infection and increased liver toxicity in PbA-infected mice. Although GSH represents an important antioxidant molecule in distinct tissue and organs, there are strong evidences demonstrating that species of the Plasmodium genus use GSH as a substrate for their reproduction in the vertebrate host [ 35 – 37 ]. Our results are in agreement with these reports since GSH treatment has induced a fast increase in parasitemia values; also, it has decreased animal survival in the PbA-infected group.…”

Genome-Wide CRISPR/Cas9 Screen Identifies New Genes Critical for Defense Against Oxidant Stress in Toxoplasma gondii

“…In addition, T. gondii uses the thiol-reduction system, including glutathione, Trx, glutaredoxin, and specific reductases, to resist oxidative damage. These enzymes, which are associated with the antioxidant system, play essential roles during parasite survival and infection ( Padín-Irizarry et al, 2016 ). However, it remains unclear whether other unidentified genes are involved in the resistance to host ROS ( Boczoń, 2002 ).…”