Functional analysis of Toxoplasma lactate dehydrogenases suggests critical roles of lactate fermentation for parasite growth in vivo |
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| Authors: | Ningbo Xia Jichao Yang Shu Ye Lihong Zhang Yanqin Zhou Junlong Zhao Laurence David Sibley Bang Shen |
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| Affiliation: | 1. State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, Hubei, China;2. Hubei Cooperative Innovation Center for Sustainable Pig Production, Wuhan, Hubei, China;3. Key Laboratory of Preventive Medicine in Hubei Province, Wuhan, Hubei, China;4. Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA |
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| Abstract: | Glycolysis was thought to be the major pathway of energy supply in both fast‐replicating tachyzoites and slowly growing bradyzoites of Toxoplasma gondii. However, its biological significance has not been clearly verified. The genome of T. gondii encodes two lactate dehydrogenases (LDHs), which are differentially expressed in tachyzoites and bradyzoites. In this study, we knocked out the two LDH genes individually and in combination and found that neither gene was required for tachyzoite growth in vitro under standard growth conditions. However, during infection in mice, Δldh1 and Δldh1 Δldh2 mutants were unable to propagate and displayed significant virulence attenuation and cyst formation defects. LDH2 only played minor roles in these processes. To further elucidate the mechanisms underlying the critical requirement of LDH in vivo, we found that Δldh1 Δldh2 mutants replicated significantly more slowly than wild‐type parasites when cultured under conditions with physiological levels of oxygen (3%). In addition, Δldh1 Δldh2 mutants were more susceptible to the oxidative phosphorylation inhibitor oligomycin A. Together these results suggest that lactate fermentation is critical for parasite growth under physiological conditions, likely because energy production from oxidative phosphorylation is insufficient when oxygen is limited and lactate fermentation becomes a key supplementation. |
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| Keywords: | cyst energy metabolism lactate fermentation LDH Toxoplasma gondii virulence |
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