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Modulation of autophagy as a therapeutic strategy for Toxoplasma gondii infection

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2022.902428

Keywords

autophagy; Toxoplasma gondii; CD40; IFN-gamma; AMPK; mTOR

Funding

  1. National Natural Science Foundation of China
  2. Natural Science Foundation of Hunan Province, China
  3. Open Sharing Fund for the Large-scale Instruments and Equipment of Central South University
  4. Science and Technology Program of Hunan Province
  5. Graduate Case base construction project of Central South University
  6. Innovation Training Program of Central South University
  7. [32170510]
  8. [2020JJ4765]
  9. [CSUZC202236]
  10. [2021ZK4154]
  11. [2020ALK91]
  12. [20220026020009]

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Toxoplasma gondii infection is a severe global health threat. By promoting host cell autophagy or attenuating the inhibition of autophagic targeting, novel therapeutic strategies against T. gondii can be developed.
Toxoplasma gondii infection is a severe health threat that endangers billions of people worldwide. T. gondii utilizes the host cell membrane to form a parasitophorous vacuole (PV), thereby fully isolating itself from the host cell cytoplasm and making intracellular clearance difficult. PV can be targeted and destroyed by autophagy. Autophagic targeting results in T. gondii killing via the fusion of autophagosomes and lysosomes. However, T. gondii has developed many strategies to suppress autophagic targeting. Accordingly, the interplay between host cell autophagy and T. gondii is an emerging area with important practical implications. By promoting the canonical autophagy pathway or attenuating the suppression of autophagic targeting, autophagy can be effectively utilized in the development of novel therapeutic strategies against T gondii. Here, we have illustrated the complex interplay between host cell mediated autophagy and T. gondii. Different strategies to promote autophagy in order to target the parasite have been elucidated. Besides, we have analyzed some potential new drug molecules from the DrugBank database using bioinformatics tools, which can modulate autophagy. Various challenges and opportunities focusing autophagy mediated T. gondii clearance have been discussed, which will provide new insights for the development of novel drugs against the parasite.

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