Publication:
Metacytofilin Is a Potent Therapeutic Drug Candidate for Toxoplasmosis

dc.contributor.authorArpron Leesombunen_US
dc.contributor.authorMasatomi Iijimaen_US
dc.contributor.authorKousuke Umedaen_US
dc.contributor.authorDaisuke Kondohen_US
dc.contributor.authorBaldorj Pagmadulamen_US
dc.contributor.authorAhmed M. Abdouen_US
dc.contributor.authorYutaka Suzukien_US
dc.contributor.authorShun Ichi Ohbaen_US
dc.contributor.authorKunio Isshikien_US
dc.contributor.authorTomoyuki Kimuraen_US
dc.contributor.authorYumiko Kubotaen_US
dc.contributor.authorRyuichi Sawaen_US
dc.contributor.authorCoh Ichi Niheien_US
dc.contributor.authorYoshifumi Nishikawaen_US
dc.contributor.otherMicrobial Chemistry Research Centeren_US
dc.contributor.otherUniversity of Tokyoen_US
dc.contributor.otherSouth Valley Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherObihiro University of Agriculture and Veterinary Medicineen_US
dc.date.accessioned2020-03-26T04:55:27Z
dc.date.available2020-03-26T04:55:27Z
dc.date.issued2020-02-18en_US
dc.description.abstract© 2019 The Author(s). Background: Toxoplasmosis, a parasitic disease caused by Toxoplasma gondii, is an important cause of miscarriage or adverse fetal effects, including neurological and ocular manifestations in humans. Current anti-Toxoplasma drugs have limited efficacy against toxoplasmosis and also have severe side effects. Therefore, novel efficacious drugs are urgently needed. Here, we identified metacytofilin (MCF) from a fungal Metarhizium species as a potential anti-Toxoplasma compound. Methods: Anti-Toxoplasma activities of MCF and its derivatives were evaluated in vitro and in vivo using nonpregnant and pregnant mice. To understand the mode of action of MCF, the RNA expression of host and parasite genes was investigated by RNAseq. Results: In vitro, MCF inhibited the viability of intracellular and extracellular T. gondii. Administering MCF intraperitoneally or orally to mice after infection with T. gondii tachyzoites increased mouse survival compared with the untreated animals. Remarkably, oral administration of MCF to pregnant mice prevented vertical transmission of the parasite. Interestingly, RNA sequencing of T. gondii-infected cells treated with MCF showed that MCF inhibited DNA replication and enhanced RNA degradation in the parasites. Conclusions: With its potent anti-T. gondii activity, MCF is a strong candidate for future drug development against toxoplasmosis.en_US
dc.identifier.citationJournal of Infectious Diseases. Vol.221, No.5 (2020), 766-774en_US
dc.identifier.doi10.1093/infdis/jiz501en_US
dc.identifier.issn15376613en_US
dc.identifier.issn00221899en_US
dc.identifier.other2-s2.0-85081684993en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/53754
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85081684993&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleMetacytofilin Is a Potent Therapeutic Drug Candidate for Toxoplasmosisen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85081684993&origin=inwarden_US

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