High-throughput phenotypic screen identifies a new family of potent anti-amoebic compounds

dc.contributor.authorSauvey C.
dc.contributor.authorMeewan I.
dc.contributor.authorEhrenkaufer G.
dc.contributor.authorBlevitt J.
dc.contributor.authorJackson P.
dc.contributor.authorAbagyan R.
dc.contributor.otherMahidol University
dc.date.accessioned2023-05-29T17:20:34Z
dc.date.available2023-05-29T17:20:34Z
dc.date.issued2023-05-01
dc.description.abstractEntamoeba histolytica is a disease-causing parasitic amoeba which affects an estimated 50 million people worldwide, particularly in socioeconomically vulnerable populations experiencing water sanitation issues. Infection with E. histolytica is referred to as amoebiasis, and can cause symptoms such as colitis, dysentery, and even death in extreme cases. Drugs exist that are capable of killing this parasite, but they are hampered by downsides such as significant adverse effects at therapeutic concentrations, issues with patient compliance, the need for additional drugs to kill the transmissible cyst stage, and potential development of resistance. Past screens of small and medium sized chemical libraries have yielded anti-amoebic candidates, thus rendering high-throughput screening a promising direction for new drug discovery in this area. In this study, we screened a curated 81,664 compound library from Janssen pharmaceuticals against E. histolytica trophozoites in vitro, and from it identified a highly potent new inhibitor compound. The best compound in this series, JNJ001, showed excellent inhibition activity against E. histolytica trophozoites with EC50 values at 0.29 μM, which is better than the current approved treatment, metronidazole. Further experimentation confirmed the activity of this compound, as well as that of several structurally related compounds, originating from both the Janssen Jump-stARter library, and from chemical vendors, thus highlighting a new structure-activity relationship (SAR). In addition, we confirmed that the compound inhibited E. histolytica survival as rapidly as the current standard of care and inhibited transmissible cysts of the related model organism Entamoeba invadens. Together these results constitute the discovery of a novel class of chemicals with favorable in vitro pharmacological properties. The discovery may lead to an improved therapy against this parasite and in all of its life stages.
dc.identifier.citationPLoS ONE Vol.18 No.5 May (2023)
dc.identifier.doi10.1371/journal.pone.0280232
dc.identifier.eissn19326203
dc.identifier.pmid37159460
dc.identifier.scopus2-s2.0-85159564156
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/82877
dc.rights.holderSCOPUS
dc.subjectMultidisciplinary
dc.titleHigh-throughput phenotypic screen identifies a new family of potent anti-amoebic compounds
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85159564156&origin=inward
oaire.citation.issue5 May
oaire.citation.titlePLoS ONE
oaire.citation.volume18
oairecerif.author.affiliationSkaggs School of Pharmacy & Pharmaceutical Sciences
oairecerif.author.affiliationJanssen Research & Development
oairecerif.author.affiliationStanford University School of Medicine
oairecerif.author.affiliationInstitute of Molecular Biosciences, Mahidol University

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