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Pharmacological and behavioral investigation of putative self-medicative plants in budongo chimpanzee diets

dc.contributor.authorFreymann, Elodie
dc.contributor.authorCarvalho, Susana
dc.contributor.authorGarbe, Leif A.
dc.contributor.authorGhazhelia, Dinda Dwi
dc.contributor.authorHobaiter, Catherine
dc.contributor.authorHuffman, Michael A.
dc.contributor.authorMuhumuza, Geresomu
dc.contributor.authorSchulz, Lena
dc.contributor.authorSempebwa, Daniel
dc.contributor.authorWald, Florian
dc.contributor.authorYikii, Eguma R.
dc.contributor.authorZuberbühler, Klaus
dc.contributor.authorSchultz, Fabien
dc.contributor.editorArmel Jackson Seukep
dc.date.accessioned2024-10-08T12:31:21Z
dc.date.available2024-10-08T12:31:21Z
dc.date.issued2024-06-20
dc.description.abstractWild chimpanzees consume a variety of plants to meet their dietary needs and maintain wellbeing. While some plants have obvious value, others are nutritionally poor and/or contain bioactive toxins which make ingestion costly. In some cases, these nutrient-poor resources are speculated to be medicinal, thought to help individuals combat illness. In this study, we observed two habituated chimpanzee communities living in the Budongo Forest, Uganda, and collected 17 botanical samples associated with putative self-medication behaviors (e.g., bark feeding, dead wood eating, and pith-stripping) or events (e.g., when consumer had elevated parasite load, abnormal urinalysis, or injury). In total, we selected plant parts from 13 species (nine trees and four herbaceous plants). Three extracts of different polarities were produced from each sample using n-hexane, ethyl acetate, and methanol/water (9/1, v/v) and introduced to antibacterial and anti-inflammatory in vitro models. Extracts were evaluated for growth inhibition against a panel of multidrug-resistant clinical isolates of bacteria, including ESKAPE strains and cyclooxygenase-2 (COX-2) inhibition activity. Pharmacological results suggest that Budongo chimpanzees consume several species with potent medicinal properties. In the antibacterial library screen, 45 out of 53 extracts (88%) exhibited ≥40% inhibition at a concentration of 256 μg/mL. Of these active extracts, 41 (91%) showed activity at ≤256μg/mL in subsequent dose-response antibacterial experiments. The strongest antibacterial activity was achieved by the n-hexane extract of Alstonia boonei dead wood against Staphylococcus aureus (IC50: 16 μg/mL; MIC: 32 μg/mL) and Enterococcus faecium (IC50: 16 μg/mL; MIC: >256 μg/mL) and by the methanol-water extract of Khaya anthotheca bark and resin against E. faecium (IC50: 16 μg/mL; MIC: 32 μg/mL) and pathogenic Escherichia coli (IC50: 16 μg/mL; MIC: 256 μg/mL). We observed ingestion of both these species by highly parasitized individuals. K. anthotheca bark and resin were also targeted by individuals with indicators of infection and injuries. All plant species negatively affected growth of E. coli. In the anti-inflammatory COX-2 inhibition library screen, 17 out of 51 tested extracts (33%) showed ≥50% COX-2 inhibition at a concentration of 5 μg/mL. Several extracts also exhibited anti-inflammatory effects in COX-2 dose-response experiments.eng
dc.identifier.doi10.1371/journal.pone.0305219
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10400.1/26020
dc.language.isoeng
dc.peerreviewedyes
dc.publisherPublic Library of Science (PLoS)
dc.relation.ispartofPLOS ONE
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titlePharmacological and behavioral investigation of putative self-medicative plants in budongo chimpanzee dietseng
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue6
oaire.citation.startPagee0305219
oaire.citation.titlePLoS ONE
oaire.citation.volume19
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85
person.familyNameCarvalho
person.givenNameSusana
person.identifier.ciencia-idC91A-A704-6E70
person.identifier.orcid0000-0003-4542-3720
person.identifier.scopus-author-id23977799600
relation.isAuthorOfPublication1f6a7971-6b67-4f1a-9b1d-f18729d02e9e
relation.isAuthorOfPublication.latestForDiscovery1f6a7971-6b67-4f1a-9b1d-f18729d02e9e

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