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Antiprotozoal activity of different Xenorhabdus and Photorhabdus bacterial secondary metabolites and identification of bioactive compounds using the easyPACId approach

  • Natural products have been proven to be important starting points for the development of new drugs. Bacteria in the genera Photorhabdus and Xenorhabdus produce antimicrobial compounds as secondary metabolites to compete with other organisms. Our study is the first comprehensive study screening the anti-protozoal activity of supernatants containing secondary metabolites produced by 5 Photorhabdus and 22 Xenorhabdus species against human parasitic protozoa, Acanthamoeba castellanii, Entamoeba histolytica, Trichomonas vaginalis, Leishmania tropica and Trypanosoma cruzi, and the identification of novel bioactive antiprotozoal compounds using the easyPACId approach (easy Promoter Activated Compound Identification) method. Though not in all species, both bacterial genera produce antiprotozoal compounds effective on human pathogenic protozoa. The promoter exchange mutants revealed that antiprotozoal bioactive compounds produced by Xenorhabdus bacteria were fabclavines, xenocoumacins, xenorhabdins and PAX peptides. Among the bacteria assessed, only P. namnaoensis appears to have acquired amoebicidal property which is effective on E. histolytica trophozoites. These discovered antiprotozoal compounds might serve as starting points for the development of alternative and novel pharmaceutical agents against human parasitic protozoa in the future.

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Author:Şebnem Hazal GülşenORCiD, Evren TilekliogluORCiD, Edna BodeORCiDGND, Harun CimenORCiD, Hatice ErtabaklarORCiD, Derya UluğORCiD, Sema ErtuğORCiD, Sebastian Leonhard WenskiGND, Mustapha TourayORCiD, Canan HazirORCiD, Duygu Kaya BilecenogluORCiD, Ibrahim YildizORCiD, Helge Björn BodeORCiDGND, Selcuk HazirORCiD
URN:urn:nbn:de:hebis:30:3-695612
DOI:https://doi.org/10.1038/s41598-022-13722-z
ISSN:2045-2322
Parent Title (English):Scientific reports
Publisher:Macmillan Publishers Limited, part of Springer Nature
Place of publication:[London]
Document Type:Article
Language:English
Date of Publication (online):2022/06/24
Date of first Publication:2022/06/24
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2023/08/11
Tag:Biotechnology; Drug discovery; Microbiology; Molecular biology; Pathogenesis
Volume:12
Issue:art. 10779
Article Number:10779
Page Number:13
First Page:1
Last Page:13
Note:
Open Access funding enabled and organized by Projekt DEAL. This study was supported by the Scientific and Technical Research Council of Turkey (TUBITAK-Project Number: 116S387) and Aydin Adnan Menderes University, Project Number: 20001).
HeBIS-PPN:512760586
Institutes:Biowissenschaften
Angeschlossene und kooperierende Institutionen / Senckenbergische Naturforschende Gesellschaft
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - CC BY - Namensnennung 4.0 International