Relative potency of a novel acaricidal compound from Xenorhabdus, a bacterial genus mutualistically associated with entomopathogenic nematodes.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
27 05 2021
Historique:
received: 13 02 2021
accepted: 17 05 2021
entrez: 28 5 2021
pubmed: 29 5 2021
medline: 9 11 2021
Statut: epublish

Résumé

Our study aimed to identify the novel acaricidal compound in Xenorhabdus szentirmaii and X. nematophila using the easyPACId approach (easy Promoter Activated Compound Identification). We determined the (1) effects of cell-free supernatant (CFS) obtained from mutant strains against T. urticae females, (2) CFS of the acaricidal bioactive strain of X. nematophila (pCEP_kan_XNC1_1711) against different biological stages of T. urticae, and females of predatory mites, Phytoseiulus persimilis and Neoseiulus californicus, (3) effects of the extracted acaricidal compound on different biological stages of T. urticae, and (4) cytotoxicity of the active substance. The results showed that xenocoumacin produced by X. nematophila was the bioactive acaricidal compound, whereas the acaricidal compound in X. szentirmaii was not determined. The CFS of X. nematophila (pCEP_kan_XNC1_1711) caused 100, 100, 97.3, and 98.1% mortality on larvae, protonymph, deutonymph and adult female of T. urticae at 7 dpa in petri dish experiments; and significantly reduced T. urticae population in pot experiments. However, the same CFS caused less than 36% mortality on the predatory mites at 7dpa. The mortality rates of extracted acaricidal compound (xenocoumacin) on the larva, protonymph, deutonymph and adult female of T. urticae were 100, 100, 97, 96% at 7 dpa. Cytotoxicity assay showed that IC

Identifiants

pubmed: 34045620
doi: 10.1038/s41598-021-90726-1
pii: 10.1038/s41598-021-90726-1
pmc: PMC8159955
doi:

Substances chimiques

Acaricides 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

11253

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Auteurs

Gamze Incedayi (G)

Department of Plant Protection, Faculty of Agriculture, Aydin Adnan Menderes University, Aydin, Turkey.

Harun Cimen (H)

Department of Biology, Faculty of Arts and Science, Aydin Adnan Menderes University, Aydin, Turkey.

Derya Ulug (D)

Department of Biology, Faculty of Arts and Science, Aydin Adnan Menderes University, Aydin, Turkey.

Mustapha Touray (M)

Department of Biology, Faculty of Arts and Science, Aydin Adnan Menderes University, Aydin, Turkey.

Edna Bode (E)

Molecular Biotechnology, Department of Biosciences, Goethe Universität Frankfurt, Max-von-Laue-Str. 9, 60438, Frankfurt am Main, Germany.

Helge B Bode (HB)

Molecular Biotechnology, Department of Biosciences, Goethe Universität Frankfurt, Max-von-Laue-Str. 9, 60438, Frankfurt am Main, Germany.
Senckenberg Gesellschaft für Naturforschung, 60325, Frankfurt am Main, Germany.
Buchmann Institute for Molecular Life Sciences (BMLS), Johann Wolfgang Goethe University, Max-von-Laue-Straße 15, 60438, Frankfurt am Main, Germany.
Department of Natural Products in Organismic Interactions, Max-Planck-Institute for Terrestrial Microbiology, 35043, Marburg, Germany.

Esra Orenlili Yaylagul (E)

Department of Nutrition and Dietetics, Faculty of Health Sciences, Aydin Adnan Menderes University, Aydin, Turkey.

Selcuk Hazir (S)

Department of Biology, Faculty of Arts and Science, Aydin Adnan Menderes University, Aydin, Turkey.

Ibrahim Cakmak (I)

Department of Plant Protection, Faculty of Agriculture, Aydin Adnan Menderes University, Aydin, Turkey. icakmak@adu.edu.tr.

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Classifications MeSH