k 2024

Impact of activation materials on Heterorhabditis bacteriophora excreted/secreted products

ŠREIBR, Sara; Jana ILGOVÁ; Pavel DOBEŠ; Jacek MARCINIAK; Jiří VOREL et. al.

Základní údaje

Originální název

Impact of activation materials on Heterorhabditis bacteriophora excreted/secreted products

Autoři

ŠREIBR, Sara (276 Německo, domácí); Jana ILGOVÁ (703 Slovensko, domácí); Pavel DOBEŠ (203 Česká republika, domácí); Jacek MARCINIAK (203 Česká republika, domácí); Jiří VOREL (203 Česká republika, domácí); Jana HURYCHOVÁ (203 Česká republika, domácí); Duarte Nuno TOUBARRO TIAGO (620 Portugalsko); Nelson SIMÕES (620 Portugalsko); Martin KAŠNÝ (203 Česká republika, domácí) a Pavel HYRŠL (203 Česká republika, domácí)

Vydání

19th Meeting of the IOBC/WPRS, Working Group Microbial and Nematode Control of Invertebrate Pests, 2024, 2024

Další údaje

Jazyk

angličtina

Typ výsledku

Prezentace na konferencích

Obor

10608 Biochemistry and molecular biology

Stát vydavatele

Portugalsko

Utajení

není předmětem státního či obchodního tajemství

Kód RIV

RIV/00216224:14310/24:00139683

Organizační jednotka

Přírodovědecká fakulta

Klíčová slova anglicky

Bioactive molecules; Heterorhabditis bacteriophora; activation; activation materials
Změněno: 8. 1. 2025 13:25, Mgr. Sara Šreibr, Ph.D.

Anotace

V originále

Entomopathogenic nematodes are obligate insect parasites that, once inside an insect host, undergo a process called activation or recovery. This process is associated with the release of excreted/secreted products (ESPs), which consist of various functional molecules. Some ESPs have been identified as immunomodulators and virulence factors, which further increased interest in their research. Understanding the functions of ESPs is crucial to comprehend the mechanism of nematodes pathogenicity and enhance their potential for biological control. This study evaluates the protein spectra of Heterorhabditis bacteriophora ESPs in relation to different activation materials. As an activation material in the in vitro activation assay, we chose three Galleria mellonella derived materials prepared with various approaches. Water and phosphate buffer was used as a control. By comparing ESPs profile between infective juveniles activated by insect-derived materials and controls, we identified several host-specific molecules. ESPs-containing samples from all treatments were analyzed using LC-MS/MS, and protein identification was conducted utilizing the in-house H. bacteriophora RNAseq database. We identified 372 proteins in total. The majority were found in the sample activated with PBS. In contrast, the lowest numbers of identified proteins were in the samples activated with insect derived material. Quantitative proteomic analysis showed significant differences in ESP composition depending on the used activation materials. Various proteins which could be involved in nematode-insect interaction were identified, such as metallopeptidase, TIL domain-containing protein and others. Interestingly, in our control groups we detected previously described immunomodulator fatty acid retinoid-binding protein. Activation materials showed a significant impact on the ESPs diversity and abundance. This implies that the way of nematode activation may play a crucial role in nematode pathogenicity. Its understanding could lead to an increase in the effectiveness of the EPN usage in biocontrol. This study was supported by the Grant Agency of the Czech Republic, project No. GAČR 23-06457S.

Návaznosti

GA23-06457S, projekt VaV
Název: Identifikace a funkční charakteristika bioaktivních molekul produkovaných entomopatogenními hlísticemi
Investor: Grantová agentura ČR, Identifikace a funkční charakteristika bioaktivních molekul produkovaných entomopatogenními hlísticemi