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Effect of commercially available Plant Defence Stimulators (PDS) on human innate immunity

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HAL Id: hal-02743600

https://hal.inrae.fr/hal-02743600

Submitted on 3 Jun 2020

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Effect of commercially available Plant Defence Stimulators (PDS) on human innate immunity

Lény Teyssier, Stéphanie Delemasure-Chalumeau, Patrick Dutartre, David Wendehenne, Olivier Lamotte, Jean-Louis Connat

To cite this version:

Lény Teyssier, Stéphanie Delemasure-Chalumeau, Patrick Dutartre, David Wendehenne, Olivier Lam- otte, et al.. Effect of commercially available Plant Defence Stimulators (PDS) on human innate immu- nity. The 2014 Innate Immunity Summit, Nov 2014, Londres, United Kingdom. 2014. �hal-02743600�

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The 2014 Innate Immunity Summit

Effect of commercially available PDS

(plant defense stimulators) on human innate immunity

Lény TEYSSIERa,c, Stéphanie DELEMASURE-CHALUMEAUb, Patrick DUTARTREb, David WENDEHENNEc, Olivier LAMOTTEd, Jean-Louis CONNATa,b

PDS (plant defence stimulators) constitute a recent alternative to pesticides used for crop protection. These compounds, also called elicitors, are of diverse nature, but they all act by stimulating innate immune system of plants. So, plants can better fight pathogens.

Introduction

We studied the pro/anti-inflammatory effect on human PBMC (peripheral blood mononuclear cells) of PDS (cf. Table1). Only the soluble fraction of PDS was studied.

Material and methods

a: INSERM U866 Lipide Nutrition Cancer, Université de Bourgogne, LPPCM, Facultés de Médecine et Pharmacie, 7 Bd Jeanne d’Arc, 21079 Dijon Cedex, France b: COHIRO Biotechnology, UFR de Médecine de Dijon, Facultés de Médecine et Pharmacie, 7 Bd Jeanne d’Arc, BP 87900, 21079 Dijon Cedex , France

c. Université de Bourgogne, UMR 1347 Agroécologie, ERL CNRS 6300, 17 Rue Sully, 21000 Dijon, France d. CNRS, UMR 1347 Agroécologie, ERL CNRS 6300, 17 Rue Sully, 21000 Dijon, France

+PDS seeding

(105

cells/wells)

Pro-

inflammatory

test culture Cell

medium cells

ELISA assay

IL-1β XTT test

Viability

There are many similarities in pathogen perception systems and cellular signalling in plants and animals. Moreover, it is well established that many elicitors stimulate both human and plant innate immunity (Zipfel and Felix, 2005)1. Therefore, it is likely that human innate immunity could be modulated by PDS.

+ elicitor

- elicitor

active ingredient IUPAC name for identified active molecule commercial formulation name

acibenzolar-S-méthyl S-methyl 1,2,3-benzothiadiazole-7-carbothioate Bion® 50 WG

seed extract of fenugreek not applicable Stifenia®

phosphonates potassium dihydrogen phosphate Etonan®

prohexadione

3,5-dioxo-4-propanoylcyclohexane-1-carboxylic

acid Regalis®

laminarin not communicated Vacciplant®

studied to be studied

Pathogen inoculation

resistant

susceptible

Table 1: List of the commercially available PDS and there respective active molecule

Discussion and perspectives

This study shows that some PDS can have cytotoxic or pro/anti- inflammatory effects on human cells. Vacciplant is cytotoxic at 0.06 and 0.2 mg/ml. Bion 50 WG is slightly cytotoxic at 0.3 and 1 mg/ml and have an anti- inflammatory effect on PBMC stimulated with LPS for the same concentrations. Stifenia is pro-inflammatory at 0.1, 0.3 and 1 mg/ml and the pro-inflammatory effect is additive with those of LPS. To further understand the mode of action of PDS that modulate IL-1β production, a caspase 1 activity assay will be used to determine the role of inflammasomes in the induction of IL-1β production in response to PDS.

incubation (20 hours)

+PDS +LPS

Anti-

inflammatory test

Results

Figure 1: Effect of PDS on PBMC viability and production of IL-1β.

Cells were treated with different concentrations of PDS and stimulated with LPS (10 ng.mL-1) when specified (+ LPS). After treatment, the cells were incubated for 20 hours. The viability values were normalized to 100% with ​​

the control treated with the vehicle (water). For each conditions, viability histograms (white) and IL-1β concentration (gray) represent the mean value of 8 technical replications. Error bars represent the standard error of each condition.Statistical analysis of differences between conditions were performed using Dunnett’s test with a significance threshold of 5%. Significant differences are indicated with an asterisk (*). For statistical analysis of the viability test, all the conditions were compared with the water control. Concerning ELISA assay statistical analysis, unstimulated PBMC treated with BION 50 WG were compared to the unstimulated control treated with the vehicle (water) whereas PBMC treated with PDS and stimulated with LPS were compared to untreated PBMC stimulated with LPS (LPS).

NA: not available, BTH: S-methyl 1,2,3-benzothiadiazole-7-carbothioate.

PBMC viability as a percentage of control cells treated with the vehicle (water)

IL-1β concentration in culture medium (pg/mL)

1) Zipfel, C., and Felix, G. (2005). Plants and animals: a different taste for microbes? Curr. Opin. Plant Biol. 8, 353–360.

IL-1β

production Caspase 1

activity Pro IL-1β Inflammasome

activation

IL-1β gene regulation The aim of this study is to evaluate pro/anti inflammatory activity of five ‑

different commercially available PDS and their respective active molecules on

human cell models.

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