Abstract

Because of the recent increase in the demand for fresh produce, contamination of raw food products has become an issue. Foodborne diseases are frequently caused by the infection of leguminous plants by human bacterial pathogens. Moreover, contamination by Vibrio cholerae, closely related with Vibrio vulnificus, has been reported in plants and vegetables. Here, we investigated the possibility of Vibrio vulnificus 96-11-17M, an opportunistic human pathogen, to infect and colonize Arabidopsis thaliana plants, resulting in typical disease symptoms at 5 and 7 days post-inoculation in vitro and in planta under artificial and favorable conditions, respectively. RNA-Seq analysis revealed 5,360, 4,204, 4,916 and 3,741 differentially expressed genes (DEGs) at 12, 24, 48 and 72 h post-inoculation, respectively, compared with the 0 h time point. Gene Ontology analysis revealed that these DEGs act in pathways responsive to chemical and hormone stimuli and plant defense. The expression of genes involved in salicylic acid (SA)-, jasmonic acid (JA)- and ethylene (ET)-dependent pathways was altered following V. vulnificus inoculation. Genetic analyses of Arabidopsis mutant lines verified that common pathogen-associated molecular pattern (PAMP) receptors perceive the V. vulnificus infection, thus activating JA and ET signaling pathways. Our data indicate that the human bacterial pathogen V. vulnificus 96-11-17M modulates defense-related genes and host defense machinery in Arabidopsis thaliana under favorable conditions.

Highlights

  • Over the past few decades, the availability of fresh foods for optimum human health has received considerable attention

  • All of the tested strains produced typical disease symptoms in Arabidopsis leaves similar to those caused by P. syringae pv. tomato (Pto) DC3000, while no disease symptoms were observed in Arabidopsis leaves inoculated with 10% phosphate buffer saline (PBS) (Fig 1A)

  • We infiltrated with V. vulnificus 96-11-17M and Pto DC3000 in Arabidopsis plants grown in soil; this was accompanied by a 15-fold increase in the total population density of V. vulnificus 96-11-17M and Pto DC3000 (Fig 1B, in planta)

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Summary

Objectives

We aimed to identify genes showing differential expression at specific time points compared with the 0 h time point

Methods
Results
Conclusion
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