Evidence map›Paper›PMID 40369434›Full record

ArticleBMC plant biology2025

Lettuce immune responses and apoplastic metabolite profile contribute to reduced internal leaf colonization by human bacterial pathogens.

Cristián Jacob, Maeli Melotto

Abstract read
In one paragraph

Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Frontiers in plant science · 2025
    Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Cristián JacobDepartamento de Ciencias Vegetales, Facultad de Agronomía y Sistemas Naturales, Pontificia Universidad Católica de Chile, Santiago, Chile. cjjacob@uc.cl.
Maeli MelottoDepartment of Plant Sciences, University of California, Davis, CA, USA. melotto@ucdavis.edu.

Funding

National Institute of Food and Agriculture 2017-67017-26180, 2020-67017-30779, and CA-D-PLS-2327-H
6 · The paper itself

Abstract

backgroundHuman bacterial pathogens such as Salmonella enterica and Escherichia coli can colonize the apoplast of leafy greens, where they may evade standard sanitization measures and persist until produce consumption. Bacterial survival in this niche is influenced by plant immune responses that may vary according to bacterial species and plant genotypes. The variability in immune responses has been associated with differences in pathogen persistence capacity within the phyllosphere. In addition, emerging evidence suggests that preexisting and inducible plant metabolites contribute to either restricting or facilitating colonization of human pathogens in plant tissues. Identifying the molecular mechanisms underlying these interactions is crucial for developing strategies to mitigate contamination in fresh produce.

resultsWe characterized whole-leaf transcriptome and apoplast metabolome profiles of three lettuce cultivars upon exposure to the human pathogenic bacteria S. enterica ser. Typhimurium 14028s and E. coli O157:H7. The lettuce genotypes Lollo Rossa and Green Towers exhibited stronger transcriptional modulation, primarily associated with defense-related processes and showed reduced bacterial survival in their apoplast. Surprisingly, Green Towers did not generate callose deposition or reactive oxygen species burst responses at levels comparable to that of Lollo Rossa, suggesting it has distinct modifications in the apoplastic conditions that restrict pathogen persistence. Apoplastic metabolomic profiling revealed specific compounds alterations in Green Towers linked to bacterial survival, indicating their potential role in this genotype's defense mechanism. In contrast, the lettuce cultivar Red Tide exhibited minimal transcriptional and metabolic modulation, lack of robust defense activation, which was accompanied by apoplastic bacterial survival.

conclusionsThis study provides evidence that lettuce cultivars exhibit distinct molecular responses that may influence the persistence of human bacterial pathogens in the leaf apoplast. The results indicate that both immune response activation and metabolite composition may contribute to restrict apoplastic bacterial persistence or growth. These findings offer novel insights into the genetic and biochemical factors shaping lettuce-pathogen interactions, which might inform breeding programs and agronomic practices aimed at enhancing food safety.

Indexed as

Escherichia coli O157LactucaMetabolomePlant DiseasesPlant ImmunityPlant LeavesSalmonella typhimuriumHumansTranscriptomeEscherichia coliFood safetyFresh produceLeaf ApoplastOmicsPlant defensePlant-microbe interactionSalmonella enterica

Identifiers

PMID40369434
PMCPMC12076921

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.