Grant Information

THE ROLE OF PHYLLOSPHERE BACTERIAL SURFACTANT PRODUCTION ON THE ATTACHMENT, MOVEMENT AND INTERNALIZATION OF HUMAN PATHOGENS ON PRODUCE

Sponsoring Institution National Institute of Food and Agriculture
Program A1301 - Foundational Program: Food-borne Pathogen Plant Interactions
Status COMPLETE
Funding Source AFRI COMPETITIVE GRANT
Division NIFA Non Formula
Reporting Frequency Annual
Project Director Lindow, Steve
Accession Number 224405
Grant Number 2011-67017-30097
Project Number CA-B-PLB-0038-FG
Proposal Number 2010-04499
Dates 2011-01-15 - 2015-01-14
Grant Year 2011
Cumulative Award Amount $490,112.00
Performing Department Microbial Biology
Recipient Organization UNIVERSITY OF CALIFORNIA, BERKELEY

BERKELEY,CA 94720
Keywords biosurfactant
escherichia coli
invasion
lettuce
salmonella enterica
spinach
tatsoi
Research Effort Applied (0%)
Basic (100%)
Developmental (0%)
Classification Parameters
Knowledge AreaSubject of InvestigationField of SciencePercent
712 - Protect Food from Contamination by Pathogenic Microorganisms, Parasites, and Naturally Occurring Toxins 1499 - Vegetables, general/other 1100 - Bacteriology 100%
Non-technical Summary

Colonization of fresh produce by human pathogens such as E. coli and Salmonella enterica is a growing food safety issue. The behavior of such human pathogens on produce is, however, strongly influenced by the other resident bacterial colonists of the plant surface. Specifically, epiphytic bacteria that produce biosurfactants that alter the interaction of water with the plant can facilitate the invasion of pathogens into the plant where they can not be decontaminated during postharvest treatments. We have developed a novel method to identify biosurfactant producers on plants that reveals that they are very common in this habitat and that they produce surfactants with unique properties that will facilitate their interactions with plants. We will use this assay to determine the seasonal and regional variation in biosurfactant producers on spinach, romaine lettuce, and tatsoi in the region of commercial leafy vegetable production in Northern California and determine the variety of biosurfactants produced. Bacteria producing different classes of biosurfactants will be assessed for their ability to enhance the invasion of E. coli and Salmonella enterica into the edible plant varieties both in greenhouse and field studies. Likewise the effect of the biosurfactants on the viability and retention of the pathogens on plants will be assessed. Understanding the contribution of such extrinsic factors as the indigenous biosurfactant-producing bacterial microflora will enable better estimates of the risks associated with contamination of human pathogens to be developed.

Goals / Objectives
The development of a novel assay to sensitively detect biosurfactant production by bacteria recovered from plants has provided evidence that they may greatly alter the nature of the plant surface, thereby altering the behavior of human pathogens, enabling them to more easily invade leaves. The objectives of this study are thus to isolate and characterize the diversity of epiphytic bacteria and their biosurfactants on produce plant species. We further will investigate the production of biosurfactants on the leaf surface, and the effect of a rich indigenous epiphytic population on the leaf's physical properties. To address the effects of indigenous biosurfactant producers on plants we will examine the effect of biosurfactant production on the attachment, movement, and internalization of human pathogens such as E. coli or Salmonella enterica.
Methods (unparsed)

Using the novel oil-spray assay for biosurfactants that we have developed, initially, we will use this assay to screen isolates obtained from field-grown baby-leaf romaine lettuce, baby flat-leaf spinach, and tatsoi from field sites in northern California. We will further characterize the variety of surfactants that these strains produce such as by determining their hydrophilic-lipophilic balance (HLB) so that in the future, the effects of novel biosurfactants on human pathogens might be easily predicted based on their properties. To enable subsequent studies of the effect of surfactants themselves on neighboring human pathogenic bacteria, we will create surfactant-deficient mutants of at least one representative strain for each observed class of biosurfactant. Biosurfactant-deficient mutants and WT strains will be tested in the greenhouse, and in field experiments to determine the role of that given surfactant in plant colonization by the bacteria. We will develop reporter gene fusions to biosurfactant-producing genes to determine conditions affecting surfactant production in culture and in planta. Direct assessment of the effects of surfactants on the properties of the leaf surface will be assessed by applying droplets of water of different sizes to leaf surfaces. Tests in the greenhouse and the field will show how biosurfactant alter the behavior of human pathogens. Initial field studies will be to characterize attachment and invasion on the three distinctive edible plant species without modification of the microbial flora to provide a baseline for subsequent studies to test the impact of surfactant producers. Invasion of these inoculated plant species by human pathogens under several controlled conditions and in the field. Plants without an altered epiphytic microbial community will be inoculated with human pathogens and their subsequent ease of removal and invasion into plants will be assessed. The effects of application of extracted biosurfactants from bacteria on the behavior of the human pathogens and of commonly used agricultural surfactants will be measured. Plants will be challenge inoculated with human pathogens after the plants are treated with the various surfactants. The effect of indigenous surfactant producers on human pathogen behavior will be measured by establishing populations of a given strain on plants under field conditions and then challenging the plants by inoculating human pathogens. Invasion and ease of removal from leaves will be assessed. Plants treated with the biosurfactants and untreated controls will be harvested and exposed to human pathogens and then subjected to postharvest storage conditions and the numbers and location of the human pathogens on these plants will be compared. The overall experimental design will be to compare human pathogen mortality, invasion, and adhesion on leaves that are A) uncolonized (colonized only with small numbers of epiphytic bacteria, and few biosurfactant producers), B) colonized with large numbers of a given surfactant producer, or C) colonized by a mutant unable to produce surfactant.

Methods
Using the novel oil-spray assay for biosurfactants that we have developed, initially, we will use this assay to screen isolates obtained from field-grown baby-leaf romaine lettuce, baby flat-leaf spinach, and tatsoi from field sites in northern California. We will further characterize the variety of surfactants that these strains produce such as by determining their hydrophilic-lipophilic balance (HLB) so that in the future, the effects of novel biosurfactants on human pathogens might be easily predicted based on their properties. To enable subsequent studies of the effect of surfactants themselves on neighboring human pathogenic bacteria, we will create surfactant-deficient mutants of at least one representative strain for each observed class of biosurfactant. Biosurfactant-deficient mutants and WT strains will be tested in the greenhouse, and in field experiments to determine the role of that given surfactant in plant colonization by the bacteria. We will develop reporter gene fusions to biosurfactant-producing genes to determine conditions affecting surfactant production in culture and in planta. Direct assessment of the effects of surfactants on the properties of the leaf surface will be assessed by applying droplets of water of different sizes to leaf surfaces. Tests in the greenhouse and the field will show how biosurfactant alter the behavior of human pathogens. Initial field studies will be to characterize attachment and invasion on the three distinctive edible plant species without modification of the microbial flora to provide a baseline for subsequent studies to test the impact of surfactant producers. Invasion of these inoculated plant species by human pathogens under several controlled conditions and in the field. Plants without an altered epiphytic microbial community will be inoculated with human pathogens and their subsequent ease of removal and invasion into plants will be assessed. The effects of application of extracted biosurfactants from bacteria on the behavior of the human pathogens and of commonly used agricultural surfactants will be measured. Plants will be challenge inoculated with human pathogens after the plants are treated with the various surfactants. The effect of indigenous surfactant producers on human pathogen behavior will be measured by establishing populations of a given strain on plants under field conditions and then challenging the plants by inoculating human pathogens. Invasion and ease of removal from leaves will be assessed. Plants treated with the biosurfactants and untreated controls will be harvested and exposed to human pathogens and then subjected to postharvest storage conditions and the numbers and location of the human pathogens on these plants will be compared. The overall experimental design will be to compare human pathogen mortality, invasion, and adhesion on leaves that are A) uncolonized (colonized only with small numbers of epiphytic bacteria, and few biosurfactant producers), B) colonized with large numbers of a given surfactant producer, or C) colonized by a mutant unable to produce surfactant.
Project Timeline Tracking

Outputs

Target Audience
The target audience for this project is other microbiologists who focus on food safety, particularly that of edible cooked vegetable crops. Another target are agronomists and farmers with a focus on the production of edible vegetable crops, and who have a need to identify management practices that would minimize the risk of contamination of their crops by human pathogens such as E. coli and Salmonella.

Changes / Problems
No major changes in the experimental design or methodology that was proposed for this research were made. The only significant change in the research as conducted as compared to what was proposed was that due to the low population sizes of applied biosurfactant producing bacteria that survive application to romaine lettuce plants in field trials conducted at Davis California due to relatively warm and dry conditions, subsequent experiments were conducted under more controlled conditions in field sites at Berkeley California.

Training & Professional Development
This project provided an excellent opportunity for a skilled microbiologist to learn more about economic practices and the issues and practices in the arena of food safety. Dr. Adrien Burch was trained in new methods of molecular microbial ecology to address the fundamental ecology of bacteria that live on edible plants. This work provided her training not only in cutting edge molecular microbial ecology methods, but it also has provided new insight into the ecology of bacteria of all kinds on edible plants.

Dissemination Streams
The results of this research have been disseminated widely at national and international meetings that focused on microbial ecology, food safety, and plant biology. These venues included oral presentations of the research at the annual meeting of the American Society for Microbiology, at the 10th International Symposium on Phyllosphere Microbiology, and invited lectures at Virginia Polytechnic University, and at the Max Plank Institute for plant breeding. In addition, results of this work has been presented at a variety of grower meetings as well as it a variety of food safety conferences by Prof. Suslow.

Next Reporting Steps
Nothing Reported


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