» Articles » PMID: 28026146

Profiling the Extended Phenotype of Plant Pathogens: Challenges in Bacterial Molecular Plant Pathology

Overview
Specialty Molecular Biology
Date 2016 Dec 28
PMID 28026146
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

One of the most fundamental questions in plant pathology is what determines whether a pathogen grows within a plant? This question is frequently studied in terms of the role of elicitors and pathogenicity factors in the triggering or overcoming of host defences. However, this focus fails to address the basic question of how the environment in host tissues acts to support or restrict pathogen growth. Efforts to understand this aspect of host-pathogen interactions are commonly confounded by several issues, including the complexity of the plant environment, the artificial nature of many experimental infection systems and the fact that the physiological properties of a pathogen growing in association with a plant can be very different from the properties of the pathogen in culture. It is also important to recognize that the phenotype and evolution of pathogen and host are inextricably linked through their interactions, such that the environment experienced by a pathogen within a host, and its phenotype within the host, is a product of both its interaction with its host and its evolutionary history, including its co-evolution with host plants. As the phenotypic properties of a pathogen within a host cannot be defined in isolation from the host, it may be appropriate to think of pathogens as having an 'extended phenotype' that is the product of their genotype, host interactions and population structure within the host environment. This article reflects on the challenge of defining and studying this extended phenotype, in relation to the questions posed below, and considers how knowledge of the phenotype of pathogens in the host environment could be used to improve disease control. What determines whether a pathogen grows within a plant? What aspects of pathogen biology should be considered in describing the extended phenotype of a pathogen within a host? How can we study the extended phenotype in ways that provide insights into the phenotypic properties of pathogens during natural infections?

Citing Articles

Metabolome profiling dissects the oat (Avena sativa L.) innate immune response to Pseudomonas syringae pathovars.

Pretorius C, Steenkamp P, Dubery I PLoS One. 2025; 20(2):e0311226.

PMID: 39899505 PMC: 11790117. DOI: 10.1371/journal.pone.0311226.


". Nitrosocosmicus" members are the dominant archaea associated with plant rhizospheres.

Lee U, Gwak J, Choi S, Jung M, Lee T, Ryu H mSphere. 2024; 9(12):e0082124.

PMID: 39530672 PMC: 11656794. DOI: 10.1128/msphere.00821-24.


Antibiotic Resistance in Plant Pathogenic Bacteria: Recent Data and Environmental Impact of Unchecked Use and the Potential of Biocontrol Agents as an Eco-Friendly Alternative.

Islam T, Haque M, Barai H, Istiaq A, Kim J Plants (Basel). 2024; 13(8).

PMID: 38674544 PMC: 11054394. DOI: 10.3390/plants13081135.


Plants as the Extended Phenotype of Endophytes-The Actual Source of Bioactive Compounds.

Rutkowska N, Drozdzynski P, Ryngajllo M, Marchut-Mikolajczyk O Int J Mol Sci. 2023; 24(12).

PMID: 37373241 PMC: 10298476. DOI: 10.3390/ijms241210096.


Elicitor-induced plant immunity relies on amino acids accumulation to delay the onset of bacterial virulence.

Zhang X, Tubergen P, Agorsor I, Khadka P, Tembe C, Denbow C Plant Physiol. 2023; 192(1):601-615.

PMID: 36715647 PMC: 10152640. DOI: 10.1093/plphys/kiad048.


References
1.
Engl C, Waite C, McKenna J, Bennett M, Hamann T, Buck M . Chp8, a diguanylate cyclase from Pseudomonas syringae pv. Tomato DC3000, suppresses the pathogen-associated molecular pattern flagellin, increases extracellular polysaccharides, and promotes plant immune evasion. mBio. 2014; 5(3):e01168-14. PMC: 4030453. DOI: 10.1128/mBio.01168-14. View

2.
Win J, Chaparro-Garcia A, Belhaj K, Saunders D, Yoshida K, Dong S . Effector biology of plant-associated organisms: concepts and perspectives. Cold Spring Harb Symp Quant Biol. 2012; 77:235-47. DOI: 10.1101/sqb.2012.77.015933. View

3.
OLeary B, Neale H, Geilfus C, Jackson R, Arnold D, Preston G . Early changes in apoplast composition associated with defence and disease in interactions between Phaseolus vulgaris and the halo blight pathogen Pseudomonas syringae Pv. phaseolicola. Plant Cell Environ. 2016; 39(10):2172-84. PMC: 5026161. DOI: 10.1111/pce.12770. View

4.
Turner J, Mitchell R . Association between Symptom Development and Inhibition of Ornithine Carbamoyltransferase in Bean Leaves Treated with Phaseolotoxin. Plant Physiol. 1985; 79(2):468-73. PMC: 1074908. DOI: 10.1104/pp.79.2.468. View

5.
Boudart G, Jamet E, Rossignol M, Lafitte C, Borderies G, Jauneau A . Cell wall proteins in apoplastic fluids of Arabidopsis thaliana rosettes: identification by mass spectrometry and bioinformatics. Proteomics. 2004; 5(1):212-21. DOI: 10.1002/pmic.200400882. View