Microbes, plant immunity, and crop science
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Rescooped by Nicolas Denancé from TAL effector science
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Gene targeting by the TAL effector PthXo2 reveals cryptic resistance gene for bacterial blight of rice - Plant J.

Gene targeting by the TAL effector PthXo2 reveals cryptic resistance gene for bacterial blight of rice - Plant J. | Microbes, plant immunity, and crop science | Scoop.it

(via T. Schreiber, thx)

Bacterial blight of rice is caused by the γ-proteobacterium Xanthomonas oryzae pv. oryzae, which utilizes a group of type III TAL (transcription activator-like) effectors to induce host gene expression and condition host susceptibility. Five SWEET genes are functionally redundant to support bacterial disease, but only two were experimentally proven targets of natural TAL effectors. Here, we report the identification of the sucrose transporter gene OsSWEET13 as the disease susceptibility gene for PthXo2 and the existence of cryptic recessive resistance to PthXo2-dependent X. oryzae pv. oryzae due to promoter variations of OsSWEET13 in japonica rice. PthXo2-containing strains induce OsSWEET13 in indica rice IR24 due to the presence of an unpredicted and undescribed effector binding site not present in the alleles in japonica rice Nipponbare and Kitaake. The specificity of effector-associated gene induction and disease susceptibility is attributable to a single nucleotide polymorphism (SNP), which is also found in a polymorphic allele of OsSWEET13 known as the recessive resistance gene xa25 from the rice cultivar Minghui 63. The mutation of OsSWEET13 with CRISPR/Cas9 technology further corroborates the requirement of OsSWEET13 expression for the state of PthXo2-dependent disease susceptibility to X. oryzae pv. oryzae. Gene profiling of a collection of 104 strains revealed OsSWEET13 induction by 42 isolates of X. oryzae pv. oryzae. Heterologous expression of OsSWEET13 in Nicotiana benthamiana leaf cells elevates sucrose concentrations in the apoplasm. The results corroborate a model whereby X. oryzae pv. oryzae enhances the release of sucrose from host cells in order to exploit the host resources.

 


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J. Exp. Bot.: Identification of a molecular dialogue between developing seeds of Medicago truncatula and seedborne xanthomonads (2015)

J. Exp. Bot.: Identification of a molecular dialogue between developing seeds of Medicago truncatula and seedborne xanthomonads (2015) | Microbes, plant immunity, and crop science | Scoop.it

Plant pathogenic bacteria disseminate and survive mainly in association with seeds. This study addresses whether seeds are passive carriers or engage a molecular dialogue with pathogens during their development. We developed two pathosystems using Medicago truncatula with Xanthomonas alfalfae subsp. alfalfae (Xaa), the natural Medicago sp. pathogen and Xanthomonas campestris pv. campestris (Xcc), a Brassicaceae pathogen. Three days after flower inoculation, the transcriptome of Xcc-infected pods showed activation of an innate immune response that was strongly limited in Xcc mutated in the type three secretion system, demonstrating an incompatible interaction of Xcc with the reproductive structures. In contrast, the presence of Xaa did not result in an activation of defence genes. Transcriptome profiling during development of infected seeds exhibited time-dependent and differential responses to Xcc and Xaa. Gene network analysis revealed that the transcriptome of Xcc-infected seeds was mainly affected during seed filling whereas that of Xaa-infected seeds responded during late maturation. The Xcc-infected seed transcriptome exhibited an activation of defence response and a repression of targeted seed maturation pathways. Fifty-one percent of putative ABSCISIC ACID INSENSITIVE3 targets were deregulated by Xcc, including oleosin, cupin, legumin and chlorophyll degradation genes. At maturity, these seeds displayed decreased weight and increased chlorophyll content. In contrast, these traits were not affected by Xaa infection. These findings demonstrate the existence of a complex molecular dialogue between xanthomonads and developing seeds and provides insights into a previously unexplored trade-off between seed development and pathogen defence.

 

Emmanuel Terrasson, Armelle Darrasse, Karima Righetti, Julia Buitink, David Lalanne, Benoit Ly Vu, Sandra Pelletier, William Bolingue, Marie-Agnès Jacques, and Olivier Leprince

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Secondary metabolites in plant innate immunity

Secondary metabolites in plant innate immunity | Microbes, plant immunity, and crop science | Scoop.it
Plant secondary metabolites carry out numerous functions in interactions between plants and a broad range of other organisms. Experimental evidence strongly supports the indispensable contribution of many constitutive and pathogen-inducible phytochemicals to plant innate immunity. Extensive studies on model plant species, particularly Arabidopsis thaliana, have brought significant advances in our understanding of the molecular mechanisms underpinning pathogen-triggered biosynthesis and activation of defensive secondary metabolites. However, despite the proven significance of secondary metabolites in plant response to pathogenic microorganisms, little is known about the precise mechanisms underlying their contribution to plant immunity. This insufficiency concerns information on the dynamics of cellular and subcellular localization of defensive phytochemicals during the encounters with microbial pathogens and precise knowledge on their mode of action. As many secondary metabolites are characterized by their in vitro antimicrobial activity, these compounds were commonly considered to function in plant defense as in planta antibiotics. Strikingly, recent experimental evidence suggests that at least some of these compounds alternatively may be involved in controlling several immune responses that are evolutionarily conserved in the plant kingdom, including callose deposition and programmed cell death.
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Perception of pathogenic or beneficial bacteria and their evasion of host immunity: pattern recognition receptors in the frontline

Perception of pathogenic or beneficial bacteria and their evasion of host immunity: pattern recognition receptors in the frontline | Microbes, plant immunity, and crop science | Scoop.it
Plants are continuously monitoring the presence of microorganisms to establish an adapted response. Plants commonly use pattern recognition receptors (PRRs) to perceive microbe- or pathogen-associated molecular patterns (MAMPs/PAMPs) which are microorganism molecular signatures. Located at the plant plasma membrane, the PRRs are generally receptor-like kinases (RLKs) or receptor-like proteins (RLPs). MAMP detection will lead to the establishment of a plant defense program called MAMP-triggered immunity (MTI). In this review, we overview the RLKs and RLPs that assure early recognition and control of pathogenic or beneficial bacteria. We also highlight the crucial function of PRRs during plant-microbe interactions, with a special emphasis on the receptors of the bacterial flagellin and peptidoglycan. In addition, we discuss the multiple strategies used by bacteria to evade PRR-mediated recognition.

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Jean-Michel Ané's curator insight, April 14, 2015 12:53 PM

Another nice review

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Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3 - PLOS One

Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3 - PLOS One | Microbes, plant immunity, and crop science | Scoop.it

Schreiber et al, 2015

AvrBs3, the archetype of the family of transcription activator-like (TAL) effectors from phytopathogenic Xanthomonas bacteria, is translocated by the type III secretion system into the plant cell. AvrBs3 localizes to the plant cell nucleus and activates the transcription of target genes. Crucial for this is the central AvrBs3 region of 17.5 34-amino acid repeats that functions as a DNA-binding domain mediating recognition in a “one-repeat-to-one base pair” manner. Although AvrBs3 forms homodi


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Rescooped by Nicolas Denancé from Plants and Microbes
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NLR Biology in Plants and Animals - Interactions, Bavaria, Germany from May 3–6, 2015

NLR Biology in Plants and Animals - Interactions, Bavaria, Germany from May 3–6, 2015 | Microbes, plant immunity, and crop science | Scoop.it

This workshop aims to draw together researchers in plant and animal NLR biology to discuss recent conceptual advances and future directions for the field. The workshop will take place at Schloss Ringberg in Bavaria, Germany from May 3–6, 2015. View the workshop poster for more information on how to register and submit an abstract.


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Nat. Commun.: Bacterial killing via a type IV secretion system (2015)

Nat. Commun.: Bacterial killing via a type IV secretion system (2015) | Microbes, plant immunity, and crop science | Scoop.it

http://www.nature.com/ncomms/2015/150306/ncomms7453/full/ncomms7453.html?WT.ec_id=NCOMMS-20150311

 

Type IV secretion systems (T4SSs) are multiprotein complexes that transport effector proteins and protein–DNA complexes through bacterial membranes to the extracellular milieu or directly into the cytoplasm of other cells. Many bacteria of the family Xanthomonadaceae, which occupy diverse environmental niches, carry a T4SS with unknown function but with several characteristics that distinguishes it from other T4SSs. Here we show that the Xanthomonas citri T4SS provides these cells the capacity to kill other Gram-negative bacterial species in a contact-dependent manner. The secretion of one type IV bacterial effector protein is shown to require a conserved C-terminal domain and its bacteriolytic activity is neutralized by a cognate immunity protein whose 3D structure is similar to peptidoglycan hydrolase inhibitors. This is the first demonstration of the involvement of a T4SS in bacterial killing and points to this special class of T4SS as a mediator of both antagonistic and cooperative interbacterial interactions.

 

Diorge P. Souza, Gabriel U. Oka, Cristina E. Alvarez-Martinez, Alexandre W. Bisson-Filho, German Dunger, Lise Hobeika, Nayara S. Cavalcante, Marcos C. Alegria, Leandro R.S. Barbosa, Roberto K. Salinas, Cristiane R. Guzzo & Chuck S. Farah

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Front. Microbiol.: rpoN1, but not rpoN2, is required for twitching motility, natural competence, growth on nitrate and virulence of Ralstonia solanacearum (2015)

Front. Microbiol.: rpoN1, but not rpoN2, is required for twitching motility, natural competence, growth on nitrate and virulence of Ralstonia solanacearum (2015) | Microbes, plant immunity, and crop science | Scoop.it
The plant pathogen Ralstonia solanacearum has two genes encoding for the sigma factor 54: rpoN1, located in the chromosome and rpoN2, located in a distinct ‘megaplasmid’ replicon. In this study, individual mutants as well as a double mutant of rpoN were created in R. solanacearum strain GMI1000 in order to determine the extent of functional overlap between these two genes. By virulence assay we observed that rpoN1 is required for virulence whereas rpoN2 is not. In addition rpoN1 controls other important functions such twitching motility, natural transformation and growth on nitrate, unlike rpoN2. The rpoN1 and rpoN2 genes have different expression pattern, the expression of rpoN1 being constitutive whereas rpoN2 expression is induced in minimal medium and in the presence of plant cells. Moreover, the expression of rpoN2 is dependent upon rpoN1. Our work therefore reveals that the two rpoN genes are not functionally redundant in R.solanacearum. A list of potential sigma 54 targets was identified in the R. solanacearum genome and suggests that multiple traits are under the control of these regulators. Based on these findings, we provide a model describing the functional connection between RpoN1and the PehR pathogenicity regulator and their dual role in the control of several R. solanacearum virulence determinants.

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Trends Plant Sci.: Rhizobium–legume symbioses: the crucial role of plant immunity (2015)

Trends Plant Sci.: Rhizobium–legume symbioses: the crucial role of plant immunity (2015) | Microbes, plant immunity, and crop science | Scoop.it

New research results have significantly revised our understanding of the rhizobium–legume infection process. For example, Nod factors (NFs), previously thought to be absolutely essential for this symbiosis, were shown to be dispensable under particular conditions. Similarly, an NF receptor, previously considered to be solely involved in symbiosis, was shown to function during plant pathogen infections. Indeed, there is a growing realization that plant innate immunity is a crucial component in the establishment and maintenance of symbiosis. We review here the factors involved in the suppression of plant immunity during rhizobium–legume symbiosis, and we attempt to place this information into context with the most recent and sometimes surprising research results.

 

Benjamin Gourion, Fathi Berrabah, Pascal Ratet, Gary Stacey

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Nature Immunology: A lectin S-domain receptor kinase mediates lipopolysaccharide sensing in Arabidopsis thaliana

Nature Immunology: A lectin S-domain receptor kinase mediates lipopolysaccharide sensing in Arabidopsis thaliana | Microbes, plant immunity, and crop science | Scoop.it

The sensing of microbe-associated molecular patterns (MAMPs) triggers innate immunity in animals and plants. Lipopolysaccharide (LPS) from Gram-negative bacteria is a potent MAMP for mammals, with the lipid A moiety activating proinflammatory responses via Toll-like receptor 4 (TLR4). Here we found that the plant Arabidopsis thaliana specifically sensed LPS of Pseudomonas and Xanthomonas. We isolated LPS-insensitive mutants defective in the bulb-type lectin S-domain-1 receptor–like kinase LORE (SD1-29), which were hypersusceptible to infection with Pseudomonas syringae. Targeted chemical degradation of LPS from Pseudomonas species suggested that LORE detected mainly the lipid A moiety of LPS. LORE conferred sensitivity to LPS onto tobacco after transient expression, which demonstrated a key function in LPS sensing and indicated the possibility of engineering resistance to bacteria in crop species.


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J. Exp. Bot.: Greasy tactics in the plant–pathogen molecular arms race (2015)

J. Exp. Bot.: Greasy tactics in the plant–pathogen molecular arms race (2015) | Microbes, plant immunity, and crop science | Scoop.it

The modification of proteins by the attachment of fatty acids is a targeting tactic involved in mechanisms of both plant immunity and bacterial pathogenesis. The plant plasma membrane (PM) is a key battleground in the war against disease-causing microbes. This membrane is armed with an array of sensor proteins that function as a surveillance system to detect invading pathogens. Several of these sensor proteins are directed to the plasma membrane through the covalent addition of fatty acids, a process termed fatty acylation. Phytopathogens secrete effector proteins into the plant cell to subvert these surveillance mechanisms, rendering the host susceptible to infection. The targeting of effectors to specific locales within plant cells, particularly the internal face of the host PM, is critical for their virulence function. Several bacterial effectors hijack the host fatty acylation machinery to be modified and directed to this contested locale. To find and fight these fatty acylated effectors the plant leverages lipid-modified intracellular sensors. This review provides examples featuring how fatty acylation is a battle tactic used by both combatants in the molecular arms race between plants and pathogens. Also highlighted is the exploitation of a specific form of host-mediated fatty acid modification, which appears to be exclusively employed by phytopathogenic effector proteins.

 

 

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Rescooped by Nicolas Denancé from Plant Biology Teaching Resources (Higher Education)
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Plants and Pathogens teaching tool updated and revised

Plants and Pathogens teaching tool updated and revised | Microbes, plant immunity, and crop science | Scoop.it

We've updated and revised TTPB22, "Plants and Pathogens". http://www.plantcell.org/site/teachingtools/TTPB22.xhtml
Lots and lots of new references, a few new case studies and some new slides too. What a fascinating and wonderful topic to have a chance to revisit!


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FEMS Microbiol. Rev.: The battle for chitin recognition in plant-microbe interactions (2015)

FEMS Microbiol. Rev.: The battle for chitin recognition in plant-microbe interactions (2015) | Microbes, plant immunity, and crop science | Scoop.it

Fungal cell walls play dynamic functions in interaction of fungi with their surroundings. In pathogenic fungi, the cell wall is the first structure to make physical contact with host cells. An important structural component of fungal cell walls is chitin, a well-known elicitor of immune responses in plants. Research into chitin perception has sparked since the chitin receptor from rice was cloned nearly a decade ago. Considering the widespread nature of chitin perception in plants, pathogens evidently evolved strategies to overcome detection, including alterations in the composition of cell walls, modification of their carbohydrate chains and secretion of effectors to provide cell wall protection or target host immune responses. Also non-pathogenic fungi contain chitin in their cell walls and are recipients of immune responses. Intriguingly, various mutualists employ chitin-derived signaling molecules to prepare their hosts for the mutualistic relationship. Research on the various types of interactions has revealed different molecular components that play crucial roles and, moreover, that various chitin-binding proteins contain dissimilar chitin-binding domains across species that differ in affinity and specificity. Considering the various strategies from microbes and hosts focused on chitin recognition, it is evident that this carbohydrate plays a central role in plant–fungus interactions.

 

Andrea Sánchez-Vallet , Jeroen R. Mesters , Bart P.H.J. Thomma

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#NLR2015 Twitter Archive: NLR BIOLOGY IN PLANTS AND ANIMALS; WORKSHOP AT SCHLOSS RINGBERG; May 2015 DAYS 1/2


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Front. Plant Sci.: Decision tools for bacterial blight resistance gene deployment in rice-based agricultural ecosystems (2015)

Front. Plant Sci.: Decision tools for bacterial blight resistance gene deployment in rice-based agricultural ecosystems (2015) | Microbes, plant immunity, and crop science | Scoop.it

Attempting to achieve long-lasting and stable resistance using uniformly deployed rice varieties is not a sustainable approach. The real situation appears to be much more complex and dynamic, one in which pathogens quickly adapt to resistant varieties. To prevent disease epidemics, deployment should be customized and this decision will require interdisciplinary actions. This perspective article aims to highlight the current progress on disease resistance deployment to control bacterial blight in rice. Although the model system rice−Xanthomonas oryzae pv. oryzae has distinctive features that underpin the need for a case-by-case analysis, strategies to integrate those elements into a unique decision tool could be easily extended to other crops.

 

Gerbert Sylvestre Dossa, Adam H. Sparks, Casiana Vera Cruz and Ricardo Oliva

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Molecular Genetics and Genomics: Full-genome identification and characterization of NBS-encoding disease resistance genes in wheat (2014)

Molecular Genetics and Genomics: Full-genome identification and characterization of NBS-encoding disease resistance genes in wheat (2014) | Microbes, plant immunity, and crop science | Scoop.it

Host resistance is the most economical, effective and ecologically sustainable method of controlling diseases in crop plants. In bread wheat, despite the high number of resistance loci that have been cataloged to date, only few have been cloned, underlying the need for genomics-guided investigations capable of providing a prompt and acute knowledge on the identity of effective resistance genes that can be used in breeding programs. Proteins with a nucleotide-binding site (NBS) encoded by the major plant disease resistance (R) genes play an important role in the responses of plants to various pathogens. In this study, a comprehensive analysis of NBS-encoding genes within the whole wheat genome was performed, and the genome scale characterization of this gene family was established. From the recently published wheat genome sequence, we used a data mining and automatic prediction pipeline to identify 580 complete ORF candidate NBS-encoding genes and 1,099 partial-ORF ones. Among complete gene models, 464 were longer than 200 aa, among them 436 had less than 70 % of sequence identity to each other. This gene models set was deeply characterized. (1) First, we have analyzed domain architecture and identified, in addition to typical domain combinations, the presence of particular domains like signal peptides, zinc fingers, kinases, heavy-metal-associated and WRKY DNA-binding domains. (2) Functional and expression annotation via homology searches in protein and transcript databases, based on sufficient criteria, enabled identifying similar proteins for 60 % of the studied gene models and expression evidence for 13 % of them. (3) Shared orthologous groups were defined using NBS-domain proteins of rice and Brachypodium distachyon. (4) Finally, alignment of the 436 NBS-containing gene models to the full set of scaffolds from the IWGSC’s wheat chromosome survey sequence enabled high-stringence anchoring to chromosome arms. The distribution of the R genes was found balanced on the three wheat sub-genomes. In contrast, at chromosome scale, 50 % of members of this gene family were localized on 6 of the 21 wheat chromosomes and ~22 % of them were localized on homeologous group 7. The results of this study provide a detailed analysis of the largest family of plant disease resistance genes in allohexaploid wheat. Some structural traits reported had not been previously identified and the genome-derived data were confronted with those stored in databases outlining the functional specialization of members of this family. The large reservoir of NBS-type genes presented and discussed will, firstly, form an important framework for marker-assisted improvement of resistance in wheat, and, secondly, open up new perspectives for a better understanding of the evolution dynamics of this gene family in grass species and in polyploid systems.


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Front. Plant Sci.: What makes Xanthomonas albilineans unique amongst xanthomonads? (2015)

Front. Plant Sci.: What makes Xanthomonas albilineans unique amongst xanthomonads? (2015) | Microbes, plant immunity, and crop science | Scoop.it

Xanthomonas albilineans causes leaf scald, a lethal disease of sugarcane. Compared to other species of Xanthomonas, X. albilineans exhibits distinctive pathogenic mechanisms, ecology and taxonomy. Its genome, which has experienced significant erosion, has unique genomic features. It lacks two loci required for pathogenicity in other plant pathogenic species of Xanthomonas: the xanthan gum biosynthesis and the Hrp-T3SS (hypersensitive response and pathogenicity-type three secretion system) gene clusters. Instead, X. albilineans harbours in its genome an SPI-1 (Salmonella pathogenicity island-1) T3SS gene cluster usually found in animal pathogens. X. albilineans produces a potent DNA gyrase inhibitor called albicidin, which blocks chloroplast differentiation, resulting in the characteristic white foliar stripe symptoms. The antibacterial activity of albicidin also confers on X. albilineans a competitive advantage against rival bacteria during sugarcane colonization. Recent chemical studies have uncovered the unique structure of albicidin and allowed us to partially elucidate its fascinating biosynthesis apparatus, which involves an enigmatic hybrid PKS/NRPS (polyketide synthase/non-ribosomal peptide synthetase) machinery.

 

Isabelle Pieretti, Alexander Pesic, Daniel Petras, Monique Royer, Roderich D. Süssmuth and Stéphane Cociancich

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Genome Announc.: Draft Genome Sequence of the Xylella fastidiosa CoDiRO Strain (2015)

We determined the draft genome sequence of the Xylella fastidiosa CoDiRO strain, which has been isolated from olive plants in southern Italy (Apulia). It is associated with olive quick decline syndrome (OQDS) and characterized by extensive scorching and desiccation of leaves and twigs.

 

Giampetruzzi A, Chiumenti M, Saponari M, Donvito G, Italiano A, Loconsole G, Boscia D, Cariddi C, Martelli GP, Saldarelli P.

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Rescooped by Nicolas Denancé from Publications from The Sainsbury Laboratory
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New Phytologist: Arabidopsis EF-Tu receptor enhances bacterial disease resistance in transgenic wheat (2015)

New Phytologist: Arabidopsis EF-Tu receptor enhances bacterial disease resistance in transgenic wheat (2015) | Microbes, plant immunity, and crop science | Scoop.it

Perception of pathogen (or microbe)-associated molecular patterns (PAMPs/MAMPs) by pattern recognition receptors (PRRs) is a key component of plant innate immunity. The Arabidopsis PRR EF-Tu receptor (EFR) recognizes the bacterial PAMP elongation factor Tu (EF-Tu) and its derived peptide elf18. Previous work revealed that transgenic expression of AtEFR in Solanaceae confers elf18 responsiveness and broad-spectrum bacterial disease resistance.In this study, we developed a set of bioassays to study the activation of PAMP-triggered immunity (PTI) in wheat. We generated transgenic wheat (Triticum aestivum) plants expressing AtEFR driven by the constitutive rice actin promoter and tested their response to elf18.We show that transgenic expression of AtEFR in wheat confers recognition of elf18, as measured by the induction of immune marker genes and callose deposition. When challenged with the cereal bacterial pathogen Pseudomonas syringae pv. oryzae, transgenic EFR wheat lines had reduced lesion size and bacterial multiplication.These results demonstrate that AtEFR can be transferred successfully from dicot to monocot species, further revealing that immune signalling pathways are conserved across these distant phyla. As novel PRRs are identified, their transfer between plant families represents a useful strategy for enhancing resistance to pathogens in crops.


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The Sainsbury Lab's curator insight, March 12, 2015 5:48 AM
Perception of pathogen (or microbe)-associated molecular patterns (PAMPs/MAMPs) by pattern recognition receptors (PRRs) is a key component of plant innate immunity. The Arabidopsis PRR EF-Tu receptor (EFR) recognizes the bacterial PAMP elongation factor Tu (EF-Tu) and its derived peptide elf18. Previous work revealed that transgenic expression of AtEFR in Solanaceae confers elf18 responsiveness and broad-spectrum bacterial disease resistance.In this study, we developed a set of bioassays to study the activation of PAMP-triggered immunity (PTI) in wheat. We generated transgenic wheat (Triticum aestivum) plants expressing AtEFR driven by the constitutive rice actin promoter and tested their response to elf18.We show that transgenic expression of AtEFR in wheat confers recognition of elf18, as measured by the induction of immune marker genes and callose deposition. When challenged with the cereal bacterial pathogen Pseudomonas syringae pv. oryzae, transgenic EFR wheat lines had reduced lesion size and bacterial multiplication.These results demonstrate that AtEFR can be transferred successfully from dicot to monocot species, further revealing that immune signalling pathways are conserved across these distant phyla. As novel PRRs are identified, their transfer between plant families represents a useful strategy for enhancing resistance to pathogens in crops.
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TAL effectors - December 2014 Molecule of the Month by David Goodsell

TAL effectors - December 2014 Molecule of the Month by David Goodsell | Microbes, plant immunity, and crop science | Scoop.it

doi: 10.2210/rcsb_pdb/mom_2014_12 (ePub Version  )


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Nature Comms: Two linked pairs of Arabidopsis TNL resistance genes independently confer recognition of bacterial effector ​AvrRps4 (2015)

Nature Comms: Two linked pairs of Arabidopsis TNL resistance genes independently confer recognition of bacterial effector ​AvrRps4 (2015) | Microbes, plant immunity, and crop science | Scoop.it

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The Sainsbury Lab's curator insight, March 6, 2015 3:09 PM

Plant immunity requires recognition of pathogen effectors by intracellular NB-LRR immune receptors encoded by Resistance (R) genes. Most R proteins recognize a specific effector, but some function in pairs that recognize multiple effectors. Arabidopsis thaliana TIR-NB-LRR proteins RRS1-R and RPS4together recognize two bacterial effectors, AvrRps4 from Pseudomonas syringae and PopP2 from Ralstonia solanacearum. However, AvrRps4, but not PopP2, is recognized in rrs1/rps4 mutants. We reveal an R gene pair that resembles and is linked to RRS1/RPS4, designated as RRS1B/RPS4B, which confers recognition of AvrRps4 but not PopP2. Like RRS1/RPS4, RRS1B/RPS4B proteins associate and activate defence genes upon AvrRps4 recognition. Inappropriate combinations (RRS1/RPS4B or RRS1B/RPS4) are non-functional and this specificity is not TIR domain dependent. Distinct putative orthologues of both pairs are maintained in the genomes of Arabidopsis thalianarelatives and are likely derived from a common ancestor pair. Our results provide novel insights into paired R gene function and evolution.

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Plant Science Summer School - University of Angers, Fr.

Plant Science Summer School - University of Angers, Fr. | Microbes, plant immunity, and crop science | Scoop.it

You will find the summer programs of the University of Angers in the field of health sciences and plant science, which will be held from June 29th to July 10th 2015. Our summer schools offer an unique opportunity for students from all over the world to enjoy Science in a beautiful environment. Each program entirely conducted in English includes conferences by international researchers, hands-on activities, visits of research facilities and biotech companies and an attractive social program. Come and meet in Angers international students who share your passion for Science!

 

Plenary conference by Prof. Gareth Williams, renowned professor.

Session 1 : Plant defense stimulation, plant protection and plant memory

Session 2 : Genomic and Bacterial diagnostic

Session 3 : Fungal foliar disease on ornamentals

Session 4: Weed control in intercropping systems

Session 5: Metabolomics and medicinal plants                                              

Session 6 : Physiology and Nutritional Quality of seeds             

Session 7: Fruit production, Fruit development and self-thinning

Session 8: Post-harvest fruit quality management

 

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MBPP2015 | 2015 Molecular Biology of Plant Pathogens Conference at the University of the West of England, Bristol on 8-9 April 2015

MBPP2015 | 2015 Molecular Biology of Plant Pathogens Conference at the University of the West of England, Bristol on 8-9 April 2015 | Microbes, plant immunity, and crop science | Scoop.it

The 2015 Molecular Biology of Plant Pathogens (MBPP) conference will be held at the University of the West of England (UWE), Bristol on the 8th-9th April 2015. This will be the 23rd MBPP conference!

 

UWE is the largest university in the South West of England with over 30,000 students and approximately 3,500 staff. UWE has a long and interesting history starting life as a Merchant Venturer’s Navigation College in 1595 and undergoing many changes before gaining University status in 1992. Today UWE attracts students from all over the UK as well as a significant number of international students from 140 countries worldwide.

 

UWE has an active research community which makes a significant contribution to advances in industry, commerce, health and technology both nationally and internationally. The organisers of this years’ MBPP conference, Professor Dawn Arnold, Dr Carrie Brady and Dr Helen Neale work within the Centre for Research in Bioscience (CRIB) which leads world-class research in areas of strategic importance including plant science, agri-food, bio-sensing and biomedicine.

 

MBPP provides an excellent forum for networking between junior and senior scientists. The primary focus is on providing PhD students and post-doctoral scientists the opportunity to give oral presentations in front of a wide range of national and international researchers.

 

There will also be three keynote talks by internationally renowned scientists Professor Pietro Spanu (Imperial College), Dr Chris Ridout (John Innes Centre) and Professor Teresa Coutinho (Forestry and Agricultural Biotechnology Institute, University of Pretoria, South Africa). Please see our biographies tab for more information on these speakers.


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Front. Microbiol.: Agroforestry leads to shifts within the gammaproteobacterial microbiome of banana plants cultivated in Central America (2015)

Front. Microbiol.: Agroforestry leads to shifts within the gammaproteobacterial microbiome of banana plants cultivated in Central America (2015) | Microbes, plant immunity, and crop science | Scoop.it

Bananas (Musa spp.) belong to the most important global food commodities, and their cultivation represents the world's largest monoculture. Although the plant-associated microbiome has substantial influence on plant growth and health, there is a lack of knowledge of the banana microbiome and its influencing factors. We studied the impact of (i) biogeography, and (ii) agroforestry on the banana-associated gammaproteobacterial microbiome analyzing plants grown in smallholder farms in Nicaragua and Costa Rica. Profiles of 16S rRNA genes revealed high abundances of Pseudomonadales, Enterobacteriales, Xanthomonadales, and Legionellales. An extraordinary high diversity of the gammaproteobacterial microbiota was observed within the endophytic microenvironments (endorhiza and pseudostem), which was similar in both countries. Enterobacteria were identified as dominant group of above-ground plant parts (pseudostem and leaves). Neither biogeography nor agroforestry showed a statistically significant impact on the gammaproteobacterial banana microbiome in general. However, indicator species for each microenvironment and country, as well as for plants grown in Coffea intercropping systems with and without agri-silvicultural production of different Fabaceae trees (Inga spp. in Nicaragua and Erythrina poeppigiana in Costa Rica) could be identified. For example, banana plants grown in agroforestry systems were characterized by an increase of potential plant-beneficial bacteria, like Pseudomonas and Stenotrophomonas, and on the other side by a decrease of Erwinia. Hence, this study could show that as a result of legume-based agroforestry the indigenous banana-associated gammaproteobacterial community noticeably shifted.

 

Martina Köberl, Miguel Dita, Alfonso Martinuz, Charles Staver, and Gabriele Berg

 

 

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Colloque SFP, 2-5 Juin 2015 - Colmar, Fr

Colloque SFP, 2-5 Juin 2015 - Colmar, Fr | Microbes, plant immunity, and crop science | Scoop.it

En agriculture, les agents phytopathogènes (champignons, virus, bactéries) sont responsables de pertes considérables de rendements et de qualité. Ces pathologies combinées avec la croissance démographique mondiale et les changements climatiques constituent un risque majeur pour la sécurité alimentaire.  Pour mettre en place des actions appropriées il est indispensable de détecter, d'identifier  et de mieux connaitre ces organismes. Après le congres de Paris en 2012, la SFP continue son compagnonnage et, cette année, le colloque se tiendra en Alsace à Colmar du 2 au 5 juin 2015 au CREF (centre de rencontres, d'échanges et de formation) au 5 Rue des jardins.

Ce colloque, est ouvert aux phytopathologistes français et étrangers. C'est une opportunité d’aborder tous les domaines de la santé des végétaux et de faciliter le dialogue entre chercheurs à thématiques différentes. Pour présenter vos travaux, vous informer des recherches récentes dans ce domaine en France et au-delà, faire des rencontres et des échanges entre collègues, venez au 9éme colloque de la SFP, qui propose un programme passionnant, tant scientifique que touristique. C'est aussi l'occasion de découvrir la gastronomie alsacienne et les richesses touristiques de Colmar.

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