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1.
PLoS Biol ; 19(8): e3001136, 2021 08.
Article in English | MEDLINE | ID: mdl-34424903

ABSTRACT

In plants, nucleotide-binding domain and leucine-rich repeat (NLR)-containing proteins can form receptor networks to confer hypersensitive cell death and innate immunity. One class of NLRs, known as NLR required for cell death (NRCs), are central nodes in a complex network that protects against multiple pathogens and comprises up to half of the NLRome of solanaceous plants. Given the prevalence of this NLR network, we hypothesised that pathogens convergently evolved to secrete effectors that target NRC activities. To test this, we screened a library of 165 bacterial, oomycete, nematode, and aphid effectors for their capacity to suppress the cell death response triggered by the NRC-dependent disease resistance proteins Prf and Rpi-blb2. Among 5 of the identified suppressors, 1 cyst nematode protein and 1 oomycete protein suppress the activity of autoimmune mutants of NRC2 and NRC3, but not NRC4, indicating that they specifically counteract a subset of NRC proteins independently of their sensor NLR partners. Whereas the cyst nematode effector SPRYSEC15 binds the nucleotide-binding domain of NRC2 and NRC3, the oomycete effector AVRcap1b suppresses the response of these NRCs via the membrane trafficking-associated protein NbTOL9a (Target of Myb 1-like protein 9a). We conclude that plant pathogens have evolved to counteract central nodes of the NRC immune receptor network through different mechanisms. Coevolution with pathogen effectors may have driven NRC diversification into functionally redundant nodes in a massively expanded NLR network.


Subject(s)
Biological Evolution , Helminth Proteins/physiology , Host-Pathogen Interactions/physiology , NLR Proteins/physiology , Solanaceae/microbiology , Cell Death , Disease Resistance
2.
J Appl Microbiol ; 129(3): 496-508, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32248611

ABSTRACT

Pepper bacterial wilt is caused by the bacterial pathogen, Ralstonia solanacearum. It is the most destructive disease of many Solanaceous crops such as potatoes, tobacco, pepper, tomatoes and eggplant and is a significant source of crop loss worldwide. Physical, cultural and chemical controls have been employed to combat this destructive disease. However, none of these strategies has been able to control the disease completely due to the broad host range and genetic diversity of the pathogen, its prolonged survival in the soil and survival on vegetation as a latent infection. Owing to co-management strategies, biological control is the best approach for human health and environmental friendly motivations. It makes use of various antagonistic rhizobacteria and epiphytic species such as Bacillus cereus, Pseudomonas putida, Bacillus subtilis, Paenibacillus macerans, Serratia marcescens, Bacillus pumilus and Pseudomonas fluorescens, which compete with and ultimately inhibit the growth of the pathogen. The possible mechanisms of biocontrol by these species involve multifaceted interactions between the host, pathogen and the antagonists. These can involve competition for nutrients and space, plant-mediated systemic resistance, siderophore production and production of extracellular cell wall degrading enzymes to inhibit or suppress the growth of the bacterial wilt agent.


Subject(s)
Crops, Agricultural/microbiology , Pest Control, Biological , Plant Diseases/microbiology , Plant Diseases/prevention & control , Solanaceae/microbiology , Antibiosis , Bacteria/classification , Bacteria/growth & development , Bacteria/metabolism , Capsicum/microbiology , Host Microbial Interactions , Ralstonia solanacearum/growth & development
3.
Plant Dis ; 104(1): 179-185, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31725343

ABSTRACT

'Candidatus Liberibacter solanacearum' (Lso), transmitted by the potato psyllid (Bactericera cockerelli), is the putative causal agent of potato zebra chip disease. The bacterial pathogen infects a wide range of solanaceous plants (both wild and cultivated species), among which are peppers, potatoes, and tomatoes. Currently there are two commonly detected, genetically distinct haplotypes of Lso (A and B) identified from potatoes in the United States. To determine whether there are interactions between Lso haplotypes and different solanaceous hosts, experiments were conducted in the greenhouse in which pepper, potato, and tomato plants were infested with psyllids carrying Lso A, B, or an A and B mix (AB) or with psyllids free of Lso. Host plants were grown in pots in cages on the greenhouse benches and infested with six psyllids per plant. In addition, eight pepper cultivars were similarly infested for deeper understanding of host-haplotype interactions. Approximately 7 weeks after infestation, adult psyllids in each cage were counted to determine the impact of Lso haplotype-host interactions on psyllid survival and plants were sampled and tested molecularly for Lso. Individual psyllids carrying haplotypes B or AB and those free of Lso copiously reproduced on all three hosts, and leaf tissue from each plant tested positive for the respective Lso except those infested with Lso-negative psyllids. However, psyllids carrying Lso A did not survive on peppers but survived and abundantly reproduced on potatoes and tomatoes. In addition, samples from peppers infested with psyllids carrying Lso A tested negative for Lso. However, peppers infested with individual psyllids carrying Lso AB tested positive for Lso A, indicating that the presence of B may be required for infection by Lso A and psyllid survival on peppers. The different pepper cultivars infested with psyllids carrying Lso A showed similar results to the haplotype-host interaction tests, suggesting that cultivar may not be a factor in Lso A-pepper host interactions. Results from these studies suggest that Lso A may affect host selection by psyllids either for nutrition or laying of eggs. Mechanisms involved in preventing psyllid reproduction on peppers, once identified, will have significant implications for potential psyllid management.


Subject(s)
Hemiptera , Host-Pathogen Interactions , Rhizobiaceae , Solanaceae , Animals , Haplotypes , Hemiptera/microbiology , Plant Diseases/microbiology , Solanaceae/microbiology
4.
Plant Biotechnol J ; 16(7): 1349-1362, 2018 07.
Article in English | MEDLINE | ID: mdl-29265643

ABSTRACT

Ralstonia solanacearum, the causal agent of bacterial wilt disease, is considered one of the most destructive bacterial pathogens due to its lethality, unusually wide host range, persistence and broad geographical distribution. In spite of the extensive research on plant immunity over the last years, the perception of molecular patterns from R. solanacearum that activate immunity in plants is still poorly understood, which hinders the development of strategies to generate resistance against bacterial wilt disease. The perception of a conserved peptide of bacterial flagellin, flg22, is regarded as paradigm of plant perception of invading bacteria; however, no elicitor activity has been detected for R. solanacearum flg22. Recent reports have shown that other epitopes from flagellin are able to elicit immune responses in specific species from the Solanaceae family, yet our results show that these plants do not perceive any epitope from R. solanacearum flagellin. Searching for elicitor peptides from R. solanacearum, we found several protein sequences similar to the consensus of the elicitor peptide csp22, reported to elicit immunity in specific Solanaceae plants. A R. solanacearum csp22 peptide (csp22Rsol ) was indeed able to trigger immune responses in Nicotiana benthamiana and tomato, but not in Arabidopsis thaliana. Additionally, csp22Rsol treatment conferred increased resistance to R. solanacearum in tomato. Transgenic A. thaliana plants expressing the tomato csp22 receptor (SlCORE) gained the ability to respond to csp22Rsol and became more resistant to R. solanacearum infection. Our results shed light on the mechanisms for perception of R. solanacearum by plants, paving the way for improving current approaches to generate resistance against R. solanacearum.


Subject(s)
Peptides/immunology , Plant Diseases/immunology , Plant Immunity , Ralstonia solanacearum/metabolism , Solanaceae/immunology , Arabidopsis/immunology , Arabidopsis/microbiology , Disease Resistance , Epitopes/immunology , Flagellin/immunology , Solanum lycopersicum/immunology , Solanum lycopersicum/microbiology , Plant Diseases/microbiology , Plant Leaves/immunology , Plant Leaves/microbiology , Plant Roots/immunology , Plant Roots/microbiology , Plants, Genetically Modified/immunology , Solanaceae/microbiology , Nicotiana/immunology , Nicotiana/microbiology
5.
World J Microbiol Biotechnol ; 34(9): 132, 2018 Aug 13.
Article in English | MEDLINE | ID: mdl-30105532

ABSTRACT

Actinomycetes, a Gram positive bacteria, well reported as a source of antibiotics, also possess potential to control various plant pathogens, besides acting as plant growth promoting agent. Chemicals in different forms are extensively being used in vegetable farming, adversely affecting the environment and consumer health. Microbial agent like actinomycetes can substantially replace these harmful chemicals, and have now started finding a place as an important input in to farming practices. Only selected vegetable crops belonging to 11 different families have been explored with use of actinomycetes as biocontrol and plant growth promoting agent till now. It provides ample opportunities to vegetable researchers, to further explore with use of this very important group of microorganisms, in order to achieve even higher production level of safe vegetables. Mycostop and Actinovate are two actinomycetes based formulations globally available for use in vegetable farming as a substitute for chemical formulations. Present review article has summarized the literature available on use of actinomycetes in vegetable farming. Existing wide gap in knowledge, and potential thrust areas for future research have also been projected.


Subject(s)
Actinobacteria/physiology , Crops, Agricultural/growth & development , Crops, Agricultural/microbiology , Plant Development , Vegetables/growth & development , Vegetables/microbiology , Agriculture , Amaranthaceae/growth & development , Amaranthaceae/microbiology , Amaryllidaceae/growth & development , Amaryllidaceae/microbiology , Antibiosis , Apiaceae/growth & development , Apiaceae/microbiology , Asparagaceae/growth & development , Asparagaceae/microbiology , Asteraceae/growth & development , Asteraceae/microbiology , Biological Control Agents , Brassicaceae/growth & development , Brassicaceae/microbiology , Cucurbitaceae/growth & development , Cucurbitaceae/microbiology , Fabaceae/growth & development , Fabaceae/microbiology , Plant Diseases/prevention & control , Solanaceae/growth & development , Solanaceae/microbiology , Zingiberaceae/growth & development , Zingiberaceae/microbiology
6.
New Phytol ; 214(4): 1657-1672, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28386988

ABSTRACT

Pathogen-associated molecular patterns (PAMPs) are detected by plant pattern recognition receptors (PRRs), which gives rise to PAMP-triggered immunity (PTI). We characterized a novel fungal PAMP, Cell Death Inducing 1 (RcCDI1), identified in the Rhynchosporium commune transcriptome sampled at an early stage of barley (Hordeum vulgare) infection. The ability of RcCDI1 and its homologues from different fungal species to induce cell death in Nicotiana benthamiana was tested following agroinfiltration or infiltration of recombinant proteins produced by Pichia pastoris. Virus-induced gene silencing (VIGS) and transient expression of Phytophthora infestans effectors PiAVR3a and PexRD2 were used to assess the involvement of known components of PTI in N. benthamiana responses to RcCDI1. RcCDI1 was highly upregulated early during barley colonization with R. commune. RcCDI1 and its homologues from different fungal species, including Zymoseptoria tritici, Magnaporthe oryzae and Neurospora crassa, exhibited PAMP activity, inducing cell death in Solanaceae but not in other families of dicots or monocots. RcCDI1-triggered cell death was shown to require N. benthamiana Brassinosteroid insensitive 1-Associated Kinase 1 (NbBAK1), N. benthamiana suppressor of BIR1-1 (NbSOBIR1) and N. benthamiana SGT1 (NbSGT1), but was not suppressed by PiAVR3a or PexRD2. We report the identification of a novel Ascomycete PAMP, RcCDI1, recognized by Solanaceae but not by monocots, which activates cell death through a pathway that is distinct from that triggered by the oomycete PAMP INF1.


Subject(s)
Ascomycota/pathogenicity , Fungal Proteins/metabolism , Host-Pathogen Interactions/physiology , Pathogen-Associated Molecular Pattern Molecules/metabolism , Solanaceae/microbiology , Amino Acid Sequence , Ascomycota/genetics , Ascomycota/physiology , Cell Death , Conserved Sequence , Fungal Proteins/genetics , Hordeum/microbiology , Phylogeny , Plant Cells/microbiology , Plant Proteins/genetics , Plant Proteins/metabolism , Solanaceae/cytology , Nicotiana/genetics , Nicotiana/microbiology , Virulence Factors/genetics , Virulence Factors/metabolism
7.
Int J Mol Sci ; 17(10)2016 Oct 02.
Article in English | MEDLINE | ID: mdl-27706100

ABSTRACT

This review provides a current summary of plant resistance inducers (PRIs) that have been successfully used in the Solanaceae plant family to protect against pathogens by activating the plant's own defence. Solanaceous species include many important crops such as potato and tomato. We also present findings regarding the molecular processes after application of PRIs, even if the number of such studies still remains limited in this plant family. In general, there is a lack of patterns regarding the efficiency of induced resistance (IR) both between and within solanaceous species. In many cases, a hypersensitivity-like reaction needs to form in order for the PRI to be efficient. "-Omics" studies have already given insight in the complexity of responses, and can explain some of the differences seen in efficacy of PRIs between and within species as well as towards different pathogens. Finally, examples of field applications of PRIs for solanaceous crops are presented and discussed. We predict that PRIs will play a role in future plant protection strategies in Solanaceae crops if they are combined with other means of disease control in different spatial and temporal combinations.


Subject(s)
Solanaceae/metabolism , Aminobutyrates/metabolism , Aminobutyrates/pharmacology , Bacteria/drug effects , Crops, Agricultural , Cyclopentanes/metabolism , Cyclopentanes/pharmacology , Ethylenes/metabolism , Ethylenes/pharmacology , Fungi/drug effects , Oxylipins/metabolism , Oxylipins/pharmacology , Reactive Oxygen Species/metabolism , Solanaceae/genetics , Solanaceae/microbiology
8.
Mol Plant Microbe Interact ; 28(8): 927-42, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25822715

ABSTRACT

The microrchidia (MORC) proteins, a subset of the GHKL ATPase superfamily, were recently described as components involved in transcriptional gene silencing and plant immunity in Arabidopsis. To assess the role of MORC1 during resistance to Phytophthora infestans in solanaceous species, we altered the expression of the corresponding MORC1 homologs in potato, tomato, and Nicotiana benthamiana. Basal resistance to P. infestans was compromised in StMORC1-silenced potato and enhanced in overexpressing lines, indicating that StMORC1 positively affects immunity. By contrast, silencing SlMORC1 expression in tomato or NbMORC1 expression in N. benthamiana enhanced basal resistance to this oomycete pathogen. In addition, silencing SlMORC1 further enhanced resistance conferred by two resistance genes in tomato. Transient expression of StMORC1 in N. benthamiana accelerated cell death induced by infestin1 (INF1), whereas SlMORC1 or NbMORC1 suppressed it. Domain-swapping and mutational analyses indicated that the C-terminal region dictates the species-specific effects of the solanaceous MORC1 proteins on INF1-induced cell death. This C-terminal region also was required for homodimerization and phosphorylation of recombinant StMORC1 and SlMORC1, and its transient expression induced spontaneous cell death in N. benthamiana. Thus, this C-terminal region likely plays important roles in both determining and modulating the biological activity of MORC1 proteins.


Subject(s)
Adenosine Triphosphatases/metabolism , Host-Pathogen Interactions/immunology , Plant Proteins/metabolism , Solanaceae/immunology , Solanaceae/microbiology , Adenosine Triphosphatases/antagonists & inhibitors , Adenosine Triphosphatases/genetics , Gene Expression Regulation, Plant , Solanum lycopersicum/immunology , Solanum lycopersicum/microbiology , Phosphorylation , Phylogeny , Phytophthora infestans/pathogenicity , Plant Diseases/immunology , Plant Diseases/microbiology , Plant Immunity , Plant Proteins/genetics , Sesquiterpenes/pharmacology , Solanum tuberosum/immunology , Solanum tuberosum/microbiology , Nicotiana/immunology , Nicotiana/microbiology
9.
Mol Biol Evol ; 31(11): 2913-28, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25086002

ABSTRACT

Ralstonia solanacearum, the causal agent of a lethal bacterial wilt plant disease, infects an unusually wide range of hosts. These hosts can further be split into plants where R. solanacearum is known to cause disease (original hosts) and those where this bacterium can grow asymptomatically (distant hosts). Moreover, this pathogen is able to adapt to many plants as supported by field observations reporting emergence of strains with enlarged pathogenic properties. To investigate the genetic bases of host adaptation, we conducted evolution experiments by serial passages of a single clone of the pathogen on three original and two distant hosts over 300 bacterial generations and then analyzed the whole-genome of nine evolved clones. Phenotypic analysis of the evolved clones showed that the pathogen can increase its fitness on both original and distant hosts although the magnitude of fitness increase was greater on distant hosts. Only few genomic modifications were detected in evolved clones compared with the ancestor but parallel evolutionary changes in two genes were observed in independent evolved populations. Independent mutations in the regulatory gene efpR were selected for in three populations evolved on beans, a distant host. Reverse genetic approaches confirmed that these mutations were associated with fitness gain on bean plants. This work provides a first step toward understanding the within-host evolutionary dynamics of R. solanacearum during infection and identifying bacterial genes subjected to in planta selection. The discovery of EfpR as a determinant conditioning host adaptation of the pathogen illustrates how experimental evolution coupled with whole-genome sequencing is a potent tool to identify novel molecular players involved in central life-history traits.


Subject(s)
Adaptation, Physiological/genetics , Genes, Bacterial , Genes, Regulator , Genome, Bacterial , Ralstonia solanacearum/genetics , Ralstonia solanacearum/pathogenicity , Brassicaceae/microbiology , Clone Cells , Fabaceae/microbiology , Geraniaceae/microbiology , Host Specificity , Host-Pathogen Interactions , Mutation , Plant Diseases/microbiology , Ralstonia solanacearum/metabolism , Selection, Genetic , Solanaceae/microbiology , Virulence
10.
Mol Genet Genomics ; 290(6): 2173-86, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26008792

ABSTRACT

Late blight caused by the oomycete Phytophthora infestans is one of the most severe threats to potato production worldwide. Numerous studies suggest that the most effective protective strategy against the disease would be to provide potato cultivars with durable resistance (R) genes. However, little is known about the origin and evolutional history of these durable R-genes in potato. Addressing this might foster better understanding of the dynamics of these genes in nature and provide clues for identifying potential candidate R-genes. Here, a systematic survey was executed at RB/Rpi-blb1 locus, an exclusive broad-spectrum R-gene locus in potato. As indicated by synteny analysis, RB/Rpi-blb1 homologs were identified in all tested genomes, including potato, tomato, pepper, and Nicotiana, suggesting that the RB/Rpi-blb1 locus has an ancient origin. Two evolutionary patterns, similar to those reported on RGC2 in Lactuca, and Pi2/9 in rice, were detected at this locus. Type I RB/Rpi-blb1 homologs have frequent copy number variations and sequence exchanges, obscured orthologous relationships, considerable nucleotide divergence, and high non-synonymous to synonymous substitutions (Ka/Ks) between or within species, suggesting rapid diversification and balancing selection in response to rapid changes in the oomycete pathogen genomes. These characteristics may serve as signatures for cloning of late blight resistance genes.


Subject(s)
Evolution, Molecular , Genes, Plant , Solanaceae/genetics , Phylogeny , Solanaceae/classification , Solanaceae/microbiology
11.
New Phytol ; 208(1): 210-23, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26009937

ABSTRACT

Plant nucleotide-binding, leucine-rich repeat (NB-LRR) proteins confer immunity to pathogens possessing the corresponding avirulence proteins. Activation of NB-LRR proteins is often associated with induction of the hypersensitive response (HR), a form of programmed cell death. NRC1 (NB-LRR Required for HR-Associated Cell Death-1) is a tomato (Solanum lycopersicum) NB-LRR protein that participates in the signalling cascade leading to resistance to the pathogens Cladosporium fulvum and Verticillium dahliae. To identify mutations in NRC1 that cause increased signalling activity, we generated a random library of NRC1 variants mutated in their nucleotide-binding domain and screened them for the ability to induce an elicitor-independent HR in Nicotiana tabacum. Screening of 1920 clones retrieved 11 gain-of-function mutants, with 10 of them caused by a single amino acid substitution. All substitutions are located in or very close to highly conserved motifs within the nucleotide-binding domain, suggesting modulation of the signalling activity of NRC1. Three-dimensional modelling of the nucleotide-binding domain of NRC1 revealed that the targeted residues are centred around the bound nucleotide. Our mutational approach has generated a wide set of novel gain-of-function mutations in NRC1 and provides insight into how the activity of this NB-LRR is regulated.


Subject(s)
Disease Resistance/genetics , Mutation , Plant Diseases/microbiology , Plant Proteins/genetics , Protein Interaction Domains and Motifs/genetics , Proteins/genetics , Solanaceae/genetics , Amino Acid Sequence , Bacterial Proteins/metabolism , Binding Sites , Cell Death , Cladosporium/metabolism , Cladosporium/pathogenicity , Genes, Plant , Leucine/metabolism , Leucine-Rich Repeat Proteins , Solanum lycopersicum/genetics , Solanum lycopersicum/metabolism , Solanum lycopersicum/microbiology , Molecular Structure , Mutagenesis , Nucleotides/metabolism , Plant Proteins/metabolism , Proteins/metabolism , Signal Transduction , Solanaceae/metabolism , Solanaceae/microbiology , Nicotiana/genetics , Nicotiana/microbiology , Verticillium/metabolism , Verticillium/pathogenicity
12.
Transgenic Res ; 24(5): 847-58, 2015 Oct.
Article in English | MEDLINE | ID: mdl-25947088

ABSTRACT

Specific homologs of the plant Mildew Locus O (MLO) gene family act as susceptibility factors towards the powdery mildew (PM) fungal disease, causing significant economic losses in agricultural settings. Thus, in order to obtain PM resistant phenotypes, a general breeding strategy has been proposed, based on the selective inactivation of MLO susceptibility genes across cultivated species. In this study, PCR-based methodologies were used in order to isolate MLO genes from cultivated solanaceous crops that are hosts for PM fungi, namely eggplant, potato and tobacco, which were named SmMLO1, StMLO1 and NtMLO1, respectively. Based on phylogenetic analysis and sequence alignment, these genes were predicted to be orthologs of tomato SlMLO1 and pepper CaMLO2, previously shown to be required for PM pathogenesis. Full-length sequence of the tobacco homolog NtMLO1 was used for a heterologous transgenic complementation assay, resulting in its characterization as a PM susceptibility gene. The same assay showed that a single nucleotide change in a mutated NtMLO1 allele leads to complete gene loss-of-function. Results here presented, also including a complete overview of the tobacco and potato MLO gene families, are valuable to study MLO gene evolution in Solanaceae and for molecular breeding approaches aimed at introducing PM resistance using strategies of reverse genetics.


Subject(s)
Ascomycota/pathogenicity , Nicotiana/genetics , Solanaceae/genetics , Amino Acid Sequence , Fungal Proteins/chemistry , Molecular Sequence Data , Phylogeny , Plants, Genetically Modified , Sequence Homology, Amino Acid , Solanaceae/microbiology , Nicotiana/microbiology
13.
Phytopathology ; 105(7): 863-71, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25822188

ABSTRACT

'Candidatus Liberibacter solanacearum' contains two solanaceous crop-infecting haplotypes, A and B. Two haplotype A draft genomes were assembled and compared with ZC1 (haplotype B), revealing inversion and relocation genomic rearrangements, numerous single-nucleotide polymorphisms, and differences in phage-related regions. Differences in prophage location and sequence were seen both within and between haplotype comparisons. OrthoMCL and BLAST analyses identified 46 putative coding sequences present in haplotype A that were not present in haplotype B. Thirty-eight of these loci were not found in sequences from other Liberibacter spp. Quantitative polymerase chain reaction (qPCR) assays designed to amplify sequences from 15 of these loci were screened against a panel of 'Ca. L. solanacearum'-positive samples to investigate genetic diversity. Seven of the assays demonstrated within-haplotype diversity; five failed to amplify loci in at least one haplotype A sample while three assays produced amplicons from some haplotype B samples. Eight of the loci assays showed consistent A-B differentiation. Differences in genome arrangements, prophage, and qPCR results suggesting locus diversity within the haplotypes provide more evidence for genetic complexity in this emerging bacterial species.


Subject(s)
Genome, Bacterial , Rhizobiaceae/genetics , Solanaceae/microbiology , Haplotypes , Molecular Sequence Data , New Zealand , United States
14.
Phytopathology ; 104(6): 586-96, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24283538

ABSTRACT

Although bacterial wilt remains a major plant disease throughout South America and the Caribbean, the diversity of prevalent Ralstonia solanacearum populations is largely unknown. The genetic and phenotypic diversity of R. solanacearum strains in French Guiana was assessed using diagnostic polymerase chain reactions and sequence-based (egl and mutS) genotyping on a 239-strain collection sampled on the families Solanaceae and Cucurbitaceae, revealing an unexpectedly high diversity. Strains were distributed within phylotypes I (46.9%), IIA (26.8%), and IIB (26.3%), with one new endoglucanase sequence type (egl ST) found within each group. Phylotype IIB strains consisted mostly (97%) of strains with the emerging ecotype (IIB/sequevar 4NPB). Host range of IIB/4NPB strains from French Guiana matched the original emerging reference strain from Martinique. They were virulent on cucumber; virulent and highly aggressive on tomato, including the resistant reference Hawaii 7996; and only controlled by eggplant SM6 and Surya accessions. The emerging ecotype IIB/4NPB is fully established in French Guiana in both cultivated fields and uncultivated forest, rendering the hypothesis of introduction via ornamental or banana cuttings unlikely. Thus, this ecotype may have originated from the Amazonian region and spread throughout the Caribbean region.


Subject(s)
Cucurbitaceae/microbiology , Genetic Variation , Genome, Bacterial/genetics , Plant Diseases/microbiology , Ralstonia solanacearum/genetics , Solanaceae/microbiology , Bacterial Proteins/genetics , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Ecotype , French Guiana , Genotype , Geography , Host Specificity , Molecular Typing , Phenotype , Phylogeny , Polymerase Chain Reaction , Ralstonia solanacearum/classification , Ralstonia solanacearum/isolation & purification , Ralstonia solanacearum/pathogenicity , Sequence Analysis, DNA , Virulence
15.
J Integr Plant Biol ; 56(12): 1164-78, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24975554

ABSTRACT

To date, only a limited number of solanaceous miRNAs have been deposited in the miRNA database. Here, genome-wide bioinformatic identification of miRNAs was performed in six solanaceous plants (potato, tomato, tobacco, eggplant, pepper, and petunia). A total of 2,239 miRNAs were identified following a range of criteria, of which 982 were from potato, 496 from tomato, 655 from tobacco, 46 from eggplant, 45 were from pepper, and 15 from petunia. The sizes of miRNA families and miRNA precursor length differ in all the species. Accordingly, 620 targets were predicted, which could be functionally classified as transcription factors, metabolic enzymes, RNA and protein processing proteins, and other proteins for plant growth and development. We also showed evidence for miRNA clusters and sense and antisense miRNAs. Additionally, five Pi starvation- and one arbuscular mycorrhiza (AM)-related cis-elements were found widely distributed in the putative promoter regions of the miRNA genes. Selected miRNAs were classified into three groups based on the presence or absence of P1BS and MYCS cis-elements, and their expression in response to Pi starvation and AM symbiosis was validated by quantitative reverse transcription-polymerase chain reaction (qRT-PCR). These results show that conserved miRNAs exist in solanaceous species and they might play pivotal roles in plant growth, development, and stress responses.


Subject(s)
MicroRNAs/genetics , Mycorrhizae/physiology , Signal Transduction/genetics , Solanaceae/genetics , Gene Expression Regulation, Plant/genetics , Gene Expression Regulation, Plant/physiology , Solanum lycopersicum/genetics , Solanum lycopersicum/microbiology , Mycorrhizae/genetics , Phosphates/metabolism , Solanaceae/microbiology , Solanaceae/physiology , Solanum melongena/genetics , Solanum melongena/microbiology , Solanum tuberosum/genetics , Solanum tuberosum/microbiology , Nicotiana/genetics , Nicotiana/microbiology
16.
New Phytol ; 200(3): 847-860, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23865782

ABSTRACT

The bacterial flagellin (FliC) epitopes flg22 and flgII-28 are microbe-associated molecular patterns (MAMPs). Although flg22 is recognized by many plant species via the pattern recognition receptor FLS2, neither the flgII-28 receptor nor the extent of flgII-28 recognition by different plant families is known. Here, we tested the significance of flgII-28 as a MAMP and the importance of allelic diversity in flg22 and flgII-28 in plant-pathogen interactions using purified peptides and a Pseudomonas syringae ∆fliC mutant complemented with different fliC alleles. The plant genotype and allelic diversity in flg22 and flgII-28 were found to significantly affect the plant immune response, but not bacterial motility. The recognition of flgII-28 is restricted to a number of solanaceous species. Although the flgII-28 peptide does not trigger any immune response in Arabidopsis, mutations in both flg22 and flgII-28 have FLS2-dependent effects on virulence. However, the expression of a tomato allele of FLS2 does not confer to Nicotiana benthamiana the ability to detect flgII-28, and tomato plants silenced for FLS2 are not altered in flgII-28 recognition. Therefore, MAMP diversification is an effective pathogen virulence strategy, and flgII-28 appears to be perceived by an as yet unidentified receptor in the Solanaceae, although it has an FLS2-dependent virulence effect in Arabidopsis.


Subject(s)
Arabidopsis Proteins/metabolism , Arabidopsis/microbiology , Flagellin/genetics , Genotype , Plant Immunity/genetics , Protein Kinases/metabolism , Pseudomonas syringae/pathogenicity , Solanaceae/microbiology , Alleles , Arabidopsis/genetics , Arabidopsis/metabolism , Arabidopsis Proteins/genetics , Gene Expression Regulation, Plant , Host-Pathogen Interactions/genetics , Solanum lycopersicum/genetics , Solanum lycopersicum/metabolism , Solanum lycopersicum/microbiology , Mutation , Plant Diseases/genetics , Protein Kinases/genetics , Pseudomonas syringae/genetics , Pseudomonas syringae/physiology , Solanaceae/genetics , Solanaceae/metabolism , Nicotiana/genetics , Nicotiana/metabolism , Nicotiana/microbiology
17.
New Phytol ; 195(4): 894-911, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22738163

ABSTRACT

The pathogenicity of the Gram-negative plant-pathogenic bacterium Xanthomonas campestris pv. vesicatoria (Xcv) is dependent on type III effectors (T3Es) that are injected into plant cells by a type III secretion system and interfere with cellular processes to the benefit of the pathogen. In this study, we analyzed eight T3Es from Xcv strain 85-10, six of which were newly identified effectors. Genetic studies and protoplast expression assays revealed that XopB and XopS contribute to disease symptoms and bacterial growth, and suppress pathogen-associated molecular pattern (PAMP)-triggered plant defense gene expression. In addition, XopB inhibits cell death reactions induced by different T3Es, thus suppressing defense responses related to both PAMP-triggered immunity (PTI) and effector-triggered immunity (ETI). XopB localizes to the Golgi apparatus and cytoplasm of the plant cell and interferes with eukaryotic vesicle trafficking. Interestingly, a XopB point mutant derivative was defective in the suppression of ETI-related responses, but still interfered with vesicle trafficking and was only slightly affected with regard to the suppression of defense gene induction. This suggests that XopB-mediated suppression of PTI and ETI is dependent on different mechanisms that can be functionally separated.


Subject(s)
Bacterial Proteins/metabolism , Bacterial Secretion Systems/genetics , Plant Immunity , Xanthomonas campestris/metabolism , Arabidopsis/genetics , Arabidopsis/immunology , Arabidopsis/microbiology , Bacterial Proteins/genetics , Cell Death , Gene Expression Regulation, Bacterial , Gene Expression Regulation, Plant , Genes, Bacterial/genetics , Genetic Association Studies , Golgi Apparatus/metabolism , Plant Cells/microbiology , Plant Immunity/genetics , Plant Proteins/metabolism , Protein Transport/genetics , Solanaceae/cytology , Solanaceae/microbiology , Virulence/genetics , Xanthomonas campestris/genetics , Xanthomonas campestris/pathogenicity
18.
Phytopathology ; 102(8): 733-40, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22533876

ABSTRACT

The genetic and phenotypic diversity of Côte d'Ivoire Ralstonia solanacearum strains was assessed on a 168-strain collection sampled on Solanaceae both in the southern lowlands and western highlands. Phylotypes I, II, and III were prevalent, though at unexpected frequencies. Phylotype I strains (87.5%) were genetically diverse and overrepresented in all agroecological areas, including highlands (AEZ III). Phylotype II strains (10.7%) only belonged to one tropical lowland-adapted broad host range lineage (IIA-35), whereas no highland-adapted potato brown rot (IIB-1) or Moko strains were detected. African phylotype III strains were rare (1.8%). They originated from a single Burkina Faso lineage (III-23) and were only found in lowlands. Three phylotype I strains were found harboring pRSC35, a plasmid identified in phylotype III strains in Cameroon. From pathogenicity tests performed on commercial varieties and tomato/eggplant/pepper references, the virulence diversity observed was high, with five pathoprofiles described. Eggplant accessions MM152 and EG203 and tomato HW7996 displayed the largest resistance spectrum and highest level. Two highly virulent phylotype I strains were able to bypass resistance of HW7996 and the eggplant reference AG91-25. Collectively, these points lead to the conclusion that the situation in Côte d'Ivoire is specific towards other African countries, and specifically from the Cameroon reference, and that within phylotype I can exist a high virulence diversity. This calls for similar studies in neighboring West African countries, linking R. solanacearum pathogen genetic diversity to strain virulence at the regional level, for the rationalization of regional resistance deployment strategies and future resistance durability studies.


Subject(s)
Ralstonia solanacearum/genetics , Ralstonia solanacearum/pathogenicity , Solanaceae/microbiology , Africa , Cote d'Ivoire , Genetic Variation , Phylogeny , Ralstonia solanacearum/classification , Virulence/genetics
19.
Phytopathology ; 102(9): 878-91, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22708726

ABSTRACT

Pathogenic isolates of Pyrenochaeta lycopersici, the causal agent of corky root rot of tomato, secrete cell death in tomato 1 (CDiT1), a homodimeric protein of 35 kDa inducing cell death after infiltration into the leaf apoplast of tomato. CDiT1 was purified by fast protein liquid chromatography, characterized by mass spectrometry and cDNA cloning. Its activity was confirmed after infiltration of an affinity-purified recombinant fusion of the protein with a C-terminal polyhistidine tag. CDiT1 is highly expressed during tomato root infection compared with axenic culture, and has a putative ortholog in other pathogenic Pleosporales species producing proteinaceous toxins that contribute to virulence. Infiltration of CDiT1 into leaves of other plants susceptible to P. lycopersici revealed that the protein affects them differentially. All varieties of cultivated tomato (Solanum lycopersicum) tested were more sensitive to CDiT1 than those of currant tomato (S. pimpinellifolium). Root infection assays showed that varieties of currant tomato are also significantly less prone to intracellular colonization of their root cells by hyphae of P. lycopersici than varieties of cultivated tomato. Therefore, secretion of this novel type of inducer of cell death during penetration of the fungus inside root cells might favor infection of host species that are highly sensitive to this molecule.


Subject(s)
Ascomycota/metabolism , Cucumis/microbiology , Gene Expression Regulation, Fungal/physiology , Plant Diseases/microbiology , Solanaceae/microbiology , Amino Acid Sequence , Ascomycota/physiology , Fungal Proteins/genetics , Fungal Proteins/metabolism , Molecular Sequence Data , Plant Leaves/microbiology , Plant Roots/microbiology
20.
Am J Bot ; 98(8): 1231-42, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21795732

ABSTRACT

In eukaryotic organisms, horizontal gene transfer (HGT) is regarded as an important though infrequent source of reticulate evolution. Many confirmed instances of natural HGT involving multicellular eukaryotes come from flowering plants. This review intends to provide a synthesis of present knowledge regarding HGT in higher plants, with an emphasis on tobacco and other species in the Solanaceae family because there are numerous detailed reports concerning natural HGT events, involving various donors, in this family. Moreover, in-depth experimental studies using transgenic tobacco are of great importance for understanding this process. Valuable insights are offered concerning the mechanisms of HGT, the adaptive role and regulation of natural transgenes, and new routes for gene trafficking. With an increasing amount of data on HGT, a synthetic view is beginning to emerge.


Subject(s)
DNA, Bacterial/genetics , DNA, Fungal/genetics , DNA, Plant/genetics , Gene Transfer, Horizontal , Nicotiana/genetics , Solanaceae/genetics , Agrobacterium/genetics , Cell Nucleus/genetics , Chloroplasts/genetics , DNA, Chloroplast/genetics , DNA, Viral/genetics , Evolution, Molecular , Mycorrhizae/genetics , Plant Viruses/genetics , Solanaceae/microbiology , Solanaceae/virology , Nicotiana/microbiology , Nicotiana/virology , Transformation, Genetic
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