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1.
Plant Signal Behav ; 7(9): 1129-31, 2012 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-22899059

RESUMO

Type III secreted effectors shape the potential of bacterial pathogens to cause disease on plants. Some effectors affect pathogen growth only in specific niches. For example, HopZ3 causes reduced epiphytic growth of Pseudomonas syringae strain B728a on Nicotiana benthamiana. This raises the question of whether genes important for effector-triggered disease resistance are needed for responses to effectors whose major effect is in the epiphytic niche. We report that SGT1b, a protein known to be important for defense activation, is essential for HopZ3-mediated suppression of PsyB728a epiphytic growth. SGT1b is required for HopZ3- and AvrB3-induced cell death in N. benthamiana plants that express the Pto resistance gene from tomato. We suggest that HopZ3 activates R gene mediated responses in N. benthamiana.


Assuntos
Proteínas de Bactérias/metabolismo , Resistência à Doença/genética , Genes de Plantas , Nicotiana/genética , Doenças das Plantas , Pseudomonas syringae , Morte Celular/genética , Solanum lycopersicum/genética , Doenças das Plantas/genética , Doenças das Plantas/microbiologia , Folhas de Planta/microbiologia , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Plantas Geneticamente Modificadas , Proteínas Serina-Treonina Quinases/genética , Pseudomonas syringae/crescimento & desenvolvimento , Pseudomonas syringae/patogenicidade , Nicotiana/metabolismo , Nicotiana/microbiologia
2.
Plant Physiol ; 158(4): 1803-18, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22319072

RESUMO

The bacterium Pseudomonas syringae pv syringae B728a (PsyB728a) uses a type III secretion system (T3SS) to inject effector proteins into plant cells, a process that modulates the susceptibility of different plants to infection. Analysis of GREEN FLUORESCENT PROTEIN-expressing PsyB728a after spray inoculation without additives under moderate relative humidity conditions permitted (1) a detailed analysis of this strain's survival and growth pattern on host (Nicotiana benthamiana) and nonhost (tomato [Solanum lycopersicum]) leaf surfaces, (2) an assessment of the role of plant defenses in affecting PsyB728a leaf surface (epiphytic) growth, and (3) the contribution of the T3SS and specific effectors to PsyB728a epiphytic survival and growth. On host leaf surfaces, PsyB728a cells initially persist without growing, and show an increased population only after 48 h, unless plants are pretreated with the defense-inducing chemical benzothiazole. During the persistence period, some PsyB728a cells induce a T3SS reporter, whereas a T3SS-deficient mutant shows reduced survival. By 72 h, rare invasion by PsyB728a to the mesophyll region of host leaves occurs, but endophytic and epiphytic bacterial growths are not correlated. The effectors HopZ3 and HopAA1 delay the onset of epiphytic growth of PsyB728a on N. benthamiana, whereas they promote epiphytic survival/growth on tomato. These effectors localize to distinct sites in plant cells and likely have different mechanisms of action. HopZ3 may enzymatically modify host targets, as it requires residues important for the catalytic activity of other proteins in its family of proteases. Thus, the T3SS, HopAA1, HopZ3, and plant defenses strongly influence epiphytic survival and/or growth of PsyB728a.


Assuntos
Proteínas de Bactérias/metabolismo , Viabilidade Microbiana , Nicotiana/microbiologia , Folhas de Planta/microbiologia , Pseudomonas syringae/crescimento & desenvolvimento , Solanum lycopersicum/microbiologia , Aminoácidos/metabolismo , Aderência Bacteriana/fisiologia , Biocatálise , Biofilmes/crescimento & desenvolvimento , Contagem de Colônia Microbiana , Proteínas de Fluorescência Verde/metabolismo , Solanum lycopersicum/imunologia , Fenótipo , Células Vegetais/microbiologia , Folhas de Planta/imunologia , Mutação Puntual/genética , Transporte Proteico , Proteínas Recombinantes de Fusão/metabolismo , Ácido Salicílico/metabolismo , Propriedades de Superfície , Nicotiana/imunologia
3.
J Bacteriol ; 188(20): 7242-56, 2006 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-17015663

RESUMO

Transcriptional profiles of Pseudomonas aeruginosa exposed to two separate copper stress conditions were determined. Actively growing bacteria subjected to a pulse of elevated copper for a short period of time was defined as a "copper-shocked" culture. Conversely, copper-adapted populations were defined as cells actively growing in the presence of elevated copper. Expression of 405 genes changed in the copper-shocked culture, compared to 331 genes for the copper-adapted cultures. Not surprisingly, there were genes identified in common to both conditions. For example, both stress conditions resulted in up-regulation of genes encoding several active transport functions. However, there were some interesting differences between the two types of stress. Only copper-adapted cells significantly altered expression of passive transport functions, down-regulating expression of several porins belonging to the OprD family. Copper shock produced expression profiles suggestive of an oxidative stress response, probably due to the participation of copper in Fenton-like chemistry. Copper-adapted populations did not show such a response. Transcriptional profiles also indicated that iron acquisition is fine-tuned in the presence of copper. Several genes induced under iron-limiting conditions, such as the siderophore pyoverdine, were up-regulated in copper-adapted populations. Interesting exceptions were the genes involved in the production of the siderophore pyochelin, which were down-regulated. Analysis of the copper sensitivity of select mutant strains confirmed the array data. These studies suggest that two resistance nodulation division efflux systems, a P-type ATPase, and a two-component regulator were particularly important for copper tolerance in P. aeruginosa.


Assuntos
Cobre/toxicidade , Perfilação da Expressão Gênica , Regulação Bacteriana da Expressão Gênica , Viabilidade Microbiana , Pseudomonas aeruginosa/efeitos dos fármacos , Pseudomonas aeruginosa/genética , Adaptação Fisiológica , Permeabilidade da Membrana Celular , Cobre/metabolismo , Homeostase , Ferro/metabolismo , Análise de Sequência com Séries de Oligonucleotídeos , Pseudomonas aeruginosa/crescimento & desenvolvimento , Pseudomonas aeruginosa/metabolismo , RNA Bacteriano/análise , RNA Bacteriano/genética , RNA Mensageiro/análise , RNA Mensageiro/genética , Transcrição Gênica , Zinco/toxicidade
4.
Mol Microbiol ; 62(1): 26-44, 2006 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16942603

RESUMO

The bacterial plant pathogen Pseudomonas syringae injects a large repertoire of effector proteins into plant cells using a type III secretion apparatus. Effectors can trigger or suppress defences in a host-dependent fashion. Host defences are often accompanied by programmed cell death, while interference with defences is sometimes associated with cell death suppression. We previously predicted the effector repertoire of the sequenced bean pathogen P. syringae pv. syringae (Psy) B728a using bioinformatics. Here we show that PsyB728a is also pathogenic on the model plant species Nicotiana benthamiana (tobacco). We confirm our effector predictions and clone the nearly complete PsyB728a effector repertoire. We find effectors to have different cell death-modulating activities and distinct roles during the infection of the susceptible bean and tobacco hosts. Unexpectedly, we do not find a strict correlation between cell death-eliciting and defence-eliciting activity and between cell death-suppressing activity and defence-interfering activity. Furthermore, we find several effectors with quantitative avirulence activities on their susceptible hosts, but with growth-promoting effects on Arabidopsis thaliana, a species on which PsyB728a does not cause disease. We conclude that P. syringae strains may have evolved large effector repertoires to extend their host ranges or increase their survival on various unrelated plant species.


Assuntos
Proteínas de Bactérias/genética , Doenças das Plantas/microbiologia , Plantas/microbiologia , Pseudomonas syringae/genética , Proteínas de Bactérias/metabolismo , Proteínas de Bactérias/fisiologia , Fabaceae/microbiologia , Regulação Bacteriana da Expressão Gênica/genética , Viabilidade Microbiana/genética , Pseudomonas syringae/metabolismo , Pseudomonas syringae/patogenicidade , Nicotiana/microbiologia , Virulência/genética
5.
Appl Environ Microbiol ; 69(4): 2313-20, 2003 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12676715

RESUMO

A study was undertaken to examine the effects of the heavy metals copper, lead, and zinc on biofilm and planktonic Pseudomonas aeruginosa. A rotating-disk biofilm reactor was used to generate biofilm and free-swimming cultures to test their relative levels of resistance to heavy metals. It was determined that biofilms were anywhere from 2 to 600 times more resistant to heavy metal stress than free-swimming cells. When planktonic cells at different stages of growth were examined, it was found that logarithmically growing cells were more resistant to copper and lead stress than stationary-phase cells. However, biofilms were observed to be more resistant to heavy metals than either stationary-phase or logarithmically growing planktonic cells. Microscopy was used to evaluate the effect of copper stress on a mature P. aeruginosa biofilm. The exterior of the biofilm was preferentially killed after exposure to elevated concentrations of copper, and the majority of living cells were near the substratum. A potential explanation for this is that the extracellular polymeric substances that encase a biofilm may be responsible for protecting cells from heavy metal stress by binding the heavy metals and retarding their diffusion within the biofilm.


Assuntos
Biofilmes/efeitos dos fármacos , Cobre/farmacologia , Metais Pesados/farmacologia , Plâncton/efeitos dos fármacos , Pseudomonas aeruginosa/efeitos dos fármacos , Animais , Biofilmes/crescimento & desenvolvimento , Farmacorresistência Bacteriana , Testes de Sensibilidade Microbiana , Plâncton/crescimento & desenvolvimento , Pseudomonas aeruginosa/crescimento & desenvolvimento
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