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Featured researches published by A. Czelleng.


Molecular Plant-microbe Interactions | 2006

Novel Extracellular Chitinases Rapidly and Specifically Induced by General Bacterial Elicitors and Suppressed by Virulent Bacteria as a Marker of Early Basal Resistance in Tobacco

Péter G. Ott; Gabriella Varga; Ágnes Szatmári; Zoltán Bozsó; Éva Klement; Katalin F. Medzihradszky; E. Besenyei; A. Czelleng; Zoltán Klement

Early basal resistance (EBR, formerly known as early induced resistance) is triggered by general bacterial elicitors. EBR has been suggested to inhibit or retard expression of the type III secretion system of pathogenic bacteria and may also prevent nonpathogenic bacteria from colonizing the plant tissue. The quickness of EBR here plays a crucial role, compensating for a low bactericidal efficacy. This inhibitory activity should take place in the cell wall, as bacteria do not enter living plant cells. We found several soluble proteins in the intercellular fluid of tobacco leaf parenchyma that coincided with EBR under different environmental (light and temperature) conditions known to affect EBR. The two most prominent proteins proved to be novel chitinases (EC 3.2.1.14) that were transcriptionally induced before and during EBR development. Their expression in the apoplast was fast and not stress-regulated as opposed to many pathogenesis-related proteins. Nonpathogenic, saprophytic, and avirulent bacteria all induced EBR and the chitinases. Studies using these chitinases as EBR markers revealed that the virulent Pseudomonas syringae pv. tabaci, being sensitive to EBR, must suppress it while suppressing the chitinases. EBR, the chitinases, as well as their suppression are quantitatively related, implying a delicate balance determining the outcome of an infection.


Current Microbiology | 2006

Identification of Virulence-Associated Genes of Pseudomonas viridiflava Activated During Infection by Use of a Novel IVET Promoter Probing Plasmid

A. Czelleng; Zoltán Bozsó; Péter G. Ott; E. Besenyei; Gabriella Varga; Ágnes Szatmári; L. Kiraly; Zoltán Klement

Analysis of virulence mechanisms of plant pathogens is often limited by the lack of genetic tools that can be used to identify genes that are preferentially expressed during their interactions with plants. In the present study, we used the newly constructed IVET (in vivoexpression technique) plasmid pIviGK and the corresponding antibiotic resistance–based selection method to identify genes that encode pathogenicity factors of the soft rot-causing bacterium Pseudomonas viridiflava. These included pel, the gene encoding pectate lyase, which is responsible for the development of soft rot symptoms. We have also isolated and characterized the gene mviNpv encoding a putative novel membrane associated virulence factor of P. viridiflava. A mutation in mviNpv was shown to influence motility as well as virulence of P. viridiflava. The mviNpv gene is expressed to a moderate level in LB media and its expression increases under inducing conditions as was shown by measuring in planta expression dynamics of the fused gfp reporter gene.


Presentations from the 6th International Conference on Pseudomonas syringae pathovars and related pathogens, Maratea, Italy, September 15-19, 2002. | 2003

Early Induced Resistance, a General, Symptomless Plant Response to Bacteria

Zoltán Klement; Zoltán Bozsó; E. Besenyei; A. Czelleng; M. L. Kecskés; Péter G. Ott

Many micro-organisms including pathogenic and saprophytic bacteria react with plant cells in the intercellular spaces inducing different defence responses. The local Early Induced Resistance (EIR) is a first line defence mechanism against bacteria. Here an overview will be given of this local, nonspecific, symptomless defence mechanism as a separate entity from the incompatible-specific Hypersensitive Response (HR). The EIR operates 1–6 h after inoculation (hpi) for about one day depending on temperature and leaf age. The EIR can be inhibited by a short heat shock (50°C for 15 sec) of leaves or by a plant protein synthesis inhibitor, cycloheximide (5 µg m1−1). In a compatible host-pathogen relationship (Pseudomonas syringae pv. tabaci/tobacco) the effect of EIR does not eventuate. However, the EIR develops simultaneously with the HR and sometimes is able to prevent it when the induction time of HR is longer than the time required for the development of the EIR (e.g. P. s. pv. phaseolicola does not induce HR in tobacco above 28°C). It seems that the EIR inhibits the metabolism of bacteria and the activity of hrp genes. Moreover, EIR activates the accumulation of H2O2 at the bacterial attachment site expressing new peroxidase isoenzymes in the initiated plant tissue. Further investigations, hopefully, will clarify the relationship of other complementary defence mechanisms like local late induced resistance (LIR) examined by Sequeira (1983) and Mazzucchi and co-workers (1979), Minardi (1995), Newman et al., (2001).


Archive | 2001

Non-specific, Peroxidase and H2O2 Associated Reactions of Tobacco Leaves after Infiltration with hrp/hrmA Mutants of P. syringae pv. syringae 61

Zoltán Bozsó; Péter G. Ott; M. L. Kecskés; A. Czelleng; Zoltán Klement

Plants recognize the infection of both pathogenic and non-pathogenic bacteria and respond with specific and non-specific defense reactions after bacterial infections. One of the specific defense responses of plants is the hypersensitive reaction (HR). The HR is accompanied by an accumulation of active oxygen species including H2O2 and other resistance associated responses. The hrp/hrc genes are indispensable for phytopathogenic bacteria to induce HR or disease in plants. The plant cells sense not only the plant pathogenic bacteria and their elicitors (harpin or avr proteins) but also the non-pathogenic and the HR-negative bacteria (non-specific reactions). During these non-specific reactions plants respond with different resistance related reactions such as induction of mRNA accumulation of several defense associated genes, and large papilla formation at the site of attachment of bacteria. The plants probably recognize the bacterial common surface molecules e.g. flagellin protein (1) or bacterial lipopolysaccharides (2, Kecskes et al., unpublished).


Plant Cell Reports | 2006

Characterisation of basal resistance (BR) by expression patterns of newly isolated representative genes in tobacco

Ágnes Szatmári; Péter G. Ott; Gabriella Varga; E. Besenyei; A. Czelleng; Zoltán Klement; Zoltán Bozsó


Journal of Phytopathology | 2005

Early Detection of Bacterium‐induced Basal Resistance in Tobacco Leaves with Diaminobenzidine and Dichlorofluorescein Diacetate

Zoltán Bozsó; Péter G. Ott; Ágnes Szatmári; A. Czelleng; Gabriella Varga; E. Besenyei; É. Sárdi; É. Bányai; Zoltán Klement


Acta Phytopathologica Et Entomologica Hungarica | 2005

Low temperature delay and inhibition of a plant defence mechanism: early basal resistance in tobacco

E. Besenyei; Péter G. Ott; Zoltán Bozsó; A. Czelleng; Ágnes Szatmári; Gabriella Varga; Zoltán Klement


Acta Phytopathologica Et Entomologica Hungarica | 2004

Isolation of in planta-Induced Genes of Pseudomonas viridiflava

A. Czelleng; Zoltán Bozsó; Péter G. Ott; E. Besenyei; Gabriella Varga; Ágnes Szatmári; Y. M. Hafez; Zoltán Klement


Archive | 2002

Cloning and characterization of peroxidases associated with generalized defense reactions of plants against bacterial pathogens

Zoltán Bozsó; E. Besenyei; Péter G. Ott; A. Czelleng; Zoltán Klement


Acta Phytopathologica Et Entomologica Hungarica | 2006

Basal resistance of plants against bacteria: From discovery to molecular characterisation

Péter G. Ott; Gabriella Varga; Ágnes Szatmári; Zoltán Bozsó; E. Besenyei; A. Czelleng; Erika Szabó

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Zoltán Bozsó

Hungarian Academy of Sciences

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Péter G. Ott

Hungarian Academy of Sciences

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E. Besenyei

Hungarian Academy of Sciences

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Zoltán Klement

Hungarian Academy of Sciences

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Ágnes Szatmári

Hungarian Academy of Sciences

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Gabriella Varga

Hungarian Academy of Sciences

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Erika Szabó

Hungarian Academy of Sciences

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M. L. Kecskés

Hungarian Academy of Sciences

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L. Kiraly

Hungarian Academy of Sciences

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