stefania tegli

Prof. stefania tegli

Dipartimento di Scienze e Tecnologie Agrarie, Alimentari Ambientali e Forestali, Laboratorio di Patologia Vegetale Molecolare, Università degli Studi di Firenze, Via della Lastruccia 10, 50019 Sesto Fiorentino, Firenze, Italy
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Research Focus & Metrics

Academic Career Length

42Years (1985-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2003 in Research in Microbiology
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Journal Article
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Stefano MocaliStefano Mocali
Stefano Mocali
EBEmanuela Bertelli
Emanuela Bertelli
FCFrancescopaolo Di Cello
Francescopaolo Di Cello
Alessio MengoniAlessio Mengoni
Alessio Mengoni
ASAlessandra Sfalanga
Alessandra Sfalanga
RFRenato Fani
Renato Fani

1 October 2002 in Letters in Applied Microbiology
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Journal Article
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stefania teglistefania tegli
stefania tegli
ASA. Sereni
A. Sereni
GSGiuseppe Surico
Giuseppe Surico

26 July 2017 in Plant Pathology
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Journal Article
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EOEbrahim Osdaghi
Ebrahim Osdaghi
STS. Mohsen Taghavi
S. Mohsen Taghavi
HHHabiballah Hamzehzarghani
Habiballah Hamzehzarghani
AFAmal Fazliarab
Amal Fazliarab
RHRobert M. Harveson
Robert M. Harveson
JLJay Ram Lamichhane
Jay Ram Lamichhane

1 November 2016 in Research in Microbiology
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Journal Article
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MCMatteo Cerboneschi
Matteo Cerboneschi
FDFrancesca Decorosi
Francesca Decorosi
CBCarola Biancalani
Carola Biancalani
MOMaria Vittoria Ortenzi
Maria Vittoria Ortenzi
SMSofia Macconi
Sofia Macconi
stefania teglistefania tegli
stefania tegli

1 June 2010 in Applied and Environmental Microbiology
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Journal Article
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IPIsabel Pérez-Martínez
Isabel Pérez-Martínez
Luis Rodríguez MorenoLuis Rodríguez Moreno
Luis Rodríguez Moreno
LLLotte Lambertsen
Lotte Lambertsen
IMIsabel M. Matas
Isabel M. Matas
Jesus MurilloJesus Murillo
Jesus Murillo
Cayo RamosCayo Ramos
Cayo Ramos
Pseudomonas savastanoipv. savastanoi strain NCPPB 3335 is a model bacterial pathogen for studying the molecular basis of disease production in woody hosts. We report the sequencing of thehrpS-to-hrpZregion of NCPPB 3335, which has allowed us to determine the phylogenetic position of this pathogen with respect to previously sequencedPseudomonas syringae hrpclusters. In addition, we constructed a mutant of NCPPB 3335, termed T3, which carries a deletion from the 3′ end of thehrpSgene to the 5′ end of thehrpZoperon. Despite its inability to multiply in olive tissues and to induce tumor formation in woody olive plants,P.savastanoipv. savastanoi T3 can induce knot formation on young micropropagated olive plants. However, the necrosis and formation of internal open cavities previously reported in knots induced by the wild-type strain were not observed in those induced byP.savastanoipv. savastanoi T3. Tagging ofP.savastanoipv. savastanoi T3 with green fluorescent protein (GFP) allowed real-time monitoring of its behavior on olive plants. In olive plant tissues, the wild-type strain formed aggregates that colonized the intercellular spaces and internal cavities of the hypertrophic knots, while the mutant T3 strain showed a disorganized distribution within the parenchyma of the knot. Ultrastructural analysis of knot sections revealed the release of extensive outer membrane vesicles from the bacterial cell surface of theP.savastanoipv. savastanoi T3 mutant, while the wild-type strain exhibited very few vesicles. This phenomenon has not been described before for any other bacterial phytopathogen during host infection.

1 January 2006 in Cell Biochemistry and Biophysics
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LPLuigia Pazzagli
Luigia Pazzagli
BPBarbara Pantera
Barbara Pantera
LCLara Carresi
Lara Carresi
CZCamilla Zoppi
Camilla Zoppi
TPThelma A. Pertinhez
Thelma A. Pertinhez
GCGianni Cappugi
Gianni Cappugi