Viviana A Rapisarda

Dr. Viviana A Rapisarda

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Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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1 August 2002 in Analytical Biochemistry
Verified
Journal Article
Closed access
Viviana A RapisardaViviana A Rapisarda
Viviana A Rapisarda
Sabrina VolentiniSabrina Volentini
Sabrina Volentini
RFRicardo N Farı́as
Ricardo N Farı́as
EMEddy M Massa
Eddy M Massa

1 July 2006 in Archives of Biochemistry and Biophysics
Verified
Journal Article
Closed access
LRLuisa Rodríguez-Montelongo
Luisa Rodríguez-Montelongo
Sabrina VolentiniSabrina Volentini
Sabrina Volentini
RFRicardo N. Farías
Ricardo N. Farías
EMEddy M. Massa
Eddy M. Massa
Viviana A RapisardaViviana A Rapisarda
Viviana A Rapisarda

1 September 2002 in Archives of Biochemistry and Biophysics
Verified
Journal Article
Closed access
Viviana A RapisardaViviana A Rapisarda
Viviana A Rapisarda
RCRosana Chehin
Rosana Chehin
Javier De Las RivasJavier De Las Rivas
Javier De Las Rivas
LRLuisa Rodrı́guez-Montelongo
Luisa Rodrı́guez-Montelongo
RFRicardo N Farı́as
Ricardo N Farı́as
EMEddy M Massa
Eddy M Massa

10 March 2011 in BioMetals
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Journal Article
Closed access
PDF file
Sabrina VolentiniSabrina Volentini
Sabrina Volentini
RFRicardo N. Farías
Ricardo N. Farías
LRLuisa Rodríguez-Montelongo
Luisa Rodríguez-Montelongo
Viviana A RapisardaViviana A Rapisarda
Viviana A Rapisarda

19 March 2014 in BMC Microbiology
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Journal Article
Open access
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MGMariana Grillo-Puertas
Mariana Grillo-Puertas
LSLici Ariane Schurig-Briccio
Lici Ariane Schurig-Briccio
LRLuisa Rodríguez-Montelongo
Luisa Rodríguez-Montelongo
MRMaría Regina Rintoul
María Regina Rintoul
Viviana A RapisardaViviana A Rapisarda
Viviana A Rapisarda
Metal tolerance in bacteria has been related to polyP in a model in which heavy metals stimulate the polymer hydrolysis, forming metal-phosphate complexes that are exported. As previously described in our laboratory, Escherichia coli cells grown in media containing a phosphate concentration >37 mM maintained an unusually high polyphosphate (polyP) level in stationary phase. The aim of the present work was to evaluate the influence of polyP levels as the involvement of low-affinity inorganic phosphate transport (Pit) system in E. coli copper tolerance.

30 November 2012 in PLOS ONE
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Journal Article
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MGMariana Grillo-Puertas
Mariana Grillo-Puertas
JVJosefina M. Villegas
Josefina M. Villegas
MRMaría R. Rintoul
María R. Rintoul
Viviana A RapisardaViviana A Rapisarda
Viviana A Rapisarda
In most natural environments, association with a surface in a structure known as biofilm is the prevailing microbial life-style of bacteria. Polyphosphate (polyP), an ubiquitous linear polymer of hundreds of orthophosphate residues, has a crucial role in stress responses, stationary-phase survival, and it was associated to bacterial biofilm formation and production of virulence factors. In previous work, we have shown that Escherichia coli cells grown in media containing a critical phosphate concentration >37 mM maintained an unusual high polyP level in stationary phase. The aim of the present work was to analyze if fluctuations in polyP levels in stationary phase affect biofilm formation capacity in E. coli. Polymer levels were modulated by the media phosphate concentration or using mutant strains in polyP metabolism. Cells grown in media containing phosphate concentrations higher than 25 mM were defective in biofilm formation. Besides, there was a disassembly of 24 h preformed biofilm by the addition of high phosphate concentration to the medium. These phenotypes were related to the maintenance or re-synthesis of polyP in stationary phase in static conditions. No biofilm formation was observed in ppk−ppx− or ppk−ppx−/ppk+ strains, deficient in polyP synthesis and hydrolysis, respectively. luxS and lsrK mutants, impaired in autoinducer-2 quorum sensing signal metabolism, were unable to form biofilm unless conditioned media from stationary phase wild type cells grown in low phosphate were used. We conclude that polyP degradation is required for biofilm formation in sufficient phosphate media, activating or triggering the production of autoinducer-2. According to our results, phosphate concentration of the culture media should be carefully considered in bacterial adhesion and virulence studies.