José Alejandro Di Conza

Prof. Dr. José Alejandro Di Conza

orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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1 February 2002 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Open access
PDF file
MRMarcela Radice
Marcela Radice
Pablo PowerPablo Power
Pablo Power
José Alejandro Di ConzaJosé Alejandro Di Conza
José Alejandro Di Conza
GGGabriel Osvaldo Gutkind
Gabriel Osvaldo Gutkind

1 July 2002 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Open access
PDF file
José Alejandro Di ConzaJosé Alejandro Di Conza
José Alejandro Di Conza
JUAN ALFONSO Ayala SerranoJUAN ALFONSO Ayala Serrano
JUAN ALFONSO Ayala Serrano
Pablo PowerPablo Power
Pablo Power
MMMarta Mollerach
Marta Mollerach
GGGabriel Osvaldo Gutkind
Gabriel Osvaldo Gutkind
The genetic organization of the region coding for CTX-M-2 in Salmonella enterica serovar Infantis was determined by PCR mapping. This gene seems to have been mobilized from the Kluyvera ascorbata chromosome to a complex sulI -type integron, similar to In6 and In7.

25 July 2018 in Frontiers in Microbiology
Verified
Journal Article
Open access
PDF file
JDJohana E. Dominguez
Johana E. Dominguez
LRLeandro M. Redondo
Leandro M. Redondo
RFRoque Figueroa-Espinosa
Roque Figueroa-Espinosa
DCDaniela Cejas
Daniela Cejas
GGGabriel Osvaldo Gutkind
Gabriel Osvaldo Gutkind
MFMariano E. Fernández-Miyakawa
Mariano E. Fernández-Miyakawa
The use of antimicrobial growth promoters (AGPs) in sub-therapeutic doses for long periods promotes the selection of resistant microorganisms and the subsequent risk of spreading this resistance to the human population and the environment. Global concern about antimicrobial resistance development and transference of resistance genes from animal to human has been rising. The goal of our research was to evaluate the susceptibility pattern to different classes of antimicrobials of colistin-resistant Escherichia coli from poultry production systems that use AGPs, and characterize the resistance determinants associated to transferable platforms. E. coli strains (n = 41) were obtained from fecal samples collected from typical Argentine commercial broiler farms and susceptibility for 23 antimicrobials, relevant for human or veterinary medicine, was determined. Isolates were tested by PCR for the presence of mcr-1, extended spectrum β-lactamase encoding genes and plasmid-mediated quinolone resistance (PMQR) coding genes. Conjugation and susceptibility patterns of the transconjugant studies were performed. ERIC-PCR and REP-PCR analysis showed a high diversity of the isolates. Resistance to several antimicrobials was determined and all colistin-resistant isolates harbored the mcr-1 gene. CTX-M-2 cefotaximase was the main mechanism responsible for third generation cephalosporins resistance, and PMQR determinants were also identified. In addition, co-transference of the qnrB determinant on the mcr-1-positive transconjugants was corroborated, which suggests that these resistance genes are likely to be located in the same plasmid. In this work a wide range of antimicrobial resistance mechanisms were identified in E. coli strains isolated from the environment of healthy chickens highlighting the risk of antimicrobial abuse/misuse in animals under intensive production systems and its consequences for public health.

1 November 2012 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Closed access
PDF file
SSS. Sennati
S. Sennati
GSG. Santella
G. Santella
José Alejandro Di ConzaJosé Alejandro Di Conza
José Alejandro Di Conza
LPLucia Pallecchi
Lucia Pallecchi
MPM. Pino
M. Pino
GGGabriel Osvaldo Gutkind
Gabriel Osvaldo Gutkind
A multicenter survey, carried out in 2010 in Argentina, showed an increased prevalence of extended-spectrum β-lactamase (ESBL)-producing enterobacteria, with some changes in the molecular epidemiology of circulating ESBLs. While enzymes of the CTX-M-2 group remain endemic, the emergence of CTX-M-15 and of enzymes of the CTX-M-8 and CTX-M-9 groups was observed. The CTX-M-15-positive isolates represented 40% of CTX-M producers and included representatives of Escherichia coli ST131 and Klebsiella pneumoniae ST11.

1 March 2019 in Veterinary Microbiology
Verified
Journal Article
Closed access
MRMaría Valeria Rumi
María Valeria Rumi
JMJavier Mas
Javier Mas
AEAlan Elena
Alan Elena
LCLouise Teixeira Cerdeira
Louise Teixeira Cerdeira
MMMaria E. Muñoz
Maria E. Muñoz
GGGabriel Osvaldo Gutkind
Gabriel Osvaldo Gutkind

1 April 2019 in Journal of Microbiological Methods
Verified
Journal Article
Closed access
RFRoque Figueroa-Espinosa
Roque Figueroa-Espinosa
ACAgustina Costa
Agustina Costa
DCDaniela Cejas
Daniela Cejas
RBRubén Barrios
Rubén Barrios
CVCarlos Vay
Carlos Vay
José Alejandro Di ConzaJosé Alejandro Di Conza
José Alejandro Di Conza