Jorge Pavan

Dr. Jorge Pavan


Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

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

Representative Publications

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1 April 2015 in Environmental Research
Verified
Journal Article
Closed access
PBP.A. Barril
P.A. Barril
TFT.M. Fumian
T.M. Fumian
VPV.E. Prez
V.E. Prez
PGP.I. Gil
P.I. Gil
LML.C. Martínez
L.C. Martínez
SNS.V. Nates
S.V. Nates

7 September 2011 in PLOS ONE
Verified
Journal Article
Open access
PDF file
ELElizabeth B. Liu
Elizabeth B. Liu
LFLeonardo Ferreyra
Leonardo Ferreyra
SFStephen L. Fischer
Stephen L. Fischer
JPJorge Pavan
Jorge Pavan
SNSilvia V. Nates
Silvia V. Nates
MJMorris S. Jones
Morris S. Jones
In February of 1996 a human adenovirus (formerly known as Ad-Cor-96-487) was isolated from the stool of an AIDS patient who presented with severe chronic diarrhea. To characterize this apparently novel pathogen of potential public health significance, the complete genome of this adenovirus was sequenced to elucidate its origin. Bioinformatic and phylogenetic analyses of this genome demonstrate that this virus, heretofore referred to as HAdV-D58, contains a novel hexon gene as well as a recombinant fiber gene. In addition, serological analysis demonstrated that HAdV-D58 has a different neutralization profile than all previously characterized HAdVs. Bootscan analysis of the HAdV-D58 fiber gene strongly suggests one recombination event.

1 December 2015 in Science of The Total Environment
Verified
Journal Article
Closed access
VPV.E. Prez
V.E. Prez
PGP.I. Gil
P.I. Gil
CTC.F. Temprana
C.F. Temprana
PCP.R. Cuadrado
P.R. Cuadrado
LML.C. Martínez
L.C. Martínez
PBP.A. Barril
P.A. Barril

1 March 2018 in Applied and Environmental Microbiology
Verified
Journal Article
Open access
PDF file
GMG. Masachessi
G. Masachessi
MPM. B. Pisano
M. B. Pisano
VPV. E. Prez
V. E. Prez
LML. C. Martínez
L. C. Martínez
JMJ. F. Michelena
J. F. Michelena
VRV. Ré
V. Ré
Water resources contaminated with wastewater are an important source for the dissemination of enteric viruses with an impact on the health of the population. The aim of the study was to assess the viral contamination of freshwater from a dam in Argentina by using infectious enterovirus detection, viral RNA amplification, and a genetic characterization of five enteric viruses associated with diarrhea and hepatitis. Enterovirus infectivity (iEV) was evaluated by cell culture and direct immunofluorescence. The detection of the viral genome of rotavirus (RV), human astrovirus (HAstV), norovirus (NoV), hepatitis A virus (HAV), and hepatitis E virus (HEV) was performed by reverse transcriptase PCR (RT-PCR). A total of 48 water samples from 4 monitoring points on the body of the dam from January to December 2012 and 66 water samples from 3 tourist beaches on the edge of the dam from October 2013 to October 2015 were collected monthly. During the first period, the overall viral frequency detection was 52.1% for group A RV, 50% for HAstV, 60.4% for NoV, 22.9% for HAV, 2.1% for HEV, and 64.6% for iEV. The overall frequency detection for the second sampling was 18.2% for RV and HAstV, 31.8% for NoV, 7.57% for HEV, and 66.7% for iEV. There was no detection of HAV during this period. The genotypes and genogroups detected through the study correlated with the most common genomic variants associated with human gastrointestinal and hepatitis illnesses. The results obtained could alert the health systems and environmental sanitation to make decisions for viral control and prevention in our environment. IMPORTANCE The study shows the impact of anthropic contamination of one of the most important tourist water resources in Argentina. This course of recreational water would be a favorable scenario for infection, as well as a reservoir for the enteric viruses, creating a risk for the population exposed to these waters. The results obtained could alert the health systems and environmental sanitation to make decisions for the control and prevention of viral diseases in this environment.

1 August 2003 in Intervirology
Verified
Journal Article
Closed access
PDF file
LMLaura C. Martínez
Laura C. Martínez
MGMiguel O. Giordano
Miguel O. Giordano
MIMaria B. Isa
Maria B. Isa
LALuis Fernando Alvarado
Luis Fernando Alvarado
JPJorge Pavan
Jorge Pavan
SNSilvia V. Nates
Silvia V. Nates
Objectives: This study was carried out in order to evaluate the efficacy of the recently developed picobirnavirus (PBV) sets of primers and to establish the phylogenetic relationships of Argentine strains with PBV strains isolated in China and the USA. Methods: Thirteen fecal specimens tested as positive for PBV by polyacrylamide gel electrophoresis were analyzed by reverse transcription-polymerase chain reaction assays using primers target to the genomic segments 2 of PBV strains isolated in China and the USA. The amplicons were sequenced and analyzed. Results: Primers derived from the China strain produced amplicons in only 4 of the 13 specimens (30.76%). No sample was revealed as positive with the primers derived from the US strain. DNA sequencing of polymerase chain reaction products differed in nucleic acid and amino acid sequences by 13.9–42.28% and 18.1–51.1%, respectively. Despite this strain diversity, three domains of conserved nucleotide sequences as well as the amino acid motif D-S-D typical of RNA-dependent RNA polymerase gene of double-strand RNA viruses were identified. Comparatively, these conserved regions were also identified in homologous PBV strains from the USA and China. Phylogenetic analysis showed no time or geographic clustering. Conclusions: These findings provide evidence that PBV may represent an emerging heterogeneous group of viruses.

1 June 1994 in Genes, Chromosomes and Cancer
Verified
Journal Article
Closed access
PDF file
FGFrancesca Gualandi
Francesca Gualandi
CMCristina Morelli
Cristina Morelli
JPJorge Pavan
Jorge Pavan
PRPaola Rimessi
Paola Rimessi
ASAlberto Sensi
Alberto Sensi
GBGiuseppe Barbanti‐Brodano
Giuseppe Barbanti‐Brodano