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Dive into the research topics where Thiago Pavoni Gomes Chagas is active.

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Featured researches published by Thiago Pavoni Gomes Chagas.


Journal of Antimicrobial Chemotherapy | 2013

Isolation of NDM-producing Providencia rettgeri in Brazil

Ana Paula D'Alincourt Carvalho-Assef; Polyana Silva Pereira; Rodolpho M. Albano; Gabriela Casemiro Berião; Thiago Pavoni Gomes Chagas; Loeci Natalina Timm; Renato Cassol Ferreira da Silva; Diego R. Falci; Marise Dutra Asensi

Laboratório de Pesquisa em Infecção Hospitalar (LAPIH), Instituto Oswaldo Cruz-FIOCRUZ, Rio de Janeiro, RJ, Brazil; Departamento de Bioquı́mica, Instituto de Biologia Roberto Alcântara Gomes, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil; Fundação Estadual de Produção e Pesquisa em Saúde (FEPPS IPB-LACEN-RS), Porto Alegre, RS, Brazil; Hospital Nossa Senhora da Conceição, Porto Alegre, RS, Brazil


Diagnostic Microbiology and Infectious Disease | 2014

Characterization of carbapenem-resistant Acinetobacter baumannii in Brazil (2008–2011): countrywide spread of OXA-23–producing clones (CC15 and CC79)

Thiago Pavoni Gomes Chagas; Karyne Rangel Carvalho; Ivson Cassiano de Oliveira Santos; Ana Paula D’Alincourt Carvalho-Assef; Marise Dutra Asensi

The study investigated the genetic relationship of carbapenem-resistant Acinetobacter baumannii clinical isolated from inpatients during 2008-2011 from 11 Brazilian states. Antimicrobial susceptibility profile was determined by disc diffusion method and Etest. Polymerase chain reaction was applied for carbapenemase genes, and ISAba1. Isolates were subjected to pulsed field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) for molecular typing. Most of the isolates showed high resistance rates to antibiotics tested. The blaOXA-51-like gene was found in all isolates, and 146 (94.2%) isolates were positive for blaOXA-23-like. In the most OXA-23-producing isolates, the blaOXA-23-like gene was accompanied by ISAba1. A total of 146 OXA-23-producing isolates were clustered into 28 genotypes by PFGE. Molecular analysis by MLST identified 13 sequence types (STs). The most prevalent PFGE profiles were designated as ST15 (CC15), ST1 (CC1), and ST79 (CC79). This study showed the widespread of clonal complexes of A. baumannii harboring the blaOXA-23-like gene in different Brazilian states.


Antimicrobial Agents and Chemotherapy | 2014

Detection of NDM-1-, CTX-M-15-, and qnrB4-Producing Enterobacter hormaechei Isolates in Brazil

Ana Paula D'Alincourt Carvalho-Assef; Polyana Silva Pereira; Rodolpho M. Albano; Gabriela Casemiro Berião; Carolina Padilha Tavares; Thiago Pavoni Gomes Chagas; Elizabeth Andrade Marques; Loeci Natalina Timm; Renato Cassol Ferreira da Silva; Diego R. Falci; Marise Dutra Asensi

Ana Paula D’Alincourt Carvalho-Assef, Polyana S. Pereira, Rodolpho M. Albano, Gabriela Casemiro Berião, Carolina Padilha Tavares, Thiago Pavoni Gomes Chagas, Elizabeth A. Marques, Loeci N. Timm, Renato C. F. Da Silva, Diego R. Falci, Marise D. Asensi Laboratório de Pesquisa em Infecção Hospitalar (LAPIH), Instituto Oswaldo Cruz-FIOCRUZ, Rio de Janeiro, RJ, Brazil; Departamento de Bioquímica, Instituto de Biologia Roberto Alcântara Gomes, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil; Departamento de Microbiologia, Imunologia e Parasitologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil; Fundação Estadual de Produção e Pesquisa em Saúde (FEPPS IPB-LACEN-RS), Porto Alegre, RS, Brazil; Hospital Nossa Senhora da Conceição, Porto Alegre, RS, Brazil


Antimicrobial Agents and Chemotherapy | 2014

First Report of NDM-1-Producing Acinetobacter baumannii Sequence Type 25 in Brazil

Marcelo Pillonetto; Lavinia N. Arend; Eliana Carolina Vespero; Marsileni Pelisson; Thiago Pavoni Gomes Chagas; Ana Paula D'Alincourt Carvalho-Assef; Marise Dutra Asensi

ABSTRACT New Delhi metallo-β-lactamase 1 (NDM-1) was first identified in Brazil in Enterobacter hormaechei and Providencia rettgeri in 2013. Here, we describe the first case of NDM-1-producing Acinetobacter baumannii sequence type 25 isolated from the urinary tract of a 71-year-old man who died of multiple complications, including A. baumannii infection. The NDM-1 gene was detected by quantitative PCR, and its sequence confirmed its presence in an ∼100-kb plasmid.


Brazilian Journal of Infectious Diseases | 2011

Diversity of genotypes in CTX-M-producing Klebsiella pneumoniae isolated in different hospitals in Brazil.

Thiago Pavoni Gomes Chagas; R. M. Alves; Deyse Christina Vallim; Liliane Miyuki Seki; Leila Carvalho Campos; Marise Dutra Asensi

OBJECTIVE The present study was undertaken to characterize CTX-M ESBL-producing Klebsiella pneumoniae collected from hospitals in different cities of Brazil. MATERIAL AND METHODS Eighty-five K. pneumoniae strains isolated from hospitalized patients in six different hospitals of three cities of Brazil were analyzed. ESBL production was confirmed by the standard double-disk synergy test and the Etest®. The MIC50 and MIC90 for ESBL-producing isolates were determined by the Etest® method. The antimicrobial susceptibilities of bacterial isolates were determined using the agar diffusion method according to the CLSI. Screening for blaTEM, blaSHV, blaCTX-M genes and class 1 integron was performed by PCR amplification. To determine the genomic diversity of CTX-M-producers, isolates were analyzed by macrorestriction profile analysis following PFGE. RESULTS AND DISCUSSION Seventy-one K. pneumoniae isolates were ESBL-producing. PCR and sequencing experiments detected 38 CTX-M-producing K. pneumoniae belonged to groups CTX-M 1, CTX-M 2, CTX-M 8 and CTX-M 9. The association of different types ESBL (CTX-M, SHV and TEM) was frequent. All K. pneumoniae isolates carried class 1 integron. PFGE analysis revealed thirty-one clonal types among CTX-M-producing isolates. The data presented herein illustrate the diversity of genotypes of CTX-M producing K. pneumoniae among Brazilians hospitals.


Brazilian Journal of Infectious Diseases | 2015

Spread of multidrug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa clones in patients with ventilator-associated pneumonia in an adult intensive care unit at a university hospital

Sabrina Royer; Ana Luiza Souza Faria; Liliane Miyuki Seki; Thiago Pavoni Gomes Chagas; Paola Amaral de Campos; Deivid William da Fonseca Batistão; Marise Dutra Asensi; Paulo Pinto Gontijo Filho; Rosineide Marques Ribas

BACKGROUND In Brazil, ventilator-associated pneumonia (VAP) caused by carbapenem resistant Acinetobacter baumannii and Pseudomonas aeruginosa isolates are associated with significant mortality, morbidity and costs. Studies on the clonal relatedness of these isolates could lay the foundation for effective infection prevention and control programs. OBJECTIVES We sought to study the epidemiological and molecular characteristics of A. baumannii vs. P. aeruginosa VAP in an adult intensive care unit (ICU). METHODS It was conducted a cohort study of patients with VAP caused by carbapenem resistant A. baumannii and P. aeruginosa during 14 months in an adult ICU. Genomic studies were used to investigate the clonal relatedness of carbapenem resistant OXA-23-producing A. baumannii and P. aeruginosa clinical isolates. The risk factors for acquisition of VAP were also evaluated. Clinical isolates were collected for analysis as were samples from the environment and were typed using pulsed field gel electrophoresis. RESULTS Multivariate logistic regression analysis identified trauma diagnosed at admission and inappropriate antimicrobial therapy as independent variables associated with the development of A. baumannii VAP and hemodialysis as independent variable associated with P. aeruginosa VAP. All carbapenem resistant clinical and environmental isolates of A. baumannii were OXA-23 producers. No MBL-producer P. aeruginosa was detected. Molecular typing revealed a polyclonal pattern; however, clone A (clinical) and H (surface) were the most frequent among isolates of A. baumannii tested, with a greater pattern of resistance than other isolates. In P. aeruginosa the most frequent clone I was multi-sensitive. CONCLUSION These findings suggest the requirement of constant monitoring of these microorganisms in order to control the spread of these clones in the hospital environment.


Diagnostic Microbiology and Infectious Disease | 2017

Carbapenem-resistant Acinetobacter pittii strain harboring blaOXA-72 from Brazil

Thiago Pavoni Gomes Chagas; Thamirys Rachel Tavares e Oliveira; Ana Paula D'Alincourt Carvalho-Assef; Rodolpho M. Albano; Marise Dutra Asensi

In this study, we report the isolation of OXA-72-producing Acinetobacter pittii in Brazil. A carbapenem-resistant A. pittii strain was recovered from a hospitalized female patient from Espírito Santo, Southeastern Brazil. PCR screening and DNA sequencing allowed us to identify the presence of blaOXA-72. We observed blaOXA-72 in a ~11kb plasmid and flanked by XerC/XerD-binding sites.


Antimicrobial Agents and Chemotherapy | 2017

Multiclonal Expansion of Klebsiella pneumoniae Isolates Producing NDM-1 in Rio de Janeiro, Brazil

Caio Augusto Martins Aires; Polyana Silva Pereira; Carlos Felipe Machado de Araujo; Thiago Pavoni Gomes Chagas; Jane Cleide Ribeiro Oliveira; Sibelle Nogueira Buonora; Rodolpho M. Albano; Ana Paula D'Alincourt Carvalho-Assef; Marise Dutra Asensi

ABSTRACT We characterized NDM-1-producing Klebsiella isolates from Rio de Janeiro, Brazil. PCR was applied for resistance and virulence determinants. The genetic context of blaNDM was determined by S1 nuclease pulsed-field gel electrophoresis (PFGE) and hybridization. Genotyping was performed by PFGE and multilocus sequence typing (MLST). Most isolates carried multiple resistance genes and remained susceptible to amikacin, fosfomycin-trometamol, polymyxin B, and tigecycline. The spread of NDM-1-producing Klebsiella pneumoniae was not associated with clonal expansion and appears to be associated with Tn3000.


Journal of global antimicrobial resistance | 2015

Detection of an NDM-1-producing Acinetobacter bereziniae strain in Brazil

Thiago Pavoni Gomes Chagas; Ana Paula D’Alincourt Carvalho-Assef; Caio Augusto Martins Aires; Rita Bertocini; Marise Dutra Asensi

This work was supported by Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ) and Oswaldo Cruz Institute (PAPES-FIOCRUZ).


Memorias Do Instituto Oswaldo Cruz | 2015

Draft genome sequence of a multidrug-resistant Acinetobacter baumannii ST15 (CC15) isolated from Brazil

Thiago Pavoni Gomes Chagas; Melise Chaves Silveira; Rodolpho M. Albano; Ana Paula D’Alincourt Carvalho-Assef; Marise Dutra Asensi

Acinetobacter baumannii is an important pathogen frequently associated with nosocomial outbreaks around the world. In Brazil, A. baumannii has become particularly problematic because of its prevalence and the carbapenems resistance. Here, we report the draft genome sequence of a multidrug-resistant A. baumannii (ST15/CC15) isolated in 2009 from the state of Espírito Santo (Southeast Brazil). We observed important resistance determinant genes in an estimated genome size of 4,102,788 bp with 3,862 predicted coding regions. A detailed report of the genomic data analysis might help to understand the specific features of highly successful strains belonged to a relevant complex clonal in different Brazilian geographical regions.

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Rodolpho M. Albano

Rio de Janeiro State University

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Liliane Miyuki Seki

Universidade Federal Rural do Rio de Janeiro

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Ana Luiza Souza Faria

Federal University of Uberlandia

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