Daniel F. M. Monte

Dr. Daniel F. M. Monte

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Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

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

Representative Publications

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28 April 2016 in Eurosurveillance
Verified
Journal Article
Open access
Miriam R. FernandesMiriam R. Fernandes
Miriam R. Fernandes
QMQuezia Moura
Quezia Moura
LSLuciana Sartori
Luciana Sartori
KSKetrin C Silva
Ketrin C Silva
MCMarcos Pv Cunha
Marcos Pv Cunha
NLNilton Lincopan
Nilton Lincopan
During a Brazilian multicentric antimicrobial resistance surveillance study, colistin resistance was investigated in 4,620 Enterobacteriaceae isolated from human, animal, food and environmental samples collected from 2000 to 2016. We present evidence that mcr-1-positive Escherichia coli has been emerging in South America since at least 2012, supporting a previous report on the possible acquisition of mcr-1-harbouring E. coli by European travellers visiting Latin American countries.

1 May 2017 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Closed access
PDF file
DMDaniel F. M. Monte
Daniel F. M. Monte
AMAndressa Mem
Andressa Mem
Miriam R. FernandesMiriam R. Fernandes
Miriam R. Fernandes
LCLouise Teixeira Cerdeira
Louise Teixeira Cerdeira
FEFernanda Esposito
Fernanda Esposito
MLMariza Landgraf
Mariza Landgraf
The detection and rapid spread of colistin-resistant Enterobacteriaceae carrying the mcr-1 gene has created an urgent need to strengthen surveillance. In this study, eight clonally unrelated colistin-resistant Escherichia coli isolates carrying mcr-1 and bla CTX-M or bla CMY-2 genes were isolated from commercial chicken meat in Brazil. Most E. coli strains carried IncX4 plasmids, previously identified in human and animal isolates. These results highlight a new reservoir of mcr-1 -harboring E. coli strains in South America.

30 July 2019 in Scientific Reports
Verified
Journal Article
Open access
PDF file
DMDaniel F. M. Monte
Daniel F. M. Monte
NLNilton Lincopan
Nilton Lincopan
HBHanna Berman
Hanna Berman
LCLouise Teixeira Cerdeira
Louise Teixeira Cerdeira
SKShivaramu Keelara
Shivaramu Keelara
MLMariza Landgraf
Mariza Landgraf
Multidrug-resistant (MDR) Salmonella enterica has been deemed a high-priority pathogen by the World Health Organization. Two hundred and sixty-four Salmonella enterica isolates recovered over a 16-year period (2000 to 2016) from the poultry and swine production chains, in Brazil, were investigated by whole-genome sequencing (WGS). Most international lineages belonging to 28 serovars, including, S. enterica serovars S. Schwarzengrund ST96, S. Typhimurium ST19, S. Minnesota ST548, S. Infantis ST32, S. Heidelberg ST15, S. Newport ST45, S. Brandenburg ST65 and S. Kentucky ST198 displayed MDR and virulent genetic backgrounds. In this regard, resistome analysis revealed presence of qnrE1 (identified for the first time in S. Typhimurium from food chain), qnrB19, qnrS1, blaCTX-M-8, blaCTX-M-2 and blaCMY-2 genes, as well as gyrA mutations; whereas ColpVC, IncHI2A, IncHI2, IncFIA, Incl1, IncA/C2, IncR, IncX1 and po111 plasmids were detected. In addition, phylogenetic analysis revealed multiple independent lineages such as S. enterica serovars S. Infantis, S. Schwarzengrund, S. Minnesota, S. Kentucky and S. Brandenburg. In brief, ocurrence and persistence of international lineages of S. enterica serovars in food production chain is supported by conserved genomes and wide virulome and resistome.

2 April 2020 in Transboundary and Emerging Diseases
Verified
Journal Article
Open access
PDF file
MCMarcelo P. N. Carvalho
Marcelo P. N. Carvalho
Miriam R. FernandesMiriam R. Fernandes
Miriam R. Fernandes
Fábio SelleraFábio Sellera
Fábio Sellera
RLRalf Lopes
Ralf Lopes
DMDaniel F. M. Monte
Daniel F. M. Monte
NLNilton Lincopan
Nilton Lincopan
CTX‐M‐type extended‐spectrum β‐lactamase (ESBL)‐producing Escherichia coli clones have been increasingly reported worldwide. In this regard, although discussions of transmission routes of these bacteria are in evidence, molecular data are lacking to elucidate the epidemiological impacts of ESBL producers in wild animals. In this study, we have screened 90 wild animals living in a surrounding area of São Paulo, the largest metropolitan city in South America, to monitor the presence of multidrug‐resistant (MDR) Gram‐negative bacteria. Using a genomic approach, we have analyzed eight ceftriaxone‐resistant E. coli. Resistome analyses revealed that all E. coli strains carried blaCTX‐M‐type genes, prevalent in human infections, besides other clinically relevant resistance genes to aminoglycosides, β‐lactams, phenicols, tetracyclines, sulfonamides, trimethoprim, fosfomycin, and quinolones. Additionally, E. coli strains belonged to international sequence types (STs) ST38, ST58, ST212, ST744, ST1158 and ST1251, and carried several virulence‐associated genes. Our findings suggest spread and adaptation of international clones of CTX‐M‐producing E. coli beyond urban settings, including wildlife from shared environments.

1 April 2019 in Current Opinion in Food Science
Verified
Journal Article
Closed access
DMDaniel F. M. Monte
Daniel F. M. Monte
NLNilton Lincopan
Nilton Lincopan
PCPaula J. Fedorka Cary
Paula J. Fedorka Cary
MLMariza Landgraf
Mariza Landgraf

30 October 2020 in PLOS ONE
Verified
Journal Article
Open access
PDF file
DMDaniel F. M. Monte
Daniel F. M. Monte
Fábio SelleraFábio Sellera
Fábio Sellera
RLRalf Lopes
Ralf Lopes
SKShivaramu Keelara
Shivaramu Keelara
MLMariza Landgraf
Mariza Landgraf
STSiddhartha Thakur
Siddhartha Thakur
International lineages, such as Salmonella Typhimurium sequence type (ST) 19, are most often associated with foodborne diseases and deaths in humans. In this study, we compared the whole-genome sequences of five S. Typhimurium strains belonging to ST19 recovered from clinical human stool samples in North Carolina, United States. Overall, S. Typhimurium strains displayed multidrug-resistant profile, being resistance to critically and highly important antimicrobials including ampicillin, ticarcillin/clavulanic acid, streptomycin and sulfisoxazole, chloramphenicol, tetracycline, respectively. Interestingly, all S. Typhimurium strains carried class 1 integron (intl1) and we were able to describe two genomic regions surrounding blaCARB-2 gene, size 4,062 bp and 4,422 bp for S. Typhimurium strains (HS5344, HS5437, and HS5478) and (HS5302 and HS5368), respectively. Genomic analysis for antimicrobial resistome confirmed the presence of clinically important genes, including blaCARB-2, aac(6’)-Iaa, aadA2b, sul1, tetG, floR, and biocide resistance genes (qacEΔ1). S. Typhimurium strains harbored IncFIB plasmid containing spvRABCD operon, as well as rck and pef virulence genes, which constitute an important apparatus for spreading the virulence plasmid. In addition, we identified several virulence genes, chromosomally located, while the phylogenetic analysis revealed clonal relatedness among these strains with S. enterica isolated from human and non-human sources obtained in European and Asian countries. Our results provide new insights into this unusual class 1 integron in virulent S. Typhimurium strains that harbors a pool of genes acting as potential hotspots for horizontal gene transfer providing readily adaptation to new surrounds, as well as being crucially required for virulence in vivo. Therefore, continuous genomic surveillance is an important tool for safeguarding human health.