Maryoris Elisa Soto Lopez

Dr. Maryoris Elisa Soto Lopez

University of Córdoba, Montería, Córdoba, Colombia
orcid

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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1 September 2015 in LWT
Verified
Journal Article
Closed access
DGDelaine Meireles Gouvêa
Delaine Meireles Gouvêa
RMRegina Célia Santos Mendonça
Regina Célia Santos Mendonça
Maryoris Elisa Soto LopezMaryoris Elisa Soto Lopez
Maryoris Elisa Soto Lopez
RCRenato Souza Cruz
Renato Souza Cruz

1 April 2016 in LWT
Verified
Journal Article
Closed access
DGDelaine Meireles Gouvêa
Delaine Meireles Gouvêa
RMRegina Célia Santos Mendonça
Regina Célia Santos Mendonça
Maryoris Elisa Soto LopezMaryoris Elisa Soto Lopez
Maryoris Elisa Soto Lopez
LBLaís Silva Batalha
Laís Silva Batalha

1 October 2017 in Colloids and Surfaces B: Biointerfaces
Verified
Journal Article
Closed access
DBDelaine M.G. Boggione
Delaine M.G. Boggione
LBLaís S. Batalha
Laís S. Batalha
Marco Tulio Pardini GontijoMarco Tulio Pardini Gontijo
Marco Tulio Pardini Gontijo
Maryoris Elisa Soto LopezMaryoris Elisa Soto Lopez
Maryoris Elisa Soto Lopez
ATAlvaro Vianna Novaes de Carvalho Teixeira
Alvaro Vianna Novaes de Carvalho Teixeira
RMRegina C.S. Mendonça
Regina C.S. Mendonça

1 March 2021 in Research in Microbiology
Verified
Journal Article
Closed access
Marco Tulio Pardini GontijoMarco Tulio Pardini Gontijo
Marco Tulio Pardini Gontijo
Pedro Marcus Pereira VidigalPedro Marcus Pereira Vidigal
Pedro Marcus Pereira Vidigal
Maryoris Elisa Soto LopezMaryoris Elisa Soto Lopez
Maryoris Elisa Soto Lopez
MBMarcelo Brocchi
Marcelo Brocchi

14 April 2025 in Viruses
Verified
Journal Article
Open access
PDF file
Maryoris Elisa Soto LopezMaryoris Elisa Soto Lopez
Maryoris Elisa Soto Lopez
FMFernando ALONSO MENDOZA Mendoza-Corvis
Fernando ALONSO MENDOZA Mendoza-Corvis
JSJose Jorge Salgado
Jose Jorge Salgado
AAAna Maria Hernandez Arteaga
Ana Maria Hernandez Arteaga
VGVíctor Javier González
Víctor Javier González
OSOmar Andrés Pérez Sierra
Omar Andrés Pérez Sierra
Food contamination by pathogenic and spoilage bacteria causes approximately 47 million cases of foodborne diseases in the United States and leads to tons of food spoilage, worsening the food loss situation worldwide. In addition, conventional preservation treatments implemented in the food industry decrease food’s nutritional and organoleptic quality. Therefore, there is a need for new alternatives to counteract food contamination without altering its characteristics. Endolysins are a promising strategy due to their unique properties, such as host specificity, synergism with other antibacterial agents, mode of action, and low probability of resistance development. These characteristics differentiate them from other antibacterial agents used in the food industry. Endolysins are enzymes produced by bacteriophages during the process of bacterial infection and lysis. This review describes the advances related to endolysin application systems in food, considering their potential for food safety and an overview of the application conditions according to the type of food and bacteria to be controlled. We also highlight the need for new studies on endolysin encapsulation and prolongation of the action time in cases of outbreaks that allow obtaining key information to improve the application of endolysins in different food matrices during food processing and storage

17 March 2022 in Viruses
Verified
Journal Article
Open access
PDF file
HHHUMBERTO MOREIRA HUNGARO
HUMBERTO MOREIRA HUNGARO
Pedro Marcus Pereira VidigalPedro Marcus Pereira Vidigal
Pedro Marcus Pereira Vidigal
ENEdilane Cristina Do Nascimento
Edilane Cristina Do Nascimento
FOFelipe Gomes da Costa Oliveira
Felipe Gomes da Costa Oliveira
Marco Tulio Pardini GontijoMarco Tulio Pardini Gontijo
Marco Tulio Pardini Gontijo
Maryoris Elisa Soto LopezMaryoris Elisa Soto Lopez
Maryoris Elisa Soto Lopez
In this study, we have presented the genomic characterisation of UFJF_PfDIW6, a novel lytic Pseudomonas fluorescens-phage with potential for biocontrol in the dairy industry. This phage showed a short linear double-stranded DNA genome (~42 kb) with a GC content of 58.3% and more than 50% of the genes encoding proteins with unknown functions. Nevertheless, UFJF_PfDIW6’s genome was organised into five functional modules: DNA packaging, structural proteins, DNA metabolism, lysogenic, and host lysis. Comparative genome analysis revealed that the UFJF_PfDIW6’s genome is distinct from other viral genomes available at NCBI databases, displaying maximum coverages of 5% among all alignments. Curiously, this phage showed higher sequence coverages (38–49%) when aligned with uncharacterised prophages integrated into Pseudomonas genomes. Phages compared in this study share conserved locally collinear blocks comprising genes of the modules’ DNA packing and structural proteins but were primarily differentiated by the composition of the DNA metabolism and lysogeny modules. Strategies for taxonomy assignment showed that UFJF_PfDIW6 was clustered into an unclassified genus in the Podoviridae clade. Therefore, our findings indicate that this phage could represent a novel genus belonging to the Podoviridae family.