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Comparative Analysis of <i>Felixounavirus</i> Genomes Including Two New Members of the Genus That Infect <i>Salmonella</i> Infantis
Indexado
WoS WOS:000686143100001
Scopus SCOPUS_ID:85110332858
DOI 10.3390/ANTIBIOTICS10070806
Año 2021
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Salmonella spp. is one of the most common foodborne pathogens worldwide; therefore, its control is highly relevant for the food industry. Phages of the Felixounavirus genus have the characteristic that one phage can infect a large number of different Salmonella serovars and, thus, are proposed as an alternative to antimicrobials in food production. Here, we describe two new members of the Felixounavirus genus named vB_Si_35FD and vB_Si_DR94, which can infect Salmonella Infantis. These new members were isolated and sequenced, and a subsequent comparative genomic analysis was conducted including 23 publicly available genomes of Felixounaviruses that infect Salmonella. The genomes of vB_Si_35FD and vB_Si_DR94 are 85,818 and 85,730 bp large and contain 129 and 125 coding sequences, respectively. The genomes did not show genes associated with virulence or antimicrobial resistance, which could be useful for candidates to use as biocontrol agents. Comparative genomics revealed that closely related Felixounavirus are found in distinct geographical locations and that this genus has a conserved genomic structure despite its worldwide distribution. Our study revealed a highly conserved structure of the phage genomes, and the two newly described phages could represent promising biocontrol candidates against Salmonella spp. from a genomic viewpoint.

Revista



Revista ISSN
Antibiotics 2079-6382

Métricas Externas



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Disciplinas de Investigación



WOS
Infectious Diseases
Pharmacology & Pharmacy
Scopus
Infectious Diseases
Biochemistry
Pharmacology (Medical)
Microbiology
Pharmacology, Toxicology And Pharmaceutics (All)
Microbiology (Medical)
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Barron-Montenegro, Rocío Mujer Universidad de Concepción - Chile
Pontificia Universidad Católica de Chile - Chile
Millennium Initiat Collaborat Res Bacterial Resis - Chile
Facultad de Medicina - Chile
Núcleo Milenio para la Investigación Colaborativa en Resistencia Antimicrobiana - Chile
2 Garcia, Rodrigo Hombre Pontificia Universidad Católica de Valparaíso - Chile
EMORY UNIV - Estados Unidos
Emory University - Estados Unidos
3 DUENAS-CAPELLI, FERNANDO ANDRES Hombre Universidad Nacional Andrés Bello - Chile
4 Rivera, D. - Millennium Initiat Collaborat Res Bacterial Resis - Chile
Universidad Nacional Andrés Bello - Chile
Núcleo Milenio para la Investigación Colaborativa en Resistencia Antimicrobiana - Chile
5 OPAZO-CAPURRO, ANDRES FELIPE Hombre Universidad de Concepción - Chile
Millennium Initiat Collaborat Res Bacterial Resis - Chile
Núcleo Milenio para la Investigación Colaborativa en Resistencia Antimicrobiana - Chile
6 Erickson, Stephen Hombre Lab Corp America Holdings - Estados Unidos
Laboratory Corporation of America Holdings - Estados Unidos
7 MORENO-SWITT, ANDREA, I Mujer Pontificia Universidad Católica de Chile - Chile
Millennium Initiat Collaborat Res Bacterial Resis - Chile
Facultad de Medicina - Chile
Núcleo Milenio para la Investigación Colaborativa en Resistencia Antimicrobiana - Chile

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Financiamiento



Fuente
Comisión Nacional de Investigación Científica y Tecnológica
Biotechnology and Biological Sciences Research Council
BBSRC
ANID Fondecyt
ANID Millennium Science Initiative/Millennium Initiative for Collaborative Research on Bacterial Resistance
CONICYT FECHA DOCTORADO/2016

Muestra la fuente de financiamiento declarada en la publicación.

Agradecimientos



Agradecimiento
We acknowledge the funding sources: 1 [ANID FONDECYT 1181167 to AIM-S], 2 [ANID Millennium Science Initiative/Millennium Initiative for Collaborative Research on Bacterial Resistance NCN17_081 to AIMS]. Genome sequencing was provided by MicrobesNG (http://www.microbesng.uk, accessed on 1 September 2017), which is supported by the BBSRC (BB/L024209/1). Rodrigo Garcia thanks CONICYT FECHA DOCTORADO/2016 21161133.
We acknowledge the funding sources: 1 [ANID FONDECYT 1181167 to AIM-S], 2 [ANID Millennium Science Initiative/Millennium Initiative for Collaborative Research on Bacterial Resistance NCN17_081 to AIMS]. Genome sequencing was provided by MicrobesNG (http://www. microbesng.uk, accessed on 1 September 2017), which is supported by the BBSRC (BB/L024209/1). Rodrigo García thanks CONICYT FECHA DOCTORADO/2016 21161133.
Funding: We acknowledge the funding sources: 1 [ANID FONDECYT 1181167 to AIM-S], 2 [ANID Millennium Science Initiative/Millennium Initiative for Collaborative Research on Bacterial Resistance NCN17_081 to AIMS]. Genome sequencing was provided by MicrobesNG (http://www. microbesng.uk, accessed on 1 September 2017), which is supported by the BBSRC (BB/L024209/1). Rodrigo García thanks CONICYT FECHA DOCTORADO/2016 21161133.

Muestra la fuente de financiamiento declarada en la publicación.