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Genomic and phenotypic characterization of Salmonella enterica serovar Kentucky

Non-typhoidal Salmonella are extremely diverse and different serovars can exhibit varied phenotypes, including host adaptation and the ability to cause clinical illness in animals and humans. In the USA, Salmonella enterica serovar Kentucky is infrequently found to cause human illness, despite being...

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Autores principales: Richards, Amber K., Kue, Song, Norris, Connor G., Shariat, Nikki W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569734/
https://www.ncbi.nlm.nih.gov/pubmed/37750759
http://dx.doi.org/10.1099/mgen.0.001089
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author Richards, Amber K.
Kue, Song
Norris, Connor G.
Shariat, Nikki W.
author_facet Richards, Amber K.
Kue, Song
Norris, Connor G.
Shariat, Nikki W.
author_sort Richards, Amber K.
collection PubMed
description Non-typhoidal Salmonella are extremely diverse and different serovars can exhibit varied phenotypes, including host adaptation and the ability to cause clinical illness in animals and humans. In the USA, Salmonella enterica serovar Kentucky is infrequently found to cause human illness, despite being the top serovar isolated from broiler chickens. Conversely, in Europe, this serovar falls in the top 10 serovars linked to human salmonellosis. Serovar Kentucky is polyphyletic and has two lineages, Kentucky-I and Kentucky-II; isolates belonging to Kentucky-I are frequently isolated from poultry in the USA, while Kentucky-II isolates tend to be associated with human illness. In this study, we analysed whole-genome sequences and associated metadata deposited in public databases between 2017 and 2021 by federal agencies to determine serovar Kentucky incidence across different animal and human sources. Of 5151 genomes, 90.3 % were from isolates that came from broilers, while 5.9 % were from humans and 3.0 % were from cattle. Kentucky-I isolates were associated with broilers, while isolates belonging to Kentucky-II and a new lineage, Kentucky-III, were more commonly associated with cattle and humans. Very few serovar Kentucky isolates were associated with turkey and swine sources. Phylogenetic analyses showed that Kentucky-III genomes were more closely related to Kentucky-I, and this was confirmed by CRISPR-typing and multilocus sequence typing (MLST). In a macrophage assay, serovar Kentucky-II isolates were able to replicate over eight times better than Kentucky-I isolates. Analysis of virulence factors showed unique patterns across these three groups, and these differences may be linked to their association with different hosts.
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spelling pubmed-105697342023-10-13 Genomic and phenotypic characterization of Salmonella enterica serovar Kentucky Richards, Amber K. Kue, Song Norris, Connor G. Shariat, Nikki W. Microb Genom Research Articles Non-typhoidal Salmonella are extremely diverse and different serovars can exhibit varied phenotypes, including host adaptation and the ability to cause clinical illness in animals and humans. In the USA, Salmonella enterica serovar Kentucky is infrequently found to cause human illness, despite being the top serovar isolated from broiler chickens. Conversely, in Europe, this serovar falls in the top 10 serovars linked to human salmonellosis. Serovar Kentucky is polyphyletic and has two lineages, Kentucky-I and Kentucky-II; isolates belonging to Kentucky-I are frequently isolated from poultry in the USA, while Kentucky-II isolates tend to be associated with human illness. In this study, we analysed whole-genome sequences and associated metadata deposited in public databases between 2017 and 2021 by federal agencies to determine serovar Kentucky incidence across different animal and human sources. Of 5151 genomes, 90.3 % were from isolates that came from broilers, while 5.9 % were from humans and 3.0 % were from cattle. Kentucky-I isolates were associated with broilers, while isolates belonging to Kentucky-II and a new lineage, Kentucky-III, were more commonly associated with cattle and humans. Very few serovar Kentucky isolates were associated with turkey and swine sources. Phylogenetic analyses showed that Kentucky-III genomes were more closely related to Kentucky-I, and this was confirmed by CRISPR-typing and multilocus sequence typing (MLST). In a macrophage assay, serovar Kentucky-II isolates were able to replicate over eight times better than Kentucky-I isolates. Analysis of virulence factors showed unique patterns across these three groups, and these differences may be linked to their association with different hosts. Microbiology Society 2023-09-26 /pmc/articles/PMC10569734/ /pubmed/37750759 http://dx.doi.org/10.1099/mgen.0.001089 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License.
spellingShingle Research Articles
Richards, Amber K.
Kue, Song
Norris, Connor G.
Shariat, Nikki W.
Genomic and phenotypic characterization of Salmonella enterica serovar Kentucky
title Genomic and phenotypic characterization of Salmonella enterica serovar Kentucky
title_full Genomic and phenotypic characterization of Salmonella enterica serovar Kentucky
title_fullStr Genomic and phenotypic characterization of Salmonella enterica serovar Kentucky
title_full_unstemmed Genomic and phenotypic characterization of Salmonella enterica serovar Kentucky
title_short Genomic and phenotypic characterization of Salmonella enterica serovar Kentucky
title_sort genomic and phenotypic characterization of salmonella enterica serovar kentucky
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569734/
https://www.ncbi.nlm.nih.gov/pubmed/37750759
http://dx.doi.org/10.1099/mgen.0.001089
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