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Shared antibiotic resistance and virulence genes in Staphylococcus aureus from diverse animal hosts

The emergence of methicillin-resistant Staphylococcus aureus (MRSA) poses an important threat in human and animal health. In this study, we ask whether resistance and virulence genes in S. aureus are homogeneously distributed or constrained by different animal hosts. We carried out whole genome sequ...

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Autores principales: Bruce, Spencer A., Smith, Joshua T., Mydosh, Jennifer L., Ball, John, Needle, David B., Gibson, Robert, Andam, Cheryl P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924228/
https://www.ncbi.nlm.nih.gov/pubmed/35292708
http://dx.doi.org/10.1038/s41598-022-08230-z
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author Bruce, Spencer A.
Smith, Joshua T.
Mydosh, Jennifer L.
Ball, John
Needle, David B.
Gibson, Robert
Andam, Cheryl P.
author_facet Bruce, Spencer A.
Smith, Joshua T.
Mydosh, Jennifer L.
Ball, John
Needle, David B.
Gibson, Robert
Andam, Cheryl P.
author_sort Bruce, Spencer A.
collection PubMed
description The emergence of methicillin-resistant Staphylococcus aureus (MRSA) poses an important threat in human and animal health. In this study, we ask whether resistance and virulence genes in S. aureus are homogeneously distributed or constrained by different animal hosts. We carried out whole genome sequencing of 114 S. aureus isolates from ten species of animals sampled from four New England states (USA) in 2017–2019. The majority of the isolates came from cats, cows and dogs. The maximum likelihood phylogenetic tree based on the alignment of 89,143 single nucleotide polymorphisms of 1173 core genes reveal 31 sequence types (STs). The most common STs were ST5, ST8, ST30, ST133 and ST2187. Every genome carried at least eight acquired resistance genes. Genes related to resistance found in all genomes included norA (fluoroquinolone), arlRS (fluoroquinolone), lmrS (multidrug), tet(38) (tetracycline) and mepAR (multidrug and tigecycline resistance). The most common superantigen genes were tsst-1, sea and sec. Acquired antibiotic resistance (n = 10) and superantigen (n = 9) genes of S. aureus were widely shared between S. aureus lineages and between strains from different animal hosts. These analyses provide insights for considering bacterial gene sharing when developing strategies to combat the emergence of high-risk clones in animals.
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spelling pubmed-89242282022-03-17 Shared antibiotic resistance and virulence genes in Staphylococcus aureus from diverse animal hosts Bruce, Spencer A. Smith, Joshua T. Mydosh, Jennifer L. Ball, John Needle, David B. Gibson, Robert Andam, Cheryl P. Sci Rep Article The emergence of methicillin-resistant Staphylococcus aureus (MRSA) poses an important threat in human and animal health. In this study, we ask whether resistance and virulence genes in S. aureus are homogeneously distributed or constrained by different animal hosts. We carried out whole genome sequencing of 114 S. aureus isolates from ten species of animals sampled from four New England states (USA) in 2017–2019. The majority of the isolates came from cats, cows and dogs. The maximum likelihood phylogenetic tree based on the alignment of 89,143 single nucleotide polymorphisms of 1173 core genes reveal 31 sequence types (STs). The most common STs were ST5, ST8, ST30, ST133 and ST2187. Every genome carried at least eight acquired resistance genes. Genes related to resistance found in all genomes included norA (fluoroquinolone), arlRS (fluoroquinolone), lmrS (multidrug), tet(38) (tetracycline) and mepAR (multidrug and tigecycline resistance). The most common superantigen genes were tsst-1, sea and sec. Acquired antibiotic resistance (n = 10) and superantigen (n = 9) genes of S. aureus were widely shared between S. aureus lineages and between strains from different animal hosts. These analyses provide insights for considering bacterial gene sharing when developing strategies to combat the emergence of high-risk clones in animals. Nature Publishing Group UK 2022-03-15 /pmc/articles/PMC8924228/ /pubmed/35292708 http://dx.doi.org/10.1038/s41598-022-08230-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bruce, Spencer A.
Smith, Joshua T.
Mydosh, Jennifer L.
Ball, John
Needle, David B.
Gibson, Robert
Andam, Cheryl P.
Shared antibiotic resistance and virulence genes in Staphylococcus aureus from diverse animal hosts
title Shared antibiotic resistance and virulence genes in Staphylococcus aureus from diverse animal hosts
title_full Shared antibiotic resistance and virulence genes in Staphylococcus aureus from diverse animal hosts
title_fullStr Shared antibiotic resistance and virulence genes in Staphylococcus aureus from diverse animal hosts
title_full_unstemmed Shared antibiotic resistance and virulence genes in Staphylococcus aureus from diverse animal hosts
title_short Shared antibiotic resistance and virulence genes in Staphylococcus aureus from diverse animal hosts
title_sort shared antibiotic resistance and virulence genes in staphylococcus aureus from diverse animal hosts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924228/
https://www.ncbi.nlm.nih.gov/pubmed/35292708
http://dx.doi.org/10.1038/s41598-022-08230-z
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