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Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification
INTRODUCTION: USA300 has remained the dominant community and healthcare associated methicillin-resistant Staphylococcus aureus (MRSA) clone in the United States and in northern South America for at least the past 20 years. In this time, it has experienced epidemic spread in both of these locations....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902376/ https://www.ncbi.nlm.nih.gov/pubmed/36761897 http://dx.doi.org/10.3389/fcimb.2023.1081070 |
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author | Bianco, Colleen M. Moustafa, Ahmed M. O’Brien, Kelsey Martin, Michael A. Read, Timothy D. Kreiswirth, Barry N. Planet, Paul J. |
author_facet | Bianco, Colleen M. Moustafa, Ahmed M. O’Brien, Kelsey Martin, Michael A. Read, Timothy D. Kreiswirth, Barry N. Planet, Paul J. |
author_sort | Bianco, Colleen M. |
collection | PubMed |
description | INTRODUCTION: USA300 has remained the dominant community and healthcare associated methicillin-resistant Staphylococcus aureus (MRSA) clone in the United States and in northern South America for at least the past 20 years. In this time, it has experienced epidemic spread in both of these locations. However, its pre-epidemic evolutionary history and origins are incompletely understood. Large sequencing databases, such as NCBI, PATRIC, and Staphopia, contain clues to the early evolution of USA300 in the form of sequenced genomes of USA300 isolates that are representative of lineages that diverged prior to the establishment of the South American epidemic (SAE) clade and North American epidemic (NAE) clade. In addition, historical isolates collected prior to the emergence of epidemics can help reconstruct early events in the history of this lineage. METHODS: Here, we take advantage of the accrued, publicly available data, as well as two newly sequenced pre-epidemic historical isolates from 1996, and a very early diverging ACME-negative NAE genome, to understand the pre-epidemic evolution of USA300. We use database mining techniques to emphasize genomes similar to pre-epidemic isolates, with the goal of reconstructing the early molecular evolution of the USA300 lineage. RESULTS: Phylogenetic analysis with these genomes confirms that the NAE and SAE USA300 lineages diverged from a most recent common ancestor around 1970 with high confidence, and it also pinpoints the independent acquisition events of the of the ACME and COMER loci with greater precision than in previous studies. We provide evidence for a North American origin of the USA300 lineage and identify multiple introductions of USA300 into South and North America. Notably, we describe a third major USA300 clade (the pre-epidemic branching clade; PEB1) consisting of both MSSA and MRSA isolates circulating around the world that diverged from the USA300 lineage prior to the establishment of the South and North American epidemics. We present a detailed analysis of specific sequence characteristics of each of the major clades, and present diagnostic positions that can be used to classify new genomes. |
format | Online Article Text |
id | pubmed-9902376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99023762023-02-08 Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification Bianco, Colleen M. Moustafa, Ahmed M. O’Brien, Kelsey Martin, Michael A. Read, Timothy D. Kreiswirth, Barry N. Planet, Paul J. Front Cell Infect Microbiol Cellular and Infection Microbiology INTRODUCTION: USA300 has remained the dominant community and healthcare associated methicillin-resistant Staphylococcus aureus (MRSA) clone in the United States and in northern South America for at least the past 20 years. In this time, it has experienced epidemic spread in both of these locations. However, its pre-epidemic evolutionary history and origins are incompletely understood. Large sequencing databases, such as NCBI, PATRIC, and Staphopia, contain clues to the early evolution of USA300 in the form of sequenced genomes of USA300 isolates that are representative of lineages that diverged prior to the establishment of the South American epidemic (SAE) clade and North American epidemic (NAE) clade. In addition, historical isolates collected prior to the emergence of epidemics can help reconstruct early events in the history of this lineage. METHODS: Here, we take advantage of the accrued, publicly available data, as well as two newly sequenced pre-epidemic historical isolates from 1996, and a very early diverging ACME-negative NAE genome, to understand the pre-epidemic evolution of USA300. We use database mining techniques to emphasize genomes similar to pre-epidemic isolates, with the goal of reconstructing the early molecular evolution of the USA300 lineage. RESULTS: Phylogenetic analysis with these genomes confirms that the NAE and SAE USA300 lineages diverged from a most recent common ancestor around 1970 with high confidence, and it also pinpoints the independent acquisition events of the of the ACME and COMER loci with greater precision than in previous studies. We provide evidence for a North American origin of the USA300 lineage and identify multiple introductions of USA300 into South and North America. Notably, we describe a third major USA300 clade (the pre-epidemic branching clade; PEB1) consisting of both MSSA and MRSA isolates circulating around the world that diverged from the USA300 lineage prior to the establishment of the South and North American epidemics. We present a detailed analysis of specific sequence characteristics of each of the major clades, and present diagnostic positions that can be used to classify new genomes. Frontiers Media S.A. 2023-01-24 /pmc/articles/PMC9902376/ /pubmed/36761897 http://dx.doi.org/10.3389/fcimb.2023.1081070 Text en Copyright © 2023 Bianco, Moustafa, O’Brien, Martin, Read, Kreiswirth and Planet https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Bianco, Colleen M. Moustafa, Ahmed M. O’Brien, Kelsey Martin, Michael A. Read, Timothy D. Kreiswirth, Barry N. Planet, Paul J. Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification |
title | Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification |
title_full | Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification |
title_fullStr | Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification |
title_full_unstemmed | Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification |
title_short | Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification |
title_sort | pre-epidemic evolution of the mrsa usa300 clade and a molecular key for classification |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902376/ https://www.ncbi.nlm.nih.gov/pubmed/36761897 http://dx.doi.org/10.3389/fcimb.2023.1081070 |
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