4.7 Article

Pre-epidemic evolution of the MRSA USA300 clade and a molecular key for classification

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2023.1081070

Keywords

USA300; SNPs; phylogenetic; epidemics; molecular key

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USA300 has been the dominant MRSA clone in the United States and Northern South America for over 20 years. This study utilizes sequencing data and newly sequenced isolates to investigate the pre-epidemic evolution of USA300. The results confirm the divergence of NAE and SAE lineages around 1970 and identify independent acquisition events of ACME and COMER loci. The study also reveals a new USA300 clade (PEB1) that predates the establishment of South and North American epidemics.
IntroductionUSA300 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. MethodsHere, 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. ResultsPhylogenetic 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.

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