# Population genomic variation in Staphylococcus aureus isolates from carriage and disease in Indigenous communities in the Southwest United States

**Authors:** Eleonora Cella, Catherine G. Sutcliffe, Del Yazzie, Annaliesa S. Anderson, Lubomira Andrew, Ladonna Becenti, George Brasinikas, Loretta Christensen, Wanda Cowboy, Sheri L. Dixon, Lindsay R. Grant, Li Hao, Robin Hubler, Hal Jones, Pierrette Montanez, Dennie Parker, Urvi Rajyaguru, Amy Rice, Eugene Romancito, Charis Salabye, Valerie L. Tenequer, Polly Thompson, Minnie Tsingine, Carol Tso, Dan VanDeRiet, Laura L. Hammitt, Taj Azarian

PMC · DOI: 10.1099/mgen.0.001666 · Microbial Genomics · 2026-03-23

## TL;DR

This study explores why Indigenous communities in the Southwest US face higher rates of Staphylococcus aureus infections by analyzing genomic data from bacterial isolates.

## Contribution

The study identifies specific S. aureus lineages associated with invasive disease in Indigenous communities, revealing geographic differences in bacterial population structure.

## Key findings

- Methicillin-resistant S. aureus accounted for 33.4% of invasive infections in the studied Indigenous communities.
- Lineages ST8 and ST97 were significantly enriched in invasive disease compared to carriage isolates.
- Invasive disease in Indigenous communities showed higher frequencies of ST8, ST97, and ST188 compared to New Hampshire isolates.

## Abstract

Indigenous populations in the USA experience disproportionately high rates of Staphylococcus aureus invasive disease, yet the drivers of this disparity remain unclear. To investigate the role of bacterial population structure, we conducted whole-genome sequencing of 589 invasive S. aureus isolates and 125 carriage isolates collected from the Navajo Nation and White Mountain Apache (N/WMA) tribal lands in the Southwest USA. We compared lineage distribution between invasive disease and carriage, and to a contemporaneous set of bloodstream isolates from New Hampshire (NH) (n=377), using a Monte Carlo simulation based on the relative frequency ratio (RFR). Methicillin-resistant S. aureus accounted for 33.4% of invasive infections in N/WMA, and the most prevalent lineages were multi-locus sequence types (STs) 8 and 5. ST8 and ST97 were significantly enriched in invasive disease relative to carriage in N/WMA, suggesting increased invasiveness. Compared to NH, invasive disease in N/WMA was associated with higher frequencies of ST8, ST97 and ST188, while ST5 and ST30 were more common in NH. These findings highlight substantial geographic variation in S. aureus population structure and suggest that lineage composition may contribute to the elevated burden of invasive disease in Indigenous communities in the Southwest US. Our study underscores the importance of integrating genomic surveillance with epidemiologic data to inform prevention strategies.

## Linked entities

- **Species:** Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Genes:** msrA [NCBI Gene 17374484], etb [NCBI Gene 17374496], blaZ [NCBI Gene 13874473]
- **Diseases:** bacteraemia (MESH:C531821), N (MESH:C536108), diabetes (MESH:D003920), invasive (MESH:D009361), AMR (MESH:D060467), skin (MESH:D012871), EMRSA-16 (MESH:C567430), skin and soft tissue infections (MESH:D018461), N/WMA disease (MESH:D000532), HACO (MESH:D003428), MRSA (MESH:D013203), CA (MESH:D003147), bacteremia (MESH:D016470), bloodstream infections (MESH:D018805), Diseases (MESH:D004194), obesity (MESH:D009765), deaths (MESH:D003643), pneumonia (MESH:D011014), S. aureus disease (MESH:D000755), EMRSA-15 (MESH:D012559), Infections (MESH:D007239)
- **Chemicals:** EDTA (MESH:D004492), oxacillin (MESH:D010068), tetracycline (MESH:D013752), fluoroquinolone (MESH:D024841), Macrolide (MESH:D018942), JHU (-), Methicillin (MESH:D008712)
- **Species:** Homo sapiens (human, species) [taxon 9606], Staphylococcus aureus (species) [taxon 1280]
- **Mutations:** Ser84 Leu

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13034078/full.md

## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC13034078/full.md

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Source: https://tomesphere.com/paper/PMC13034078