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Improved Genomic Prediction of Staphylococcus epidermidis Isolation Sources with a Novel Polygenic Score
K Taylor Hellmann1, Lavanya Challagundla2, Barry M Gray3
1Department of Cell and Molecular Biology, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Abstract:
Staphylococcus epidermidis infections can be challenging to diagnose due to the species frequent contamination of clinical specimens and indolent course of infection. Nevertheless, S. epidermidis is the major cause of late-onset sepsis among premature infants and of intravascular infection in all age groups. Prior work has shown that bacterial virulence factors, antimicrobial resistances, and strains have up to 80% in-sample accuracy to distinguish hospital from community sources, but are unable to distinguish true bacteremia from blood culture contamination. Here, a phylogeny-informed genome-wide association study of 88 isolates was used to estimate effect sizes of particular genomic variants for isolation sources. A "polygenic score" was calculated for each isolate as the summed effect sizes of its repertoire of genomic variants. Predictive models of isolation sources based on polygenic scores were tested with in-samples and out-samples from prior studies of different patient populations. Polygenic scores from accessory genes (AGs) distinguished hospital from community sources with the highest accuracy to date, up to 98% for in-samples and 65% to 91% for various out-samples, whereas scores from single nucleotide polymorphisms (SNPs) had lower accuracy. Scores from AGs and SNPs achieved the highest in-sample accuracy to date, up to 76%, in distinguishing infection from contaminant sources within a hospital. Model training and testing data sets with more similar population structures resulted in more accurate predictions. This study reports the first use of a polygenic score for predicting a complex bacterial phenotype and shows the potential of this approach for enhancing S. epidermidis diagnosis.
Insights
A new polygenic score method accurately distinguishes Staphylococcus epidermidis hospital vs. community sources and infection vs. contamination, improving diagnosis. This approach shows promise for bacterial infection identification.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Staphylococcus epidermidis causes challenging infections, including sepsis in premature infants and intravascular infections.
- Distinguishing true infections from contamination is difficult, impacting diagnosis and treatment.
- Previous methods struggle to differentiate true bacteremia from blood culture contamination.
Purpose of the Study:
- To develop and validate a polygenic score for predicting Staphylococcus epidermidis isolation sources.
- To assess the accuracy of polygenic scores in distinguishing hospital vs. community origins and infection vs. contamination.
- To evaluate the utility of genome-wide association studies in predicting complex bacterial phenotypes.
Main Methods:
- A phylogeny-informed genome-wide association study (GWAS) was conducted on 88 S. epidermidis isolates.
- Polygenic scores were calculated based on the summed effect sizes of genomic variants (accessory genes and SNPs).
- Predictive models were trained and tested using in-sample and out-sample data from diverse patient populations.
Main Results:
- Polygenic scores from accessory genes achieved high accuracy (up to 98% in-sample, 65-91% out-sample) in distinguishing hospital from community sources.
- Scores from accessory genes and SNPs reached 76% in-sample accuracy for differentiating infection from contamination.
- Model accuracy improved with more similar population structures in training and testing datasets.
Conclusions:
- This study introduces the first polygenic score approach for predicting complex bacterial phenotypes in S. epidermidis.
- The polygenic score method demonstrates significant potential for enhancing the diagnosis of S. epidermidis infections.
- Accurate source prediction is crucial for effective clinical management of S. epidermidis.
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