# Doing more with less: Genomic quasi-G-primes differentiate septic from healthy patients

**Authors:** Congzhou M. Sha, Michail Patsakis, Ioannis Mouratidis, Xiaoyuan Wei, Taejung Chung, Jasna Kovac, Ilias Georgakopoulos-Soares

PMC · DOI: 10.1371/journal.pone.0341828 · PLOS One · 2026-02-06

## TL;DR

This paper introduces genomic quasi-G-primes to quickly and efficiently distinguish septic from healthy patients using DNA sequencing.

## Contribution

The novel concept of genomic quasi-G-primes enables efficient and accurate differentiation of sepsis from healthy states.

## Key findings

- Genomic quasi-G-primes were validated in controlled Staphylococcus aureus sequencing experiments.
- The method outperforms existing taxonomic classification approaches in distinguishing septic from healthy patients.
- The approach is space-efficient and suitable for modest hardware.

## Abstract

Sepsis is a life-threatening state of disseminated infection, and treatment requires knowledge of the organism responsible. The gold standard for sepsis diagnosis is blood culture, which requires days of growth. Next-generation sequencing has been proposed as an alternative; however, existing methods may lack sensitivity. In this work, we explore the idea of genomic quasi-G-primes, which are short DNA sequences specific to a single species within a group of relevant species. We first validated the genomic quasi-G-prime classification in controlled Staphylococcus aureus sequencing experiments, and then applied the same approach to blood-derived sequencing data from septic and healthy patients, where genomic quasi-G-prime profiles distinguished disease states. Our method is highly space-efficient, permitting fast classification on modest hardware and enabling it to outperform existing taxonomic classification approaches in this task.

## Linked entities

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

## Full-text entities

- **Diseases:** bacteremia (MESH:D016470), septic (MESH:D001170), genetic diseases (MESH:D030342), infectious disease (MESH:D003141), Sepsis (MESH:D018805), cancer (MESH:D009369), infection (MESH:D007239)
- **Chemicals:** PBS (MESH:D007854), methicillin (MESH:D008712), cephalosporins (MESH:D002511), vancomycin (MESH:D014640), BHI agar (-), ceftriaxone (MESH:D002443), cefepime (MESH:D000077723)
- **Species:** Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562], Pseudomonas (RNA similarity group I, genus) [taxon 286], Enterococcus (genus) [taxon 1350], Haemophilus (genus) [taxon 724], Staphylococcus aureus (species) [taxon 1280]
- **Mutations:** T2T

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12880686/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12880686/full.md

## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12880686/full.md

---
Source: https://tomesphere.com/paper/PMC12880686