Fast hospital discharge rates blur within-hospital ‘transmission footprint’ in bacterial genomes, as showcased with Staphylococcus aureus

The relatively slow mutation rates of bacterial pathogens impose severe limitations on phylodynamic analysis of bacterial outbreaks. However, whole-genome sequencing may enable accurate inference of bacterial transmission dynamics in health-care settings. We simulated the epidemic dynamics of a Staphylococcus aureus lineage using a stochastic model with a hospital and community compartment connected by patient admission and discharge. We generated synthetic genomic sequences and performed Bayesian phylodynamic inference on a proportion of samples from each simulated outbreak. When samples are obtained from both compartments, hospital transmission rate ([Formula: see text]) and community transmission rate ([Formula: see text]) are accurately estimated, if [Formula: see text] is on the same scale as the discharge rate. If [Formula: see text] is substantially lower than the discharge rate, a robust quantification of within-hospital transmission dynamics is challenging. Excluding samples from the community resulted in a notable underestimation of [Formula: see text] when [Formula: see text]. When transmission was 'community-driven', but sampling was restricted to hospital cases only, estimates are closer to the true [Formula: see text], if hospital sampling proportion is known. Otherwise, [Formula: see text] estimates reflected the transmission dynamics within the community. When using genomic data to estimate bacterial transmission rates in a health-care setting, it is essential to take into account the surrounding community. Many infections related to nosocomial outbreaks will not be observed within the hospital due to fast discharge rates. In the absence of usable genomic data from the community, alternative estimates of community transmission rates from publicly available data should be incorporated. Transmission rate estimates from nosocomial genomes alone need to be interpreted with care.

Authors

Institutions

Publication Details

Journal
PLoS Computational Biology
Published
2026-03-16
DOI
https://doi.org/10.1371/journal.pcbi.1013982
Primary Topic
Antimicrobial Resistance in Staphylococcus
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Fast hospital discharge rates blur within-hospital ‘transmission footprint’ in bacterial genomes, as showcased with Staphylococcus aureus

Hugo Sax, Mathilde Boumasmoud, Sanni Översti, Roger D. Kouyos et al.
PLoS Computational Biology
Antimicrobial Resistance in Staphylococcus
article

Fast hospital discharge rates blur within-hospital ‘transmission footprint’ in bacterial genomes, as showcased with Staphylococcus aureus

Hugo Sax, Mathilde Boumasmoud, Sanni Översti, Roger D. Kouyos, Huldyrch F. Günthard, Denise Kühnert, Annelies S. Zinkernagel
article en

Abstract

The relatively slow mutation rates of bacterial pathogens impose severe limitations on phylodynamic analysis of bacterial outbreaks. However, whole-genome sequencing may enable accurate inference of bacterial transmission dynamics in health-care settings. We simulated the epidemic dynamics of a Staphylococcus aureus lineage using a stochastic model with a hospital and community compartment connected by patient admission and discharge. We generated synthetic genomic sequences and performed Bayesian phylodynamic inference on a proportion of samples from each simulated outbreak. When samples are obtained from both compartments, hospital transmission rate ([Formula: see text]) and community transmission rate ([Formula: see text]) are accurately estimated, if [Formula: see text] is on the same scale as the discharge rate. If [Formula: see text] is substantially lower than the discharge rate, a robust quantification of within-hospital transmission dynamics is challenging. Excluding samples from the community resulted in a notable underestimation of [Formula: see text] when [Formula: see text]. When transmission was 'community-driven', but sampling was restricted to hospital cases only, estimates are closer to the true [Formula: see text], if hospital sampling proportion is known. Otherwise, [Formula: see text] estimates reflected the transmission dynamics within the community. When using genomic data to estimate bacterial transmission rates in a health-care setting, it is essential to take into account the surrounding community. Many infections related to nosocomial outbreaks will not be observed within the hospital due to fast discharge rates. In the absence of usable genomic data from the community, alternative estimates of community transmission rates from publicly available data should be incorporated. Transmission rate estimates from nosocomial genomes alone need to be interpreted with care.

PLoS Computational BiologyVol. 22(3)
University of Bern (CH), University of Zurich (CH), Robert Koch Institute (DE), University Hospital of Bern (CH), ETH Zurich (CH), University Hospital of Zurich (CH), Max Planck Institute for Evolutionary Anthropology (DE), Max Planck Institute for the Science of Human History (DE), Max Planck Institute of Geoanthropology
Good health and well-being
Openalex Percentile: Top 21%
Antimicrobial Resistance in Staphylococcus
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.