Transcriptome profile of delayed mortality in patients with invasive group A Streptococcal disease

Background Our aim was to study the pathophysiological mechanisms of early (<7 days) and delayed sepsis mortality by transcriptome profiling of cases with invasive group A Streptococcal (iGAS) infections and possibly find predictors for delayed mortality. Methods We recruited cases with iGAS from June 2018 to June 2020. Whole blood samples were collected at the early timepoint (within two days after admission, timepoint A) and later timepoint (a week later, timepoint B) to perform transcriptome analysis. A comparison of gene expression against disease course was done using weighted genome correlation network analysis. Results We recruited 45 patients. Eight patients died within 90 days, four of whom within the first week. After RNA quality control 34 and 31 subjects at timepoints A and B remained, respectively. The gene expression profiles associated with a severe disease course differed markedly between timepoints A and B. High expression of necroptosis factors and low expression of HLA genes at timepoint B was associated with death. Conclusions The seemingly different gene expression profile over time among patients with a severe iGAS disease may suggest distinct pathophysiological mechanisms for early and delayed sepsis mortality. However, as our sample size was small, these findings must be considered with caution and should not be interpreted as predictive.

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Publication Details

Journal
PLoS ONE
Published
2026-08-18
DOI
https://doi.org/10.1371/journal.pone.0356286
Primary Topic
Streptococcal Infections and Treatments
Type
article
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article

Transcriptome profile of delayed mortality in patients with invasive group A Streptococcal disease

Emilia Lönnqvist, Kaisu Rantakokko‐Jalava, Ville Kailankangas, Jarmo Oksi et al.
PLoS ONE
Streptococcal Infections and Treatments
article

Transcriptome profile of delayed mortality in patients with invasive group A Streptococcal disease

Emilia Lönnqvist, Kaisu Rantakokko‐Jalava, Ville Kailankangas, Jarmo Oksi, Jaana Vuopio, Kirsi Gröndahl‐Yli‐Hannuksela, Johanna Vilhonen, Shintaro Katayama, Juha Kere, Tapio Seiskari, Jaana Syrjänen, Mari Hannele Tervaniemi
article en

Abstract

Background Our aim was to study the pathophysiological mechanisms of early (<7 days) and delayed sepsis mortality by transcriptome profiling of cases with invasive group A Streptococcal (iGAS) infections and possibly find predictors for delayed mortality. Methods We recruited cases with iGAS from June 2018 to June 2020. Whole blood samples were collected at the early timepoint (within two days after admission, timepoint A) and later timepoint (a week later, timepoint B) to perform transcriptome analysis. A comparison of gene expression against disease course was done using weighted genome correlation network analysis. Results We recruited 45 patients. Eight patients died within 90 days, four of whom within the first week. After RNA quality control 34 and 31 subjects at timepoints A and B remained, respectively. The gene expression profiles associated with a severe disease course differed markedly between timepoints A and B. High expression of necroptosis factors and low expression of HLA genes at timepoint B was associated with death. Conclusions The seemingly different gene expression profile over time among patients with a severe iGAS disease may suggest distinct pathophysiological mechanisms for early and delayed sepsis mortality. However, as our sample size was small, these findings must be considered with caution and should not be interpreted as predictive.

PLoS ONEVol. 21(8)
Good health and well-being
Openalex Percentile: Top 7%
Streptococcal Infections and Treatments
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Transcriptome profile of delayed mortality in patients with invasive group A Streptococcal disease — Emilia Lönnqvist, Kaisu Rantakokko‐Jalava, et al. · PLoS ONE (2026) | TGRS Research Map | TGRS