Evidence map›Paper›PMID 41779744›Full record

ArticlePloS one2026

Shifting from an expected to an opportunistic pathogen: Comparison of cases of infant late and very late onset group B streptococcal (GBS) infection in a Canadian city over a 27-year period.

Isoken Isah, Sneha Suresh, Gregory J Tyrrell, Manoj Kumar, Joan L Robinson

Abstract readComparative Study
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Isoken IsahDepartment of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.
Sneha SureshDepartment of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.
Gregory J TyrrellDepartment of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.ORCID https://orcid.org/0000-0002-5276-2416
Manoj KumarDepartment of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.
Joan L RobinsonDepartment of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.ORCID https://orcid.org/0000-0001-9831-5681

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite decades of study, the characteristics of infants with invasive group B streptococcus (GBS) late onset disease (LOD) (onset day 7-89 of life) and in particular very late onset disease (VLOD) (after day 89 of life) are not well described. MATERIALS AND

methodsThis was a retrospective cohort study of infants hospitalized in four Edmonton hospitals April 1, 1994 through June 30, 2022 with LOD or VLOD GBS invasive disease. Data were collected on demographics, day of onset of infection, clinical manifestations and outcomes.

resultsThere were 115 episodes of LOD in 111 infants of which 50 infants (45%) were preterm. Onset of initial LOD infection was on median day 27 (IQR 19-40.5) of life. All but one infant was bacteremic while 38/111 (34%) had proven and 17/111 (15%) had possible GBS meningitis. Five of 111 (5%) died before hospital discharge with all deaths probably due to GBS. There were 11 episodes of VLOD in 11 infants (8 [73%] preterm) presenting on median day 116 (IQR 103-138) (range 93-207) of life. Three (27%) had GBS meningitis. All 11 survived to discharge. As compared with infants with LOD, those with VLOD were less likely to be born vaginally (n = 3/11 [27%] versus n = 72/111 [65%] p = 0.036), more likely to be mechanically ventilated during their birth hospitalization (n = 5/11 [45%] versus n = 17/111 [15%]; p = 0.039), and more likely to have serious infection with other pathogens during their GBS admission (n = 3/11 [27%] versus n = 4/111 [4%]); p = 0.032). Serotype III accounted for 78% of LOD and 64% of VLOD cases.

conclusionGBS remains a significant cause of infant morbidity and mortality. Infants with VLOD appear to have more complex medical histories prior to GBS infection than those with LOD. There is increasing evidence that GBS may sometimes be an opportunistic pathogen in infants over 89 days of age. This speaks of the need for increased surveillance for VLOD with further research into its epidemiology and underlying immunologic determinants.

Indexed as

Streptococcal InfectionsStreptococcus agalactiaeAge of OnsetCanadaFemaleHumansInfantInfant, NewbornMaleRetrospective Studies

Identifiers

PMID41779744
PMCPMC12959668

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