Molecular determinants of Escherichia coli causing neonatal invasive infection following vertical transmission.

Authors

Liang Gao, Jia Yin Wu, Xue Rong Huang, Xue Yan Lin, Dan Tong Lin, Yao Zhu, Xin Zhu Lin, Ji Dong Lai

Published in

Frontiers in cellular and infection microbiology. Volume 16. Pages 1855839. Epub Jun 15, 2026.

Abstract

Escherichia coli (E. coli) is a leading cause of life-threatening neonatal invasive infections via vertical transmission. However, the bacterial molecular features that distinguish invasive infection from asymptomatic colonization following vertical transmission remain unclear in genomically confirmed mother-neonate pairs.
A single-center retrospective case-control study enrolled 43 mother-neonate pairs with genome sequencing-confirmed clonal E. coli vertical transmission (average nucleotide identity, ANI ≥99.99%) between January 2020 and June 2025. Pairs were stratified into an invasive infection group (n = 27) and a colonization group (n = 16) based on neonatal clinical outcomes. Genomic characterization, including multilocus sequence typing (MLST), serotyping, and virulence gene profiling, was performed on maternal E. coli isolates. The Boruta algorithm was used for feature selection, and a Bayesian logistic regression model was constructed to identify independent predictors of invasive infection.
No significant differences were observed in baseline clinical characteristics between the two groups. ST95 was exclusively detected in the invasive infection group (29.6% vs. 0%, P = 0.018). The virulence genes neuA (63% vs. 13%), neuS (59% vs. 13%), iutA (78% vs. 38%), and kpsMT II (93% vs. 63%) were significantly more prevalent in the invasive infection group (all raw P < 0.05). Bayesian modeling identified four independent predictors: ST95 [odds ratio (OR) = 6.05, 90% credible interval (CrI): 0.82-66.7, posterior probability P(OR>1) = 0.85], neuA (OR = 4.95, 90%CrI: 1.65-16.44, P(OR>1) = 0.96), kpsMT II (OR = 4.48, 90%CrI: 1.35-16.44, P(OR>1) = 0.95), and iutA (OR = 3.32, 90%CrI: 1.22-9.03, P(OR>1) = 0.93). Notably, all ST95 isolates (100%) co-harbored neuA, kpsMT II, and iutA, forming a distinct "clonal virulence complex." The model exhibited good predictive performance (AUC = 0.847, 95%CI: 0.727-0.954), while the composite virulence burden score showed no intergroup difference (P = 0.208).
The ST95 E. coli clonal virulence complex (co-harboring neuA/kpsMT II and iutA) is strongly associated with invasive infection following vertical transmission. This signature represents a potential candidate marker for clinical risk stratification of neonates at high risk of E. coli invasive infection, with potential implications for precision monitoring and intervention in perinatal care.

PMID:
42376323
Bibliographic data and abstract were imported from PubMed on 30 Jun 2026.

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