# The Bacterial Swiss Army Knife: ExPEC Utilizes Multiple Resistance Mechanisms to Counteract Host Immune Responses

**Authors:** Eveline Weerdenburg, Susan King, Joyce Lübbers, Elise Hovingh, Todd Davies, Jeroen Geurtsen, Germie van den Dobbelsteen, Jan Poolman

PMC · DOI: 10.3390/vaccines14010051 · Vaccines · 2025-12-31

## TL;DR

This paper reviews how ExPEC bacteria use various defenses to resist the human immune system and cause infections outside the intestines.

## Contribution

The paper provides a comprehensive overview of ExPEC's resistance mechanisms against host immune responses.

## Key findings

- ExPEC uses surface polysaccharides and outer membrane proteins to resist immune defenses.
- Cytotoxins and proteases help ExPEC neutralize host immune responses.
- These mechanisms allow ExPEC to survive in extraintestinal environments.

## Abstract

Extraintestinal pathogenic Escherichia coli (ExPEC) is a major cause of infections of the urinary tract, the bloodstream, and other non-intestinal sites in humans. ExPEC often resists the bactericidal action of human immune defenses including complement, antimicrobial peptides, antibodies, and cell-mediated killing. This review provides an overview of the main host defense strategies, and the mechanisms and molecules ExPEC engages to resist these human immune responses. Surface-exposed polysaccharides, outer membrane proteins, cytotoxins, and proteases are all part of the bacterial arsenal of defenses that can neutralize many of the host’s immune defenses. These factors work in concert to enable ExPEC to survive and thrive in extraintestinal environments of the human body.

## Linked entities

- **Species:** Escherichia coli (taxon 562)

## Full-text entities

- **Diseases:** infections of (MESH:D007239)
- **Chemicals:** polysaccharides (MESH:D011134)
- **Species:** Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

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## References

260 references — full list in the complete paper: https://tomesphere.com/paper/PMC12846712/full.md

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Source: https://tomesphere.com/paper/PMC12846712