# Fever enhances host bacterial defence while limiting mitochondrial damage

**Authors:** Yonghan Wu, Elijah Rowe, Albert Siryaporn, Steven P. Gross

PMC · DOI: 10.21203/rs.3.rs-8724408/v1 · Research Square · 2026-02-06

## TL;DR

Fever helps fight bacterial infections by boosting antimicrobial peptides while protecting mitochondria.

## Contribution

Fever enhances AMP antibacterial activity while reducing mitochondrial damage in warm-blooded animals.

## Key findings

- AMP activity is temperature-sensitive and optimized for host body temperatures.
- Fever increases AMP efficacy against bacteria while minimizing mitochondrial damage.
- Cold-blooded animals avoid mitochondrial damage through different mechanisms.

## Abstract

The fever response is triggered during infection and inflammation, but the importance of this response for the function of antimicrobial peptides (AMPs) remains unknown. We discovered that the activity of the human AMP LL-37 is temperature-dependent and were curious as to why. Its temperature-dependent activity is not an enzymatic accident, as AMPs from other animals with different body temperatures have distinct temperature sensitivities. We find that in general, AMP temperature sensitivities are tuned to animals’ body temperatures, and that for animals that can induce fever or raise their body temperature, this is used to increase the AMP’s antibacterial efficacy. This effect reflects a careful balance between optimizing antibacterial killing while minimizing mitochondrial damage. In contrast, cold-blooded animals that are unable to raise their body temperature use a different strategy to avoid mitochondrial damage. Together, this study suggests that fever is beneficial for antimicrobial defence by raising AMP activity towards bacteria while reducing mitochondrial damage when pathogens are absent.

## Linked entities

- **Proteins:** CAMP (cathelicidin antimicrobial peptide)

## Full-text entities

- **Genes:** CAMP (cathelicidin antimicrobial peptide) [NCBI Gene 820] {aka CAP-18, CAP18, CRAMP, FALL-39, FALL39, HSD26}
- **Diseases:** mitochondrial damage (MESH:D028361), infection (MESH:D007239), Fever (MESH:D005334), inflammation (MESH:D007249)
- **Chemicals:** AMP (MESH:D000089882)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12889834/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12889834/full.md

## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12889834/full.md

---
Source: https://tomesphere.com/paper/PMC12889834