# Proteome profiling of Campylobacter jejuni 81–176 at 37 °C and 42 °C by label-free mass spectrometry

**Authors:** Annika Dreyer, Wycliffe O. Masanta, Raimond Lugert, Wolfgang Bohne, Uwe Groß, Andreas Leha, Mohammed Dakna, Christof Lenz, Andreas E. Zautner

PMC · DOI: 10.1186/s12866-024-03348-8 · BMC Microbiology · 2024-05-31

## TL;DR

This study compares how the bacterium Campylobacter jejuni adapts its protein production at avian (42°C) and human (37°C) body temperatures.

## Contribution

The paper provides a detailed proteomic comparison of C. jejuni at two temperatures and incubation times using label-free mass spectrometry.

## Key findings

- 37.1–47.3% of quantifiable proteins showed significant differential regulation between 37°C and 42°C incubation.
- Proteins related to replication, DNA synthesis, and metabolism were upregulated at 42°C, while chaperone and DNA uptake proteins were upregulated at 37°C.
- The proteomic response at 37°C suggests adaptation to lower temperatures and increased DNA acquisition competence.

## Abstract

The main natural reservoir for Campylobacter jejuni is the avian intestinal tract. There, C. jejuni multiplies optimally at 42 °C – the avian body temperature. After infecting humans through oral intake, the bacterium encounters the lower temperature of 37 °C in the human intestinal tract. Proteome profiling by label-free mass spectrometry (DIA-MS) was performed to examine the processes which enable C. jejuni 81–176 to thrive at 37 °C in comparison to 42 °C. In total, four states were compared with each other: incubation for 12 h at 37 °C, for 24 h at 37 °C, for 12 h at 42 °C and 24 h at 42 °C.

It was shown that the proteomic changes not only according to the different incubation temperature but also to the length of the incubation period were evident when comparing 37 °C and 42 °C as well as 12 h and 24 h of incubation. Altogether, the expression of 957 proteins was quantifiable. 37.1 − 47.3% of the proteins analyzed showed significant differential regulation, with at least a 1.5-fold change in either direction (i.e. log2 FC ≥ 0.585 or log2 FC ≤ -0.585) and an FDR-adjusted p-value of less than 0.05. The significantly differentially expressed proteins could be arranged in 4 different clusters and 16 functional categories.

The C. jejuni proteome at 42 °C is better adapted to high replication rates than that at 37 °C, which was in particular indicated by the up-regulation of proteins belonging to the functional categories “replication” (e.g. Obg, ParABS, and NapL), “DNA synthesis and repair factors” (e.g. DNA-polymerase III, DnaB, and DnaE), “lipid and carbohydrate biosynthesis” (e.g. capsular biosynthesis sugar kinase, PrsA, AccA, and AccP) and “vitamin synthesis, metabolism, cofactor biosynthesis” (e.g. MobB, BioA, and ThiE). The relative up-regulation of proteins with chaperone function (GroL, DnaK, ClpB, HslU, GroS, DnaJ, DnaJ-1, and NapD) at 37 °C in comparison to 42 °C after 12 h incubation indicates a temporary lower-temperature proteomic response. Additionally the up-regulation of factors for DNA uptake (ComEA and RecA) at 37 °C compared to 42 °C indicate a higher competence for the acquisition of extraneous DNA at human body temperature.

The online version contains supplementary material available at 10.1186/s12866-024-03348-8.

## Linked entities

- **Proteins:** obg (GTPase ObgE), napL (periplasmic protein), dnaB (replication helicase subunit), dnaE (DNA polymerase III subunit alpha), GLRX5 (glutaredoxin 5), ACACA (acetyl-CoA carboxylase alpha), ND-ACP (NADH dehydrogenase (ubiquinone) acyl carrier protein), mobB (molybdopterin-guanine dinucleotide biosynthesis protein), bioA (adenosylmethionine--8-amino-7-oxononanoate aminotransferase BioA), thiE (thiamine-phosphate pyrophosphorylase), groL (molecular chaperone GroEL), dnaK (heat shock protein 70), CLPB (ClpB family mitochondrial disaggregase), hslU (ATP-dependent protease ATP-binding subunit HslU), groS (co-chaperonin GroES), DNAJB6 (DnaJ heat shock protein family (Hsp40) member B6), DnaJ-1 (DnaJ-like-1), napD (nitrate reductase biosynthesis protein NapD), comEA (membrane bound high-affinity DNA-binding receptor), RAD51 (RAD51 recombinase)
- **Species:** Campylobacter jejuni (taxon 197), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** RAD51 (RAD51 recombinase) [NCBI Gene 5888] {aka BRCC5, FANCR, HRAD51, HsRad51, HsT16930, MRMV2}, DNAJA2 (DnaJ heat shock protein family (Hsp40) member A2) [NCBI Gene 10294] {aka CPR3, DJ3, DJA2, DNAJ, DNJ3, HIRIP4}, GPR3 (G protein-coupled receptor 3) [NCBI Gene 2827] {aka ACCA}, GLRX5 (glutaredoxin 5) [NCBI Gene 51218] {aka C14orf87, FLB4739, GRX5, PR01238, PRO1238, PRSA}
- **Chemicals:** carbohydrate (MESH:D002241), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606], Campylobacter jejuni (species) [taxon 197]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11140963/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC11140963/full.md

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Source: https://tomesphere.com/paper/PMC11140963