# Role of microplastics in the survival and antimicrobial susceptibility of Campylobacter jejuni

**Authors:** Irene Ortega-Sanz, Andreja Rajkovic

PMC · DOI: 10.3389/fmicb.2025.1717297 · 2026-01-05

## TL;DR

This study shows that microplastics help Campylobacter jejuni survive in the environment and increase their antibiotic susceptibility.

## Contribution

The study reveals how microplastics influence C. jejuni biofilm formation and antimicrobial susceptibility through genetic analysis.

## Key findings

- C. jejuni strains rapidly colonize microplastics within 24 hours, with varying attachment densities.
- The peb3 gene is critical for biofilm formation on microplastics, while capA, capB, cj1725, and porA enhance it.
- Cells from microplastic-associated biofilms showed up to 4.6 log2-fold increased antibiotic susceptibility.

## Abstract

Microplastics (MPs) are a global concern due to their persistence in the environment and capacity to carry pollutants and pathogenic microorganisms. Given recent evidence on the co-occurrence of MPs and Campylobacter spp., the leading cause of foodborne gastrointestinal infections worldwide, this study investigates the role of MPs in Campylobacter jejuni contamination and their impact on antimicrobial susceptibility. The potential of five C. jejuni isolates from different origin (poultry, water, and human) to form biofilms on MPs over time (24 h, 48 h, and 72 h) was evaluated using traditional culture-dependent methods, including the reference strain C. jejuni subsp. jejuni strain NCTC 11168. The effect of MPs on the antimicrobial susceptibility of C. jejuni cells detached from MP-associated biofilms was also assessed using Etest strips. To comprehensively understand the interactions between the MPs and the bacteria, whole-genome sequencing was performed to explore the presence of adherence and biofilm-associated genes, as well as antibiotic resistance genes. The strains rapidly colonized the MPs within 24 h, exhibiting varying attachment densities over time ranging from 1.09 to 5.78 log CFU/MP, with strain NCTC 11168 identified as the strongest biofilm former overall. Furthermore, the abundance of adherence and biofilm formation genes was consistent with their abilities to form biofilm on MPs. The gene peb3 played a critical role in determining biofilm formation levels on MPs, while specific combinations of capA, capB, cj1725, and porA were linked to enhanced biofilm development. Similarly, the presence of antibiotic resistance determinants aligned with the phenotypic resistance, and only one strain (ST-6209/CC464) exhibited resistance to ciprofloxacin, nalidixic acid, and tetracycline. Notably, antimicrobial susceptibility of cells detached from MP-biofilms was increased by up to 4.6 log2-fold compared to planktonic counterparts. The findings indicate that MPs can facilitate the persistence of C. jejuni in the environment while simultaneously increasing their susceptibility to antibiotics. Further research with larger cohorts is needed to validate these preliminary observations in order to support the development of effective policies addressing MP pollution and food safety.

## Linked entities

- **Genes:** peb3 (major antigenic peptide PEB3) [NCBI Gene 904613], Capa (Capability) [NCBI Gene 43541], CAPZB (capping actin protein of muscle Z-line subunit beta) [NCBI Gene 832], Cj1725 (periplasmic protein) [NCBI Gene 905202], pora (P450 (cytochrome) oxidoreductase a) [NCBI Gene 568202]
- **Chemicals:** ciprofloxacin (PubChem CID 2764), nalidixic acid (PubChem CID 4421), tetracycline (PubChem CID 54675776)
- **Species:** Campylobacter jejuni (taxon 197), Campylobacter jejuni subsp. jejuni (taxon 32022)

## Full-text entities

- **Diseases:** gastrointestinal infections (MESH:D005767)
- **Chemicals:** tetracycline (MESH:D013752), nalidixic acid (MESH:D009268), MP (MESH:D000080545), ciprofloxacin (MESH:D002939)
- **Species:** Campylobacter jejuni (species) [taxon 197], Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12813274/full.md

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Source: https://tomesphere.com/paper/PMC12813274