{"title":"Ecology and antimicrobial resistance of Campylobacter in wildlife: insights into specialist and generalist lineages and zoonotic potential.","authors":"Manel Gharbi, Mohamed Salah Abbassi","doi":"10.1093/lambio/ovag031","DOIUrl":null,"url":null,"abstract":"<p><p>Wildlife is a critical reservoir of Campylobacter species, particularly C. jejuni and C. coli, carrying diverse genetic lineages, virulence factors, and antimicrobial resistance (AMR) genes. Birds, especially migratory and synanthropic species, are the primary carriers, though mammals, reptiles, and other vertebrates also contribute to maintenance and dissemination. Wildlife-associated strains include both host-specific lineages and generalist clonal complexes (e.g. ST21, ST45, and ST828) capable of crossing wildlife, livestock, humans, and environmental interfaces, reflecting high zoonotic potential. Virulence factors, including motility, adhesion and invasion proteins (CadF, CiaB), and cytolethal distending toxin (CDT), facilitate colonization and survival, while efflux pumps and stress-response genes enhance persistence under antibiotic pressure. AMR is widespread, with resistance to fluoroquinolones, macrolides, tetracyclines, and multidrug phenotypes, driven by anthropogenic contamination, environmental reservoirs, and horizontal gene transfer. Key resistance determinants include gyrA mutations, tet(O), erm(B), cmeABC efflux pumps, and β-lactamases. Despite advances, knowledge gaps remain, particularly for non-avian hosts, environmental reservoirs, and resistance mechanisms. A One Health approach integrating microbiology, genomics, ecology, and epidemiology is essential to map transmission pathways, monitor emerging resistance, and guide interventions to reduce the public health impact of zoonotic and antibiotic-resistant Campylobacter.</p>","PeriodicalId":17962,"journal":{"name":"Letters in Applied Microbiology","volume":" ","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2026-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Letters in Applied Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/lambio/ovag031","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Wildlife is a critical reservoir of Campylobacter species, particularly C. jejuni and C. coli, carrying diverse genetic lineages, virulence factors, and antimicrobial resistance (AMR) genes. Birds, especially migratory and synanthropic species, are the primary carriers, though mammals, reptiles, and other vertebrates also contribute to maintenance and dissemination. Wildlife-associated strains include both host-specific lineages and generalist clonal complexes (e.g. ST21, ST45, and ST828) capable of crossing wildlife, livestock, humans, and environmental interfaces, reflecting high zoonotic potential. Virulence factors, including motility, adhesion and invasion proteins (CadF, CiaB), and cytolethal distending toxin (CDT), facilitate colonization and survival, while efflux pumps and stress-response genes enhance persistence under antibiotic pressure. AMR is widespread, with resistance to fluoroquinolones, macrolides, tetracyclines, and multidrug phenotypes, driven by anthropogenic contamination, environmental reservoirs, and horizontal gene transfer. Key resistance determinants include gyrA mutations, tet(O), erm(B), cmeABC efflux pumps, and β-lactamases. Despite advances, knowledge gaps remain, particularly for non-avian hosts, environmental reservoirs, and resistance mechanisms. A One Health approach integrating microbiology, genomics, ecology, and epidemiology is essential to map transmission pathways, monitor emerging resistance, and guide interventions to reduce the public health impact of zoonotic and antibiotic-resistant Campylobacter.
期刊介绍:
Journal of & Letters in Applied Microbiology are two of the flagship research journals of the Society for Applied Microbiology (SfAM). For more than 75 years they have been publishing top quality research and reviews in the broad field of applied microbiology. The journals are provided to all SfAM members as well as having a global online readership totalling more than 500,000 downloads per year in more than 200 countries. Submitting authors can expect fast decision and publication times, averaging 33 days to first decision and 34 days from acceptance to online publication. There are no page charges.