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Genomic tailoring of autogenous poultry vaccines to reduce Campylobacter from farm to fork

Abstract:
Campylobacter is a leading cause of food-borne gastroenteritis worldwide, linked to the consumption of contaminated poultry meat. Targeting this pathogen at source, vaccines for poultry can provide short-term caecal reductions in Campylobacter numbers in the chicken intestine. However, this approach is unlikely to reduce Campylobacter in the food chain or human incidence. This is likely as vaccines typically target only a subset of the high genomic strain diversity circulating among chicken flocks, and rapid evolution diminishes vaccine efficacy over time. To address this, we used a genomic approach to develop a whole-cell autogenous vaccine targeting isolates harbouring genes linked to survival outside of the host. We hyper-immunised a whole major UK breeder farm to passively target offspring colonisation using maternally-derived antibody. Monitoring progeny, broiler flocks revealed a near-complete shift in the post-vaccination Campylobacter population with an ~50% reduction in isolates harbouring extra-intestinal survival genes and a significant reduction of Campylobacter cells surviving on the surface of meat. Based on these findings, we developed a logistic regression model that predicted that vaccine efficacy could be extended to target 65% of a population of clinically relevant strains. Immuno-manipulation of poultry microbiomes towards less harmful commensal isolates by competitive exclusion, has major potential for reducing pathogens in the food production chain.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41541-024-00879-z

Authors


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Role:
Author
ORCID:
0000-0001-8888-0812
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Role:
Author
ORCID:
0000-0002-3399-2136
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Role:
Author
ORCID:
0000-0002-9563-6348
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-6376-5121


Publisher:
Nature Research
Journal:
npj Vaccines More from this journal
Volume:
9
Issue:
1
Article number:
105
Publication date:
2024-06-12
Acceptance date:
2024-04-19
DOI:
EISSN:
2059-0105


Language:
English
Pubs id:
2007834
Local pid:
pubs:2007834
Source identifiers:
2036974
Deposit date:
2024-06-12
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