Susceptibility of broiler chickens to Campylobacter: impacts of the gut environment and immune status on colonisation
Lead Research Organisation:
University of Leicester
Department Name: Genetics
Abstract
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Technical Summary
Chicken is the main source of human Campylobacter and this threat must be reduced. The proposed work will determine mechanisms behind the delay before broiler chickens become Campylobacter-positive in housed flocks. The project is in partnership with poultry producers to identify cost-effective control measures to protect chickens against Campylobacter.
Past work suggested that maternal antibodies provide chicks with some protection against Campylobacter in early life. However, this was done in isolation and other protective factors were not studied. Campylobacter-negative chicks can have gut bacteria that inhibit C. jejuni. In most flocks, the 'protective bacteria' were not present when birds reached 3-4 weeks of age and flocks rapidly became Campylobacter-positive.
We will determine whether maternally-derived antibodies and/or gut microbiota and/or gut architecture is the most important in determining broiler susceptibility to Campylobacter. We will study Ross 308 birds, the most common type in the UK. The field studies will relate changes in naturally acquired maternal anti-Campylobacter antibodies and gut microbiota with events in flock management, like diet change and with the presence of Campylobacter. State of the art techniques will be used to determine microbiota.
Laboratory experiments will test field-generated hypotheses in a controlled manner. B-cell deficient breeders will be produced by surgical bursectomy. This creates B-cell- and thus antibody-deficient hens. These will be used to form breeding flocks producing progeny deficient in maternal antibodies. We can then determine definitively the role of maternal antibodies in the resistance of chicks to Campylobacter. We will use modelling to investigate dynamics of chicken gut microbiota and its impact and maternal antibodies as direct and proximal drivers of colonisation in commercial chicken production. These models will be used to identify targets for mitigating Campylobacter colonisation.
Past work suggested that maternal antibodies provide chicks with some protection against Campylobacter in early life. However, this was done in isolation and other protective factors were not studied. Campylobacter-negative chicks can have gut bacteria that inhibit C. jejuni. In most flocks, the 'protective bacteria' were not present when birds reached 3-4 weeks of age and flocks rapidly became Campylobacter-positive.
We will determine whether maternally-derived antibodies and/or gut microbiota and/or gut architecture is the most important in determining broiler susceptibility to Campylobacter. We will study Ross 308 birds, the most common type in the UK. The field studies will relate changes in naturally acquired maternal anti-Campylobacter antibodies and gut microbiota with events in flock management, like diet change and with the presence of Campylobacter. State of the art techniques will be used to determine microbiota.
Laboratory experiments will test field-generated hypotheses in a controlled manner. B-cell deficient breeders will be produced by surgical bursectomy. This creates B-cell- and thus antibody-deficient hens. These will be used to form breeding flocks producing progeny deficient in maternal antibodies. We can then determine definitively the role of maternal antibodies in the resistance of chicks to Campylobacter. We will use modelling to investigate dynamics of chicken gut microbiota and its impact and maternal antibodies as direct and proximal drivers of colonisation in commercial chicken production. These models will be used to identify targets for mitigating Campylobacter colonisation.
Planned Impact
Campylobacter is the most important food borne zoonosis in the UK and the wider EU. In the UK it is estimated that there are 700000 cases of infection each year and that chicken-associated Campylobacter infection costs the UK economy ~£1 billion per year. Chicken is overwhelmingly the most important vehicle for human infection and is believed to be responsible for up to 80% of infections. ~80% of chickens on sale in the UK are Campylobacter-positive. Contaminated chicken presents two health threats. Surface contamination levels can be very high and contamination of deep muscle and liver tissues has been reported in up to 27 and 60% of samples tested respectively. The project seeks to better understand the processes that occur during the early development of chickens that leads them to become colonised by Campylobacter.
We seek to accurately determine when broiler flocks first become Campylobacter-positive, as there is a delay before this happens, and will be investigating the roles in this process of maternally acquired anti-Campylobacter antibodies and changes in gut microbiota and gut architecture for the first time all together. Such processes that are driven by bird age and/or diet and this project proposes to study these by laboratory studies, but also importantly in the field on commercial farms. By determining the reasons for changes to susceptibility to this major zoonotic pathogen, we will be able to identify farm-based control measures that will reduce levels of Campylobacter in UK poultry and not rely on biosecurity alone. In particular, our work will importantly inform studies on the use of vaccines and the use of pre- and/or probiotics. The project is in partnership with the UK poultry industry and all major UK retailers. Thus the beneficial impacts of our work can quickly be transferred to stakeholders.
We seek to accurately determine when broiler flocks first become Campylobacter-positive, as there is a delay before this happens, and will be investigating the roles in this process of maternally acquired anti-Campylobacter antibodies and changes in gut microbiota and gut architecture for the first time all together. Such processes that are driven by bird age and/or diet and this project proposes to study these by laboratory studies, but also importantly in the field on commercial farms. By determining the reasons for changes to susceptibility to this major zoonotic pathogen, we will be able to identify farm-based control measures that will reduce levels of Campylobacter in UK poultry and not rely on biosecurity alone. In particular, our work will importantly inform studies on the use of vaccines and the use of pre- and/or probiotics. The project is in partnership with the UK poultry industry and all major UK retailers. Thus the beneficial impacts of our work can quickly be transferred to stakeholders.
Organisations
People |
ORCID iD |
Julian Ketley (Principal Investigator) |
Publications
Elgamoudi BA
(2018)
New approach to distinguishing chemoattractants, chemorepellents and catabolised chemoeffectors for Campylobacter jejuni.
in Journal of microbiological methods
Elgamoudi BA
(2018)
Lighting up my life: a LOV-based fluorescent reporter for Campylobacter jejuni.
in Research in microbiology
Elgamoudi Bassam Abusalama
(2016)
The role of transducer-like proteins in Campylobacter jejuni
Jama Abdullahi Said
(2015)
CJ0700 is a remote Chez Orthologue involved in Campylobacter jejuni chemotaxis signal transduction
Lacharme-Lora L
(2017)
B lymphocytes play a limited role in clearance of Campylobacter jejuni from the chicken intestinal tract.
in Scientific reports
Wanford J
(2017)
Simulating phase variation: a practical approach to teaching mutation and diversity
in Journal of Biological Education
Description | Our findings suggest that any Campylobacter vaccine relying solely on an antibody response is unlikely to be effective in broiler chickens. In the study chemical inhibition of the production of antibody-producing white blood cells (B lymphocytes) in broiler chicks was undertaken before introducing C.jejuni infection at the age of three weeks. Bacterial levels were then monitored in the gut for the next nine weeks. We found that an antibody-associated drop in bacteria levels only became apparent after seven weeks which suggests that the adaptive immune response in the gut only begins to mature at six weeks of age. |
Exploitation Route | Vaccines that focus on a cell-mediated immune response, or alternatively some way of speeding up the production of antibodies in broiler chickens, may offer more promising routes to controlling Campylobacter. |
Sectors | Agriculture, Food and Drink |
Description | Project partner has shared this data with their industry links. |
First Year Of Impact | 2017 |
Sector | Agriculture, Food and Drink |
Impact Types | Policy & public services |
Description | Masterclass on the microbiome |
Form Of Engagement Activity | Participation in an open day or visit at my research institution |
Part Of Official Scheme? | No |
Geographic Reach | National |
Primary Audience | Public/other audiences |
Results and Impact | As part of a University offer day event I gave a presentation on the Microbiome. I discussed issues to do with the effect of production techniques and personal dietry behaviour with parents. |
Year(s) Of Engagement Activity | 2018 |
Description | Pint of Science (Leicester) |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | Regional |
Primary Audience | Public/other audiences |
Results and Impact | Approximately 40 members of the general public attended a PhD-student PE activity named the "Pint-of-Science" where general talks are given in pubs. My presentation on the microbiome generated many questions and a discussion on maintaining a healthy microbiota. |
Year(s) Of Engagement Activity | 2019 |
Description | Publication in Food Safety Magazine |
Form Of Engagement Activity | A magazine, newsletter or online publication |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Professional Practitioners |
Results and Impact | Spotlight article in the US Food Safety Magazine |
Year(s) Of Engagement Activity | 2016 |