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Random sorting of Campylobacter jejuni phase variants due to a narrow bottleneck during colonization of broiler chickens

Phase variation (PV), involving stochastic switches in gene expression, is exploited by the human pathogen Campylobacter jejuni to adapt to different environmental and host niches. Phase-variable genes of C. jejuni modulate expression of multiple surface determinants, and hence may influence host co...

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Autores principales: Wanford, Joseph J., Lango-Scholey, Lea, Nothaft, Harald, Hu, Yue, Szymanski, Christine M., Bayliss, Christopher D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097035/
https://www.ncbi.nlm.nih.gov/pubmed/29856309
http://dx.doi.org/10.1099/mic.0.000669
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author Wanford, Joseph J.
Lango-Scholey, Lea
Nothaft, Harald
Hu, Yue
Szymanski, Christine M.
Bayliss, Christopher D.
author_facet Wanford, Joseph J.
Lango-Scholey, Lea
Nothaft, Harald
Hu, Yue
Szymanski, Christine M.
Bayliss, Christopher D.
author_sort Wanford, Joseph J.
collection PubMed
description Phase variation (PV), involving stochastic switches in gene expression, is exploited by the human pathogen Campylobacter jejuni to adapt to different environmental and host niches. Phase-variable genes of C. jejuni modulate expression of multiple surface determinants, and hence may influence host colonization. Population bottlenecks can rapidly remove the diversity generated by PV, and strict single-cell bottlenecks can lead to propagation of PV states with highly divergent phenotypes. Using a combination of high-throughput fragment size analysis and comparison with in vivo and in silico bottleneck models, we have characterized a narrow population bottleneck during the experimental colonization of broiler chickens with C. jejuni strain 81-176. We identified high levels of variation in five PV genes in the inoculum, and subsequently, massively decreased population diversity following colonization. Each bird contained a dominant five-gene phasotype that was present in the inoculum indicative of random sorting through a narrow, non-selective bottleneck during colonization. These results are evidence of the potential for confounding effects of PV on in vivo studies of Campylobacter colonization factors and poultry vaccine studies. Our results are also an argument for population bottlenecks as mediators of stochastic variability in the propensity to survive through the food chain and cause clinical human disease.
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spelling pubmed-60970352018-08-20 Random sorting of Campylobacter jejuni phase variants due to a narrow bottleneck during colonization of broiler chickens Wanford, Joseph J. Lango-Scholey, Lea Nothaft, Harald Hu, Yue Szymanski, Christine M. Bayliss, Christopher D. Microbiology (Reading) Research Article Phase variation (PV), involving stochastic switches in gene expression, is exploited by the human pathogen Campylobacter jejuni to adapt to different environmental and host niches. Phase-variable genes of C. jejuni modulate expression of multiple surface determinants, and hence may influence host colonization. Population bottlenecks can rapidly remove the diversity generated by PV, and strict single-cell bottlenecks can lead to propagation of PV states with highly divergent phenotypes. Using a combination of high-throughput fragment size analysis and comparison with in vivo and in silico bottleneck models, we have characterized a narrow population bottleneck during the experimental colonization of broiler chickens with C. jejuni strain 81-176. We identified high levels of variation in five PV genes in the inoculum, and subsequently, massively decreased population diversity following colonization. Each bird contained a dominant five-gene phasotype that was present in the inoculum indicative of random sorting through a narrow, non-selective bottleneck during colonization. These results are evidence of the potential for confounding effects of PV on in vivo studies of Campylobacter colonization factors and poultry vaccine studies. Our results are also an argument for population bottlenecks as mediators of stochastic variability in the propensity to survive through the food chain and cause clinical human disease. Microbiology Society 2018-06 2018-06-01 /pmc/articles/PMC6097035/ /pubmed/29856309 http://dx.doi.org/10.1099/mic.0.000669 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wanford, Joseph J.
Lango-Scholey, Lea
Nothaft, Harald
Hu, Yue
Szymanski, Christine M.
Bayliss, Christopher D.
Random sorting of Campylobacter jejuni phase variants due to a narrow bottleneck during colonization of broiler chickens
title Random sorting of Campylobacter jejuni phase variants due to a narrow bottleneck during colonization of broiler chickens
title_full Random sorting of Campylobacter jejuni phase variants due to a narrow bottleneck during colonization of broiler chickens
title_fullStr Random sorting of Campylobacter jejuni phase variants due to a narrow bottleneck during colonization of broiler chickens
title_full_unstemmed Random sorting of Campylobacter jejuni phase variants due to a narrow bottleneck during colonization of broiler chickens
title_short Random sorting of Campylobacter jejuni phase variants due to a narrow bottleneck during colonization of broiler chickens
title_sort random sorting of campylobacter jejuni phase variants due to a narrow bottleneck during colonization of broiler chickens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097035/
https://www.ncbi.nlm.nih.gov/pubmed/29856309
http://dx.doi.org/10.1099/mic.0.000669
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