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Multiple factors interact to produce responses resembling spectrum of human disease in Campylobacter jejuni infected C57BL/6 IL-10(-/- )mice

BACKGROUND: Campylobacter jejuni infection produces a spectrum of clinical presentations in humans – including asymptomatic carriage, watery diarrhea, and bloody diarrhea – and has been epidemiologically associated with subsequent autoimmune neuropathies. This microorganism is genetically variable a...

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Autores principales: Bell, Julia A, St Charles, Jessica L, Murphy, Alice J, Rathinam, Vijay AK, Plovanich-Jones, Anne E, Stanley, Erin L, Wolf, John E, Gettings, Jenna R, Whittam, Thomas S, Mansfield, Linda S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2669091/
https://www.ncbi.nlm.nih.gov/pubmed/19296832
http://dx.doi.org/10.1186/1471-2180-9-57
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author Bell, Julia A
St Charles, Jessica L
Murphy, Alice J
Rathinam, Vijay AK
Plovanich-Jones, Anne E
Stanley, Erin L
Wolf, John E
Gettings, Jenna R
Whittam, Thomas S
Mansfield, Linda S
author_facet Bell, Julia A
St Charles, Jessica L
Murphy, Alice J
Rathinam, Vijay AK
Plovanich-Jones, Anne E
Stanley, Erin L
Wolf, John E
Gettings, Jenna R
Whittam, Thomas S
Mansfield, Linda S
author_sort Bell, Julia A
collection PubMed
description BACKGROUND: Campylobacter jejuni infection produces a spectrum of clinical presentations in humans – including asymptomatic carriage, watery diarrhea, and bloody diarrhea – and has been epidemiologically associated with subsequent autoimmune neuropathies. This microorganism is genetically variable and possesses genetic mechanisms that may contribute to variability in nature. However, relationships between genetic variation in the pathogen and variation in disease manifestation in the host are not understood. We took a comparative experimental approach to explore differences among different C. jejuni strains and studied the effect of diet on disease manifestation in an interleukin-10 deficient mouse model. RESULTS: In the comparative study, C57BL/6 interleukin-10(-/- )mice were infected with seven genetically distinct C. jejuni strains. Four strains colonized the mice and caused disease; one colonized with no disease; two did not colonize. A DNA:DNA microarray comparison of the strain that colonized mice without disease to C. jejuni 11168 that caused disease revealed that putative virulence determinants, including loci encoding surface structures known to be involved in C. jejuni pathogenesis, differed from or were absent in the strain that did not cause disease. In the experimental study, the five colonizing strains were passaged four times in mice. For three strains, serial passage produced increased incidence and degree of pathology and decreased time to develop pathology; disease shifted from watery to bloody diarrhea. Mice kept on an ~6% fat diet or switched from an ~12% fat diet to an ~6% fat diet just before infection with a non-adapted strain also exhibited increased incidence and severity of disease and decreased time to develop disease, although the effects of diet were only statistically significant in one experiment. CONCLUSION: C. jejuni strain genetic background and adaptation of the strain to the host by serial passage contribute to differences in disease manifestations of C. jejuni infection in C57BL/6 IL-10(-/- )mice; differences in environmental factors such as diet may also affect disease manifestation. These results in mice reflect the spectrum of clinical presentations of C. jejuni gastroenteritis in humans and contribute to usefulness of the model in studying human disease.
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spelling pubmed-26690912009-04-15 Multiple factors interact to produce responses resembling spectrum of human disease in Campylobacter jejuni infected C57BL/6 IL-10(-/- )mice Bell, Julia A St Charles, Jessica L Murphy, Alice J Rathinam, Vijay AK Plovanich-Jones, Anne E Stanley, Erin L Wolf, John E Gettings, Jenna R Whittam, Thomas S Mansfield, Linda S BMC Microbiol Research article BACKGROUND: Campylobacter jejuni infection produces a spectrum of clinical presentations in humans – including asymptomatic carriage, watery diarrhea, and bloody diarrhea – and has been epidemiologically associated with subsequent autoimmune neuropathies. This microorganism is genetically variable and possesses genetic mechanisms that may contribute to variability in nature. However, relationships between genetic variation in the pathogen and variation in disease manifestation in the host are not understood. We took a comparative experimental approach to explore differences among different C. jejuni strains and studied the effect of diet on disease manifestation in an interleukin-10 deficient mouse model. RESULTS: In the comparative study, C57BL/6 interleukin-10(-/- )mice were infected with seven genetically distinct C. jejuni strains. Four strains colonized the mice and caused disease; one colonized with no disease; two did not colonize. A DNA:DNA microarray comparison of the strain that colonized mice without disease to C. jejuni 11168 that caused disease revealed that putative virulence determinants, including loci encoding surface structures known to be involved in C. jejuni pathogenesis, differed from or were absent in the strain that did not cause disease. In the experimental study, the five colonizing strains were passaged four times in mice. For three strains, serial passage produced increased incidence and degree of pathology and decreased time to develop pathology; disease shifted from watery to bloody diarrhea. Mice kept on an ~6% fat diet or switched from an ~12% fat diet to an ~6% fat diet just before infection with a non-adapted strain also exhibited increased incidence and severity of disease and decreased time to develop disease, although the effects of diet were only statistically significant in one experiment. CONCLUSION: C. jejuni strain genetic background and adaptation of the strain to the host by serial passage contribute to differences in disease manifestations of C. jejuni infection in C57BL/6 IL-10(-/- )mice; differences in environmental factors such as diet may also affect disease manifestation. These results in mice reflect the spectrum of clinical presentations of C. jejuni gastroenteritis in humans and contribute to usefulness of the model in studying human disease. BioMed Central 2009-03-18 /pmc/articles/PMC2669091/ /pubmed/19296832 http://dx.doi.org/10.1186/1471-2180-9-57 Text en Copyright ©2009 Bell et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Bell, Julia A
St Charles, Jessica L
Murphy, Alice J
Rathinam, Vijay AK
Plovanich-Jones, Anne E
Stanley, Erin L
Wolf, John E
Gettings, Jenna R
Whittam, Thomas S
Mansfield, Linda S
Multiple factors interact to produce responses resembling spectrum of human disease in Campylobacter jejuni infected C57BL/6 IL-10(-/- )mice
title Multiple factors interact to produce responses resembling spectrum of human disease in Campylobacter jejuni infected C57BL/6 IL-10(-/- )mice
title_full Multiple factors interact to produce responses resembling spectrum of human disease in Campylobacter jejuni infected C57BL/6 IL-10(-/- )mice
title_fullStr Multiple factors interact to produce responses resembling spectrum of human disease in Campylobacter jejuni infected C57BL/6 IL-10(-/- )mice
title_full_unstemmed Multiple factors interact to produce responses resembling spectrum of human disease in Campylobacter jejuni infected C57BL/6 IL-10(-/- )mice
title_short Multiple factors interact to produce responses resembling spectrum of human disease in Campylobacter jejuni infected C57BL/6 IL-10(-/- )mice
title_sort multiple factors interact to produce responses resembling spectrum of human disease in campylobacter jejuni infected c57bl/6 il-10(-/- )mice
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2669091/
https://www.ncbi.nlm.nih.gov/pubmed/19296832
http://dx.doi.org/10.1186/1471-2180-9-57
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