J Med Microbiol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hodgson, A. E.
Right arrow Articles by Leach, S. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hodgson, A. E.
Right arrow Articles by Leach, S. A.
Agricola
Right arrow Articles by Hodgson, A. E.
Right arrow Articles by Leach, S. A.

The Journal of Medical Microbiology, Vol 47, Issue 9 799-809, Copyright © 1998 by Society for General Microbiology


JOURNAL ARTICLE

Experimental campylobacter infection and diarrhoea in immunodeficient mice

A. E. Hodgson, B. W. McBride, M. J. Hudson, G. Hall and S. A. Leach
Centre for Applied Microbiology and Research, Salisbury, Wiltshire.

The responses of previously untested immunodeficient mouse strains to campylobacter infection are described. Three strains of adult immunodeficient mice (SCID-Beige, C.B-17-SCID-Beige and RAG-2) were inoculated intragastrically with Campylobacter jejuni NCTC 11168. All mice became heavily colonised, but none developed clinical signs of disease. Immunocompetent BALB/c mice inoculated similarly had much lower colonisation levels. The co-administration of iron dextran had no effect on colonisation levels nor the development of clinical signs of disease. In contrast, C.B-17-SCID-Beige mice, when inoculated with one of a series of 10 clinical isolates of C. jejuni, were more heavily colonised for extended periods (up to 5 months) and approximately 10-20% of the mice became ill with diarrhoea. C. jejuni was detected in mouse faeces throughout at levels of 10(7)-10(9) cfu/g. All mice killed whilst ill with diarrhoea displayed histopathological lesions typical of human campylobacteriosis. Severe pathology was limited to the large intestine and was suggestive of an acute, bacteria-induced inflammation. Although blood was detected in the diarrhoeal stools, no evidence of mucosal epithelial cell invasion was found by immunohistology. No pathology was detected in tissue sections from any of the animals that had not developed signs of disease following C. jejuni inoculation. These immunodeficient mouse strains are readily, and heavily, colonised as adults by C. jejuni. The diarrhoea, although sporadic, was reproducibly produced, and could provide the basis for pathogenicity studies.


This article has been cited by other articles:


Home page
J Med MicrobiolHome page
N. A. Al-Banna, T. A. Junaid, T. C. Mathew, R. Raghupathy, and M. J. Albert
Histopathological and ultrastructural studies of a mouse lung model of Campylobacter jejuni infection
J. Med. Microbiol., February 1, 2008; 57(2): 210 - 217.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
R. O. Watson, V. Novik, D. Hofreuter, M. Lara-Tejero, and J. E. Galan
A MyD88-Deficient Mouse Model Reveals a Role for Nramp1 in Campylobacter jejuni Infection
Infect. Immun., April 1, 2007; 75(4): 1994 - 2003.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
L. S. Mansfield, J. A. Bell, D. L. Wilson, A. J. Murphy, H. M. Elsheikha, V. A. K. Rathinam, B. R. Fierro, J. E. Linz, and V. B. Young
C57BL/6 and Congenic Interleukin-10-Deficient Mice Can Serve as Models of Campylobacter jejuni Colonization and Enteritis
Infect. Immun., March 1, 2007; 75(3): 1099 - 1115.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
C. Chang and J. F. Miller
Campylobacter jejuni Colonization of Mice with Limited Enteric Flora
Infect. Immun., September 1, 2006; 74(9): 5261 - 5271.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
J. G. Fox, A. B. Rogers, M. T. Whary, Z. Ge, N. S. Taylor, S. Xu, B. H. Horwitz, and S. E. Erdman
Gastroenteritis in NF-{kappa}B-Deficient Mice Is Produced with Wild-Type Camplyobacter jejuni but Not with C. jejuni Lacking Cytolethal Distending Toxin despite Persistent Colonization with Both Strains
Infect. Immun., February 1, 2004; 72(2): 1116 - 1125.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
E. C. Gaynor, S. Cawthraw, G. Manning, J. K. MacKichan, S. Falkow, and D. G. Newell
The Genome-Sequenced Variant of Campylobacter jejuni NCTC 11168 and the Original Clonal Clinical Isolate Differ Markedly in Colonization, Gene Expression, and Virulence-Associated Phenotypes
J. Bacteriol., January 15, 2004; 186(2): 503 - 517.
[Abstract] [Full Text] [PDF]


Home page
J Med MicrobiolHome page
D. PURDY, C.M. BUSWELL, A.E. HODGSON, K. McALPINE, I. HENDERSON, and S.A. LEACH
Characterisation of cytolethal distending toxin (CDT) mutants of Campylobacter jejuni
J. Med. Microbiol., May 1, 2000; 49(5): 473 - 479.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
V. B. Young, C. A. Dangler, J. G. Fox, and D. B. Schauer
Chronic Atrophic Gastritis in SCID Mice Experimentally Infected with Campylobacter fetus
Infect. Immun., April 1, 2000; 68(4): 2110 - 2118.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL J MED MICROBIOL MICROBIOLOGY J GEN VIROL ALL SGM JOURNALS
Copyright © 1998 Society for General Microbiology.