|
|
||||||||
and Its Target Genes and the Age-Specific Response to Enteric Salmonella Infection1
Mucosal Immunology Laboratory, Pediatric Gastroenterology and Nutrition Unit, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA 02129
Young infants are highly susceptible to systemic dissemination of enteric pathogens such as Salmonella typhimurium when compared with older individuals. The mechanisms underlying this differential susceptibility have not been defined clearly. To better understand this phenomenon, we examined the responses of adult mice and preweaned pups to oral infection by S. typhimurium. We found clear age-specific differences, namely, an attenuated intestinal inflammatory response and a higher systemic bacterial burden in the pups compared with the adults. To elucidate the molecular basis for these differences, we obtained a microarray-based profile of gene expression in the small intestines of uninfected adult and preweaned animals. The results indicated a striking age-dependent increase in the intestinal expression of a number of IFN-
-regulated genes involved in antimicrobial defense. This finding was confirmed by real-time quantitative PCR, which also demonstrated an age-dependent increase in intestinal expression of IFN-
. The developmental up-regulation of the IFN-
-regulated genes was dependent on both IFN-
and a normal commensal microflora, as indicated by experiments in IFN-
-knockout mice and germfree mice, respectively. However, the increase in expression of IFN-
itself was independent of the commensal flora. The functional importance of IFN-
in the immunological maturation of the intestine was confirmed by the observation that the response of adult IFN-
-knockout animals to S. typhimurium infection resembled that of the wild-type pups. Our findings thus reveal a novel role for IFN-
in the developmental regulation of antimicrobial responses in the intestine.
This article has been cited by other articles:
![]() |
L. Wang, E. E. Johnson, H. N. Shi, W. A. Walker, M. Wessling-Resnick, and B. J. Cherayil Attenuated Inflammatory Responses in Hemochromatosis Reveal a Role for Iron in the Regulation of Macrophage Cytokine Translation J. Immunol., August 15, 2008; 181(4): 2723 - 2731. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Harrington, C. V. Srikanth, R. Antony, S. J. Rhee, A. L. Mellor, H. N. Shi, and B. J. Cherayil Deficiency of Indoleamine 2,3-Dioxygenase Enhances Commensal-Induced Antibody Responses and Protects against Citrobacter rodentium-Induced Colitis Infect. Immun., July 1, 2008; 76(7): 3045 - 3053. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Jupelli, M. N. Guentzel, P. A. Meier, G. Zhong, A. K. Murthy, and B. P. Arulanandam Endogenous IFN-{gamma} Production Is Induced and Required for Protective Immunity against Pulmonary Chlamydial Infection in Neonatal Mice J. Immunol., March 15, 2008; 180(6): 4148 - 4155. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Weng, D. Huntley, I-F. Huang, O. Foye-Jackson, L. Wang, A. Sarkissian, Q. Zhou, W. A. Walker, B. J. Cherayil, and H. N. Shi Alternatively Activated Macrophages in Intestinal Helminth Infection: Effects on Concurrent Bacterial Colitis J. Immunol., October 1, 2007; 179(7): 4721 - 4731. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Echeverry, K. Schesser, and B. Adkins Murine Neonates Are Highly Resistant to Yersinia enterocolitica following Orogastric Exposure Infect. Immun., May 1, 2007; 75(5): 2234 - 2243. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. F. Ortega-Cava, S. Ishihara, M. A. K. Rumi, M. M. Aziz, H. Kazumori, T. Yuki, Y. Mishima, I. Moriyama, C. Kadota, N. Oshima, et al. Epithelial Toll-Like Receptor 5 Is Constitutively Localized in the Mouse Cecum and Exhibits Distinctive Down-Regulation during Experimental Colitis Clin. Vaccine Immunol., January 1, 2006; 13(1): 132 - 138. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |