Altered Innate Defenses in the Neonatal Gastrointestinal Tract in Response to Colonization by Neuropathogenic Escherichia coli

被引:41
作者
Birchenough, George M. H. [1 ]
Johansson, Malin E. V. [2 ]
Stabler, Richard A. [3 ]
Dalgakiran, Fatma [1 ]
Hansson, Gunnar C. [2 ]
Wren, Brendan W. [3 ]
Luzio, J. Paul [4 ]
Taylor, Peter W. [1 ]
机构
[1] UCL, Sch Pharm, London, England
[2] Univ Gothenburg, Mucin Biol Grp, Gothenburg, Sweden
[3] London Sch Hyg & Trop Med, London WC1, England
[4] Univ Cambridge, Cambridge Inst Med Res, Cambridge, England
基金
瑞典研究理事会; 英国医学研究理事会;
关键词
K1 CAPSULAR POLYSACCHARIDE; PANETH CELLS; BACTERIAL-MENINGITIS; MOLECULAR ANALYSIS; POLYSIALIC ACID; EXPRESSION; MICROBIOTA; INFECTION; NEWBORN; HOST;
D O I
10.1128/IAI.00268-13
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Two-day-old (P2), but not 9-day-old (P9), rat pups are susceptible to systemic infection following gastrointestinal colonization by Escherichia coli K1. Age dependency reflects the capacity of colonizing K1 to translocate from gastrointestinal (GI) tract to blood. A complex GI microbiota developed by P2, showed little variation over P2 to P9, and did not prevent stable K1 colonization. Substantial developmental expression was observed over P2 to P9, including upregulation of genes encoding components of the small intestinal (alpha-defensins Defa24 and Defa-rs1) and colonic (trefoil factor Tff2) mucus barrier. K1 colonization modulated expression of these peptides: developmental expression of Tff2 was dysregulated in P2 tissues and was accompanied by a decrease in mucin Muc2. Conversely, alpha-defensin genes were upregulated in P9 tissues. We propose that incomplete development of the mucus barrier during early neonatal life and the capacity of colonizing K1 to interfere with mucus barrier maturation provide opportunities for neuropathogen translocation into the bloodstream.
引用
收藏
页码:3264 / 3275
页数:12
相关论文
共 75 条
[1]   6 WIDESPREAD BACTERIAL CLONES AMONG ESCHERICHIA-COLI K1 ISOLATES [J].
ACHTMAN, M ;
MERCER, A ;
KUSECEK, B ;
POHL, A ;
HEUZENROEDER, M ;
AARONSON, W ;
SUTTON, A ;
SILVER, RP .
INFECTION AND IMMUNITY, 1983, 39 (01) :315-335
[2]   The probiotic Escherichia coli strain Nissle 1917 interferes with invasion of human intestinal epithelial cells by different enteroinvasive bacterial pathogens [J].
Altenhoefer, A ;
Oswald, S ;
Sonnenborn, U ;
Enders, C ;
Schulze, J ;
Hacker, J ;
Oelschlaeger, TA .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2004, 40 (03) :223-229
[3]   Comparative Analysis of Human Gut Microbiota by Barcoded Pyrosequencing [J].
Andersson, Anders F. ;
Lindberg, Mathilda ;
Jakobsson, Hedvig ;
Backhed, Fredrik ;
Nyren, Pal ;
Engstrand, Lars .
PLOS ONE, 2008, 3 (07)
[4]   Acidobactetia phylum sequences in uranium-contaminated subsurface sediments greatly expand the known diversity within the phylum [J].
Barns, Susan M. ;
Cain, Elizabeth C. ;
Sommerville, Leslie ;
Kuske, Cheryl R. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (09) :3113-3116
[5]   Muc2 Protects against Lethal Infectious Colitis by Disassociating Pathogenic and Commensal Bacteria from the Colonic Mucosa [J].
Bergstrom, Kirk S. B. ;
Kissoon-Singh, Vanessa ;
Gibson, Deanna L. ;
Ma, Caixia ;
Montero, Marinieve ;
Sham, Ho Pan ;
Ryz, Natasha ;
Huang, Tina ;
Velcich, Anna ;
Finlay, B. Brett ;
Chadee, Kris ;
Vallance, Bruce A. .
PLOS PATHOGENS, 2010, 6 (05)
[6]   Paneth cells, antimicrobial peptides and maintenance of intestinal homeostasis [J].
Bevins, Charles L. ;
Salzman, Nita H. .
NATURE REVIEWS MICROBIOLOGY, 2011, 9 (05) :356-368
[7]   Molecular analysis of the bacterial microbiota in the human stomach [J].
Bik, EM ;
Eckburg, PB ;
Gill, SR ;
Nelson, KE ;
Purdom, EA ;
Francois, F ;
Perez-Perez, G ;
Blaser, MJ ;
Relman, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (03) :732-737
[8]   Epidemiology, Diagnosis, and Antimicrobial Treatment of Acute Bacterial Meningitis [J].
Brouwer, Matthijs C. ;
Tunkel, Allan R. ;
van de Beek, Diederik .
CLINICAL MICROBIOLOGY REVIEWS, 2010, 23 (03) :467-+
[9]   PANETH CELL-DIFFERENTIATION IN THE DEVELOPING INTESTINE OF NORMAL AND TRANSGENIC MICE [J].
BRY, L ;
FALK, P ;
HUTTNER, K ;
OUELLETTE, A ;
MIDTVEDT, T ;
GORDON, JI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (22) :10335-10339
[10]  
CHAMBERS JA, 1994, J CELL SCI, V107, P413