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Infection and Immunity, October 1998, p. 4917-4923, Vol. 66, No. 10
Department of Biological
Sciences1 and
Gastrointestinal Research
Group,2 University of Calgary, Calgary,
Alberta, Canada T2N 1N4
Received 10 March 1998/Returned for modification 15 June
1998/Accepted 21 July 1998
The increased intestinal absorption induced by epidermal growth
factor (EGF) is associated with diffuse lengthening of brush border
microvilli. The aim of this study was to examine the in vivo effects of
oral administration of EGF during infection with enteropathogenic
Escherichia coli. New Zealand White rabbits (4 weeks old)
received orogastric EGF daily starting 3 days prior to infection with
enteropathogenic E. coli RDEC-1 and were compared with
sham-treated infected animals and uninfected controls. Weight gain,
food intake, fecal E. coli, and stool consistency were
assessed daily. On day 10, segments of jejunum, ileum, proximal, and
distal colon were assessed for gram-negative bacterial colonization, disaccharidase activities, and epithelial ultrastructure. Effects of
EGF on E. coli RDEC-1 proliferation were studied in vitro. E. coli RDEC-1 caused diarrhea and reduced weight gain.
Seven days postinfection, the small and large intestines were colonized with numerous bacteria, brush border microvilli were disrupted, and
maltase and sucrase activities were significantly reduced in the
jejunum. Daily treatment with EGF prevented the occurrence of diarrhea
and reduction of weight gain. These effects were associated with
significant inhibition of E. coli colonization in the small and large intestine, improved jejunal maltase and sucrase activities and reduced microvillous injury. EGF did not affect the proliferation of E. coli in vitro. The findings suggest that EGF protects
the gastrointestinal tract against colonization by enteropathogenic E. coli.
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Effects of Orally Administered Epidermal Growth
Factor on Enteropathogenic Escherichia coli Infection
in Rabbits
*
Corresponding author. Mailing address: University of
Calgary, Dept. of Biological Sciences, 2500 University Dr. NW, Calgary, AB, Canada T2N 1N4. Phone: (403) 220-2817. Fax: (403) 289-9311. E-mail:
aburet{at}acs.ucalgary.ca.
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