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Infection and Immunity, July 2008, p. 3141-3149, Vol. 76, No. 7
0019-9567/08/$08.00+0 doi:10.1128/IAI.01743-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Stephen D. Kachman,2
Michael A. Scott,3
You Zhou,1
David H. Francis,4 and
Rodney A. Moxley1*
Departments of Veterinary & Biomedical Sciences,1 Statistics, University of Nebraska—Lincoln, Lincoln, Nebraska 68583,2 Department of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, Michigan 48824,3 Department of Veterinary Science, South Dakota State University, Brookings, South Dakota 570074
Received 28 December 2007/ Returned for modification 1 April 2008/ Accepted 11 April 2008
In swine, the most common and severe enterotoxigenic Escherichia coli (ETEC) infections are caused by strains that express K88 (F4)+ fimbriae, heat-labile enterotoxin (LT), heat-stable enterotoxin b (STb), and enteroaggregative E. coli heat-stable toxin 1. Previous studies based on a design that involved enterotoxin genes cloned into a nontoxigenic fimbriated strain have suggested that LT but not STb plays an important role in dehydrating diarrheal disease in piglets <1 week old and also enhances bacterial colonization of the intestine. In the present study, we compared these two toxins in terms of importance for piglets >1 week old with a study design that involved construction of isogenic single- and double-deletion mutants and inoculation of 9-day-old F4ac receptor-positive gnotobiotic piglets. Based on the postinoculation percent weight change per h and serum bicarbonate concentrations, the virulence of the STb– mutant (
estB) did not significantly differ from that of the parent. However, deletion of the LT genes (
eltAB) in the STb– mutant resulted in a complete abrogation of weight loss, dehydration, and metabolic acidosis in inoculated pigs, and LT complementation restored the virulence of this strain. These results support the hypothesis that LT is a more significant contributor than STb to the virulence of F4+ ETEC infections in young F4ac receptor-positive pigs less than 2 weeks old. However, in contrast to previous studies with gnotobiotic piglets, there was no evidence that the expression of LT enhanced the ability of the F4+ ETEC strain to colonize the small intestine.
Published ahead of print on 21 April 2008.
Present address: Vaccine and Infectious Disease Organization, University of Saskatchewan, 120 Veterinary Road, Saskatoon, Saskatchewan, S7N 5E3 Canada.
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