Differentiation of F18ab+ from F18ac+ Escherichia coli by Single-Strand Conformational Polymorphism Analysis of the Major Fimbrial Subunit Gene (fedA)

Authors

Brad T. Bosworth, Enteric Diseases and Food Safety Research UnitFollow
Evelyn A. Dean-Nystrom, National Animal Disease Center
Thomas A. Casey, National Animal Disease Center
Holly L. Neibergs, University of LouisvilleFollow

Date of this Version

5-1998

Citation

CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 5(3): (May 1998), p. 299–302

Abstract

Toxin-producing Escherichia coli expressing F18 fimbriae colonizes the small intestines of weaned pigs and causes diarrhea, edema disease, or both. The F18 family is composed of two antigenic variants, F18ab and F18ac. Because many strains do not express F18 fimbriae in vitro, identification and differentiation of these two variants are difficult. Single-strand conformational polymorphism (SSCP) analysis is a rapid method for identifying genetic mutations and polymorphisms. The F18 major fimbrial subunit genes (fedA) of 138 strains were amplified by PCR, and genetic differences were detected by SSCP analysis. The SSCP analysis of the fedA gene differentiated F18ab⁺ strains from F18ac⁺ strains. Most strains classified as F18ab⁺ by SSCP analysis contained Shiga toxin 2e and enterotoxin genes. Most strains classified as F18ac⁺ by SSCP analysis contained only enterotoxin genes. The SSCP analysis was a useful method for predicting the antigenicity of F18⁺ E. coli and could also be used for analysis of other virulence genes in E. coli and other pathogenic bacteria.