INTRODUCTION

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Enterotoxigenic Escherichia coli (ETEC) and E. coli organisms that produce Shiga toxin 2e (STEC) colonize the porcine small intestine and cause diarrhea and edema disease, respectively. The fimbrial adhesins of K99, F41, K88, and 987P fimbriae mediate adherence and promote ETEC colonization of the neonatal pig's small intestine. Of these four fimbriae, only K88 is frequently detected in ETEC isolated from both weaned and neonatal pigs (24). The F18 fimbria mediates colonization of both ETEC and STEC in weaned, but not neonatal, pigs. The F18 fimbrial family is composed of two antigenic variants, F18ab and F18ac, and has been previously referred to as F107, 2134P, Av24, and 8813 (1-4, 11, 14, 15, 19, 20, 25).

Differentiation of strains expressing F18ab from those expressing F18ac may be important in development and selection of effective vaccines for ETEC and STEC infections in weaned pigs. Differentiation of strains producing F18ab and F18ac is also important because of a correlation between the type of toxin produced and clinical sequelae in infected swine. F18ab⁺ strains are generally STEC and are associated with edema disease, while F18ac⁺ strains are generally ETEC and are associated with diarrhea (4, 15, 26). Monospecific polyclonal antisera and the monoclonal antibody 6C7/C1, which is specific for F18ac⁺ strains, can differentiate between these two antigenic variants (3, 4, 15, 19). However, serologic differentiation is not always possible because many strains do not express F18 when cultured in vitro under standard culture conditions (1, 8, 25, 26). The gene encoding the major fimbrial subunit of F18 (fedA) in both F18ab⁺ and F18ac⁺ strains has been sequenced, and differences have been found (9). A PCR-restriction fragment length polymorphism (RFLP) test consisting of amplification of the fedA gene followed by digestion with the restriction enzyme NgoMI has been used to differentiate F18ab⁺ from F18ac⁺ strains (9, 15, 19). This PCR-RFLP test avoided the problems of serologic differentiation, which requires in vitro pilus expression, and was based upon the DNA sequences of seven different fedA genes, fedA and fedA.1 to fedA.6 (9). These seven different sequences were determined by sequencing of the fedA genes of only 10 unique strains (9), demonstrating that the fedA gene is highly polymorphic.

Single-strand conformational polymorphism (SSCP) analysis can rapidly identify polymorphisms in a gene and is useful when a large number of samples are being analyzed. Single-strand DNA migrates according to size and shape in a nondenaturing gel. The shape is dependent upon folding due to intermolecular interactions which are DNA sequence dependent (5). The major objective of this study was to determine if SSCP analysis of the fedA gene could differentiate F18ab⁺ from F18ac⁺ strains.

	MATERIALS AND METHODS

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Bacterial strains and SSCP analysis. Identification of fedA⁺ strains in the E. coli collection at the National Animal Disease Center was done by colony blot hybridization with a 510-bp DNA fragment bearing fedA (7). The presence of genes encoding Shiga toxin 2e (Stx2e) and enterotoxins (LT, STa, and STb) was determined by colony blot hybridization (13, 18). A total of 138 unique fedA⁺ strains were analyzed for polymorphisms in fedA by SSCP analysis as previously described (16). Bacterial DNA was isolated by boiling approximately 10⁶ CFU in 30 µl of water for 5 min. The fedA gene was amplified by PCR with fedA-specific primers (sense strand, 5'-GTGAAAAGACTAGTGTTTATTTC-3', and antisense strand, 5'-CTTGTAAGTAACCGCGTAAGC-3') as previously described (7). The 10-µl reaction mixture contained a 1.0 µM concentration of each primer, a 70.0 µM concentration of each deoxynucleoside triphosphate, 2.5 mM MgCl₂, 0.1 µl of [-³²P]dATP (10 µCi/µl), 2 U of Taq polymerase (Promega, Madison, Wis.), and 5 µl of bacterial DNA. A solution containing 5 µl of an amplified product, 1 µl of a 0.1% sodium dodecyl sulfate-0.1 M EDTA solution, and 5 µl of a stop solution (95% formamide; United States Biochemicals, Cleveland, Ohio) was denatured by being heated to 95°C for 5 min. Three microliters of the denatured solution was loaded on a nondenaturing gel and subjected to electrophoresis at 5 W overnight at room temperature. SSCPs were detected by autoradiography of the nondenaturing gel.

DNA sequencing. The fedA gene was amplified by PCR as described above except that no radioactive nucleotides were included and the concentration for each deoxynucleoside triphosphate was increased to 200 µM. The amplified gene was cloned into the PCRII vector and transformed into a recipient strain according to the instructions of the manufacturer of the kit used in the procedure (TA cloning kit; Invitrogen Co., San Diego, Calif.). Three clones for each fedA gene were sequenced with the T7 Sequenase kit (version 2.0; United States Biochemicals) in both directions to ensure that the DNA sequence contained no PCR-generated artifacts. The LASERGENE DNA program (DNASTAR Inc., Madison, Wis.) was used to predict antigenicity of the major fimbrial subunit on the basis of hydrophilicity, surface probability, flexibility, and secondary structure by the method of Jameson and Wolf (10).

Immunoassay. Bacterial strains were grown overnight on Trypticase soy agar at 37°C in 5% CO₂. Expression of F18ac fimbriae was detected by a colony blot immunoassay with the monoclonal antibody 6C7/C1, as previously described (3).

	RESULTS

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SSCP and analysis of deduced amino acids. The SSCP analysis of 138 fedA⁺ strains identified 19 different fedA genes. The fedA gene migrated as three bands corresponding to single-stranded DNA molecules (Fig. 1, upper two bands) and nondenatured double-stranded DNA (Fig. 1, lower band). The SSCP analysis determined that the major fimbrial subunit gene in 125 of the 138 strains was one of the following fedA genes: fedA, fedA.1, fedA.2, fedA.3, fedA.7, and fedA.8 (Fig. 1). Each of the fedA genes of the remaining 13 strains had a unique migration pattern and the DNA sequences were not determined.

View larger version (56K): [in this window] [in a new window]   FIG. 1.   Autoradiograph showing results of an SSCP analysis of the following fedA genes on a nondenaturing gel: fedA (lane A), fedA.1 (lane B), fedA.2 (lane C), fedA.3 (lane D), fedA.7 (lane E), and fedA.8 (lane F). The top two bands are denatured single-stranded DNA, and the bottom band is nondenatured double-stranded DNA. The denatured single-stranded DNA and nondenatured double-stranded DNA in lane A are shown by arrowheads and an arrow, respectively.

View larger version (35K): [in this window] [in a new window]   FIG. 2.   Deduced amino acid sequences (single-letter designation) of the major fimbrial subunit genes fedA and fedA.1, -2, -3, -7, and -8. Amino acid differences are shown, and identical amino acids are represented as dashes. The putative leader peptide is underlined and the predicted antigenic regions are double underlined.

Predicted antigenicity. Computer analysis of the deduced amino acid sequences of all six fedA genes identified the same two regions as highly antigenic. One of the regions was homologous in all six (Fig. 2, amino acids 151 to 160). The other region predicted to be antigenic in all six had a variable amino acid composition (amino acids 116 to 130 [Fig. 2]). The major difference in this region was that fedA genes in F18ac⁺ strains encoded an additional amino acid (proline) not encoded by fedA genes found in F18ab⁺ strains.

Classification of unique fedA genes. The SSCP analysis demonstrated that the fedA genes of F18ab⁺ strains migrate differently than the fedA genes of F18ac⁺ strains. The migration of the uppermost band was slower for fedA and -1 (F18ab⁺ strains) than it was for fedA.2, -3, -7, and -8 (F18ac⁺ strains) (Fig. 1). This difference in migration was used to predict the antigenicity of the 13 strains with unique fedA genes that migrated differently during SSCP analysis than did fedA and fedA.1, -2, -3, -7, and -8. Nine of 11 strains with unique fedA genes classified as F18ac⁺ by this criterion reacted with monoclonal antibody 6C7/C1. Neither of the two strains with unique fedA genes classified as F18ab⁺ by this criterion reacted with the F18ac-specific monoclonal antibody.

Toxin profile and antigenicity. None of the 73 strains identified as F18ab⁺ by SSCP analysis reacted with monoclonal antibody 6C7/C1 (Table 1). Sixty-one of 73 strains (84%) contained the Stx2e gene, while 60 of 73 strains (82%) contained one or more enterotoxin (LT, STa, or STb) genes. Three strains were nontoxigenic.

	DISCUSSION

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Identification of and differentiation between F18ab⁺ and F18ac⁺ strains by serologic techniques are not always possible, because some strains do not express fimbriae when cultured in vitro under standard culture conditions (1, 8, 25, 26). Recently, Wittig et al. reported that in vitro fimbria expression is possible with nonconventional culture techniques (25, 26). Microaerobic culture is required, and some strains require agar containing alizarin yellow and eosin for fimbria expression, which varies from colony to colony for some strains (25).

The DNA sequences of the major fimbrial subunit genes fedA and fedA.1 to -6 were used by Imberechts et al. (9) to develop a PCR-RFLP test that differentiates F18ab⁺ from F18ac⁺ strains. fedA and fedA.1, present in F18ab⁺ strains, do not contain a proline-encoding triplet (CCG) and are resistant to digestion with restriction enzyme NgoMI, which recognizes GCCGGC. fedA.2 to -6, present in F18ac⁺ strains, contain a proline-encoding triplet and are digested by the restriction enzyme NgoMI (9). fedA.7 and -8 also contained this proline-encoding triplet and were classified as F18ac⁺ in the present study. However, fedA.7 and -8 would not be digested by NgoMI because of differences in the base pairs adjacent to the proline-encoding triplet. Strains with these fedA genes would be misclassified as F18ab⁺ by the PCR-RFLP test proposed by Imberechts et al. (9). The accuracy of this PCR-RFLP test when used to classify strains with fedA genes of undetermined sequence identified in the present study or strains with fedA genes not yet identified is unknown.

Others have recently used SSCP analysis to detect genetic polymorphisms in bacterial, viral, and protozoal genes (6, 12, 22, 23). In RFLP analysis, genetic differences in only the recognition site of the restriction enzyme are recognized, while SSCP analysis can detect differences anywhere in the amplified gene. The sensitivity of SSCP analysis to DNA differences is inversely correlated with the size of the amplified product and can be affected by the conditions used with the nondenaturing gel, such as temperature of electrophoresis. It has been estimated that SSCP analysis can detect >80% of single base substitutions in amplicons of 400 bp (5). We analyzed an approximately 500-bp amplicon because it contained the entire open reading frame of the major fimbrial subunit gene. Samples were analyzed on a nondenaturing gel at room temperature as previously described (16). While not all single base substitutions may have been identified in an amplicon of this size under the conditions we used, SSCP analysis differentiated between fedA genes that differed by only two bases (fedA versus fedA.1, fedA.2 versus fedA.3, and fedA.7 versus fedA.8).

SSCP analysis differentiated F18ab⁺ strains from F18ac⁺ strains and identified 19 variations of the fedA gene. Most, but not all, of the strains classified as F18ac⁺ by SSCP analysis reacted with monoclonal antibody 6C7/C1, while none of the strains classified as F18ab⁺ reacted with 6C7/C1. This confirms the specificity of 6C7/C1 for F18ac⁺ E. coli (4, 15) and demonstrates the usefulness of SSCP analysis in differentiating strains that do not express F18 in vitro.

Sixty-one of 73 strains designated F18ab⁺ by SSCP analysis contained the Stx2e gene (STEC) and could cause edema disease. A number of these strains also contained one or more enterotoxin genes and could also cause diarrhea. Diarrhea is occasionally a component of edema disease in field outbreaks and may be caused by strains producing both Stx2e and enterotoxins (17). Only 8 of 65 strains classified as F18ac⁺ by SSCP analysis were STEC, while more than 90% were ETEC. This confirms that F18ab⁺ strains are commonly STEC, while F18ac⁺ strains are frequently ETEC (4, 15, 26).

We were able to classify the 13 strains with unique fedA genes as either F18ab⁺ or F18ac⁺ by SSCP analysis. The upper single-stranded DNA molecules of fedA genes from strains classified as F18ac⁺ migrated farther in the nondenaturing gel than did those from strains classified as F18ab⁺. It is possible that the increased migration of one of the single-stranded fedA DNA molecules in F18ac⁺ strains is due to the proline-encoding triplet (CCG) or its complementary sequence, which is absent in fedA genes of F18ab⁺ strains. This additional triplet could significantly modify folding of the single-stranded DNA, resulting in increased mobility on the nondenaturing gel.

The major difference between fedA genes of F18ab⁺ and F18ac⁺ strains was an additional proline-encoding triplet in the fedA genes of F18ac⁺ strains, and this proline was in a region predicted by this study to be antigenic. This proline may affect antigenicity as a part of the epitope or may indirectly affect antigenicity by modifying secondary structure (9). Recently, it has been shown that inoculation with either F18ab⁺ or F18ac⁺ strains reduces shedding in swine that are subsequently challenged with either the homologous or heterologous F18 antigenic variant (21). Future studies should be directed at determining which amino acids compose the shared epitope(s) of F18ab and F18ac fimbriae. Sequencing several fedA genes increases the likelihood of identifying this shared epitope(s) and should lead to vaccines that prevent disease caused by either F18ab⁺ or F18ac⁺ E. coli.