1887

Abstract

Summary: A deletion mutation in , the gene encoding the structural subunit protein of CS1 fimbriae of enterotoxigenic of serotype O6:K15:H16 or H -, was constructed in the subcloned CS1 genetic determinant. The mutation resulted in the abolition of CS1 fimbrial adhesiveness. Complementation, involving the determinant with the deletion mutation and the gene encoding the structural subunit protein, CsoA, expressed from compatible plasmids, restored the expression and adhesive ability of CS1 fimbriae. In addition, -complementation was achieved between the determinant with the aforementioned deletion mutation and the gene encoding the structural subunit protein (CfaB) of CFA/I fimbriae, resulting in the expression of CFA/I fimbriae. The observation that heterologous assembly was possible between these two fimbrial systems, together with the knowledge that the adhesin of CFA/I fimbriae is the structural subunit, was exploited to investigate whether CsoA had adhering properties. A deletion mutation in was created in the CFA/I fimbrial determinant. Complementation of this mutation with resulted in expression of the CsoA antigen on the bacterial cell surface and restoration of bacterial adherence. As no minor subunits act as the adhesin in CFA/I fimbriae, adhesion was mediated by CsoA. Nucleotide sequencing of the DNA region downstream from confirmed the absence of genes encoding minor subunits which might act as the adhesin. Two open reading frames were revealed which encoded proteins sharing considerable homology with proteins encoded by corresponding ORFs in the CFA/I fimbrial operon. These proteins underlie the functional similarities between the CS1 and CFA/I fimbrial systems, allowing heterologous expression of their respective subunits.

Loading

Article metrics loading...

/content/journal/micro/10.1099/13500872-141-11-2849
1995-11-01
2019-11-13
Loading full text...

Full text loading...

http://instance.metastore.ingenta.com/content/journal/micro/10.1099/13500872-141-11-2849
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error