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Infection and Immunity, October 2007, p. 4687-4696, Vol. 75, No. 10
0019-9567/07/$08.00+0     doi:10.1128/IAI.00009-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Functional Consequences of Sequence Variation in Bundlin, the Enteropathogenic Escherichia coli Type IV Pilin Protein{triangledown}

Paula J. Fernandes,{dagger} Qin Guo, and Michael S. Donnenberg*

Division of Infectious Diseases, University of Maryland School of Medicine, 20 Penn Street, Baltimore, Maryland 21201

Received 3 January 2007/ Returned for modification 16 March 2007/ Accepted 10 July 2007

The bundle-forming pilus (BFP) of enteropathogenic Escherichia coli (EPEC) is an important virulence factor. We examined the role of divergent alleles of bfpA encoding bundlin, the BFP pilin protein, in pilus biogenesis, pilus interactions, and immune responses. We found that the BFP biogenesis machine from an EPEC strain that expresses one bundlin type is capable of assembling all other bundlin types. Furthermore, we found that EPEC strains expressing divergent bundlin types are capable of forming mixed autoaggregates, suggesting that different pilin types can intertwine. However, we found that there was a marked difference between alleles in immunogenicity in both rabbits and mice of a peptide derived from a region of bundlin undergoing apparent diversifying selection. In addition, despite a high degree of cross-reactivity between divergent bundlin proteins, in both mice and rabbits responses appeared to be stronger against the homologous pilin protein than against the heterologous protein. This result was verified using sera from a volunteer study, which demonstrated that the human antibody responses after an initial challenge with live EPEC were stronger against the homologous bundlin protein than against a divergent bundlin protein. However, a repeat challenge induced equivalent responses. These results are consistent with the hypothesis that human immune responses against bundlin exert selective pressure on bfpA sequence divergence.

* Corresponding author. Mailing address: Division of Infectious Diseases, University of Maryland School of Medicine, HSF2 S403D, 20 Penn Street, Baltimore, MD 21201. Phone: (410) 706-7562. Fax: (410) 706-8700. E-mail: mdonnenb{at}umaryland.edu

{triangledown} Published ahead of print on 16 July 2007.

Editor: V. J. DiRita

{dagger} Present address: Association of Public Health Laboratories, 8515 Georgia Avenue, Suite 700, Silver Spring, MD 20910.

Infection and Immunity, October 2007, p. 4687-4696, Vol. 75, No. 10
0019-9567/07/$08.00+0     doi:10.1128/IAI.00009-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

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