An official website of the United States government.

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Genetic Basis of Resistance to Food-Borne Bacterial Pathogens

Objective

Specific Aims: 1. Prepare rabbit hyperimmune sera to hexahistidine-tagged cytolethal distending toxin sub-units of Campylobacter jejuni, Escherichia coli, and Helicobacter hepaticus. 2. Identify cytolethal distending toxin target tissues/cells by overlay immunohistochemical binding assay and confirmation of cellular susceptibilities by fluorescent activated cell sorter analysis.

More information

Campylobacter jejuni and Eschericha coli are leading causes of food-borne bacterial infections in humans worldwide. Helicobacter hepaticus is a related pathogen that causes liver infections and cancer in susceptible mouse strains. A newly discovered toxin known as cytolethal distending toxin is shared among these pathogens. Identification of the receptor(s)for these microbial toxins in susceptible pigs and susceptible and resistant inbred strains of mice will provide the tools necessary for implementation of genetic selection of livestock resistant to food-borne bacterial diseases, and basic understanding of mechanisms for important bacterial diseases of humans and animals.
<p>
Produce hyperimmune rabbit sera to purified His6-tagged cytolethal distending toxin sub-units A, B and C from each microbe. Use the rabbit hyperimmune sera to identify cytolethal distending toxin target cells by overlay immunohistochemistry binding assay with tissues obtained from all major organs of newborn and adult conventional pigs and from inbred strains of mice of both sexes. Cellular susceptibilities to the toxin will be confirmed by indirect staining of single cell suspensions isolated from selected tissues of pigs and mice with individual or combinations of each sub-unit, rabbit antisera, and fluorescent activated cell sorter analysis. A recombinant flagellar bacterial protein will be included in all assays as a negative control.

Investigators
Duhamel, George
Institution
University of Nebraska - Lincoln
Start date
2005
End date
2007
Project number
NEB-14-137
Accession number
203810
Commodities