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Journal of Clinical Microbiology, July 1998, p. 2043-2045, Vol. 36, No. 7
Vaccine Testing Unit, Department of
International Health, Johns Hopkins University, Baltimore,
Maryland1;
Department of Medical
Microbiology, Red Cross War Memorial Children's Hospital, Cape
Town, South Africa2;
Enteric
Diseases Program, Naval Medical Research Institute, Bethesda,
Maryland3; and
Department of
Epidemiology, University of Texas School of Public Health, Houston,
Texas4
Received 10 December 1997/Returned for modification 24 February
1998/Accepted 30 March 1998
Campylobacter jejuni with Gm1 ganglioside in the core
of its lipopolysaccharide has been associated with Guillain-Barré
syndrome. Since this epitope may be of considerable
pathophysiologic importance and since this ganglioside binds cholera
toxin, a rapid screening assay to detect bacteria that bind cholera
toxin as an indication of Gm1 on their surfaces was developed. In the
assay, bacterial lawns were grown on agar plates, harvested with
phosphate-buffered saline, boiled, and incubated with a standard
concentration of cholera B subunit. Preparations from strains with Gm1
were observed to inhibit the binding of cholera B subunit to Gm1 in a
microtiter enzyme-linked immunosorbent assay. By using this assay with
two groups of strains, 37 positive strains were detected among the 197 tested. Species with positive isolates included C. jejuni, Campylobacter coli, and Helicobacter pylori.
The assay is capable of testing large numbers of isolates and should
prove useful in future clinical and epidemiological studies of bacteria
with this epitope.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Microtiter Assay for Detecting
Campylobacter spp. and Helicobacter pylori with
Surface Gangliosides Which Bind Cholera Toxin
*
Corresponding author. Mailing address: Johns Hopkins
University Vaccine Testing Unit, 550 N. Broadway, Suite 1001, Baltimore, MD 21205. Phone: (410) 955-0053. Fax: (410) 614-9483. E-mail: dsack{at}jhsph.edu.
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