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Clinical and Vaccine Immunology, May 2006, p. 561-567, Vol. 13, No. 5
1071-412X/06/$08.00+0     doi:10.1128/CVI.13.5.561-567.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Use of Miniaturized Protein Arrays for Escherichia coli O Serotyping

Muna F. Anjum,1* James D. Tucker,1 Katherine A. Sprigings,1 Martin J. Woodward,1 and Ralf Ehricht2

Department of Food and Environmental Safety, Veterinary Laboratories Agency-Weybridge, New Haw, Addlestone, Surrey KT15 3NB, United Kingdom,1 CLONDIAG Chip Technologies GmbH, Jena, Germany2

Received 27 July 2005/ Returned for modification 14 September 2005/ Accepted 16 February 2006

Serological typing of Escherichia coli O antigens is a well-established method used for differentiation and identification of O serotypes commonly associated with disease. In this feasibility study, we have developed a novel somatic antibody-based miniaturized microarray chip, using 17 antisera, which can be used to detect bound whole-cell E. coli antigen with its corresponding immobilized antibody, to assess the feasibility of this approach. The chip was tested using the related 17 control strains, and the O types found by the microarray chip showed 100% correlation with the O types found by conventional typing. A blind trial was performed in which 100 E. coli isolates that had been O serotyped previously by the conventional assay were tested by the array approach. Overall, the O serotypes of 88% of isolates were correctly identified by the microarray method. For several isolates, ambiguity of O-type designation by microarray arose due to increased sensitivity of this method, allowing signal intensities of cross-reactions to be quantified. Investigation of discrepancies between conventional and microarray O serotyping indicated that some isolates upon storage had become untypeable and, therefore, gave poor signal intensity when tested by the microarray or retested by conventional means. For all 20 serotype O26 and O157 isolates, the apparent discrepancy in O serotyping was analyzed further by a third independent test, which confirmed the microarray results. Therefore, the use of miniaturized protein arrays increases the speed and efficiency of O serotyping in a cost-effective manner, and these preliminary findings suggest the microarray approach may have a higher accuracy than those of traditional O-serotyping methods.


* Corresponding author. Mailing address: Department of Food and Environmental Safety, Veterinary Laboratories Agency-Weybridge, New Haw, Addlestone, Surrey KT15 3NB, United Kingdom. Phone: 44 (0)1932 359476. Fax: 44 (0)1932 357268. E-mail: m.anjum{at}vla.defra.gsi.gov.uk.


Clinical and Vaccine Immunology, May 2006, p. 561-567, Vol. 13, No. 5
1071-412X/06/$08.00+0     doi:10.1128/CVI.13.5.561-567.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




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