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Journal of Clinical Microbiology, July 2004, p. 3262-3271, Vol. 42, No. 7
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.7.3262-3271.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Detection and Genotyping of Entamoeba histolytica, Entamoeba dispar, Giardia lamblia, and Cryptosporidium parvum by Oligonucleotide Microarray

Zheng Wang,* Gary J. Vora, and David A. Stenger

Center for Bio/Molecular Science & Engineering, Naval Research Laboratory, Washington, D.C. 20375

Received 7 January 2004/ Returned for modification 11 February 2004/ Accepted 28 March 2004

Entamoeba histolytica, Giardia lamblia, and Cryptosporidium parvum are the most frequently identified protozoan parasites causing waterborne disease outbreaks. The morbidity and mortality associated with these intestinal parasitic infections warrant the development of rapid and accurate detection and genotyping methods to aid public health efforts aimed at preventing and controlling outbreaks. In this study, we describe the development of an oligonucleotide microarray capable of detecting and discriminating between E. histolytica, Entamoeba dispar, G. lamblia assemblages A and B, and C. parvum types 1 and 2 in a single assay. Unique hybridization patterns for each selected protozoan were generated by amplifying six to eight diagnostic sequences/organism by multiplex PCR; fluorescent labeling of the amplicons via primer extension; and subsequent hybridization to a set of genus-, species-, and subtype-specific covalently immobilized oligonucleotide probes. The profile-based specificity of this methodology not only permitted for the unequivocal identification of the six targeted species and subtypes, but also demonstrated its potential in identifying related species such as Cryptosporidium meleagridis and Cryptosporidium muris. In addition, sensitivity assays demonstrated lower detection limits of five trophozoites of G. lamblia. Taken together, the specificity and sensitivity of the microarray-based approach suggest that this methodology may provide a promising tool to detect and genotype protozoa from clinical and environmental samples.

* Corresponding author. Mailing address: Center for Bio/Molecular Science & Engineering, Naval Research Laboratory, 4555 Overlook Ave. SW, Washington, DC 20375. Phone: (202) 404-1007. Fax: (202) 767-9594. E-mail: zwang{at}cbmse.nrl.navy.mil.

Journal of Clinical Microbiology, July 2004, p. 3262-3271, Vol. 42, No. 7
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.7.3262-3271.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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