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pubmed-article:9766898pubmed:abstractTextThe development of a polymerase chain reaction (PCR) based fingerprinting method for the characterization of Giardia duodenalis isolates is described. The method uses three different PCRs; one is specific for the A ("Polish") major group of G. duodenalis isolates, another is specific for the B ("Belgian") group of isolates; and one amplifies a fragment of the glutamate dehydrogenase gene present in all G. duodenalis isolates. The PCRs perform highly sensitively on DNA from cultured trophozoites. Isolates were further characterized by restriction-fragment-length polymorphism (RFLP) analysis of the PCR products. In this way, representative isolates from the A and B groups could be grouped together into a number of subgroups. The stability of the genotypes with time and the reproducibility of the two methods were tested on cloned and subcloned lines from a number of isolates and proved to be highly satisfactory. The PCR/RFLP method was evaluated on cysts derived from a number of human patients. It is concluded that the PCR fingerprinting method described in this paper provides a reliable characterization method for Giardia isolates and has the potential to be used as a direct method of typing G. duodenalis cysts from feces.lld:pubmed
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pubmed-article:9766898pubmed:authorpubmed-author:van KnapenFFlld:pubmed
pubmed-article:9766898pubmed:authorpubmed-author:HomanW LWLlld:pubmed
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pubmed-article:9766898pubmed:articleTitleCharacterization of Giardia duodenalis by polymerase-chain-reaction fingerprinting.lld:pubmed
pubmed-article:9766898pubmed:affiliationMicrobiological Laboratory of Health Protection, National Institute of Public Health and the Environment, Bilthoven, The Netherlands. wieger.homan@rivm.nllld:pubmed
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