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Species-specific identification of human hookworms by PCR of the mitochondrial cytochrome oxidase I gene.
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- Author(s): Zhan B;Zhan B; Li T; Xiao S; Zheng F; Hawdon JM
- Source:
The Journal of parasitology [J Parasitol] 2001 Oct; Vol. 87 (5), pp. 1227-9.- Publication Type:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.- Language:
English - Source:
- Additional Information
- Source: Publisher: American Society of Parasitologists [etc.] Country of Publication: United States NLM ID: 7803124 Publication Model: Print Cited Medium: Print ISSN: 0022-3395 (Print) Linking ISSN: 00223395 NLM ISO Abbreviation: J Parasitol Subsets: MEDLINE
- Publication Information: Original Publication: Lawrence, Kans. [etc.] American Society of Parasitologists [etc.]
- Subject Terms: Ancylostoma/*classification ; Ancylostomiasis/*parasitology ; DNA, Helminth/*genetics ; Electron Transport Complex IV/*genetics ; Necator americanus/*classification ; Necatoriasis/*parasitology; Ancylostoma/enzymology ; Ancylostoma/genetics ; Animals ; Base Sequence ; China ; Cricetinae ; DNA, Helminth/chemistry ; DNA, Helminth/isolation & purification ; DNA, Mitochondrial/chemistry ; DNA, Mitochondrial/genetics ; DNA, Mitochondrial/isolation & purification ; Electron Transport Complex IV/chemistry ; Humans ; Mesocricetus ; Molecular Sequence Data ; Necator americanus/enzymology ; Necator americanus/genetics ; Polymerase Chain Reaction/methods ; Sensitivity and Specificity ; Sequence Homology, Nucleic Acid ; Species Specificity
- Abstract: Significant differences in the life histories of the human hookworms Ancylostoma duodenale and Necator americanus necessitate their differentiation for epidemiological studies and the design of control programs. Current methods of identification require time-consuming, labor-intensive techniques. A polymerase chain reaction (PCR)-based method that enables rapid species identification is described. The mitochondrial cytochrome oxidase I genes of both species were sequenced, and species-specific primer sets were designed. The primers were used in PCR to amplify 585-bp fragments of the cytochrome oxidase gene from individual hookworm eggs, larvae, and adults. The technique was also able to identify mixed infections containing equal amounts of eggs from each species. The technique is rapid, technically simple, and sensitive and will permit the accurate identification of human hookworms in epidemiological field studies.
- Grant Information: AI-32726 United States AI NIAID NIH HHS; P50 AI-39461 United States AI NIAID NIH HHS
- Accession Number: 0 (DNA, Helminth)
0 (DNA, Mitochondrial)
EC 1.9.3.1 (Electron Transport Complex IV) - Publication Date: Date Created: 20011107 Date Completed: 20011204 Latest Revision: 20071114
- Publication Date: 20240513
- Accession Number: 10.1645/0022-3395(2001)087[1227:SSIOHH]2.0.CO;2
- Accession Number: 11695411
- Source:
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