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dc.contributor.authorDent, Arlene E.
dc.contributor.authorYohn, Christopher T.
dc.contributor.authorZimmerman, Peter A.
dc.contributor.authorVulule, John M.
dc.contributor.authorKazura, James W.
dc.contributor.authorMoormann, Ann M.
dc.date2022-08-11T08:10:40.000
dc.date.accessioned2022-08-23T17:15:50Z
dc.date.available2022-08-23T17:15:50Z
dc.date.issued2007-08-11
dc.date.submitted2010-06-08
dc.identifier.citationAm J Trop Med Hyg. 2007 Aug;77(2):250-5. <a href="http://www.ajtmh.org/cgi/reprint/77/2/250">Link to article on publisher's site</a>
dc.identifier.issn0002-9637 (Linking)
dc.identifier.pmid17690395
dc.identifier.urihttp://hdl.handle.net/20.500.14038/47256
dc.description.abstractThe merozoite surface protein-1 (MSP-1) is a blood stage antigen currently being tested as a vaccine against Plasmodium falciparum malaria. Determining the MSP-1(19) haplotype(s) present during infection is essential for assessments of MSP-1 vaccine efficacy and studies of protective immunity in human populations. The C-terminal fragment (MSP-1(19)) has four predominant haplotypes based on point mutations resulting in non-synonymous amino acid changes: E-TSR (PNG-MAD20 type), E-KNG (Uganda-PA type), Q-KNG (Wellcome type), and Q-TSR (Indo type). Current techniques using direct DNA sequencing are laborious and expensive. We present an MSP-1(19) allele-specific polymerase chain reaction (PCR)/ligase detection reaction-fluorescent microsphere assay (LDR-FMA) that allows simultaneous detection of the four predominant MSP-1(19) haplotypes with a sensitivity and specificity comparable with other molecular methods and a semi-quantitative determination of haplotype contribution in mixed infections. Application of this method is an inexpensive, accurate, and high-throughput alternative to distinguish the predominant MSP-1(19) haplotypes in epidemiologic studies.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=17690395&dopt=Abstract">Link to Article in PubMed</a>
dc.rightsCopyright © 2007 by The American Society of Tropical Medicine and Hygiene.
dc.subjectAdult
dc.subjectAnimals
dc.subjectChild
dc.subjectDNA, Protozoan
dc.subjectFluorescent Dyes
dc.subjectHaplotypes
dc.subjectHumans
dc.subjectKenya
dc.subjectMalaria Vaccines
dc.subjectMalaria, Falciparum
dc.subjectMerozoite Surface Protein 1
dc.subjectMicrospheres
dc.subjectPlasmodium falciparum
dc.subjectPolymerase Chain Reaction
dc.subjectPrevalence
dc.subjectRNA, Ribosomal, 18S
dc.subjectSensitivity and Specificity
dc.subjectBiostatistics
dc.subjectEpidemiology
dc.subjectHealth Services Research
dc.subjectImmunology and Infectious Disease
dc.subjectPediatrics
dc.titleA polymerase chain reaction/ligase detection reaction fluorescent microsphere assay to determine Plasmodium falciparum MSP-119 haplotypes
dc.typeJournal Article
dc.source.journaltitleThe American journal of tropical medicine and hygiene
dc.source.volume77
dc.source.issue2
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1399&amp;context=qhs_pp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/qhs_pp/399
dc.identifier.contextkey1347930
refterms.dateFOA2022-08-23T17:15:50Z
html.description.abstract<p>The merozoite surface protein-1 (MSP-1) is a blood stage antigen currently being tested as a vaccine against Plasmodium falciparum malaria. Determining the MSP-1(19) haplotype(s) present during infection is essential for assessments of MSP-1 vaccine efficacy and studies of protective immunity in human populations. The C-terminal fragment (MSP-1(19)) has four predominant haplotypes based on point mutations resulting in non-synonymous amino acid changes: E-TSR (PNG-MAD20 type), E-KNG (Uganda-PA type), Q-KNG (Wellcome type), and Q-TSR (Indo type). Current techniques using direct DNA sequencing are laborious and expensive. We present an MSP-1(19) allele-specific polymerase chain reaction (PCR)/ligase detection reaction-fluorescent microsphere assay (LDR-FMA) that allows simultaneous detection of the four predominant MSP-1(19) haplotypes with a sensitivity and specificity comparable with other molecular methods and a semi-quantitative determination of haplotype contribution in mixed infections. Application of this method is an inexpensive, accurate, and high-throughput alternative to distinguish the predominant MSP-1(19) haplotypes in epidemiologic studies.</p>
dc.identifier.submissionpathqhs_pp/399
dc.contributor.departmentDepartment of Pediatrics
dc.contributor.departmentDepartment of Quantitative Health Sciences
dc.source.pages250-5


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