A polymerase chain reaction/ligase detection reaction fluorescent microsphere assay to determine Plasmodium falciparum MSP-119 haplotypes
| dc.contributor.author | Dent, Arlene E. | |
| dc.contributor.author | Yohn, Christopher T. | |
| dc.contributor.author | Zimmerman, Peter A. | |
| dc.contributor.author | Vulule, John M. | |
| dc.contributor.author | Kazura, James W. | |
| dc.contributor.author | Moormann, Ann M. | |
| dc.date | 2022-08-11T08:10:40.000 | |
| dc.date.accessioned | 2022-08-23T17:15:50Z | |
| dc.date.available | 2022-08-23T17:15:50Z | |
| dc.date.issued | 2007-08-11 | |
| dc.date.submitted | 2010-06-08 | |
| dc.identifier.citation | Am 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.issn | 0002-9637 (Linking) | |
| dc.identifier.pmid | 17690395 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14038/47256 | |
| dc.description.abstract | 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. | |
| dc.language.iso | en_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.rights | Copyright © 2007 by The American Society of Tropical Medicine and Hygiene. | |
| dc.subject | Adult | |
| dc.subject | Animals | |
| dc.subject | Child | |
| dc.subject | DNA, Protozoan | |
| dc.subject | Fluorescent Dyes | |
| dc.subject | Haplotypes | |
| dc.subject | Humans | |
| dc.subject | Kenya | |
| dc.subject | Malaria Vaccines | |
| dc.subject | Malaria, Falciparum | |
| dc.subject | Merozoite Surface Protein 1 | |
| dc.subject | Microspheres | |
| dc.subject | Plasmodium falciparum | |
| dc.subject | Polymerase Chain Reaction | |
| dc.subject | Prevalence | |
| dc.subject | RNA, Ribosomal, 18S | |
| dc.subject | Sensitivity and Specificity | |
| dc.subject | Biostatistics | |
| dc.subject | Epidemiology | |
| dc.subject | Health Services Research | |
| dc.subject | Immunology and Infectious Disease | |
| dc.subject | Pediatrics | |
| dc.title | A polymerase chain reaction/ligase detection reaction fluorescent microsphere assay to determine Plasmodium falciparum MSP-119 haplotypes | |
| dc.type | Journal Article | |
| dc.source.journaltitle | The American journal of tropical medicine and hygiene | |
| dc.source.volume | 77 | |
| dc.source.issue | 2 | |
| dc.identifier.legacyfulltext | https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1399&context=qhs_pp&unstamped=1 | |
| dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/qhs_pp/399 | |
| dc.identifier.contextkey | 1347930 | |
| refterms.dateFOA | 2022-08-23T17:15:50Z | |
| 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.submissionpath | qhs_pp/399 | |
| dc.contributor.department | Department of Pediatrics | |
| dc.contributor.department | Department of Quantitative Health Sciences | |
| dc.source.pages | 250-5 |
