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dc.contributor.authorMedeiros, Jansen Fernandes
dc.contributor.authorAlmeida, Tatiana Amaral Pires
dc.contributor.authorSilva, Lucyane Bastos Tavares
dc.contributor.authorRubio Muñoz, Jose Miguel 
dc.contributor.authorCrainey, James Lee
dc.contributor.authorPessoa, Felipe Arley Costa
dc.contributor.authorLuz, Sergio Luiz Bessa
dc.date.accessioned2017-09-04T16:34:56Z
dc.date.available2017-09-04T16:34:56Z
dc.date.issued2015-05-20
dc.identifier.citationParasit Vectors. 2015; 8:280
dc.identifier.urihttp://hdl.handle.net/20.500.12105/4853
dc.description.abstractBACKGROUND: Mansonella ozzardi is a poorly understood human filarial parasite with a broad distribution throughout Latin America. Most of what is known about its parasitism has come from epidemiological studies that have estimated parasite incidence using light microscopy. Light microscopy can, however, miss lighter, submicroscopic, infections. In this study we have compared M. ozzardi incidence estimates made using light microscopy, with estimates made using PCR. METHODS: 214 DNA extracts made from Large Volume Venous Blood Samples (LVVBS) were taken from volunteers from two study sites in the Rio Solimões region: Codajás [n = 109] and Tefé [n = 105] and were subsequently assayed for M. ozzardi parasitism using a diagnostic PCR (Mo-dPCR). Peripheral finger-prick blood samples were taken from the same individuals and used for microscopic examination. Finger-prick blood, taken from individuals from Tefé, was also used for the creation of FTAcard dried blood spots (DBS) that were subsequently subjected to Mo-dPCR. RESULTS: Overall M. ozzardi incidence estimates made with LVVBS PCRs were 1.8 times higher than those made using microscopy (44.9% [96/214] compared with 24.3% [52/214]) and 1.5 times higher than the PCR estimates made from FTAcard DBS (48/105 versus 31/105). PCR-based detection of FTAcard DBS proved 1.3 times more sensitive at diagnosing infections from peripheral blood samples than light microscopy did: detecting 24/105 compared with 31/105. PCR of LVVBS reported the fewest number of false negatives, detecting: 44 of 52 (84.6%) individuals diagnosed by microscopy; 27 of 31 (87.1%) of those diagnosed positive from DBSs and 17 out of 18 (94.4%) of those diagnosed as positive by both alternative methodologies. CONCLUSIONS: In this study, Mo-dPCR of LVVBS was by far the most sensitive method of detecting M. ozzardi infections and detected submicroscopic infections. Mo-dPCR FTAcard DBS also provided a more sensitive test for M. ozzardi diagnosis than light microscopy based diagnosis did and thus in settings where only finger-prick assays can be carried-out, it may be a more reliable method of detection. Most existing M. ozzardi incidence estimates, which are often based on light microscope diagnosis, are likely to dramatically underestimate true M. ozzardi parasitism incidence levels.
dc.description.sponsorshipJansen Fernandes de Medeiros had financial support from edital PPSUS FAPEAM/SUSAM/MS/CNPq 007/2009. FAPEAM also provided finical support for the work of: Tatiana Amaral Pires de Almeida; Lucyane Bastos Tavares da Silva and J. Lee Crainey. The authors would like to thank Ricardo Mota and personal at Tefé for their technical assistance and two referees for their useful comments, which have helped to improve the manuscript. This paper is contribution number 23 of the Research Programme on Infectious Disease Ecology in the Amazon (RP-IDEA) of the Instituto Leônidas and Maria Deane—Fiocruz Amazônia.
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.isversionofPublisher's version
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectMansonelliasis
dc.subjectMansonella ozzardi
dc.subjectPCR-detection
dc.subjectSubmicroscopic
dc.subjectFTA®cards
dc.titleA field trial of a PCR-based Mansonella ozzardi diagnosis assay detects high-levels of submicroscopic M. ozzardi infections in both venous blood samples and FTA® card dried blood spots
dc.typeArtículo
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID25990611
dc.format.volume8
dc.format.number1
dc.format.page280
dc.identifier.doi10.1186/s13071-015-0889-z
dc.description.peerreviewed
dc.identifier.e-issn1756-3305
dc.relation.publisherversionhttps://doi.org/10.1186/s13071-015-0889-z
dc.identifier.journalParasites & Vectors
dc.repisalud.centroISCIII::Centro Nacional de Microbiología::Área de Bacteriología, Micología Y Parasitología::Servicio de Parasitología::Unidad de Malaria y Protozoos Emergentes
dc.repisalud.institucionISCIII
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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