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dc.contributor.authorMartín Martín, María Jesús 
dc.contributor.authorRayner, Julian C
dc.contributor.authorGagneux, Pascal
dc.contributor.authorBarnwell, John W
dc.contributor.authorVarki, Ajit
dc.date.accessioned2025-09-05T07:30:02Z
dc.date.available2025-09-05T07:30:02Z
dc.date.issued2005-09-06
dc.identifier.citationMartin MJ, Rayner JC, Gagneux P, Barnwell JW, Varki A. Evolution of human-chimpanzee differences in malaria susceptibility: relationship to human genetic loss of N-glycolylneuraminic acid. Proc Natl Acad Sci U S A. 2005 Sep 6;102(36):12819-24. doi: 10.1073/pnas.0503819102.es_ES
dc.identifier.issn0027-8424
dc.identifier.urihttp://hdl.handle.net/10366/166958
dc.description.abstractChimpanzees are the closest evolutionary cousins of humans, sharing >99% identity in most protein sequences. Plasmodium falciparum is the major worldwide cause of malaria mortality. Plasmodium reichenowi, a morphologically identical and genetically very similar parasite, infects chimpanzees but not humans. Conversely, experimental P. falciparum infection causes brief moderate parasitization and no severe infection in chimpanzees. This surprising host specificity remains unexplained. We modified and enhanced traditional methods for measuring sialic acid (Sia)-dependent recognition of glycophorins by merozoite erythrocyte-binding proteins, eliminating interference caused by endogenous Sias on transfected cells, and by using erythroleukemia cells to allow experimental manipulation of Sia content. We present evidence that these remarkable differences among such closely related host-parasite pairs is caused by species-specific erythrocyte-recognition profiles, apparently related to the human-specific loss of the common primate Sia N-glycolylneuraminic acid. The major merozoite-binding protein erythrocyte-binding antigen-175 of P. falciparum apparently evolved to take selective advantage of the excess of the Sia N-acetylneuraminic acid (the precursor of N-glycolylneuraminic acid) on human erythrocytes. The contrasting preference of P. reichenowi erythrocyte-binding antigen-175 for N-glycolylneuraminic acid is likely the ancestral condition. The surprising ability of P. falciparum to cause disease in New World Aotus monkeys (geographically isolated from P. falciparum until arrival of peoples from the Old World) can be explained by parallel evolution of a human-like Sia expression pattern in these distantly related primates. These results also have implications for the prehistory of hominids and for the genetic origins and recent emergence of P. falciparum as a major human pathogen.es_ES
dc.language.isoenges_ES
dc.publisherhttps://www.pnas.org/doi/full/10.1073/pnas.0503819102es_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMalariaes_ES
dc.subjectSialic acides_ES
dc.subjectEvolutiones_ES
dc.subject.meshGenetic Predisposition to Disease *
dc.subject.meshTransfection *
dc.subject.meshPan troglodytes *
dc.subject.meshErythrocytes *
dc.subject.meshHumans *
dc.subject.meshNeuraminidase *
dc.subject.meshNeuraminic Acids *
dc.subject.meshCell Line *
dc.subject.meshMicroscopy *
dc.subject.meshMalaria *
dc.subject.meshHost-Parasite Interactions *
dc.subject.meshPlasmodium falciparum *
dc.subject.meshAnimals *
dc.subject.meshSpecies Specificity *
dc.subject.meshN-Acetylneuraminic Acid *
dc.titleEvolution of human-chimpanzee differences in malaria susceptibility: relationship to human genetic loss of N-glycolylneuraminic acides_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1073/PNAS.0503819102es_ES
dc.subject.unesco2403 Bioquímicaes_ES
dc.identifier.doi10.1073/pnas.0503819102
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccesses_ES
dc.identifier.pmid16126901
dc.identifier.essn1091-6490
dc.journal.titleProceedings of the National Academy of Sciences of the United States of Americaes_ES
dc.volume.number102es_ES
dc.issue.number36es_ES
dc.page.initial12819es_ES
dc.page.final12824es_ES
dc.type.hasVersioninfo:eu-repo/semantics/draftes_ES
dc.subject.decsácidos neuramínicos *
dc.subject.decsmalaria *
dc.subject.decshumanos *
dc.subject.decsneuraminidasa *
dc.subject.decslínea celular *
dc.subject.decstransfección *
dc.subject.decsmicroscopía *
dc.subject.decsespecificidad de especies *
dc.subject.decsanimales *
dc.subject.decsPlasmodium falciparum *
dc.subject.decsinteracciones huésped-parásito *
dc.subject.decsácido N-acetilneuramínico *
dc.subject.decseritrocitos *
dc.subject.decspredisposición genética a la enfermedad *
dc.subject.decsPan troglodytes *


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