Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/118196
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dc.creatorLima, C-
dc.creatorMesquita, J-
dc.creatorBrancal, H-
dc.creatorVahlenkamp, T-
dc.creatorTeixeira, AR-
dc.creatorCardoso, L-
dc.creatorAmorim, C-
dc.creatorSantarém, N-
dc.creatorCordeiro-da-Silva, A-
dc.date.accessioned2019-01-08T09:55:08Z-
dc.date.available2019-01-08T09:55:08Z-
dc.date.issued2017-
dc.identifier.issn0031-1820-
dc.identifier.urihttps://repositorio-aberto.up.pt/handle/10216/118196-
dc.description.abstractCanine leishmaniosis (CanL) is a major veterinary concern and a public health issue. Serological data are essential for disease management. Several antigens used in serological assays have specificity related problems preventing relevant seropositivity values establishment. Herein we report significant seropositivity level disparity in a study cohort with 384 dogs from eight countries, for antigens traditionally used in CanL - soluble promastigote Leishmania antigens (SPLA) and K39 recombinant protein (rK39): 43·8 and 2·9% for SPLA and rK39, respectively. To better understand the reasons for this disparity, CanL-associated serological response was characterized using, for complement serological evaluation, a ubiquitous antigen - soluble Escherichia coli antigens (SECAs). Using cohorts of CanL dogs and dogs without clinical evidences of CanL from non-endemic regions of Portugal, the serological response of CanL animals followed specific trend of seropositivity rK39 > SPLA > SECA absent in non-diseased animals. Using receiver operating characteristic curve analysis, these characteristic trends were converted in ratios, SPLA/SECA, rK39/SECA and rK39/SPLA, that presented high predictive for discriminating the CanL cohort that was potentiated when applied in a scoring system involving positivity to four out of five predictors (rK39, SPLA, SPLA/SECA, rK39/SECA and rK39/SPLA). In fact, this approach discriminated CanL with similar sensitivity/specificity as reference antigens, diminishing seropositivity in European cohort to 1·8%. Ultimately, non-related antigens like SECA and seropositivity ratios between antigens enable different perspectives into serological data focusing on the search of characteristic serological signatures and not simple absolute serology values contributing to comprehensive serological status characterization.-
dc.description.sponsorshipThis work was financed by FEDER–Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020–Operacional Programme for Competitiveness and Internationalisation (POCI), Portugal 2020, and by Portuguese funds through FCT Fundação para a Ciência e a Tecnologia/Ministério da Ciência, Tecnologia e Ensino Superior in the framework of the project‘Institute for Research and Innovation in Health Sciences’(POCI-01-0145-FEDER-007274) and from the European Community’s Seventh Framework Programme under grant agreement No. 603181 [Clinical Studies on a Multivalent Vaccine for Human Visceral Leishmaniasis (MuLeVaClin)]. ‘This article is a result of the project NORTE-01-0145-FEDER-000012, supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF)’. C.L. and N.S. were supported by BD SFRH/BD/89183/2012 and European Community’s Seventh Framework Programme under grant agreement No. 602773 (Project KINDRED), respectively.-
dc.language.isoeng-
dc.publisherCambridge University Press-
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F89183%2F2012/PT-
dc.relation.ispartofParasitology, vol.144(10), p. 1384-1393-
dc.rightsopenAccess-
dc.subject.meshAdenosine Triphosphatases/blood-
dc.subject.meshAnimals-
dc.subject.meshAntigens, Bacterial/blood-
dc.subject.meshAntigens, Protozoan/blood-
dc.subject.meshBacterial Proteins/blood-
dc.subject.meshDog Diseases/diagnosis-
dc.subject.meshDog Diseases/immunology-
dc.subject.meshDogs-
dc.subject.meshEnzyme-Linked Immunosorbent Assay/veterinary-
dc.subject.meshEscherichia coli/immunology-
dc.subject.meshLeishmania infantum/isolation & purification-
dc.subject.meshLeishmaniasis, Visceral/diagnosis-
dc.subject.meshLeishmaniasis, Visceral/immunology-
dc.subject.meshLeishmaniasis, Visceral/veterinary-
dc.subject.meshPortugal-
dc.subject.meshProtozoan Proteins/blood-
dc.subject.meshRecombinant Proteins/blood-
dc.subject.meshSEC Translocation Channels/blood-
dc.subject.meshSensitivity and Specificity-
dc.titleThe use of Escherichia coli total antigens as a complementary approach to address seropositivity to Leishmania antigens in canine leishmaniosis-
dc.typeArtigo em Revista Científica Internacional-
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde-
dc.identifier.doi10.1017/S0031182017000713-
dc.relation.publisherversionhttps://www.cambridge.org/core/journals/parasitology/article/use-of-escherichia-coli-total-antigens-as-a-complementary-approach-to-address-seropositivity-to-leishmania-antigens-in-canine-leishmaniosis/A8D231DB5EC4B4CCE10A067404AA5C6F-
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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