The use of Escherichia coli total antigens as a complementary approach to address seropositivity to Leishmania antigens in canine leishmaniosis

Autor: Luís Cardoso, João R. Mesquita, Ana Rafaela Teixeira, Nuno Santarém, Anabela Cordeiro da Silva, Hugo Brancal, Célia G. Amorim, Carla Lima, Thomas W. Vahlenkamp
Přispěvatelé: Instituto de Investigação e Inovação em Saúde
Rok vydání: 2017
Předmět:
Protozoan Proteins
Recombinant Proteins/blood
Serology
law.invention
0403 veterinary science
0302 clinical medicine
law
Protozoan Proteins/blood
Antigens
Bacterial/blood

Dog Diseases
Leishmania infantum
Adenosine Triphosphatases
SEC Translocation Channels/blood
Dog Diseases/diagnosis
biology
Leishmaniasis
Visceral/diagnosis

Leishmania infantum/isolation & purification
04 agricultural and veterinary sciences
Dog Diseases/immunology
Recombinant Proteins
3. Good health
Infectious Diseases
Cohort
Recombinant DNA
Leishmaniasis
Visceral

Enzyme-Linked Immunosorbent Assay/veterinary
040301 veterinary sciences
030231 tropical medicine
Antigens
Protozoan

Enzyme-Linked Immunosorbent Assay
Sensitivity and Specificity
03 medical and health sciences
Dogs
Bacterial Proteins
Antigen
parasitic diseases
Escherichia coli
medicine
Animals
Adenosine Triphosphatases/blood
Bacterial Proteins/blood
Antigens
Bacterial

SecA Proteins
Escherichia coli/immunology
Portugal
Leishmaniasis
Antigens
Protozoan/blood

biology.organism_classification
Leishmania
medicine.disease
Virology
Leishmaniasis
Visceral/immunology

Parasitology
Immunology
Animal Science and Zoology
Leishmaniasis
Visceral/veterinary

SEC Translocation Channels
Zdroj: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
ISSN: 1469-8161
0031-1820
Popis: Canine 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. This 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.
Databáze: OpenAIRE