Immunization with inactivated antigens of Neospora caninum induces toll-like receptors 3, 7, 8 and 9 in maternal-fetal interface of infected pregnant heifers

Neospora caninum is an obligate parasite and a major cause of abortion in cattle. Pregnancy failures appear to be associated with weak innate defences on the maternal-fetal interface during infection with N. caninum. Herein, we studied the gene expression of Toll-like receptors (TLRs) in pregnant he...

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Autor principal: Marin, M.S
Otros Autores: Hecker, Y.P, Quintana, S., Pérez, S.E, Leunda, M.R, Cantón, G.J, Cobo, E.R, Moore, D.P, Odeón, A.C
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Elsevier B.V. 2017
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024 7 |2 cas  |a gamma interferon, 82115-62-6; toll like receptor 9, 352486-49-8, 390883-32-6; toll like receptor, 409141-78-2; Antigens, Protozoan; Toll-Like Receptors 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a VPARD 
100 1 |a Marin, M.S. 
245 1 0 |a Immunization with inactivated antigens of Neospora caninum induces toll-like receptors 3, 7, 8 and 9 in maternal-fetal interface of infected pregnant heifers 
260 |b Elsevier B.V.  |c 2017 
270 1 0 |m Marin, M.S.; Instituto Nacional de Tecnología Agropecuaria (INTA), Estación Experimental Agropecuaria Balcarce, Ruta 226 Km 73.5, Balcarce, Argentina; email: marin.maia@inta.gob.ar 
506 |2 openaire  |e Política editorial 
504 |a Almeria, S., Serrano-Pérez, B., Darwich, L., Mur-Novales, R., Garcia-Ispierto, I., Cabezón, O., López-Gatius, F., Cytokine gene expression in aborting and non-aborting dams and in their foetuses after experimental infection with Neospora caninum at 110 days of gestation (2016) Vet. Parasitol., 227, pp. 138-142 
504 |a Bartley, P.M., Katzer, F., Rocchi, M.S., Maley, S.W., Benavides, J., Nath, M., Pang, Y., Innes, E.A., Development of maternal and foetal immune responses in cattle following experimental challenge with Neospora caninum at day 210 of gestation (2013) Vet. Res., 3, pp. 44-91 
504 |a Basso, W., Venturini, L., Venturini, M.C., Hill, D.E., Kwok, O.C.H., Shen, S.K., Dubey, J.P., First isolation of Neospora caninum from the feces of a naturally infected dog (2001) J. Parasitol., 87, pp. 612-618 
504 |a Beiting, D.P., Peixoto, L., Akopyants, N.S., Beverley, S.M., Wherry, E.J., Christian, D.A., Hunter, C.A., Roos, D.S., Differential induction of TLR3-dependent innate immune signaling by closely related parasite species (2014) PLoS One, 9, p. e88398 
504 |a Cóceres, V.M., Alonso, A.M., Alomar, M.L., Corvi, M.M., Rabbit antibodies against Toxoplasma Hsp20 are able to reduce parasite invasion and gliding motility in Toxoplasma gondii and parasite invasion in Neospora caninum (2012) Exp. Parasitol., 132, pp. 274-281 
504 |a Cannas, A., Naguleswaran, A., Müller, N., Eperon, S., Gottstein, B., Hemphill, A., Vaccination of mice against experimental Neospora caninum infection using NcSAG1- and NcSRS2-based recombinant antigens and DNA vaccines (2003) Parasitology, 126, pp. 303-312 
504 |a Chaouat, G., Zourbas, S., Ostojic, S., Ostojic, S., Lappree-Delage, G., Dubanchet, S., Ledee, N., Martal, J., A brief review of recent data on some cytokine expressions at the materno–interface which might challenge the classical Th1/Th2 dichotomy (2002) J. Reprod. Immunol., 53, pp. 241-256 
504 |a Dubey, J.P., Schares, G., Neosporosis in animals-the last five years (2011) Vet. Parasitol., 180, pp. 90-108 
504 |a Dubey, J.P., Hattel, A.L., Lindsay, D.S., Topper, M.J., Neonatal Neospora caninum infection in dogs: isolation of the causative agent and experimental transmission (1988) J. Am. Vet. Med. Assoc., 193, pp. 1259-1263 
504 |a Dubey, J.P., Review of Neospora caninum and neosporosis in animals (2003) Korean J. Parasitol., 41, pp. 1-16 
504 |a Ghosh, D., Stumhofer, J.S., Do you see what I see: recognition of protozoan parasites by toll-like receptors (2013) Curr. Immunol. Rev., 9, pp. 129-140 
504 |a Haddad, J.P., Dohoo, I.R., VanLeewen, J.A., A review of Neospora caninum in dairy and beef cattle–a Canadian perspective (2005) Can. Vet. J., 46, pp. 230-243 
504 |a Hecker, Y.P., Moore, D.P., Quattrocchi, V., Regidor-Cerrillo, J., Verna, A., Leunda, M.R., Morrell, E., Campero, C.M., Immune response and protection provided by live tachyzoites and native antigens from the NC-6 Argentina strain of Neospora caninum in pregnant heifers (2013) Vet. Parasitol., 197, pp. 436-446 
504 |a Hecker, Y.P., Cóceres, V., Wilkowsky, S.E., Jaramillo Ortiz, J.M., Morrell, E., Verna, A., Ganuza, A., Moore, D.P., A Neospora caninum vaccine using recombinant proteins fails to prevent fetal infection in pregnant cattle after experimental challenge (2014) Vet. Immunol. Immunopathol., 162, pp. 142-153 
504 |a Hecker, Y.P., Cantón, G., Regidor-Cerrillo, J., Chianini, F., Morrell, E., Lischinsky, L., Ortega-Mora, L.M., Moore, D.P., Cell mediated immune responses in the placenta following challenge of vaccinated pregnant heifers with Neospora caninum (2015) Vet. Parasitol., 214, pp. 247-254 
504 |a Hemphill, A., Vonlaufen, N., Naguleswaran, A., Cellular and immunological basis of the host-parasite relationship during infection with Neospora caninum (2006) Parasitology, 133, pp. 261-278 
504 |a Huang, P., Liao, M., Zhang, H., Lee, E.G., Nishikawa, Y., Xuan, X., Dense granule protein NcGRA7, a new marker for the serodiagnosis of Neospora caninum infection in aborting cows (2007) Clin. Vacc. Immunol., 14, pp. 1640-1643 
504 |a Innes, E.A., Wright, S.E., Maley, S., Rae, A., Schock, A., Kirvar, E., Bartley, P., Buxton, D., Protection against vertical transmission in bovine neosporosis (2001) Int. J. Parasitol., 31, pp. 1523-1534 
504 |a Innes, E.A., Andrianarivo, A.G., Björkman, C., Williams, D.J.L., Conrad, P.A., Immune responses to Neospora caninum and prospects for vaccination (2002) Trends Parasitol., 18, pp. 497-504 
504 |a Innes, E.A., The host-parasite relationship in pregnant cattle infected with Neospora caninum (2007) Parasitology, 134, pp. 1903-1910 
504 |a Koga, K., Mor, G., Expression and function of toll-like receptors at the maternal-fetal interface (2008) Reprod. Sci., 15, pp. 231-242 
504 |a Marin, M.S., Quintana, S., Faverín, C., Leunda, M.R., Odeón, A.C., Pérez, S.E., Toll-like receptor activation and expression in bovine alpha-herpesvirus infections (2014) Res. Vet. Sci., 96, pp. 196-203 
504 |a Marin, M.S., Hecker, Y.P., Quintana, S., Pérez, S.E., Leunda, M.R., Cantón, G.J., Cobo, E.R., Odeón, A.C., Toll-like receptors 3, 7 and 8 are upregulated in the placental caruncle and fetal spleen of Neospora caninum experimentally infected cattle (2017) Vet. Parasitol., 236, pp. 58-61 
504 |a McGuire, K., Manuja, A., Russell, G., Springbett, A., Craigmile, S., Nichani, A., Malhotra, D., Glass, E., Quantitative analysis of pro-inflammatory cytokine mRNA expression in Theileria annulata-infected cell lines derived from resistant and susceptible cattle (2004) Vet. Immunol. Immunopathol., 99, pp. 87-98 
504 |a Mineo, T.W., Oliveira, C.J., Gutierrez, F.R., Silva, J.S., Recognition by Toll-like receptor 2 induces antigen-presenting cell activation and Th1 programming during infection by Neospora caninum (2010) Immunol. Cell Biol., 88, pp. 825-833 
504 |a Nishikawa, Y., Zhang, H., Ikehara, Y., Kojima, N., Xuan, X., Yokoyama, N., Immunization with oligomannose-coated liposome-entrapped dense granule protein 7 protects dams and offspring from Neospora caninum infection in mice (2009) Clin. Vacc. Immunol., 16, pp. 792-797 
504 |a Pérez, S., Analysis of Bovine Tonsils and Trigeminal Ganglia Following Infection with Bovine Herpesvirus Type 1 (BHV-1) or a BHV-1 Latency-related Mutant Strain (Doctoral Thesis) (2006), p. 313. , University of Nebrasca-Lincoln USA; Paun, A., Bankoti, R., Joshi, T., Pitha, P.M., Stäger, S., Critical Role of IRF-5 in the Development of T helper 1 responses to Leishmania donovani infection (2011) PLoS Pathog., 7, p. e1001246 
504 |a Pfaffl, M., Horgan, G., Demplfle, L., Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR (2002) Nucleic Acids Res., 30, p. e36 
504 |a Raghupathy, R., Th-1 type immunity is incompatible with successful pregnancy (1997) Immunol. Today, 18, pp. 478-482 
504 |a Reichel, M.P., Ayanegui-Alcérreca, M.A., Gondim, L.F.P., Ellis, J.T., What is theglobal economic impact of Neospora caninum in cattle–the billion dollar question (2013) Int. J. Parasitol., 43, pp. 133-142 
504 |a Ribeiro, D.P., Freitas, M.M., Cardoso, M.R., Pajuaba, A.C., Silva, N.M., Mineo, T.W., Silva, J.S., Silva, D.A., CpG-ODN combined with Neospora caninum lysate, but not with excreted-secreted antigen, enhances protection against infection in mice (2009) Vaccine, 27, pp. 2570-2579 
504 |a Trees, A.J., Williams, D.J.L., Endogenous and exogenous transplacental infection in Neospora caninum and Toxoplasma gondii (2005) Trends Parasitol., 2, pp. 558-561 
520 3 |a Neospora caninum is an obligate parasite and a major cause of abortion in cattle. Pregnancy failures appear to be associated with weak innate defences on the maternal-fetal interface during infection with N. caninum. Herein, we studied the gene expression of Toll-like receptors (TLRs) in pregnant heifers immunized with different vaccine formulations against N. caninum before mating and then challenged the heifers with live N. caninum on day 70 of gestation. TLR7 and TLR8 expression was upregulated in the placental caruncle of infected-pregnant heifers previously exposed to live N. caninum as immunogen. However, TLR7 and 8 expression in both placenta and caruncle as well as, TLR3 and 9 expression in caruncle were upregulated when heifers were previously immunized with inactivated soluble whole antigens and recombinant NcSAG1, NcHSP20 and NcGRA7 proteins. All dams were carrying viable fetuses when they were culled at day 104 of gestation. Upregulation of TLR7 and IFNγ expression was detected in fetal spleen when their mothers where previously vaccinated with soluble antigens and recombinant NcSAG1, NcHSP20 and NcGRA7 proteins. These studies demonstrate that soluble or recombinant NcSAG1, NcHSP20 and NcGRA7 antigens induce key TLRs expression at the maternal-fetal interface, probably triggering damaging inflammatory cellular immune responses associated with abortion. Previous infection with N. caninum seems to attenuate the innate immune response at the maternal-fetal interface, which could favour pregnancy maintenance and perpetuation of the disease. This finding represents novel information on how N. caninum vaccination and infection modulate TLRs expression at the placenta and fetal spleen, the possible role in the pregnancy outcomes and transplacental transmission of the protozoa. © 2017 Elsevier B.V.  |l eng 
536 |a Detalles de la financiación: European Environment Agency 
536 |a Detalles de la financiación: Instituto Nacional de Tecnología Agropecuaria, PNSA-115053, 2013-0393, PICTs 2008-1421 
536 |a Detalles de la financiación: Faculty of Veterinary Medicine, Cairo University 
536 |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica 
536 |a Detalles de la financiación: This study was financially supported by INTA, Specific Project PNSA-115053 and PICTs 2008-1421 and 2013-0393 (ANPCyT). We especially thank Emily Boucher (University of Calgary, Faculty of Veterinary Medicine) for revising and editing the manuscript and Susana Pereyra (INTA, EEA Balcarce, Argentina) for her contribution and support to the study. 
593 |a Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rivadavia 1917, Buenos Aires, C1033AAJ, Argentina 
593 |a Instituto Nacional de Tecnología Agropecuaria (INTA), Estación Experimental Agropecuaria Balcarce, Ruta 226 Km 73.5, Balcarce, Buenos Aires, 7620, Argentina 
593 |a Centro de Investigación en Abejas Sociales, Departamento de Biología, Facultad de Ciencias Exactas y Naturales, UNMDP, Funes 3350, Mar del Plata, Buenos Aires, 7600, Argentina 
593 |a Centro de Investigación Veterinaria de Tandil (CIVETAN, CONICET-CICPBA), Facultad de Ciencias Veterinarias, UNCPBA, Paraje Arroyo Seco s/n, Tandil, Buenos Aires, 7000, Argentina 
593 |a Production Animal Health, Faculty of Veterinary Medicine, University of Calgary, Canada 
690 1 0 |a CATTLE 
690 1 0 |a MATERNAL-FETAL INTERFACE 
690 1 0 |a NEOSPORA CANINUM 
690 1 0 |a TOLL-LIKE RECEPTOR EXPRESSION 
690 1 0 |a VACCINE 
690 1 0 |a GAMMA INTERFERON 
690 1 0 |a HEAT SHOCK PROTEIN 20 
690 1 0 |a INACTIVATED VACCINE 
690 1 0 |a PARASITE ANTIGEN 
690 1 0 |a PROTEIN GRA7 
690 1 0 |a PROTEIN SAG1 
690 1 0 |a TOLL LIKE RECEPTOR 3 
690 1 0 |a TOLL LIKE RECEPTOR 7 
690 1 0 |a TOLL LIKE RECEPTOR 8 
690 1 0 |a TOLL LIKE RECEPTOR 9 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a PARASITE ANTIGEN 
690 1 0 |a TOLL LIKE RECEPTOR 
690 1 0 |a ABORTION 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ANIMAL MODEL 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a BREEDING 
690 1 0 |a CELLULAR IMMUNITY 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DAM (ANIMAL) 
690 1 0 |a FEMALE 
690 1 0 |a FETUS 
690 1 0 |a HEIFER 
690 1 0 |a IMMUNITY 
690 1 0 |a INFLAMMATION 
690 1 0 |a INNATE IMMUNITY 
690 1 0 |a MATERNAL FETAL INTERFACE 
690 1 0 |a NEOSPOROSIS 
690 1 0 |a NONHUMAN 
690 1 0 |a PROTEIN EXPRESSION 
690 1 0 |a SPLEEN 
690 1 0 |a UPREGULATION 
690 1 0 |a VACCINATION 
690 1 0 |a ANIMAL 
690 1 0 |a BOVINE 
690 1 0 |a CATTLE DISEASE 
690 1 0 |a COCCIDIOSIS 
690 1 0 |a IMMUNIZATION 
690 1 0 |a IMMUNOLOGY 
690 1 0 |a METABOLISM 
690 1 0 |a NEOSPORA 
690 1 0 |a PARASITOLOGY 
690 1 0 |a PREGNANCY 
690 1 0 |a PREGNANCY COMPLICATION 
690 1 0 |a VETERINARY 
690 1 0 |a ANIMALS 
690 1 0 |a ANTIGENS, PROTOZOAN 
690 1 0 |a CATTLE 
690 1 0 |a CATTLE DISEASES 
690 1 0 |a COCCIDIOSIS 
690 1 0 |a FEMALE 
690 1 0 |a IMMUNITY, CELLULAR 
690 1 0 |a IMMUNIZATION 
690 1 0 |a NEOSPORA 
690 1 0 |a PREGNANCY 
690 1 0 |a PREGNANCY COMPLICATIONS, PARASITIC 
690 1 0 |a TOLL-LIKE RECEPTORS 
650 1 7 |2 spines  |a PLACENTA 
650 1 7 |2 spines  |a PLACENTA 
700 1 |a Hecker, Y.P. 
700 1 |a Quintana, S. 
700 1 |a Pérez, S.E. 
700 1 |a Leunda, M.R. 
700 1 |a Cantón, G.J. 
700 1 |a Cobo, E.R. 
700 1 |a Moore, D.P. 
700 1 |a Odeón, A.C. 
773 0 |d Elsevier B.V., 2017  |g v. 243  |h pp. 12-17  |p Vet. Parasitol.  |x 03044017  |w (AR-BaUEN)CENRE-7124  |t Veterinary Parasitology 
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