Bovine neosporosis; Mono- and binucleate cells; PAGs; Placental damage
Abstract :
[en] Neospora caninum is an obligate intracellular protozoan that causes abortion in cattle worldwide. Plasma concentrations of pregnancy-associated glycoprotein 1 (PAG-1), produced by binucleate trophoblast cells, are used for pregnancy diagnosis and as a marker of foetal-placental well-being, while PAG-2, produced by both mono- and binucleate trophoblast cells, may serve as an indicator of abortion risk. In prior work, natural N. caninum infection was found to modify plasma PAG-1 and PAG-2 patterns. The present study examines PAG-1 and PAG-2 dynamics and trophoblast cell populations following experimental infection with N. caninum. The study population was comprised of 17 N. caninum seronegative Holstein-Friesian heifers. On day 110 of gestation, 6 heifers were inoculated intravenously with 10(7) taquyzoites of N. canimum. Plasma samples for PAG-1 and PAG-2 determinations were collected on days 0, 7, 14, 21 and 42 post infection. During the study course, pregnancy was normally expressed in all controls while three infected heifers lost their foetuses. All heifers were euthanised on day 42 post infection and placentome samples from the 14 non-aborting heifers were collected to examine trophoblast cell populations. Plasma PAG-1 and PAG-2 concentrations in non-infected heifers increased until the day of euthanasia while non-aborting infected heifers showed a temporary fall in PAG-1 (P<0.004) and PAG-2 (P<0.002) concentrations from 7 to 14 days post infection (dpi). The two dams aborting at 14 and 21 dpi and a third dam with a mummified foetus upon euthanasia showed dramatic PAG-1 and PAG-2 reductions from 14 dpi to undetectable levels upon euthanasia. A stereological study of placentomes revealed significantly higher relative proportions of mono- (P=0.035) and binucleate (P=0.029) trophoblast cells at 42 dpi in non-infected heifers than infected non-aborting heifers. According to our findings, following experimental N. caninum infection on day 110 of gestation, non-aborting heifers showed a brief reversible drop in plasma PAG-1 and 2 concentrations two weeks later and reduced proportions of bi- and mono-nucleate trophoblast cells 42 days after infection. In aborting dams, dramatically reduced PAG levels were related to severe placental damage and a non-viable pregnancy.
Research Center/Unit :
FARAH - Fundamental and Applied Research for Animals and Health - ULiège
Disciplines :
Veterinary medicine & animal health
Author, co-author :
Mur-Novales, R.; University of Lleida, Spain > Department of Animal Production
Serrano-Perez, B.; University of Lleida, Spain > Department of Animal Production
Garcia-Ispierto, I.; University of Lleida, Spain > Department of Animal Production
Melo de Sousa, Noelita ; Université de Liège > Département des sciences fonctionnelles (DSF) > Département des sciences fonctionnelles (DSF)
Beckers, Jean-François ; Université de Liège > Département des sciences fonctionnelles (DSF) > Département des sciences fonctionnelles (DSF)
Almeria, S.; Universitat Autònoma de Barcelona (UAB), 08193, Bellaterra, Barcelona, Spain > Departament de Sanitat i Anatomia Animals
Lopez-Gatius, F.; University of Lleida, Spain > Agrotecnio Centre
Language :
English
Title :
Experimental Neospora caninum infection modifies trophoblast cell populations and plasma pregnancy-associated glycoprotein 1 and 2 dynamics in pregnant dairy heifers.
Publication date :
2016
Journal title :
Veterinary Parasitology
ISSN :
0304-4017
eISSN :
1873-2550
Publisher :
Elsevier, Netherlands
Volume :
216
Pages :
7-12
Peer reviewed :
Peer Reviewed verified by ORBi
Funders :
This study was supported by a grant from the SpanishMINECO (AGL2012-39830-C02-01/02) and FEDER. Ramón Mur-Novales was supported by a FPI grant from the Spanish Ministryof Science and Innovation, MICINN, BES-2013-063215.
Almería S., López-Gatius F. Markers related to the diagnosis and to the risk of abortion in bovine neosporosis. Res. Vet. Sci. 2015, 100:169-175.
Almería S., Ferrer D., Pabón M., Castellà J., Manas S. Red foxes (Vulpes vulpes) are natural intermediate host of Neospora caninum. Vet. Parasitol. 2002, 107:287-294.
Almeria S., Serrano-Perez B., Darwich L., Araujo R.N., Lopez-Gatius F., Dubey J.P., et al. Maternal and fetal immune response patterns in heifers experimentally infected with Neospora caninum in the second trimester of pregnancy-a descriptive study. Vet. Parasitol. 2014, 204:146-152.
Almería S., Serrano B., Darwich L., Domingo M., Mur R., Regidor-Cerrillo J., Cabezón O., Pérez-Maillo M., Lopez-Helguera I., Fernández-Aguilar X., Puig M., Ortega-Mora L.M., García-Ispierto I., Dubey J.P., López Gatius F. Foetal death in naive heifers inoculated with Neospora caninum isolate Nc-Spain7 at 110 days of pregnancy. Vet. Parasitol. 2015, (submitted for publication).
Bartley P.M., Katzer F., Rocchi M.S., Maley S.W., Benavides J., Nath M., Pang Y., Cantón G., Thomson J., Chianini F., Innes E.A. Development of maternal and foetal immune responses in cattle following experimental challenge with Neospora caninum at day 210 of gestation. Vet. Res. 2013, 44:91.
Beckers J.F., Dewulf M., Verstegen J., Wouters-Ballman P., Ectors F. Isolation of a bovine chorionic gonadotrophin (bCG). Theriogenology 1988, 29:218.
Dubey J.P., Schares G. Neosporosis in animals-the last five years. Vet. Parasitol. 2011, 180:90-108.
Dubey J.P., Schares G., Ortega-Mora L.M. Epidemiology and control of neosporosis and Neospora caninum. Clin. Microbiol. Rev. 2007, 20:323-367.
García-Ispierto I., Nogareda C., Yániz J.L., Almería S., Martíinez-Bello D., de Sousa N.M., Beckers J.F., López-Gatius F. Neospora caninum and Coxiella burnetii seropositivity are related to endocrine pattern changes during gestation in lactating dairy cows. Theriogenology 2010, 74:212-220.
García-Ispierto I., Almería S., Serrano B., de Sousa,N M., Beckers J.F., López-Gatius F. Plasma concentrations of pregnancy-associated glycoproteins measured using anti-bovine PAG-2 antibodies on day 120 of gestation predict abortion in dairy cows naturally infected with Neospora caninum. Reprod. Domest. Anim. 2013, 48:613-618.
Innes E.A., Wright S., Bartley P., Maley S., Macaldowie C., Esteban-Redondo I., Buxton D. The host-parasite relationship in bovine neosporosis. Vet. Immunol. Immunopathol. 2005, 108:29-36.
Kannekens E.M., Murray R.D., Howard C.V., Currie J. A stereological method for estimating the feto-maternal exchange surface area in the bovine placentome at 135 days gestation. Res. Vet. Sci. 2006, 81:127-133.
López-Gatius F., Pabon M., Almería S. Neospora caninum infection does not affect early pregnancy in dairy cattle. Theriogenology 2004, 62:606-613.
López-Gatius F., Garbayo J.M., Santolaria P., Yániz J., Ayad A., de Sousa N.M., Beckers J.F. Milk production correlates negatively with plasma concentrations of pregnancy-associated glycoprotein (PAG) during the early fetal period in high producing dairy cows with live fetuses. Domest. Anim. Endocrinol. 2007, 32:29-42.
López-Gatius F., Garbayo J.M., Santolaria P., Yániz J.L., Almería S., Ayad A., de Sousa N.M., Beckers J.F. Plasma pregnancy-associated glycoprotein-1 (PAG-1) concentrations during gestation in Neospora-infected dairy cows. Theriogenology 2007, 67:502-508.
Maley S.W., Buxton D., Macaldowie C.N., Anderson I.E., Wright S.E., Bartley P.M., Esteban-Redondo I., Hamilton C.M., Storsety A.K., Innes E.A. Characterization of the immune response in the placenta of cattle experimentally infected with Neospora caninum in early gestation. J. Comp. Pathol. 2006, 135:130-141.
Regidor-Cerrillo J., Arranz-Solís D., Benavides J., Gómez-Bautista M., Castro-Hermida J.A., Mezo M., Pérez V., Ortega-Mora L.M., Gónzalez-Warleta M. Neospora caninum infection during early pregnancy in cattle: how the isolate influences infection dynamics, clinical outcome and peripheral and local immune responses. Vet. Res. 2014, 45:10-25.
Reichel M.P., Ayanegui-Alcerreca M.Alejandra, Gondim L.F., Ellis J.T. What is the global economic impact of Neospora caninum in cattle-the billion dollar question. Int. J. Parasitol. 2013, 43:133-142.
Rosbottom A., Guy C.S., Gibney E.H., Smith R.F., Valarcher J.F., Taylor G., Williams D.J.L. Peripheral immune responses in pregnant cattle following Neospora caninum infection. Parasite Immunol. 2007, 29:219-228.
Rosbottom A., Gibney E.H., Kaiser P., Hartley C., Smith R.F., Robinson R., Kipar A., Williams D.J.L. Up regulation of the maternal immune response in the placenta of cattle naturally infected with Neospora caninum. PLoS One 2011, 6:e15799.
Thorell J.I., Johansson B.G. Enzymatic iodination of polypeptides with 125I to high specific activity. Biochim. Biophys. Acta 1971, 251:363-369.
Touzard E., Reinaud P., Dubois O., Guyader-Joly C., Humblot P., Ponsart C., Charpigny G. Specific expression patterns and cell distribution of ancient and modern PAG in bovine placenta during pregnancy. Reproduction 2013, 146:347-362.
Vaitukaitis J., Robbins J.B., Nieschlag E., Ross G.T. A method for producing specific antisera with small doses of immunogen. J. Clin. Endocrinol. Metab. 1971, 33:988-991.
Wallace R.M., Pohler K.G., Smith M.F., Green J.A. Placental PAGs: gene origins, expression patterns, and use as markers of pregnancy. Reproduction 2015, 149:R115-R126.