This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Adams D.S., Crawford T.B., Banks K.L., McGuire T.C., Perryman L.E.: Immune responses of goats persistently infected with caprine arthritis-encephalitis virus. Infect Immun 1980, 28, 421–227, doi: 10.1128/iai.28.2.421-427.1980.AdamsD.S.CrawfordT.B.BanksK.L.McGuireT.C.PerrymanL.E.Immune responses of goats persistently infected with caprine arthritis-encephalitis virus19802842122710.1128/iai.28.2.421-427.1980.Open DOISearch in Google Scholar
Adams D.S., Klevjer-Anderson P., Carlson J.L., McGuire T.C., Gorham J.R.: Transmission and control of caprine arthritisencephalitis virus. Am J Vet Res 1983, 44, 1670–1675.AdamsD.S.Klevjer-AndersonP.CarlsonJ.L.McGuireT.C.GorhamJ.R.Transmission and control of caprine arthritisencephalitis virus19834416701675Search in Google Scholar
Ahmad A., Morisset R., Thomas R., Menezes J.: Evidence for a defect of antibody-dependent cellular cytotoxic (ADCC) effector function and anti-HIV gp120/41-specific ADCC-mediating antibody titres in HIV-infected individuals. J Acquir Immune Defic Syndr 1994, 7, 428–437.AhmadA.MorissetR.ThomasR.MenezesJ.Evidence for a defect of antibody-dependent cellular cytotoxic (ADCC) effector function and anti-HIV gp120/41-specific ADCC-mediating antibody titres in HIV-infected individuals19947428437Search in Google Scholar
Altman D.G., Machin D., Bryant T.N., Gardner M.J.: Statistics with Confidence: Confidence Intervals and Statistical Guidelines, Second Edition, BMJ Books, London, 2000.AltmanD.G.MachinD.BryantT.N.GardnerM.J.BMJ BooksLondon2000Search in Google Scholar
Alvarez V., Arranz J., Daltabuit-Test M., Leginagoikoa I., Juste R.A., Amorena B., de Andrés D., Luján L.L., Badiola J.J., Berriatua E. Relative contribution of colostrum from Maedi-Visna virus (MVV) infected ewes to MVV-seroprevalence in lambs. Res Vet Sci 2005, 78, 237–243, doi: 10.1016/j.rvsc.2004.09.006.AlvarezV.ArranzJ.Daltabuit-TestM.LeginagoikoaI.JusteR.A.AmorenaB.deAndrés D.LujánL.L.BadiolaJ.J.BerriatuaE.Relative contribution of colostrum from Maedi-Visna virus (MVV) infected ewes to MVV-seroprevalence in lambs20057823724310.1016/j.rvsc.2004.09.006.Open DOISearch in Google Scholar
Alvarez V., Daltabuit-Test M., Arranz J., Leginagoikoa I., Juste R.A., Amorena B., de Andrés D., Luján L.L., Badiola J.J., Berriatua E.: PCR detection of colostrum-associated Maedi-Visna virus (MVV) infection and relationship with ELISA-antibody status in lambs. Res Vet Sci 2006, 80, 226–234, doi: 10.1016/j.rvsc.2005.05.008.AlvarezV.Daltabuit-TestM.ArranzJ.LeginagoikoaI.JusteR.A.AmorenaB.de AndrésD.LujánL.L.BadiolaJ.J.BerriatuaE.PCR detection of colostrum-associated Maedi-Visna virus (MVV) infection and relationship with ELISA-antibody status in lambs20068022623410.1016/j.rvsc.2005.05.008.Open DOISearch in Google Scholar
Barquero N., Arjona A., Domenech A., Toural C., de las Heras A., Fernández-Garayzabal J.F., Ruiz-Santa Quiteria J.A., Gomez-Lucia E.: Diagnostic performance of PCR and ELISA on blood and milk samples and serological survey for small ruminant lentiviruses in central Spain. Vet Rec 2011, 168, 20, doi: 10.1136/vr.c4951.BarqueroN.ArjonaA.DomenechA.TouralC.de lasHeras A.Fernández-GarayzabalJ.F.Ruiz-SantaQuiteria J.A.Gomez-LuciaE.Diagnostic performance of PCR and ELISA on blood and milk samples and serological survey for small ruminant lentiviruses in central Spain20111682010.1136/vr.c4951.Open DOISearch in Google Scholar
Berriatua E., Alvarez V., Extramiana B., González L., Daltabuit M., Juste R.A.: Transmission and control implications of seroconversion to Maedi-Visna virus in Basque dairy-sheep flocks. Prev Vet Med 2003, 60, 265–279, doi: 10.1016/s0167-5877(03)00163-6.BerriatuaE.AlvarezV.ExtramianaB.GonzálezL.DaltabuitM.JusteR.A.Transmission and control implications of seroconversion to Maedi-Visna virus in Basque dairy-sheep flocks20036026527910.1016/s0167-5877(03)00163-6.Open DOISearch in Google Scholar
Blacklaws B.A., Berriatua E., Torsteinsdottir S., Watt N.J., de Andrés D., Klein D., Harkiss G.D.: Transmission of small ruminant lentiviruses. Vet Microbiol 2004, 101, 199–208, doi: 10.1016/j.vetmic.2004.04.006.BlacklawsB.A.BerriatuaE.TorsteinsdottirS.WattN.J.de AndrésD.KleinD.HarkissG.D.Transmission of small ruminant lentiviruses200410119920810.1016/j.vetmic.2004.04.006.Open DOISearch in Google Scholar
Broughton-Neiswanger L.E., White S.N., Knowles D.P., Mousel M.R., Lewis G.S., Herndon D.R., Herrmann-Hoesing L.M.: Non-maternal transmission is the major mode of ovine lentivirus transmission in a ewe flock: a molecular epidemiology study. Infect Genet Evol 2010, 10, 998–1007, doi: 10.1016/j.meegid. 2010.06.007.Broughton-NeiswangerL.E.WhiteS.N.KnowlesD.P.MouselM.R.LewisG.S.HerndonD.R.Herrmann-HoesingL.M.Non-maternal transmission is the major mode of ovine lentivirus transmission in a ewe flock: a molecular epidemiology study201010998100710.1016/j.meegid.2010.06.007.Open DOISearch in Google Scholar
Cardinaux L., Zahno M.L., Deubelbeiss M., Zanoni R., Vogt H.R., Bertoni G.: Virological and phylogenetic characterization of attenuated small ruminant lentivirus isolates eluding efficient serological detection. Vet Microbiol 2013, 162, 572–581, doi: 10.1016/j.vetmic.2012.11.017.CardinauxL.ZahnoM.L.DeubelbeissM.ZanoniR.VogtH.R.BertoniG.Virological and phylogenetic characterization of attenuated small ruminant lentivirus isolates eluding efficient serological detection201316257258110.1016/j.vetmic.2012.11.017.Open DOISearch in Google Scholar
Colitti B., Coradduzza E., Puggioni G., Capucchio M.T., Reina R., Bertolotti L., Rosati S.: A new approach for Small Ruminant Lentivirus full genome characterization revealed the circulation of divergent strains. PLoS One 2019, 14, e0212585, doi: 10.1371/journal.pone.0212585.ColittiB.CoradduzzaE.PuggioniG.CapucchioM.T.ReinaR.BertolottiL.RosatiS.A new approach for Small Ruminant Lentivirus full genome characterization revealed the circulation of divergent strains201914e021258510.1371/journal.pone.0212585.Open DOISearch in Google Scholar
Conover W.J., Iman R.L.: Rank transformations as a bridge between parametric and nonparametric statistics. Am Stat 1984, 35, 124–129, doi: 10.2307/2683975.ConoverW.J.ImanR.L.Rank transformations as a bridge between parametric and nonparametric statistics19843512412910.2307/2683975.Open DOISearch in Google Scholar
Czopowicz M., Szaluś-Jordanow O., Mickiewicz M., Moroz A., Witkowski L., Markowska-Daniel I., Reczyńska D., Bagnicka E., Kaba J.: Decline of maternal antibodies to small ruminant lentivirus in goat kids. Anim Sci J 2018, 89, 1364–1370, doi: 10.1111/asj.13038.CzopowiczM.Szaluś-JordanowO.MickiewiczM.MorozA.WitkowskiL.Markowska-DanielI.ReczyńskaD.BagnickaE.KabaJ.Decline of maternal antibodies to small ruminant lentivirus in goat kids2018891364137010.1111/asj.13038.Open DOISearch in Google Scholar
de Andrés X., Ramírez H., Bertolotti L., San Román B., Glaria I., Crespo H., Jáuregui P., Minguijón E., Juste R.A., Leginagoikoa I., Pérez M., Luján L.L., Badiola J.J., Polledo L., García-Marín J.F., Riezu J.I., Borrás-Cuesta F., de Andrés D., Rosati S., Reina R., Amorena B.: An insight into a combination of ELISA strategies to diagnose small ruminant lentivirus infections. Vet Immunol Immunopathol 2013, 152, 277–288, doi: 10.1016/j.vetimm.2012.12.017.deAndrés X.RamírezH.BertolottiL.SanRomán B.GlariaI.CrespoH.JáureguiP.MinguijónE.JusteR.A.LeginagoikoaI.PérezM.LujánL.L.BadiolaJ.J.PolledoL.García-MarínJ.F.RiezuJ.I.Borrás-CuestaF.deAndrés D.RosatiS.ReinaR.AmorenaB.An insight into a combination of ELISA strategies to diagnose small ruminant lentivirus infections201315227728810.1016/j.vetimm.2012.12.017.Open DOISearch in Google Scholar
De Regge N., Cay B.: Development, validation and evaluation of added diagnostic value of a q(RT)-PCR for the detection of genotype A strains of small ruminant lentiviruses. J Virol Methods 2013, 194, 250–257, doi: 10.1016/j.jviromet.2013.09.001.De ReggeN.CayB.Development, validation and evaluation of added diagnostic value of a q(RT)-PCR for the detection of genotype A strains of small ruminant lentiviruses201319425025710.1016/j.jviromet.2013.09.001.Open DOISearch in Google Scholar
East N.E., Rowe J.D., Dahlberg J.E., Theilen G.H., Pedersen N.C.: Modes of transmission of caprine arthritis-encephalitis virus infection. Small Rumin Res 1993, 10, 251–262, doi: 10.1016/0921-4488(93)90130-A.EastN.E.RoweJ.D.DahlbergJ.E.TheilenG.H.PedersenN.C.Modes of transmission of caprine arthritis-encephalitis virus infection19931025126210.1016/0921-4488(93)90130-A.Open DOISearch in Google Scholar
Ellis T.M., Carman H., Robinson W.F., Wilcox G.E.: The effect of colostrum-derived antibody on neo-natal transmission of caprine arthritis-encephalitis virus infection. Aust Vet J 1986, 63, 242–245, doi: 10.1111/j.1751-0813.1986.tb02984.x.EllisT.M.CarmanH.RobinsonW.F.WilcoxG.E.The effect of colostrum-derived antibody on neo-natal transmission of caprine arthritis-encephalitis virus infection19866324224510.1111/j.1751-0813.1986.tb02984.x.Open DOISearch in Google Scholar
Ellis T.M., Robinson W.F., Wilcox G.E.: Characterisation, experimental infection and serological response to caprine retrovirus. Aust Vet J 1983, 60, 321–326, doi: 10.1111/j.1751-0813.1983.tb02831.x.EllisT.M.RobinsonW.F.WilcoxG.E.Characterisation, experimental infection and serological response to caprine retrovirus19836032132610.1111/j.1751-0813.1983.tb02831.x.Open DOISearch in Google Scholar
Ellis T.M., Robinson W.F., Wilcox G.E.: The pathology and aetiology of lung lesions in goats infected with caprine arthritis– encephalitis virus. Aust Vet J 1988, 65, 69–73, doi: 10.1111/j.1751-0813.1988.tb07361.x.EllisT.M.RobinsonW.F.WilcoxG.E.The pathology and aetiology of lung lesions in goats infected with caprine arthritis– encephalitis virus198865697310.1111/j.1751-0813.1988.tb07361.x.Open DOISearch in Google Scholar
Furtado Araújo J., Andrioli A., Pinheiro R.R., Sider L.H., de Sousa A.L.M., de Azevedo D.A.A., Peixoto R.M., Lima A.M.C., Damasceno E.M., Souza S.C.R., Teixeira M.F.D.S.: Vertical transmissibility of small ruminant lentivirus. PLoS One 2020, 15, e0239916, doi: 10.1371/journal.pone.0239916.FurtadoAraújo J.AndrioliA.PinheiroR.R.SiderL.H.de SousaA.L.M.de AzevedoD.A.A.PeixotoR.M.LimaA.M.C.DamascenoE.M.SouzaS.C.R.TeixeiraM.F.D.S.Vertical transmissibility of small ruminant lentivirus202015e023991610.1371/journal.pone.0239916.Open DOISearch in Google Scholar
Gjerset B., Jonassen C.M., Rimstad E.: Natural transmission and comparative analysis of small ruminant lentiviruses in the Norwegian sheep and goat populations. Virus Res 2007, 125, 153–161, doi: 10.1016/j.virusres.2006.12.014.GjersetB.JonassenC.M.RimstadE.Natural transmission and comparative analysis of small ruminant lentiviruses in the Norwegian sheep and goat populations200712515316110.1016/j.virusres.2006.12.014.Open DOISearch in Google Scholar
Grego E., Profiti M., Giammarioli M., Giannino L., Rutili D., Woodall C., Rosati S.: Genetic heterogeneity of small ruminant lentiviruses involves immunodominant epitope of capsid antigen and affects sensitivity of single-strain-based immunoassay. Clin Diagn Lab Immunol 2002, 9, 828–832, doi: 10.1128/cdli.9.4.828-832.2002.GregoE.ProfitiM.GiammarioliM.GianninoL.RutiliD.WoodallC.RosatiS.Genetic heterogeneity of small ruminant lentiviruses involves immunodominant epitope of capsid antigen and affects sensitivity of single-strain-based immunoassay2002982883210.1128/cdli.9.4.828-832.2002.Open DOISearch in Google Scholar
Hanson J., Hydbring E., Olsson K.: A long term study of goats naturally infected with caprine arthritis-encephalitis virus. Acta Vet Scand 1996, 37, 31–39, doi: 10.1186/BF03548117.HansonJ.HydbringE.OlssonK.A long term study of goats naturally infected with caprine arthritis-encephalitis virus199637313910.1186/BF03548117.Open DOISearch in Google Scholar
Hasegawa M.Y., Lara M.D.C.C.D.S.H., Lobos E.M.C.V., Gaeta N.C., Hayashi M., Shirayama L., Castro R.D.S., Gregory L.: An experimental study on the vertical transmission of caprine arthritis-encephalitis virus from naturally infected females to their offspring. Small Rumin Res 2017, 149, 23–27, doi: 10.1016/j.smallrumres.2017.01.010.HasegawaM.Y.LaraM.D.C.C.D.S.H.LobosE.M.C.V.GaetaN.C.HayashiM.ShirayamaL.CastroR.D.S.GregoryL.An experimental study on the vertical transmission of caprine arthritis-encephalitis virus from naturally infected females to their offspring2017149232710.1016/j.smallrumres.2017.01.010.Open DOISearch in Google Scholar
Herrmann L.M., Cheevers W.P., McGuire T.C., Adams D.S., Hutton M.M., Gavin W.G., Knowles D.P.: Competitive-inhibition enzyme-linked immunosorbent assay for detection of serum antibodies to caprine arthritis-encephalitis virus: diagnostic tool for successful eradication. Clin Diagn Lab Immunol 2003, 10, 267–271, doi: 10.1128/cdli.10.2.267-271.2003.HerrmannL.M.CheeversW.P.McGuireT.C.AdamsD.S.HuttonM.M.GavinW.G.KnowlesD.P.Competitive-inhibition enzyme-linked immunosorbent assay for detection of serum antibodies to caprine arthritis-encephalitis virus: diagnostic tool for successful eradication20031026727110.1128/cdli.10.2.267-271.2003.Open DOISearch in Google Scholar
Herrmann-Hoesing L.M., Palmer G.H., Knowles D.P.: Evidence of proviral clearance following postpartum transmission of an ovine lentivirus. Virology 2007, 362, 226–234, doi: 10.1016/j.virol.2006.12.021.Herrmann-HoesingL.M.PalmerG.H.KnowlesD.P.Evidence of proviral clearance following postpartum transmission of an ovine lentivirus200736222623410.1016/j.virol.2006.12.021.Open DOISearch in Google Scholar
Kaba J., Bagnicka E., Czopowicz M., Nowicki M., Witkowski L., Szaluś-Jordanow O.: Long-term study on the spread of caprine arthritis-encephalitis in a goat herd. Centr Eur J Immunol 2011, 36, 170–173.KabaJ.BagnickaE.CzopowiczM.NowickiM.WitkowskiL.Szaluś-JordanowO.Long-term study on the spread of caprine arthritis-encephalitis in a goat herd201136170173Search in Google Scholar
Kaba J., Rola M., Materniak M., Kuźmak J., Nowicki M.: Isolation and characterization of caprine arthritis encephalitis virus in goats from Poland. Pol J Vet Sci 2009, 12, 183–188.KabaJ.RolaM.MaterniakM.KuźmakJ.NowickiM.Isolation and characterization of caprine arthritis encephalitis virus in goats from Poland200912183188Search in Google Scholar
Kazmi S.H., Naglik J.R., Sweet S.P., Evans R.W., O’Shea S., Banatvala J.E., Challacombe S.J.: Comparison of human immunodeficiency virus type 1-specific inhibitory activities in saliva and other human mucosal fluids. Clin Vaccine Immunol 2006, 13, 1111–1118, doi: 10.1128/CDLI.00426-05.KazmiS.H.NaglikJ.R.SweetS.P.EvansR.W.O’SheaS.BanatvalaJ.E.ChallacombeS.J.Comparison of human immunodeficiency virus type 1-specific inhibitory activities in saliva and other human mucosal fluids2006131111111810.1128/CDLI.00426-05.Open DOISearch in Google Scholar
Kramski M., Center R.J., Wheatley A.K., Jacobson J.C., Alexander M.R., Rawlin G., Purcell D.F.: Hyperimmune bovine colostrum as a low-cost, large-scale source of antibodies with broad neutralizing activity for HIV-1 envelope with potential use in microbicides. Antimicrob Agents Chemother 2012, 56, 4310–4319, doi: 10.1128/AAC.00453-12.KramskiM.CenterR.J.WheatleyA.K.JacobsonJ.C.AlexanderM.R.RawlinG.PurcellD.F.Hyperimmune bovine colostrum as a low-cost, large-scale source of antibodies with broad neutralizing activity for HIV-1 envelope with potential use in microbicides2012564310431910.1128/AAC.00453-12.Open DOISearch in Google Scholar
Kramski M., Lichtfuss G.F., Navis M., Isitman G., Wren L., Rawlin G., Center R.J., Jaworowski A., Kent S.J., Purcell D.F.: Anti-HIV-1 antibody-dependent cellular cytotoxicity mediated by hyperimmune bovine colostrum IgG. Eur J Immunol 2012, 42, 2771–2781, doi: 10.1002/eji.201242469.KramskiM.LichtfussG.F.NavisM.IsitmanG.WrenL.RawlinG.CenterR.J.JaworowskiA.KentS.J.PurcellD.F.Anti-HIV-1 antibody-dependent cellular cytotoxicity mediated by hyperimmune bovine colostrum IgG2012422771278110.1002/eji.201242469.Open DOISearch in Google Scholar
Lacerenza D., Giammarioli M., Grego E., Marini C., Profiti M., Rutili D., Rosati S.: Antibody response in sheep experimentally infected with different small ruminant lentivirus genotypes. Vet Immunol Immunopathol 2006, 112, 264–271, doi: 10.1016/j.vetimm.2006.03.016.LacerenzaD.GiammarioliM.GregoE.MariniC.ProfitiM.RutiliD.RosatiS.Antibody response in sheep experimentally infected with different small ruminant lentivirus genotypes200611226427110.1016/j.vetimm.2006.03.016.Open DOISearch in Google Scholar
Larruskain A., Jugo B.M.: Retroviral infections in sheep and goats: small ruminant lentiviruses and host interaction. Viruses 2013, 5, 2043–2061, doi: 10.3390/v5082043.LarruskainA.JugoB.M.Retroviral infections in sheep and goats: small ruminant lentiviruses and host interaction201352043206110.3390/v5082043.Open DOISearch in Google Scholar
Leroux C., Lerondelle C., Chastang J., Mornex J.F.: RT-PCR detection of lentiviruses in milk or mammary secretions of sheep or goats from infected flocks. Vet Res 1997, 28, 115–121.LerouxC.LerondelleC.ChastangJ.MornexJ.F.RT-PCR detection of lentiviruses in milk or mammary secretions of sheep or goats from infected flocks199728115121Search in Google Scholar
MacKenzie R.W., Oliver R.E., Rooney J.P., Kagei H.: A successful attempt to raise goat kids free of infection with caprine arthritis encephalitis virus in an endemically infected goat herd. N Z Vet J 1987, 35, 184–186, doi: 10.1080/00480169./1987.35440.MacKenzieR.W.OliverR.E.RooneyJ.P.KageiH.A successful attempt to raise goat kids free of infection with caprine arthritis encephalitis virus in an endemically infected goat herd19873518418610.1080/00480169./1987.35440.Open DOISearch in Google Scholar
Marinho R.C., Martins G.R., Souza K.C., Sousa A.L.M., Silva S.T.C., Nobre J.A., Teixeira M.F.S.: Duplex nested-PCR for detection of small ruminant lentiviruses. Braz J Microbiol 2018, 49, 83–92, doi: 10.1016/j.bjm.2018.04.013.MarinhoR.C.MartinsG.R.SouzaK.C.SousaA.L.M.SilvaS.T.C.NobreJ.A.TeixeiraM.F.S.Duplex nested-PCR for detection of small ruminant lentiviruses201849839210.1016/j.bjm.2018.04.013.Open DOISearch in Google Scholar
McNeilly T.N., Baker A., Brown J.K., Collie D., MacLachlan G., Rhind S.M., Harkiss G.D.: Role of alveolar macrophages in respiratory transmission of visna/maedi virus. J Virol 2008, 82, 1526–1536, doi: 10.1128/JVI.02148-07.McNeillyT.N.BakerA.BrownJ.K.CollieD.MacLachlanG.RhindS.M.HarkissG.D.Role of alveolar macrophages in respiratory transmission of visna/maedi virus2008821526153610.1128/JVI.02148-07.Open DOISearch in Google Scholar
McNeilly T.N., Tennant P., Luján L.L., Pérez M., Harkiss G.D.: Differential infection efficiencies of peripheral lung and tracheal tissues in sheep infected with Visna/maedi virus via the respiratory tract. J Gen Virol 2007, 88, 670–679, doi: 10.1099/vir.0.82434-0.McNeillyT.N.TennantP.LujánL.L.PérezM.HarkissG.D.Differential infection efficiencies of peripheral lung and tracheal tissues in sheep infected with Visna/maedi virus via the respiratory tract20078867067910.1099/vir.0.82434-0.Open DOISearch in Google Scholar
Michiels R., Adjadj N.R., De Regge N.: Phylogenetic Analysis of Belgian Small Ruminant Lentiviruses Supports Cross Species Virus Transmission and Identifies New Subtype B5 Strains. Pathogens 2020, 9, E183, doi: 10.3390/pathogens9030183.MichielsR.AdjadjN.R.De ReggeN.Phylogenetic Analysis of Belgian Small Ruminant Lentiviruses Supports Cross Species Virus Transmission and Identifies New Subtype B5 Strains20209E18310.3390/pathogens9030183.Open DOISearch in Google Scholar
Michiels R., Roels S., Vereecke N., Mathijs E., Mostin L., De Regge N.: Species-Specific Humoral Immune Responses in Sheep and Goats upon Small Ruminant Lentivirus Infections Inversely Correlate with Protection against Virus Replication and Pathological Lesions. Int J Mol Sci 2021, 22, 9824, doi: 10.3390/ijms22189824.MichielsR.RoelsS.VereeckeN.MathijsE.MostinL.De ReggeN.Species-Specific Humoral Immune Responses in Sheep and Goats upon Small Ruminant Lentivirus Infections Inversely Correlate with Protection against Virus Replication and Pathological Lesions202122982410.3390/ijms22189824.Open DOISearch in Google Scholar
Michiels R., Van Mael E., Quinet C., Adjadj N.R., Cay A.B., De Regge N.: Comparative Analysis of Different Serological and Molecular Tests for the Detection of Small Ruminant Lentiviruses (SRLVs) in Belgian Sheep and Goats. Viruses 2018, 10, 696, doi: 10.3390/v10120696.MichielsR.VanMael E.QuinetC.AdjadjN.R.CayA.B.De ReggeN.Comparative Analysis of Different Serological and Molecular Tests for the Detection of Small Ruminant Lentiviruses (SRLVs) in Belgian Sheep and Goats20181069610.3390/v10120696.Open DOISearch in Google Scholar
Minguijón E., Reina R., Pérez M., Polledo L., Villoria M., Ramírez H., Leginagoikoa I., Badiola J.J., García-Marín J.F., de Andrés D., Luján L.L., Amorena B., Juste R.A.: Small ruminant lentivirus infections and diseases. Vet Microbiol 2015, 181, 75–89, doi: 10.1016/j.vetmic.2015.08.007.MinguijónE.ReinaR.PérezM.PolledoL.VilloriaM.RamírezH.LeginagoikoaI.BadiolaJ.J.García-MarínJ.F.deAndrés D.LujánL.L.AmorenaB.JusteR.A.Small ruminant lentivirus infections and diseases2015181758910.1016/j.vetmic.2015.08.007.Open DOISearch in Google Scholar
Moroz A., Czopowicz M., Sobczak-Filipiak M., Dolka I., Rzewuska M., Kizerwetter-Świda M., Chrobak-Chmiel D., Mickiewicz M., Witkowski L., Szaluś-Jordanow O., Nalbert T., Potârniche A.V., Barszcz K., Markowska-Daniel I., Puchała R., Bagnicka E., Kaba J.: The Prevalence of Histopathological Features of Pneumonia in Goats with Symptomatic Caprine Arthritis-Encephalitis. Pathogens 2022, 11, 629, doi: 10.3390/pathogens11060629.MorozA.CzopowiczM.Sobczak-FilipiakM.DolkaI.RzewuskaM.Kizerwetter-ŚwidaM.Chrobak-ChmielD.MickiewiczM.WitkowskiL.Szaluś-JordanowO.NalbertT.PotârnicheA.V.BarszczK.Markowska-DanielI.PuchałaR.BagnickaE.KabaJ.The Prevalence of Histopathological Features of Pneumonia in Goats with Symptomatic Caprine Arthritis-Encephalitis20221162910.3390/pathogens11060629.Open DOISearch in Google Scholar
Nogarol C., Bertolotti L., Klevar S., Profiti M., Gjerset B., Rosati S.: Serological characterization of small ruminant lentiviruses: A complete tool for serotyping lentivirus infection in goat. Small Rumin Res 2019, 176, 42–46, doi: 10.1016/j.smallrumres.2019.05.010.NogarolC.BertolottiL.KlevarS.ProfitiM.GjersetB.RosatiS.Serological characterization of small ruminant lentiviruses: A complete tool for serotyping lentivirus infection in goat2019176424610.1016/j.smallrumres.2019.05.010.Open DOISearch in Google Scholar
Nowicka D., Czopowicz M., Mickiewicz M., Szaluś-Jordanow O., Witkowski L., Bagnicka E., Kaba J.: Diagnostic performance of ID screen MVV-CAEV Indirect Screening ELISA in identifying small ruminant lentiviruses-infected goats. Pol J Vet Sci 2014, 17, 501–506, doi: 10.2478/pjvs-2014-0072.NowickaD.CzopowiczM.MickiewiczM.Szaluś-JordanowO.WitkowskiL.BagnickaE.KabaJ.Diagnostic performance of ID screen MVV-CAEV Indirect Screening ELISA in identifying small ruminant lentiviruses-infected goats20141750150610.2478/pjvs-2014-0072.Open DOISearch in Google Scholar
Olech M., Kuźmak J.: Compartmentalization of Subtype A17 of Small Ruminant Lentiviruses between Blood and Colostrum in Infected Goats Is Not Exclusively Associated to the env Gene. Viruses 2019, 11, 270, doi: 10.3390/v11030270.OlechM.KuźmakJ.Compartmentalization of Subtype A17 of Small Ruminant Lentiviruses between Blood and Colostrum in Infected Goats Is Not Exclusively Associated to the env Gene20191127010.3390/v11030270.Open DOISearch in Google Scholar
Olech M., Kuźmak J.: Molecular Characterization of Small Ruminant Lentiviruses in Polish Mixed Flocks Supports Evidence of Cross Species Transmission, Dual Infection, a Recombination Event, and Reveals the Existence of New Subtypes within Group A. Viruses 2021, 13, 2529, doi: 10.3390/v13122529.OlechM.KuźmakJ.Molecular Characterization of Small Ruminant Lentiviruses in Polish Mixed Flocks Supports Evidence of Cross Species Transmission, Dual Infection, a Recombination Event, and Reveals the Existence of New Subtypes within Group A202113252910.3390/v13122529.Open DOISearch in Google Scholar
Olech M., Valas S., Kuźmak J.: Epidemiological survey in single-species flocks from Poland reveals expanded genetic and antigenic diversity of small ruminant lentiviruses. PLoS One 2018, 13, e0193892, doi: 10.1371/journal.pone.0193892.OlechM.ValasS.KuźmakJ.Epidemiological survey in single-species flocks from Poland reveals expanded genetic and antigenic diversity of small ruminant lentiviruses201813e019389210.1371/journal.pone.0193892.Open DOISearch in Google Scholar
Peterhans E., Greenland T., Badiola J.J., Harkiss G.D., Bertoni G., Amorena B., Eliaszewicz M., Juste R.A., Krassnig R., Lafont J.P., Lenihan P., Pétursson G., Pritchard G., Thorley J., Vitu C., Mornex J.F., Pépin M.: Routes of transmission and consequences of small ruminant lentiviruses (SRLVs) infection and eradication schemes. Vet Res 2004, 35, 257–274, doi: 10.1051/vetres:2004014.PeterhansE.GreenlandT.BadiolaJ.J.HarkissG.D.BertoniG.AmorenaB.EliaszewiczM.JusteR.A.KrassnigR.LafontJ.P.LenihanP.PéturssonG.PritchardG.ThorleyJ.VituC.MornexJ.F.PépinM.Routes of transmission and consequences of small ruminant lentiviruses (SRLVs) infection and eradication schemes20043525727410.1051/vetres:2004014.Open DOISearch in Google Scholar
Pisoni G., Bertoni G., Manarolla G., Vogt H.R., Scaccabarozzi L., Locatelli C., Moroni P.: Genetic analysis of small ruminant lentiviruses following lactogenic transmission. Virology 2010, 407, 91–99, doi: 10.1016/j.virol.2010.08.004.PisoniG.BertoniG.ManarollaG.VogtH.R.ScaccabarozziL.LocatelliC.MoroniP.Genetic analysis of small ruminant lentiviruses following lactogenic transmission2010407919910.1016/j.virol.2010.08.004.Open DOISearch in Google Scholar
Rachid A., Croisé B., Russo P., Vignoni M., Lacerenza D., Rosati S., Kuźmak J., Valas S.: Diverse host-virus interactions following caprine arthritis-encephalitis virus infection in sheep and goats. J Gen Virol 2013, 94, 634–642, doi: 10.1099/vir.0.044768-0.RachidA.CroiséB.RussoP.VignoniM.LacerenzaD.RosatiS.KuźmakJ.ValasS.Diverse host-virus interactions following caprine arthritis-encephalitis virus infection in sheep and goats20139463464210.1099/vir.0.044768-0.Open DOISearch in Google Scholar
Reina R., Juganaru M.M., Profiti M., Cascio P., Cerruti F., Bertolotti L., De Meneghi D., Amorena B., Rosati S.: Immunological parameters in goats experimentally infected with SRLV genotype E, strain Roccaverano. Vet Immunol Immunopathol 2011, 139, 237–244, doi: 10.1016/j.vetimm.2010.11.001.ReinaR.JuganaruM.M.ProfitiM.CascioP.CerrutiF.BertolottiL.De MeneghiD.AmorenaB.RosatiS.Immunological parameters in goats experimentally infected with SRLV genotype E, strain Roccaverano201113923724410.1016/j.vetimm.2010.11.001.Open DOISearch in Google Scholar
Rimstad E., East N.E., Torten M., Higgins J., DeRock E., Pedersen N.C.: Delayed seroconversion following naturally acquired caprine arthritis-encephalitis virus infection in goats. Am J Vet Res 1993, 54, 1858–1862.RimstadE.EastN.E.TortenM.HigginsJ.DeRockE.PedersenN.C.Delayed seroconversion following naturally acquired caprine arthritis-encephalitis virus infection in goats1993541858186210.2460/ajvr.1993.54.11.1858Search in Google Scholar
Rowe J.D., East N.E.: Risk factors for transmission and methods for control of caprine arthritis-encephalitis virus infection. Vet Clin North Am Food Anim Pract 1997, 13, 35–53.RoweJ.D.EastN.E.Risk factors for transmission and methods for control of caprine arthritis-encephalitis virus infection199713355310.1016/S0749-0720(15)30363-79071745Search in Google Scholar
Rowe J.D., East N.E., Franti C.E., Thurmond M.C., Pedersen N.C., Theilen G.H.: Risk factors associated with the incidence of seroconversion to caprine arthritis-encephalitis virus in goats on California dairies. Am J Vet Res 1992, 53, 2396–2403.RoweJ.D.EastN.E.FrantiC.E.ThurmondM.C.PedersenN.C.TheilenG.H.Risk factors associated with the incidence of seroconversion to caprine arthritis-encephalitis virus in goats on California dairies1992532396240310.2460/ajvr.1992.53.12.2396Search in Google Scholar
Rowe J.D., East N.E., Thurmond M.C., Franti C.E., Pedersen N.C.: Cohort study of natural transmission and two methods for control of caprine arthritis-encephalitis virus infection in goats on a California dairy. Am J Vet Res 1992, 53, 2386–2395.RoweJ.D.EastN.E.ThurmondM.C.FrantiC.E.PedersenN.C.Cohort study of natural transmission and two methods for control of caprine arthritis-encephalitis virus infection in goats on a California dairy1992532386239510.2460/ajvr.1992.53.12.2386Search in Google Scholar
Sanjosé L., Pinczowski P., Crespo H., Pérez M., Glaria I., Gimeno M., de Andrés D., Amorena B., Luján L.L., Reina R.: Diagnosing infection with small ruminant lentiviruses of genotypes A and B by combining synthetic peptides in ELISA. Vet J 2015, 204, 88–93, doi: 10.1016/j.tvjl.2015.01.012.SanjoséL.PinczowskiP.CrespoH.PérezM.GlariaI.GimenoM.de AndrésD.AmorenaB.LujánL.L.ReinaR.Diagnosing infection with small ruminant lentiviruses of genotypes A and B by combining synthetic peptides in ELISA2015204889310.1016/j.tvjl.2015.01.012.Open DOISearch in Google Scholar
Sartwell P.E.: The distribution of incubation periods of infectious disease. Historical Paper, 1949. Am J Epidemiol 1995, 141, 386–394, doi: 10.1093/oxfordjournals.aje.a117440.SartwellP.E.The distribution of incubation periods of infectious disease199514138639410.1093/oxfordjournals.aje.a117440.Open DOISearch in Google Scholar
Schaer J., Cvetnic Z., Sukalic T., Dörig S., Grisiger M., Iscaro C., Feliziani F., Pfeifer F., Origgi F., Zanoni R.G., Abril C.E.: Evaluation of Serological Methods and a New Real-Time Nested PCR for Small Ruminant Lentiviruses. Pathogens 2022, 11, 129, doi: 10.3390/pathogens11020129.SchaerJ.CvetnicZ.SukalicT.DörigS.GrisigerM.IscaroC.FelizianiF.PfeiferF.OriggiF.ZanoniR.G.AbrilC.E.Evaluation of Serological Methods and a New Real-Time Nested PCR for Small Ruminant Lentiviruses20221112910.3390/pathogens11020129.Open DOISearch in Google Scholar
Shah C., Böni J., Huder J.B., Vogt H.R., Mühlherr J., Zanoni R., Miserez R., Lutz H., Schüpbach J.: Phylogenetic analysis and reclassification of caprine and ovine lentiviruses based on 104 new isolates: evidence for regular sheep-to-goat transmission and worldwide propagation through livestock trade. Virology 2004, 319, 12–26, doi: 10.1016/j.virol.2003.09.047.ShahC.BöniJ.HuderJ.B.VogtH.R.MühlherrJ.ZanoniR.MiserezR.LutzH.SchüpbachJ.Phylogenetic analysis and reclassification of caprine and ovine lentiviruses based on 104 new isolates: evidence for regular sheep-to-goat transmission and worldwide propagation through livestock trade2004319122610.1016/j.virol.2003.09.047.Open DOISearch in Google Scholar
Souza T.S., Pinheiro R.R., Costa J.N., Lima C.C., Andrioli A., Azevedo D.A., Santos V.W., Furtado Araújo J., Sousa A.L., Pinheiro D.N., Fernandes F.M., Costa Neto A.O.: Interspecific transmission of small ruminant lentiviruses from goats to sheep. Braz J Microbiol 2015, 46, 867–874, doi: 10.1590/S1517-838246320140402.SouzaT.S.PinheiroR.R.CostaJ.N.LimaC.C.AndrioliA.AzevedoD.A.SantosV.W.FurtadoAraújo J.SousaA.L.PinheiroD.N.FernandesF.M.CostaNeto A.O.Interspecific transmission of small ruminant lentiviruses from goats to sheep20154686787410.1590/S1517-838246320140402.Open DOISearch in Google Scholar
Torsteinsdóttir S., Matthíasdóttir S., Vidarsdóttir N., Svansson V., Pétursson G.: Intratracheal inoculation as an efficient route of experimental infection with maedi-visna virus. Res Vet Sci 2003, 75, 245–247, doi: 10.1016/s0034-5288(03)00098-5.TorsteinsdóttirS.MatthíasdóttirS.VidarsdóttirN.SvanssonV.PéturssonG.Intratracheal inoculation as an efficient route of experimental infection with maedi-visna virus20037524524710.1016/s0034-5288(03)00098-5.Open DOISearch in Google Scholar
Wilkerson M.J., Davis W.C., Baszler T.V., Cheevers W.P.: Immunopathology of chronic lentivirus-induced arthritis. Am J Pathol 1995, 146, 1433–1443.WilkersonM.J.DavisW.C.BaszlerT.V.CheeversW.P.Immunopathology of chronic lentivirus-induced arthritis199514614331443Search in Google Scholar
Zanoni R.G.: Phylogenetic analysis of small ruminant lentiviruses. J Gen Virol 1998, 79, 1951–1961, doi: 10.1099/0022-1317-79-8-1951.ZanoniR.G.Phylogenetic analysis of small ruminant lentiviruses1998791951196110.1099/0022-1317-79-8-1951.Open DOISearch in Google Scholar