Ackermann M, Engels M (2006) Pro and contra IBR-eradication. Vet Microbiol 113:293–302. https://doi.org/10.1016/j.vetmic.2005.11.043

Article  PubMed  Google Scholar 

Araujo IL, Dummer LA, Rodrigues PRC, dos Santos AG, Jr FG, Cunha RC, Leite FPL (2018) Immune responses in bovines to recombinant glycoprotein D of bovine herpesvirus type 5 as vaccine antigen. Vaccine 36:7708–7714. https://doi.org/10.1016/j.vaccine.2018.10.080

Bashir S, Singh R, Sharma B, Yadav SK (2011) Development of a sandwich ELISA for the detection of bovine herpesvirus type 1. Asian Pac J Trop Med 4:363–366. https://doi.org/10.1016/S1995-7645(11)60104-1

Article  CAS  PubMed  Google Scholar 

Cao Y, Li K, Wang S, Fu Y, Sun P, Li P, Bai X, Zhang J, Ma X, Xing X, Zhou S, Bao H, Li D, Chen Y, Li Z, Lu Z, Liu Z (2019) Implication of broadly neutralizing bovine monoclonal antibodies in the development of an enzyme-linked immunosorbent assay for detecting neutralizing antibodies against foot-and-mouth disease virus serotype O. J Clin Microbiol 57:e01030-e1119. https://doi.org/10.1128/JCM.01030-19

Article  CAS  PubMed  PubMed Central  Google Scholar 

Cao Y, Li K, Xing X, Zhu G, Fu Y, Bao H, Bai X, Sun P, Li P, Zhang J, Ma X, Wang J, Zhao Z, Li D, Liu Z, Lu Z (2022) Development and validation of a competitive ELISA based on bovine monoclonal antibodies for the detection of neutralizing antibodies against foot-and-mouth disease virus serotype A. J Clin Microbiol 60:e0214221. https://doi.org/10.1128/jcm.02142-21

Article  CAS  PubMed  Google Scholar 

Chen X, Wang X, Qi Y, Wen X, Li C, Liu X, Ni H (2018) Meta analysis of prevalence of bovine herpes virus 1 in cattle in Mainland China. Acta Trop 187:37–43. https://doi.org/10.1016/j.actatropica.2018.07.024

Article  PubMed  Google Scholar 

Collins JK, Ayers VK, Carman J (1988) Evaluation of an antigen-capture ELISA for the detection of bovine herpesvirus type 1 shedding from feedlot cattle. Vet Microbiol 16:101–107. https://doi.org/10.1016/0378-1135(88)90034-x

Article  CAS  PubMed  Google Scholar 

Friguet B, Djavadi-Ohaniance L, Pages J, Bussard A, Goldberg M (1983) A convenient enzyme-linked immunosorbent assay for testing whether monoclonal antibodies recognize the same antigenic site. Application to hybridomas specific for the beta 2-subunit of Escherichia coli tryptophan synthase. J Immunol Methods 60:351–358. https://doi.org/10.1016/0022-1759(83)90292-2

Article  CAS  PubMed  Google Scholar 

Jambunathan N, Clark CM, Musarrat F, Chouljenko VN, Rudd J, Kousoulas KG (2021) Two sides to every story: herpes simplex type-1 viral glycoproteins gB, gD, gH/gL, gK, and cellular receptors function as key players in membrane fusion. Viruses 13:1849. https://doi.org/10.3390/v13091849

Article  CAS  PubMed  PubMed Central  Google Scholar 

Jones C, Chowdhury S (2007) A review of the biology of bovine herpesvirus type 1 (BHV-1), its role as a cofactor in the bovine respiratory disease complex and development of improved vaccines. Anim Health Res Rev 8:187–205. https://doi.org/10.1017/S146625230700134X

Article  PubMed  Google Scholar 

Jones C (2019) Bovine herpesvirus 1 counteracts immune responses and immune-surveillance to enhance pathogenesis and virus transmission. Front Immunol 10:1008. https://doi.org/10.3389/fimmu.2019.01008

Article  CAS  PubMed  PubMed Central  Google Scholar 

Keil GM, Höhle C, Giesow K, König P (2005) Engineering glycoprotein B of bovine herpesvirus 1 to function as transporter for secreted proteins: a new protein expression approach. J Virol 79:791–799. https://doi.org/10.1128/JVI.79.2.791-799.2005

Article  CAS  PubMed  PubMed Central  Google Scholar 

Kit S, Otsuka H, Kit M (1992) Blocking ELISA for distinguishing infectious bovine rhinotracheitis virus (IBRV)-infected animals from those vaccinated with a gene-deleted marker vaccine. J Virol Methods 40:45–56. https://doi.org/10.1016/0166-0934(92)90006-Y

Article  CAS  PubMed  PubMed Central  Google Scholar 

Kit S, Otsuka H, Kit M (1993) Differential diagnostic blocking ELISA for use in conjunction with modified-live IBRV gIII-deleted marker vaccine. J Vet Diagn Invest 5:440–443. https://doi.org/10.1177/104063879300500325

Article  CAS  PubMed  Google Scholar 

Kramps JA, Magdalena J, Quak J, Weerdmeester K, Kaashoek MJ, Maris-Veldhuis MA, Rijsewijk FA, Keil G, van Oirschot JT (1994) A simple, specific, and highly sensitive blocking enzyme-linked immunosorbent assay for detection of antibodies to bovine herpesvirus 1. J Clin Microbiol 32:2175–2181. https://doi.org/10.1128/jcm.32.9.2175-2181.1994

Article  CAS  PubMed  PubMed Central  Google Scholar 

Kramps JA, Quak S, Weerdmeester K, van Oirschot JT (1993) Comparative study on sixteen enzyme-linked immunosorbent assays for the detection of antibodies to bovine herpesvirus 1 in cattle. Vet Microbiol 35:11–21. https://doi.org/10.1016/0378-1135(93)90112-k

Article  CAS  PubMed  Google Scholar 

Krawczyk A, Krauss J, Eis-Hübinger AM, Däumer MP, Schwarzenbacher R, Dittmer U, Schneweis KE, Jäger D, Roggendorf M, Arndt MAE (2011) Impact of valency of a glycoprotein B-specific monoclonal antibody on neutralization of herpes simplex virus. J Virol 85:1793–1803. https://doi.org/10.1128/JVI.01924-10

Article  CAS  PubMed  Google Scholar 

Lin J, Chen RH, Yang MJ, Zhu YM, Xue F (2021) Isolation and molecular characterization of bovine herpesvirus 4 from cattle in mainland China. Arch Virol 166:619–626. https://doi.org/10.1007/s00705-020-04896-w

Article  CAS  PubMed  PubMed Central  Google Scholar 

Liu D, Li K, Zhang L, Lan Y, Wang X, Zhang H, Wang L, Gui R, Han Z, Jang W, Sizhu S, Li J (2017) Seroprevalence investigation of bovine ephemeral fever in yaks in Tibetan Plateau of China from 2012 to 2015. Trop Anim Health Prod 49:227–230. https://doi.org/10.1007/s11250-016-1172-9

Article  PubMed  Google Scholar 

Liu XB, Yu GW, Gao XY, Huang JL, Qin LT, Ni HB, Lyu C (2021) Intranasal delivery of plasmids expressing bovine herpesvirus 1 gB/gC/gD proteins by polyethyleneimine magnetic beads activates long-term immune responses in mice. Virol J 18:60. https://doi.org/10.1186/s12985-021-01536-w

Article  CAS  PubMed  PubMed Central  Google Scholar 

Luo Y, Xiong D, Li HH, Qiu SP, Lin CL, Chen Q, Huang CH, Yuan Q, Zhang J, Xia NS (2016) Development of an HSV-1 neutralization test with a glycoprotein D specific antibody for measurement of neutralizing antibody titer in human sera. Virol J 13:44. https://doi.org/10.1186/s12985-016-0508-4

Article  CAS  PubMed  PubMed Central  Google Scholar 

Madavaraju K, Koganti R, Volety I, Yadavalli T, Shukla D (2020) Herpes simplex virus cell entry mechanisms: an update. Front Cell Infect Microbiol 10:617578. https://doi.org/10.3389/fcimb.2020.617578

Article  PubMed  Google Scholar 

Marawan MA, Deng M, Wang C, Chen Y, Hu C, Chen J, Chen X, Chen H, Guo A (2021) Characterization of BoHV-1 gG-/tk-/gE- mutant in differential protein expression, virulence, and immunity. Vet Sci 8:253. https://doi.org/10.3390/vetsci8110253

Article  PubMed  PubMed Central  Google Scholar 

Martin Beer, Dastjerdl A (2018) OIE Terrestrial Manual. Chapter 3.4.11 Infectious bovine rhinotracheitis/infectious pustular vulvovaginitis. In: Manual of diagnostic tests and vaccines for terrestrial animals. Office Intl Des Epizooties, Paris, pp 1139–1157

Nandi S, Kumar M (2011) Comparison of ELISA and virus neutralization test in assaying serum antibodies to bovine herpesvirus 1. Acta Virol 55:175–177. https://doi.org/10.4149/av_2011_02_175

Panasiuk M, Rychłowski M, Derewońko N, Bieńkowska-Szewczyk K (2018) Tunneling nanotubes as a novel route of cell-to-cell spread of herpesviruses. J Virol 92:e00090-e118. https://doi.org/10.1128/JVI.00090-18

Article  CAS  PubMed  PubMed Central  Google Scholar 

Pastenkos G, Lee B, Pritchard SM, Nicola AV (2018) Bovine herpesvirus 1 entry by a low-pH endosomal pathway. J Virol 92:e00839-e918. https://doi.org/10.1128/JVI.00839-18

Article  CAS  PubMed  PubMed Central  Google Scholar 

Petrini S, Iscaro C, Righi C (2019) Antibody responses to bovine alphaherpesvirus 1 (BoHV-1) in passively immunized calves. Viruses 11:23. https://doi.org/10.3390/v11010023

Article  CAS  PubMed  PubMed Central  Google Scholar 

Quattrocchi V, Soria I, Langellotti CA, Gnazzo V, Gammella M, Moore DP, Zamorano PI (2017) A DNA vaccine formulated with chemical adjuvant provides partial protection against bovine herpes virus infection in cattle. Front Immunol 8:37. https://doi.org/10.3389/fimmu.2017.00037

Article  CAS  PubMed  PubMed Central  Google Scholar 

Sarangi LN, Reddy RVC, Rana SK, Naveena T, Ponnanna NM, Sharma GK (2021) Sero-diagnostic efficacy of various ELISA kits for diagnosis of infectious bovine rhinotracheitis (IBR) in cattle and buffaloes in India. Vet Immunol Immunopathol 241:110324. https://doi.org/10.1016/j.vetimm.2021.110324

Article  CAS  PubMed  Google Scholar 

Schröder C, Keil GM (1999) Bovine herpesvirus 1 requires glycoprotein H for infectivity and direct spreading and glycoproteins gH (W450) and gB for glycoprotein D-independent cell-to-cell spread. J Gen Virol 80:57–61. https://doi.org/10.1099/0022-1317-80-1-57

Article  Google Scholar 

Schröder C, Linde G, Fehler F, Keil GM (1997) From essential to beneficial: glycoprotein D loses importance for replication of bovine herpesvirus 1 in cell culture. J Virol 71:25–33. https://doi.org/10.1128/jvi.71.1.25-33

Article  PubMed  PubMed Central  Google Scholar 

Su V, Knutson A, Lau K, Kurata W, Berestecky J, Lau AF (2009) Generation and characterization of mouse monoclonal antibodies against CIP75, an UbL-UBA domain-containing protein. Hybridoma (larchmt) 28:79–84. https://doi.org/10.1089/hyb.2008.0082

Article  CAS  PubMed  Google Scholar 

Tian R, Ju F, Yu M, Liang Z, Xu Z, Zhao M, Qin Y, Lin Y, Huang X, Chang Y, Li S, Ren W, Lin C, Xia N, Huang C (2022) A potent neutralizing and protective antibody against a conserved continuous epitope on HSV glycoprotein D. Antiviral Res 201:105298. https://doi.org/10.1016/j.antiviral.2022.105298

Article  CAS  PubMed  Google Scholar 

Toussaint JF, Coen L, Letellier C, Dispas M, Gillet L, Vanderplasschen A, Kerkhofs P (2005) Genetic immunisation of cattle against bovine herpesvirus 1: glycoprotein gD confers higher protection than glycoprotein gC or tegument protein VP8. Vet Res 36:529–544. https://doi.org/10.1051/vetres:2005015