| 
              
              
              Open Access  
 
              
              
              
              Research 
              
              
(Published 
				online: 05-12-2016)  
              5. 
				
              Phylogenetic analysis of glycoprotein B gene 
              sequences of bovine herpesvirus 1 isolates from India reveals the 
              predominance of subtype 1.1. -
              
              
              S. S. Patil, A. Prajapati, D. Hemadri, K. P. Suresh, G. S. Desai, 
              G. B. Manjunatha Reddy, B. M. Chandranaik, S. Ranganatha
              
              
              and H. Rahman 
              
              Veterinary World, 9(12): 1364-1369   
              
   
                
                
doi: 
              
				
				10.14202/vetworld.2016.1364-1369 
                
                
                S. S. Patil:
                
              
                ICAR-National 
                Institute of Veterinary Epidemiology and Disease Informatics, 
                Bengaluru - 560 064, Karnataka, India; sharanspin123@rediffmail.com 
              
              A. Prajapati:
              
              
              ICAR-National 
              Institute of Veterinary Epidemiology and Disease Informatics, 
              Bengaluru - 560 064, Karnataka, India; avi75prajapati@gmail.com 
              
              D. Hemadri:
              
              
              ICAR-National 
              Institute of Veterinary Epidemiology and Disease Informatics, 
              Bengaluru - 560 064, Karnataka, India; divakar.hemadri@gmail.com 
              
              K. P. Suresh:
              
              
              ICAR-National 
              Institute of Veterinary Epidemiology and Disease Informatics, 
              Bengaluru - 560 064, Karnataka, India; suresh.KP@icar.gov.in 
              
              G. S. Desai:
              
              
              ICAR-National 
              Institute of Veterinary Epidemiology and Disease Informatics, 
              Bengaluru - 560 064, Karnataka, India; gurusdesai@rediffmail.com 
              
              G. B. Manjunatha Reddy:
              
              
              ICAR-National 
              Institute of Veterinary Epidemiology and Disease Informatics, 
              Bengaluru - 560 064, Karnataka, India; suresh.KP@icar.gov.in 
              
              B. M. Chandranaik:
              
              
              Institute of Animal 
              Health and Veterinary Biologicals, Bengaluru - 560 024, Karnataka, 
              India; dinglychandru@yahoo.co.in 
              
              S. Ranganatha:
              
              
              Institute of Animal 
              Health and Veterinary Biologicals, Bengaluru - 560 024, Karnataka, 
              India; srangavetco@gmail.com 
              
              H. Rahman:
              
              
              Division of Animal 
              Sciences, Indian Council of Agriculture Research, Krishi Bhawan, 
              New Delhi - 110 001, India; hricar@gmail.com   
              
              Received: 06-06-2016, Accepted: 17-10-2016, Published online: 
              05-12-2016   
				
              	
              	Corresponding author: 
              	
				S. S. Patil, 
                e-mail: sharanspin123@rediffmail.com 
 
              Citation: 
              
              Patil SS, Prajapati A, Hemadri D, Suresh KP, Desai GS, Reddy GBM, 
              Chandranaik BM, Ranganatha S, Rahman H (2016) Phylogenetic 
              analysis of glycoprotein B gene sequences of bovine herpesvirus 1 
              isolates from India reveals the predominance of subtype 1.1., 
              Veterinary World, 9(12): 1364-1369. 
 
              
				Abstract 
 
              Aim: 
              This study was 
              conducted for the isolation and molecular characterization of 
              bovine herpesvirus 1 (BoHV-1) isolated from the nasal and vaginal 
              swabs collected from naturally infected cattle showing clinical 
              symptoms of the respiratory disease.  
              Materials and 
              Methods: 
              Isolation of 
              BoHV-1 virus performed on clinical samples collected from 65 
              cattle from five states of India. The BoHV-1 isolates were further 
              confirmed by polymerase chain reaction (PCR) using primers 
              specific for glycoprotein B (gB) genomic region. PCR amplification 
              was performed using previously published gB gene-specific primer 
              pairs. gB PCR amplicons obtained from all isolates were sequenced, 
              and phylogenetic analysis was performed using software. 
               
              Results: 
              A total of 12 
              samples were found positive in cell culture isolation. 11 isolates 
              showed the visible cytopathic effect on Madin-Darby bovine kidney 
              after 72 h. Partial sequence analysis of gB gene of all isolates 
              revealed 99.0-100% homology between them. All isolates showed 
              99.2-99.8% homology with Cooper stain.  
              Conclusion:
              
              BoHV-1.1 is the predominant circulating subtype of BoHV in India, 
              and all isolates have homology with Cooper stain.  
              
              Keywords: 
              
              bovine herpesvirus 1-1, glycoprotein B, India, infectious bovine 
              rhinotracheitis, phylogenetic analysis, sequencing, subtype 1.1. 
 
              References 
 
                
                  | 1. MacLachlan, N.J. and Dubovi, E.J. (2011) Fenner's 
                  Veterinary Virology. 4th ed. Academic Press, London. |  
                  |  |  
                  | 2. Nandi, S., Kumar, M., Manohar, M. and Chauhan, R.S. (2009) 
                  Bovine herpes virus infections in cattle. Anim. Health Res. 
                  Rev., 10: 85-98. https://doi.org/10.1017/S1466252309990028
 PMid:19558751
 |  
                  |  |  
                  | 3. Raaperi, K., Bougeard, S., Aleksejev, A., Orro, T. and 
                  Viltrop, A. (2012) Association of herd BHV-1 seroprevalence 
                  with respiratory disease in young stock in Estonian dairy 
                  cattle. Res. Vet. Sci., 93: 641-648. https://doi.org/10.1016/j.rvsc.2011.10.015
 PMid:22100246
 |  
                  |  |  
                  | 4. Muylkens, B., Thiry, J., Kirten, P., Schynts, F. and Thiry, 
                  E. (2007) Bovine herpesvirus 1 infection and infectious bovine 
                  rhinotracheitis. Vet. Res., 38: 181-209. https://doi.org/10.1051/vetres:2006059
 PMid:17257569
 |  
                  |  |  
                  | 5. Biswas, S., Bandyopadhyay, S., Dimri, U. and Patra, P.H. 
                  (2013) Bovine herpesvirus-1 (BHV-1) - A re-emerging concern in 
                  livestock: A revisit to its biology, epidemiology, diagnosis, 
                  and prophylaxis. Vet. Q., 33: 68-81. https://doi.org/10.1080/01652176.2013.799301
 |  
                  |  |  
                  | 6. Mehrotra, M.L., Rajya, B.S. and Kumar, S. (1976) Infectious 
                  bovine rhinotracheitis (IBR) - keratoconjunctivitis in calves. 
                  Indian J. Vet. Pathol., 1: 70-73. |  
                  |  |  
                  | 7. Renukaradhya, G.J., Rajasekar, M. and Raghavan, R. (1996) 
                  Prevalence of infectious bovinerhinotracheitis in Southern 
                  India. Rev. Sci. Tech., 15: 1021-1028. https://doi.org/10.20506/rst.15.3.970
 PMid:9025147
 |  
                  |  |  
                  | 8. Renukaradhya, G.J., Isloor, S. and Rajasekhar, M. (2002) 
                  Epidemiology, zoonotic aspects, vaccination and 
                  control/eradication of brucellosis in India. Vet. Microbiol., 
                  90: 183-195. https://doi.org/10.1016/S0378-1135(02)00253-5
 |  
                  |  |  
                  | 9. Koppad, K.K., Patil, S.S., Shome, R., Desai, G.S., Bhure, 
                  S., Gajendragad, M.R., Tiwari, C.B. and Prabhudas, K. (2007) 
                  Seroprevalence of infectious bovine rhinotracheitis in 
                  Karnataka. Indian Vet. J., 84: 569-572. |  
                  |  |  
                  | 10. Trangadia, B., Rana, S., Mukherjee, F. and Srinivasan, V. 
                  (2010) Prevalence of brucellosis and infectious bovine 
                  rhinotracheitis in organized dairy farms in India. Trop. Anim. 
                  Health Prod., 42: 203-207. https://doi.org/10.1007/s11250-009-9407-7
 PMid:19644761
 |  
                  |  |  
                  | 11. Chandranaik, B.M., Rathnamma, D., Patil, S.S., Ranganath, 
                  S., Kovi, R.C., Akhila, D.S., Isloor, S., Renukaprasad, C. and 
                  Prabhudas, K. (2014a) Cloning of partial glycoprotein B gene 
                  and molecular epidemiology studies of bovine herpes virus-1 
                  isolates. Indian J. Anim. Sci., 84: 108-114. |  
                  |  |  
                  | 12. Krishnamoorthy, P., Patil, S.S., Shome, R. and Rahman, H. 
                  (2015) Sero-epidemiology of infectious bovine rhinotracheitis 
                  and brucellosis in organised dairy farms in southern India. 
                  Indian J. Anim. Sci., 85: 7. |  
                  |  |  
                  | 13. Patil, S.S., Prajapati, A., Krishnamoorthy, P., Desai, G.S., 
                  Reddy, G.B.M., Suresh, K.P. and Rahman, H. (2015) 
                  Seroprevalence of Infectious bovine rhinotracheitis in 
                  organized dairy farms in India. Indian J. Anim. Res., DOI: 
                  18805/ijar.7084. https://doi.org/10.18805/ijar.7084
 |  
                  |  |  
                  | 14. Chandranaik, B.M., Shivaraj, C., Sanjeev, K. and 
                  Renukaprasad, C. (2010) Isolation of BHV-1 from bovine semen 
                  and application of real time isolation of BHV-1 from bovine 
                  semen and application of real time PCR for diagnosis of IBR/IPV 
                  from clinical samples. Vet. Arch., 80: 467-475. |  
                  |  |  
                  | 15. Ravishankar, C., Nandi, S., Chander, V. and Mohapatra, T.K. 
                  (2012) Glycoprotein C gene based molecular subtyping of a 
                  bovine herpesvirus -1 isolate from Uttar Pradesh, India. 
                  Indian J. Virol., 23: 402-406. https://doi.org/10.1007/s13337-012-0116-x
 PMid:24293834 PMCid:PMC3550786
 |  
                  |  |  
                  | 16. Surendra, K.S.N., Rana, S.K., Subramanian, B.M., Reddy, 
                  R.V.C., Sharma, G.K. and Srinivasan, V.A. (2015) Phylogenetic 
                  analysis of bovine herpesvirus isolate of India. Adv. Anim. 
                  Vet. Sci., 3: 451-460. https://doi.org/10.14737/journal.aavs/2015/3.8.451.460
 |  
                  |  |  
                  | 17. Babiuk, L.A., L'ltalien, J., van Drunen Little-van den 
                  Hurk, S., Zamb, T., Lawman, M.J.P., Hughes, G. and Gifford, 
                  G.A. (1987) Protection of cattle from bovine herpesvirus type 
                  1 (BHV-1) infection by immunization with individual viral 
                  glycoproteins. Virology, 159: 57-66. https://doi.org/10.1016/0042-6822(87)90347-3
 |  
                  |  |  
                  | 18. Clinton, J. and Chowdhury, S. (2010) Bovine herpesvirus 
                  type 1 (BHV-1) is an important cofactor in the bovine 
                  respiratory disease complex. Vet. Clin. Food Anim., 26: 
                  303-321. https://doi.org/10.1016/j.cvfa.2010.04.007
 PMid:20619186
 |  
                  |  |  
                  | 19. Hutchings, D.L., van Drunen Little-van den Hurk, S. and 
                  Babiuk, L.A. (1990) Lymphocyte proliferative responses to 
                  separated bovine herpesvirus 1 proteins in immune cattle. J. 
                  Virol., 64: 5114-5122. PMid:2168990 PMCid:PMC248003
 |  
                  |  |  
                  | 20. Ros, C. and Belák, S. (1999) Studies of genetic 
                  relationships between bovine, caprine, cervine, and 
                  rangiferine alphaherpes viruses and improved molecular methods 
                  for virus detection and identification. J. Clin. Microbiol., 
                  37: 1247-153. PMid:10203465 PMCid:PMC84742
 |  
                  |  |  
                  | 21. Page, R.D. (1996) Tree view: An application to display 
                  phylogenetic trees on personal computers. Comput. Appl., 12: 
                  357-358. https://doi.org/10.1093/bioinformatics/12.4.357
 |  
                  |  |  
                  | 22. Das, P., Mohanty, N.N., Ranganatha, S., Ranabijuli, S., 
                  Sarangi, L.N. and Panda, H.K.A. (2014) Comparative evaluation 
                  of avidin-biotin ELISA and micro SNT for detection of 
                  antibodies to infectious bovine rhinotracheitis in cattle 
                  population of Odisha, India. Vet. World, 7: 548-552. https://doi.org/10.14202/vetworld.2014.548-552
 |  
                  |  |  
                  | 23. Rodríguez, M.M., Landa, A.H. and Valle, B.M. (2009) 
                  Development and evaluation of a polymerase chain reaction 
                  assay to detect bovine herpesvirus 1. Span. J. Agric. Res., 7: 
                  59-66. https://doi.org/10.5424/sjar/2009071-398
 |  
                  |  |  
                  | 24. Sobhy, N.M., Mor, S.K., Mohammed, M.E.M., Bastawecy, I.M., 
                  Fakhry, H.M., Youssef, C.R.B. and Goyal, S.M. (2014) 
                  Comparative molecular characterization of bovine herpesvirus-1 
                  strains from Egypt and the United States. Life Sci. J., 11: 
                  493-499. |  
                  |  |  
                  | 25. Mahajan, V., Banga, H.S., Deka, D., Filia, G. and Gupta, 
                  A. (2013) Comparison of diagnostic tests for diagnosis of 
                  infectious bovine rhinotracheitis in natural cases of bovine 
                  abortion. J. Comp. Pathol., 149: 391-401. https://doi.org/10.1016/j.jcpa.2013.05.002
 PMid:23885803
 |  
                  |  |  
                  | 26. Traesel, C.K., Bernardes, L.M., Spilki, F.R., Weiblen, R. 
                  and Flores, E.F. (2015) Sequence analysis of the 59 third of 
                  glycoprotein C gene of South American bovine herpesviruses 1 
                  and 5 Brazilian. J. Med. Biol. Res., 48: 470-478. https://doi.org/10.1590/1414-431X20144266
 PMid:25760029 PMCid:PMC4445672
 |  
                  |  |  
                  | 27. Majumder, S., Pandey, A.B. and Ramakrishnan, A.N. (2014) 
                  Sequence and phylogenetic analysis of glycoprotein B gene of 
                  Indian isolate of bovine herpesvirus 1. Adv. Anim. Vet. Sci., 
                  2: 19-23. https://doi.org/10.14737/journal.aavs/2014/2.2s.19.22
 |  
                  |  |  
                  | 28. Patil, S.S., Hemadri, D., Sreekala, K., Veeresh, H., 
                  Chandranaik, B.M. and Prabhudas, K. (2012) Genetic 
                  characterization of bovine herpesvirus1(BoHV-1) isolates from 
                  India. Indian J. Anim. Sci., 82: 848-850. |  
                  |  |  
                  | 29. Chandranaik, B.M., Rathnamma, D., Patil, S.S., Ranganath, 
                  S., Ramesh, C.K., Akhila, D.S., Isloor, S., Renukaprasad, C. 
                  and Prabhudas, K. (2014b) Epidemiology of bovine herpes virus- 
                  1 under different housing practices in cattle breeding 
                  station. Indian J. Anim. Sci., 84: 103-107. |  
                  |  |  
                  | 30. Sreenivasa, B.P., Natarjan, C. and Rasool, T.J. (1996) 
                  Restriction endonuclease analysis of DNA from Indian isolates 
                  of bovine herpesvirus 1. Acta Virol., 40: 315-318. PMid:9171462
 |  
                  |  |  
                  | 31. Spilki, F.R., Esteves, P.A., Lima, M., Franco, A.C., 
                  Chiminazzo, C., Flores, E.F., Weiblen, R., Driemeier, D. and 
                  Roehe, P.M. (2004). Comparative pathogenicity of bovine 
                  herpesvirus 1 (BHV-1) subtypes 1 (BHV-1.1) and 2a (BHV-1.2a). 
                  Pesqui. Vet. Bras., 24: 43-49. https://doi.org/10.1590/S0100-736X2004000100010
 |  
                  |  |  
                  | 32. Esteves, P.A., Dellagostin, O.A., Pinto, L.S., Silva, 
                  A.D., Spilki, F.R., Ciacci-Zanella, J.R., Hübner, S.O., 
                  Puentes, R., Maisonnave, J., Franco, A.C., Rijsewijk, F.A., 
                  Batista, H.B., Teixeira, T.F., Dezen, D., Oliveira, A.P., 
                  David, C., Arns, C.W. and Roehe, P.M. (2008) Phylogenetic 
                  comparison of the carboxy-terminal region glycoprotein C (gC) 
                  of bovine herpesviruses (BoHV). Virus Res., 131(1): 16-22. https://doi.org/10.1016/j.virusres.2007.08.004
 PMid:17889957
 |  
                  |  |  
                  | 33. Saha, T., Guha, C., Chakraborty, D., Pal, B., Biswas, U., 
                  Chatterjee, A., Koenig, P. and Beer, M. (2010) Isolation and 
                  characterization of BoHV-1 from cattle in West Bengal India. 
                  Iran. J. Vet. Sci., Technol., 2: 1-8. |  
                  |  |  
                  | 34. Engels, M., Giuliani, C., Wild, P., Beck, T.M., Loepfe, E. 
                  and Wyler, R. (1986) The genome of bovine herpesvirus 1 
                  (BHV-1) strains exhibiting a neuropathogenic potential 
                  compared to known BHV-1 strains by restriction site mapping 
                  and cross-hybridization. Virus Res., 6: 57-73. https://doi.org/10.1016/0168-1702(86)90057-2
 |  
                  |  |  
                  | 35. Claus, M.P., Alfieri, A.F., Folgueras-Flatschart, A.V., 
                  Wosiacki, S.R., Medici, K.C. and Alfieri, A.A. (2005) Rapid 
                  detection and differentiation of bovine herpesvirus 1 and 5 
                  glycoprotein C gene in clinical specimens by multiplex PCR. J. 
                  Virol., 128: 183-188. https://doi.org/10.1016/j.jviromet.2005.05.001
 |  
                  |  |  
                  | 36. Alegre, M., Nanni, M. and Fondevila, N. (2001) Development 
                  of a multiplex polymerase chain reaction for the 
                  differentiation of bovine herpesvirus-1 and 5. J. Vet. Med. 
                  Infect. Dis. Vet., 48(8): 613-621. https://doi.org/10.1046/j.1439-0450.2001.00489.x
 |  |