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Monodon Baculovirus of Shrimp

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Abstract

Among the viruses infecting penaeid shrimp, monodon-type baculovirus (MBV) otherwise known as Penaeus monodon singly enveloped nuclear polyhedrosis virus (PmSNPV), is one of the widely reported and well described viruses. It is a rod-shaped, enveloped, double-stranded DNA virus, and considered till recently, as the type A baculovirus. Besides MBV, two strains of SNPV are reported—plebejus baculovirus and bennettae baculovirus. MBV was reported to be originated from Taiwan and has wide geographic distribution and is reported to be enzootic in wild penaeids of the Indo-pacific coasts of Asia. The virus also has diverse host-range including a variety of cultured and captured shrimp species and freshwater prawn, Macrobrachium rosenbergii. MBV has been reported in all life stages of P. monodon with late larval, postlarval and young juvenile as the most susceptible stages/ages. However, MBV has not been documented in early larval stages. Although MBV has been reported to be tolerated well by shrimp, the infection has been attributed to decreased productivity. The target organs or tissues of MBV are the hepatopancreatic tubules and duct epithelium of postlarvae, juveniles and adults, and the anterior midgut epithelium of very young postlarvae. The prominent clinical sign of infection is the presence of multiple spherical inclusion bodies in the hepatopancreas and midgut epithelial cells. The major mode of transmission of the virus is horizontal through oral exposure to occlusion bodies, contaminated tissues or fomites. Minor morphometric variation of the virus has been reported among different isolates. The rod-shaped enveloped virus particles range from 265–324 nm in length and 42–77 nm in diameter. Although complete genome sequence of MBV is not available, nucleic acid of MBV is circular, double-stranded DNA with a genome size ranging from 80 to 160 kbp. The virus codes for a 53 kDa major polyhedrin polypeptide and two minor 47 and 49 kDa polypeptides. A variety of diagnostic tools have been reported for this virus including real-time PCR and LAMP-based detection. Taxonomic position is still uncertain and International Committee on Taxonomy of Viruses lists MBV as a tentative species named PemoNPV in the genus Nucleopolyhedrovirus. However, according to the latest genomic information on the virus, it has been suggested to create a new group of non-occluded bacilliform viruses called nudiviruses with MBV as one of the members. The aim of the current work is to describe the knowledge on the status, distribution and host-range, pathology, transmission, virus structure and morphogenesis, genomic characteristics, diagnosis and the latest taxonomic position of MBV.

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References

  1. Alavandi SV, Vijayan KK, Rajendran KV. Shrimp diseases, their prevention and control. Central Institute of Brackishwater Aquaculture (CIBA). Bulletin. 1995;3:1–17.

    Google Scholar 

  2. Ambipillai L, Sobhana KS, George KC, Sanil NK. Histopathological survey of cultured shrimps in Cochin, Kerala. J Mar Biol Ass India. 2003;45:178–85.

    Google Scholar 

  3. Anderson IG, Shariff M, Nash G, Nash M. Mortalities of juvenile shrimp, Penaeus monodon, associated with Penaeus monodon baculovirus, cytoplasmic reo-like virus, and ricketssial and bacterial infections, from Malaysian brackishwater ponds. Asian Fish Sci. 1987;1:47–64.

    Google Scholar 

  4. Baticados MCL. Diseases of prawns in Philippines. SEAFDEC Asian Aquaculture. 1988;10:1–8.

    Google Scholar 

  5. Baticados MCL, Cruz-Lacierda ER, de la Cruz MC, Duremdez-Fernandez RC, Gacutan RQ, Lavilla-Pitogo CR, Lio-Po GD. Diseases of penaeid shrimps in the Philippines. Aquaculture extension manual no. 16. Aquaculture Department, Southeast Asian Fisheries Development Center (SEAFDEC), Tigbauan, Iloilo, Philippines. 1990. p. 46.

  6. Baticados MCL, Lavilla-Pitogo CR, Paner MG, de la Pena LD, Tendencia EA. Occurrence and pathology of Penaeus monodon baculovirus infection in hatcheries and ponds in Philippines. Bamidegh. 1991;43:35–41.

    Google Scholar 

  7. Belcher CR, Young PR. Colourimetric PCR-based detection of monodon baculovirus in whole Penaeus monodon postlarvae. J Virol Methods. 1998;74:21–9.

    Article  PubMed  CAS  Google Scholar 

  8. Boonsanongchokying C, Sang-oum W, Sithigorngul P, Sriurairatana S, Flegel TW. Production of monoclonal antibodies to polyhedrin of monodon baculovirus (MBV) from shrimp. Sci Asia. 2006;32:371–6.

    Article  CAS  Google Scholar 

  9. Brock JA. Pathogen considerations for peaneid shrimp imported into Hawai. Aquaculture Development Program, Hawai. 1983.

  10. Brock JA, Lightner DV. Diseases of crustacea. Diseases caused by microorganisms. In: Kinne O, editor. Diseases of marine animals, vol. 3. Hamburg: Biologische Anstalt Helgoland; 1990. p. 245–349.

    Google Scholar 

  11. Caipang CMA, Sibonga MFJ, Amar MJA, Geduspan JS. Development of a polymerase chain reaction (PCR) assay for the detection of Philippine isolates of the Penaeus monodon-type Baculovirus (MBV). Curr Res J Biol Sci. 2011;3:416–20.

    CAS  Google Scholar 

  12. Caipang CMA, Sibonga MFJ, Geduspan JS. Partial sequence of the genomic DNA from a Philippine isolate of the Penaeus monodon-type baculovirus (MBV) and comparison with other geographical isolates. AACL bioflux. 2011;4:387–93.

    Google Scholar 

  13. Chaivisuthangkura P, Tawilert C, Tejangkura T, Rukpratanporn S, Longyant S, Sithigorngul W, Sithigorngul P. Molecular isolation and characterization of a novel occlusion body protein gene from Penaeus monodon nucleopolyhedrovirus. Virology. 2008;381:261–7.

    Article  PubMed  CAS  Google Scholar 

  14. Chaivisuthangkura P, Srisuk C, Rukpratanporn S, Longyanta S, Sridulyakula P, Sithigorngul P. Rapid and sensitive detection of Penaeus monodon nucleopolyhedrovirus by loop-mediated isothermal amplification. J Virol Methods. 2009;162:188–93.

    Article  PubMed  CAS  Google Scholar 

  15. Chang PS, Wang YC, Lo CF, Kou GH, Chen SN. Purification and biochemical characteristics of occlusion body of Penaeus monodon-type baculovirus (MBV). Fish Pathol. 1992;27:127–30.

    Article  Google Scholar 

  16. Chang PS, Lo CF, Kou GH, Lu CC, Chen SN. Purification and amplification of DNA from Penaeus monodon type baculovirus (MBV). J Invertebr Pathol. 1993;62:116–20.

    Article  PubMed  CAS  Google Scholar 

  17. Chanratchakool P, Turnbull JF, Funge-Smith S, MacRae IH, Limsuwan C. Health management in shrimp ponds. Bangkok: Aquatic Animal Health Research Institute; 1998.

    Google Scholar 

  18. Chayaburakul K, Nash G, Pratanpipat P, Sriurairatana S, Withyachumnarnkul B. Multiple pathogens found in growth-retarded black tiger shrimp Penaeus monodon cultivated in Thailand. Dis Aquat Organ. 2004;60:89–96.

    Article  PubMed  Google Scholar 

  19. Chen SN, Kou GH. Infection of cultured cells from the lymphoid organ of Penaeus monodon Fabricius by monodon-type baculovirus (MBV). J Fish Dis. 1989;12:73–6.

    Article  Google Scholar 

  20. Chen SN, Chang PS, Kou GH, Lightner DV. Studies on virogenesis and cytopathology of Penaeus monodon baculovirus (MBV) in the giant tiger prawn (Penaeus monodon) and the red tail prawn (Penaeus penecillatus). Fish Pathol. 1989;24:89–100.

    Article  Google Scholar 

  21. Chen SN, Chang PS, Kou GH. Infection route and eradication of Penaeus monodon baculovirus (MBV) in larval giant tiger prawn Penaeus monodon. In: Fulks W, Main KL, editors. Diseases of cultured shrimp in Asia and United States. Honolulu: The Oceanic Institute; 1992. p. 177–84.

    Google Scholar 

  22. Cheng CH, Liu SM, Chow TY, Hsiao YY, Wang DP, Huang JJ, Chen HH. Analysis of the complete genome sequence of the Hz-1 virus suggests that it is related to members of the Baculoviridae. J Virol. 2002;76:9024–34.

    Article  PubMed  CAS  Google Scholar 

  23. Colorni A. Penaeid pathology in Israel: Problems and research. In: Advances in tropical aquaculture, Tahiti. Actes de Colloque 9 AQUACOP IFREMER. 1989. p. 89–96.

  24. Colorni A, Samocha T, Colorni B. Pathogenic viruses introduced into mariculture systems by imported penaeid shrimp. Bamidgeh. 1987;39:21–8.

    Google Scholar 

  25. Couch JA. An enzootic nuclear polyhedrosis virus of pink shrimp: ultrastructure, prevalence, and enhancement. J Invertebr Pathol. 1974;24:311–31.

    Article  PubMed  CAS  Google Scholar 

  26. Couch JA. Viral diseases of invertebrates other than insects. In: Davidson EW, editor. Pathogenesis of invertebrate microbial diseases. Totowa: Allanheld, Osmun Publisher; 1981. p. 127–60.

    Google Scholar 

  27. Couch JA. Baculoviridae. Nuclear polyhedrosis viruses. Part 2. Nuclear polyhedrosis viruses of invertebrates other than insects. In: Adams JR, Bonami JR, editors. Atlas of invertebrate viruses. Boca Raton: CRC Press; 1991. p. 205–26.

    Google Scholar 

  28. de la Pena LD, Lavilla-Pitogo CR, Villar CBR, Paner MG. Prevalence of economically-important viral diseases in wild shrimp (Penaeus monodon) in the Philippines. In: Nagasawa K, editor. Recent advances in diagnosis and control of fish and shrimp diseases in Southeast Asia. Iloilo: SEAFDEC Aquaculture Department; 2005.

    Google Scholar 

  29. Diamant A, Colorni A. Viral infections of penaeid shrimp in Israel and use of acridine orange fluorescence as a rapid diagnostic method. In: Third international EAFP conference, Bergen, Norway, 31 Aug–3 Sept, 1987.

  30. Doubrovsky A, Paynter JL, Sambhi SK, Atherton JG, Lester RJG. Observations on the ultrastructure of baculovirus in Australian Penaeus monodon and Penaeus merguiensis. Aust J Mar Freshw Res. 1988;39:743–9.

    Article  Google Scholar 

  31. Fegan DF, Flegal TW, Sriurairatana S, Waiakrutra M. The occurrence, development and histopathology of monodon baculovirus in Penaeus monodon in Southern Thailand. Aquaculture. 1991;96:205–17.

    Article  Google Scholar 

  32. Felix S, Devaraj M. Incidence of destructive MBV and IHHNV in a commercial shrimp hatchery. Seaf Export J. 1993;25:13–8.

    Google Scholar 

  33. Flegel TW. Special topic review: major viral diseases of the black tiger prawn (Penaeus monodon) in Thailand. World J Microbiol Biotechnol. 1997;13:433–42.

    Article  Google Scholar 

  34. Flegel TW. Detection of major penaeid shrimp viruses in Asia, a historical perspective with emphasis on Thailand. Aquaculture. 2006;258:1–33.

    Article  Google Scholar 

  35. Flegel TW, Pasharawipas T. Active viral accommodation: a new concept for crustacean response to viral pathogens. In: Flegel TW, editor. Advances in shrimp biotechnology. Bangkok: National Center for Genetic Engineering and Biotechnology; 1998. p. 245–50.

    Google Scholar 

  36. Flegel TW, Fegan DF, Kongsom S, Vuthikornudomkit S, Sriurairatana S, Boonyaratpalin S, Chantanachookhin C, Vickers J, Macdonald OD. Occurrence, diagnosis and treatment of shrimp diseases in Thailand. In: Fulks W, Main KL, editors. Diseases of cultured penaeid shrimp in Asia and the United States. Honolulu: Oceanic Institute; 1992. p. 57–112.

    Google Scholar 

  37. Flegel TW, Thamavit V, Pasharawipas T, Alday-Sans V. Statistical correlation between severity of hepatopancreatic parvovirus infection and stunting of farmed black tiger shrimp (Penaeus monodon). Aquaculture. 1999;174:197–206.

    Article  Google Scholar 

  38. Flegel TW, Tirasak P, Linda N, Vitaya T, Suraphol K. Effects of hepatopancreatic parvovirus (HPV), monodon baculovirus (MBV) and multiple viral infections on cultivated shrimp in Thailand. In: Proceedings of the 3rd national symposium on marine shrimp, 8–9 Nov 2001. Bangkok: Queen Sirikit National Convention Center; 2001. p.48–63.

  39. Flegel TW, Nielsen L, Thamavit V, Kongtim S, Pasharawipas T. Presence of multiple viruses in non-diseased, cultivated shrimp at harvest. Aquaculture. 2004;240:55–68.

    Article  Google Scholar 

  40. Gangnonngiw W, Laisutisan K, Sriurairatana S, Senapin S, Chuchird N, Limsuwan C, Chaivisuthangkura P, Flegel TW. Monodon baculovirus (MBV) infects the freshwater prawn Macrobrachium rosenbergii cultivated in Thailand. Virus Res. 2010;148:24–30.

    Article  PubMed  CAS  Google Scholar 

  41. Gunalan B, Soundarapandian P, Dinakaran GK. Effect of different stocking densities on the MBV infected seeds of black tiger shrimp, Penaeus monodon (Fabricius). Asian J Agric Sci. 2010;2:5–8.

    Google Scholar 

  42. Hao NV. Study on diseases in Penaeus monodon cultured in Tra Vinh Province, Vietnam. Report of UNDP Project (VIE/96/025). 1999.

  43. Hsu YL, Wang KH, Yang YH, Tung MC, Hu CH, Lo CF, Wang CH, Hsu T. Diagnosis of Penaeus monodon-type baculovirus by PCR and by ELISA of occlusion bodies. Dis Aquat Organ. 2000;40:93–9.

    Article  PubMed  CAS  Google Scholar 

  44. Johnson PT, Lightner DV. The rod-shaped nuclear viruses of crustaceans: gut-infecting species. Dis Aquat Organ. 1988;4:123–41.

    Article  Google Scholar 

  45. Karunasagar I, Otta SK, Karunasagar I. Monodon baculovirus and bacterial speticaemia associated with mass mortality of cultivated shrimp (P. monodon) from the east coast of India. Indian J Virol. 1998;14:27–30.

    Google Scholar 

  46. Lester RJG, Doubrovsky A, Paynter JL, Sambhi SK, Atherton JG. Light and electron microscope evidence of baculovirus infection in the prawn Penaeus plebejus. Dis Aquat Organ. 1987;3:217–9.

    Article  Google Scholar 

  47. Liao I. A culture study on grass prawn, Penaeus monodon, in Taiwan- the patterns, the problems and the prospects. J Fish Soc Taiwan. 1977;5:11–29.

    Google Scholar 

  48. Liao IC, Su MS, Chang CF. Diseases of Penaeus monodon in Taiwan: a review from 1977 to 1991. In: Fulks W, Main KL, editors. Diseases of cultured penaeid shrimp in Asia and the United States. Honolulu: Oceanic Institute; 1992. p. 113–37.

    Google Scholar 

  49. Lightner DV. A review of the diseases of cultured penaeid shrimps and prawns with emphasis on recent discoveries and developments. In: Proceedings of the first international conference on the culture of penaeid prawns/shrimps, Iloilo City, Philippines. 1985; p.79–103.

  50. Lightner DV. Diseases of cultured penaeid shrimp and prawns. In: Sinderman CJ, Lightner DV, editors. Disease diagnosis and control in North American marine aquaculture. Amsterdam: Elsevier; 1988. p. 8–127.

    Google Scholar 

  51. Lightner DV. A handbook of shrimp pathology and diagnostic procedures for diseases of cultured penaeid shrimp. Baton Rouge: World Aquaculture Society; 1996.

    Google Scholar 

  52. Lightner DV, Redman RM. A baculovirus-caused disease of the penaeid shrimp, Penaeus monodon. J Invertebr Pathol. 1981;38:299–302.

    Article  Google Scholar 

  53. Lightner DV, Redman RM. Geographic distribution, hosts, and diagnostic procedures for the penaeid virus diseases of concern to shrimp culturists in the Americas. In: DeLoach P, Dougherty WJ, Davidson MA, editors. Frontiers of shrimp research. Amsterdam: Elsevier; 1991. p. 173–96.

    Google Scholar 

  54. Lightner DV, Redman RM. Penaeid virus diseases of the shrimp culture industry of the Americas. In: Fast AW, Lester LJ, editors. Culture of marine shrimp: principles and practices. Amsterdam: Elsevier; 1992. p. 569–88.

    Google Scholar 

  55. Lightner DV, Redman RM. Shrimp diseases and current diagnostic methods. Aquaculture. 1998;164:201–20.

    Article  Google Scholar 

  56. Lightner DV, Redman RM, Bell TA. Observation on the geographic distribution, pathogenesis and morphology of the baculovirus from Penaeus monodon Fabricius. Aquaculture. 1983;32:209–33.

    Article  Google Scholar 

  57. Lightner DV, Hedrick RP, Fryer JL, Chen SN, Lia IC, Kou GH. A survey of cultured penaeid shrimps in Taiwan for viral and other important diseases. Fish Pathol. 1987;22:127–40.

    Article  Google Scholar 

  58. Lightner DV, Bell TA, Redman RM. A review of the known host, geographic range and current diagnostic procedures for the virus diseases of cultured penaeid shrimps. Advances in Topical Aquaculture. Tahiti, AQUACOP, IFREMER, Centre de Brest, Plouzane, France, Actes de Colloque. 1990;9:113–26.

  59. Lightner DV, Bell TA, Redman RM, Mohney LL, Natividad JM, Rukyani A, Poernomo A. A review of some major diseases of economic significance in penaeid prawns/shrimps of the Americas and Indopacific. In: Shariff M, Subasinghe RP, Arthur JR, editors. Diseases in Asian aquaculture I. Manila: Fish Health section, Asian Fisheries Society; 1992. p. 57–80.

    Google Scholar 

  60. Lin CK. Prawn culture in Taiwan, what went wrong? World Aquac. 1989;20:19–20.

    Google Scholar 

  61. Lu CC, Tang FJK, Kou GH, Chen SN. Development of a Penaeus monodon-type baculovirus (MBV) DNA probe by polymerase chain reaction and sequence analysis. J Fish Dis. 1993;16:551–9.

    Article  CAS  Google Scholar 

  62. Lu CC, Tang KFJ, Kou GH, Chen SN. Detection of Penaeus monodon-type baculovirus (MBV) infection in Penaeus monodon fabricius by in situ hybridization. J Fish Dis. 1995;18:337–45.

    Article  Google Scholar 

  63. Lu CC, Tang KFJ, Chen SN. Morphogenesis of the membranous labyrinth in penaeid shrimp cells infected with Penaeus monodon baculovirus (MBV). J Fish Dis. 1996;19:357–64.

    Article  Google Scholar 

  64. Manisseri MK, Spann KM, Lester RJG. Iodine as a disinfectant against monodon baculovirus (MBV). Asian Fish Sci. 1999;12:105–11.

    Google Scholar 

  65. Manivannan S, Otta SK, Karunasagar I, Karunasagar I. Multiple viral infection in Penaeus monodon shrimp postlarvae in an Indian hatchery. Dis Aquat Organ. 2002;48:233–6.

    Article  PubMed  Google Scholar 

  66. Manivannan S, Kennedy B, Karunasagar I, Karunasagar I. Prevalence of monodon baculovirus in wild Metapenaeus species along the southwest coast of India. Aquaculture. 2004;232:63–7.

    Article  Google Scholar 

  67. Mari J, Bonami JR, Poulos B, Lightner DV. Preliminary characterization and partial cloning of the genome of a baculovirus from Penaeus monodon (PmSNPV = MBV). Dis Aquat Organ. 1993;16:207–15.

    Article  CAS  Google Scholar 

  68. Mayo MA. A summary of taxonomic changes recently approved by ICTV. Arch Virol. 2002;147:1655–6.

    Article  PubMed  CAS  Google Scholar 

  69. Nash G, Poemomo A, Nash MB. Baculovirus infection in brackishwater pond cultured Penaeus monodon fabricius in Indonesia. Aquaculture. 1988;73:1–6.

    Article  Google Scholar 

  70. Nash M, Nash G, Anderson IG, Shariff M. A reo-like virus observed in the tiger prawn, Penaeus monodon Fabricius, from Malaysia. J Fish Dis. 1988;11:531–5.

    Article  Google Scholar 

  71. Natividad JM. The Penaeus monodon baculovirus (MBV): its epizootiology, prevention and control in penaeid shrimp hatcheries and grow-out ponds in the Philippines. Ph.D. Dissertation, School of Renewable Natural Resources, University of Arizona. 1991.

  72. Natividad JM, Lightner DV. Susceptibility of the different larval and postlarval stages of the black tiger prawn, Penaeus monodon Fabricius, to monodon baculovirus (MBV). In: Shariff M, Subasinghe RP, Arthur JR, editors. Diseases in Asian aquaculture 1. Manila: Fish Health Section, Asian Fisheries Society; 1992. p. 111–25.

    Google Scholar 

  73. Natividad KDT, Migo MVP, Albaladejo JD, Magbanua JPV, Nomura N, Matsumura M. Simultaneous PCR detection of two shrimp viruses (WSSV and MBV) in postlarvae of Penaeus monodon in the Philippines. Aquaculture. 2006;257:142–9.

    Article  CAS  Google Scholar 

  74. Nimitphak T, Meemetta W, Arunrut N, Senapin S, Kiatpathomchai W. Rapid and sensitive detection of Penaeus monodon nucleopolyhedrovirus (PemoNPV) by loop-mediated isothermal amplification combined with lateral-flow dipstick. Mol Cell Probe. 2010;24:1–5.

    Article  CAS  Google Scholar 

  75. Oanh DTH, Phuong NT. Prevalence of white spot syndrome virus (WSSV) and monodon baculovirus (MBV) infection in Penaeus monodon postlarvae in Vietnam. In: Walker P, Lester R, Bondad-Reantaso MG, editors. Diseases in Asian aquaculture V. Manila: Fish Health Section, Asian Fisheries Society; 2005. p. 395–404.

    Google Scholar 

  76. Otta SK, Karunasagar I, Karunasagar I. Detection of monodon baculovirus and white spot syndrome virus in apparently healthy Penaeus monodon postlarvae from India by polymerase chain reaction. Aquaculture. 2003;220:59–67.

    Article  Google Scholar 

  77. Panchayuthapani D. A survey of shrimp disease in India. In: Flegel TW, Mac Rae IH, editors. Diseases in Asian aquaculture III. Manila: Asian Fisheries Society; 1997. p. 225–32.

    Google Scholar 

  78. Paynter JL, Vickers JE, Lester RJG. Experimental transmission of Penaeus monodon type baculovirus (MBV). In: Shariff M, Subasinghe RP, Arthur JR, editors. Diseases in Asian aquaculture I. Manila: Fish Health Section, Asian Fisheries Society; 1992. p. 97–110.

    Google Scholar 

  79. Poulos BT, Mari J, Bonami JR, Redman R, Lightner DV. Use of nonradioactively labeled DNA probes for the detection of a baculovirus from Penaeus monodon by in situ hybridization on fixed tissue. J Virol Methods. 1994;49:187–94.

    Article  PubMed  Google Scholar 

  80. Ramasamy P, Brennan GP, Jayakumar R. A record and prevalence of monodon baculovirus from postlarval Penaeus monodon in Madras. India Aquac. 1995;130:129–35.

    Google Scholar 

  81. Ramasamy P, Rajan PR, Purushothaman V, Brennan GP. Ultrastructure and pathogenesis of monodon baculovirus (PmSNPV) in cultured larvae and natural brooders of Peneaus monodon. Aquaculture. 2000;184:45–66.

    Article  Google Scholar 

  82. Sano T, Nishimura T, Oguma K, Momoyama K, Takeno N. Baculovirus infection of cultured Kuruma shrimp, Penaeus japonicus, in Japan. Fish Pathol. 1981;15:185–91.

    Article  Google Scholar 

  83. Satidkanitkul A, Sithigorngul P, Sang-oum W, Rukpratanporn S, Sriurairatana S, Withayachumnarnkul B, Flegel TW. Synthetic peptide used to develop antibodies for detection of polyhedrin from monodon baculovirus (MBV). Dis Aquat Organ. 2005;65:79–84.

    Article  PubMed  CAS  Google Scholar 

  84. Spann KM, Lester RJG. Baculovirus of Metapenaeus bennettae from the Moreton Bay region of Australia. Dis Aquat Organ. 1996;27:53–8.

    Article  Google Scholar 

  85. Spann KM, Lester RJG, Paynter JL. Efficiency of chlorine as a disinfectant against monodon baculovirus (MBV). Asian Fish Sci. 1993;6:295–301.

    Google Scholar 

  86. Sridulyakul P, Suwannaka T, Chaivisuthangkura P, Longyant S, Rukpratanporn S, Sithigorngul P. Penaeus monodon nucleopolyhedrovirus detection using monoclonal antibodies specific to recombinant polyhedrin protein. Aquaculture. 2011;321:216–22.

    Article  CAS  Google Scholar 

  87. Summers MD. Characterization of shrimp baculovirus. EPA-600/3-77-130. National Technical Information Service, Springfield, VA 22161. 1977.

  88. Sundararaj A, Murali Manohar BB, Rubby Renchitt Sheela P, Selvaraj D, Ravishankar B. Occurrence of monodon baculovirus infection in shrimp in Tamil Nadu. Indian J Fish. 1996;43:103–5.

    Google Scholar 

  89. Surachetpong W, Poulos BT, Tang KFJ, Lightner DV. Improvement of PCR method for the detection of monodon baculovirus (MBV) in penaeid shrimp. Aquaculture. 2005;249:69–75.

    Article  CAS  Google Scholar 

  90. Tangtongpiroj J. A virus disease of black tiger prawn. Fisheries News. 1989;13:25–9.

    Google Scholar 

  91. Theilmann DA, Blissard GW, Bonning B, Jehle J, O’Reilly DR, Rohrmann GF, Thiem S, Vlak JM. Family Baculoviridae. In: Fauquet CM, Mayo MA, Maniloff J, Desselberger U, Ball LA, editors. Virus taxonomy eighth report of the international committee on taxonomy of viruses. Amsterdam: Elsevier; 2005. p. 177–85.

    Google Scholar 

  92. Thikiew N. A serious MBV outbreak in the black tiger prawn. Livest Prod Mag. 1990;7:13–6.

    Google Scholar 

  93. Thurman RB, Lightner DV, Bell TA, Hazanow S. Unique physiochemical properties of the occluded penaeid shrimp baculoviruses and their use in diagnosis of infections. J Aquat Anim Health. 1990;2:128–31.

    Article  Google Scholar 

  94. Turnbull JF, Larkins PE, Matondang R, Mc Padden C. Histopathological disease survey of cultured shrimps in North-East Sumatra, Indonesia. J Fish Dis. 1994;17:57–65.

    Article  Google Scholar 

  95. Uma A, Prabhakar T, Koteeswaran A, Karunasagar I, Karunasagar I. Prevalence of hepatopancreatic parvovirus (HPV) in Penaeus monodon postlarvae from commercial shrimp hatcheries in Tamilnadu, southeast coast of India. Asian Fish Sci. 2006;19:113–6.

    Google Scholar 

  96. Uma A, Ramanathan N, Saravanabava K. A study by PCR on the prevalence of white spot syndrome virus, monodon baculovirus and hepatopancreatic parvovirus infection in Penaeus monodon post larvae in Tamil Nadu, southeast coast of India. Asian Fish Sci. 2007;20:227–39.

    Google Scholar 

  97. Umesha RK, Uma A, Otta SK, Karunasagar I, Karunasagar I. Detection by PCR of hepatopancreatic parvovirus (HPV) and other viruses in hatchery-reared Penaeus monodon postlarvae. Dis Aquat Organ. 2003;57:141–6.

    Article  PubMed  CAS  Google Scholar 

  98. Umesha KR, Chakraborty A, Venugopal MN, Nagarajappa M, Karunasagar I, Karunasagar I. Occurrence of multiple viruses in Penaeus monodon shrimp ponds and their effects on shrimp production. In: Bondad-Reantaso MG, Mohan CV, Crumlish M, Subasinghe RP, editors. Diseases in Asian aquaculture VI. Manila: Fish Health Section Asian Fisheries Society; 2008. p. 389–98.

    Google Scholar 

  99. van Hulten MC, Witteveldt J, Peters S, Kloosterboer N, Tarchini R, Fiers M, Sandbrink H, Lankhorst RK, Vlak JM. The white spot syndrome virus DNA geneome sequence. Virology. 2001;286:7–22.

    Article  PubMed  CAS  Google Scholar 

  100. Vaseeharan B, Ramasamy P. Abundance of potentially pathogenic micro-organisms in Penaeus monodon larvae rearing systems in India. Microbiol Res. 2004;158:299–308.

    Article  Google Scholar 

  101. Vickers JE, Lester RJG, Spradbrow PB, Pemberton JM. Detection of Penaeus monodon-type baculovirus (MBV) in digestive glands of postlarval prawns using polymerase chain reaction. In: Shariff M, Subasinghe RP, Arthur JR, editors. Diseases in Asian aquaculture, vol. I. Manila: Fish Health Section, Asian Fisheries Society Philippines; 1992. p. 127–33.

    Google Scholar 

  102. Vickers JE, Paynter JL, Spradbrow PB, Lester RJG. An impression smear method for rapid detection of Penaeus monodon-type baculovirus (MBV) in Australian prawns. J Fish Dis. 1993;16:507–11.

    Article  Google Scholar 

  103. Vickers JE, Webb R, Young PR. Monodon baculovirus from Australia: ultrastructural observations. Dis Aquat Organ. 2000;39:169–76.

    Article  PubMed  CAS  Google Scholar 

  104. Vijayan KK, Alavandi SV, Rajendran KV, Alagarswami K. Prevalence and histopathology of monodon baculovirus (MBV) infection in Penaeus monodon and P. indicus in shrimp farms in the South-east coast of India. Asian Fish Sci. 1995;8:267–72.

    Google Scholar 

  105. Vogt G. Transformation of anterior midgut and hepatopancreas cells by monodon baculovirus (MBV) in Penaeus monodon postlarvae. Aquaculture. 1992;107:239–48.

    Article  Google Scholar 

  106. Wang Y, Jehle JA. Nudiviruses and other large, double-stranded circular DNA viruses of invertebrates: new insights on an old topic. J Invertebr Pathol. 2009;101:187–93.

    Article  PubMed  CAS  Google Scholar 

  107. Wang CS, Tang KFJ, Kou GH, Chen SN. Light and electron microscopic evidence of white spot disease in the giant tiger shrimp, Penaeus monodon (Fabricius), and the kuruma shrimp, Penaeus japonicus (Bate), cultured in Taiwan. J Fish Dis. 1997;20:323–31.

    Article  Google Scholar 

  108. Wang Y, Kleespies RG, Huger AM, Jehle JA. The genome of Gryllus bimaculatus nudivirus indicates an ancient diversification of baculovirus-related nonoccluded nudiviruses of insects. J Virol. 2007;81:5395–406.

    Article  PubMed  CAS  Google Scholar 

  109. Wang Y, Kleespies RG, Ramle MB, Jehle JA. Sequencing of the large dsDNA genome of Oryctes rhinoceros nudivirus using multiple displacement amplification of nanogram amounts of virus DNA. J Virol Methods. 2008;152:106–8.

    Article  PubMed  CAS  Google Scholar 

  110. Wyban J. World shrimp farming revolution: Industry impact of domestication, breeding and widespread use of specific pathogen free Penaeus vannamei. In: Craig L, Browdy and Darryl EJ (eds), The Rising Tide, Proceedings of the special session on sustainable shrimp farming, World Aquaculture. 2009; p. 12–21.

  111. Wyban JA, Sweeny JN. Shrimp health maintenance. In: Intensive shrimp production technology. The Oceanic Institute, Hawaii. 1991;103–12.

  112. Yan D, Tang KFJ, Lightner DV. Development of a real-time PCR assay for detection of monodon baculovirus (MBV) in penaeid shrimp. J Invertebr Pathol. 2009;102:97–100.

    Article  PubMed  CAS  Google Scholar 

  113. Yang F, He J, Lin X, Li Q, Pan D, Zhang X, Xu X. Complete genome sequence of the shrimp white spot bacilliform virus. J Virol. 2001;75:11811–20.

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

The first and second authors (KVR and MM) thank the Director, CIFE, for providing necessary support. The last author (IK) is thankful to the Karnataka Veterinary, Animal and Fisheries Sciences University, Bidar, for providing necessary facilities.

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Correspondence to K. V. Rajendran.

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Rajendran, K.V., Makesh, M. & Karunasagar, I. Monodon Baculovirus of Shrimp. Indian J. Virol. 23, 149–160 (2012). https://doi.org/10.1007/s13337-012-0086-z

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