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2010 | 13 | 4 |

Tytuł artykułu

Equine herpesvirus type 1 (EHV-1) replication in primary murine neurons culture

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Equine herpesvirus-1 (EHV-1) infections cause significant economic losses for equine industries worldwide as a result of abortion, respiratory illness, and neurologic disease in all breeds of horses. The occurrence of abortions caused by EHV-1 has repeatedly been confirmed in Poland, but neurological manifestations of the infection have not been described yet. Also it is unknown how the infection of neurons with non-neuropathogenic strains is regulated. To further understand the virus- neuron interaction we studied two strains of EHV-1 in murine primary neuron cell cultures. Both strains were isolated from aborted fetuses: Rac-H, a reference strain isolated by Woyciechowska in 1959 (Woyciechowska 1960) and Jan-E isolated by Bańbura et al. (Bańbura et al. 2000). Upon infection of primary murine neuronal cell cultures with Jan-E or Rac-H strains, a cytopathic effect was observed, manifested by a changed morphology and disintegration of the cell monolayer. Positive results of immunofluorescence, nPCR and real-time PCR tests indicated high virus concentration in neurons, meaning that both EHV-1 strains were likely to replicate in mouse neurons in vitro without the need for adaptation. Moreover, we demonstrated that some neurons may survive (limited) virus replication during primary infection, and these neurons (eight weeks p.i.) harbour EHV-1 and were still able to transmit infection to other cells.

Wydawca

-

Rocznik

Tom

13

Numer

4

Opis fizyczny

p.701-708,fig.,ref.

Twórcy

autor
  • Division of Virology, Department of Preclinical Science, Faculty of Veterinary Medicine, Warsaw University of Life Science (SGGW), Ciszewskiego 8, 02-786 Warsaw, Poland
autor
autor
autor
autor

Bibliografia

  • Allen GP (2007) Development of a real-time polymerase chain reaction assay for rapid diagnosis of neuropathogenic strains of equine herpesvirus-1. J Vet Diagn Invest 19: 69-72.
  • Awan AR, Chong YC, Field HJ (1990) The pathogenesis of equine herpesvirus type 1 in the mouse: a new model for studying host responses to the infection. J Gen Virol 71: 1131-1140.
  • Bańbura M, Chmielewska A, Tucholska A, Malicki K (1998) Test PCR w diagnostyce wirusowego zakaźnego ronienia klaczy. Med Weter 54: 772-774.
  • Bańbura M, Sendecka H, Chmielewska A, Tucholska A (2000) Histopathological changes and exspression of latency-related RNA in the central nervous systems of mice latently infected with a field isolate of EHV-1. Med Weter 56: 804-808.
  • Bańbura MW (2003) Productive nad latent infections with equine herpesvirus type 1 (EHV-1). Treatises and monographs. Publications of Warsaw Agricultural University.
  • Baxi MK, Efstathiou S, Lawrence G, Whalley JM, Slater JD (1995) The detection of latency-associated transcript of equine herpesvirus 1 in ganglionic neurons. J Gen Virol 76: 3113-3118.
  • Borchers K, Slater J (1993) A nested PCR for the detection and differentiation of EHV-1 and EHV-4. J Virol Methods 45: 331-336.
  • Bryans JT, Allen GP (1989) Herpesviral Diseases of the Horse. In: Wittman G (ed) Herpesvirus Diseases of Cattle, Horses and Pigs. Kluwer Academic Publishers, Boston/Dodrecht/London, pp. 176-229.
  • Ch’ng TH and Enquist LW (2005) Neuron-to-cell spread of pseudorabies virus in a compartmented neuronal culture system. J Virol 79: 10875-10889.
  • Chesters PM (1997) Detection of latency-associated transcripts of equide herpesvirus 1 in equine leukocytes but not in trigeminal ganglia. J Virol 71: 3437-3443.
  • Delhon GA, González MJ, Murcia PR (2002) Susceptibility of sensory neurons to apoptosis following infection by bovine herpesvirus type 1. J Gen Virol 83: 2257-2267.
  • Dzieciątkowski T, Przybylski M, Cymerys J, Turowska A, Chmielewska A, Tucholska A, Banbura MW (2009) Equine herpesvirus type 1 quantification in different types of samples by a real-time PCR. Pol J Vet Sci 12: 311-315.
  • Geenen K, Favoreel HW, Nauwynck HJ (2005) Higher resistance of porcine trigeminal ganglion neurons towards pseudorabies virus-induced cell death compared with other porcine cell types in vitro. J Gen Virol 86: 1251-1260.
  • Geiger KD, Gurushanthaiah D, Howes EL, Lewandowski GA, Reed JC, Bloom FE, Sarvetnick NE (1999) Cytokine-mediated survival from lethal herpes simplex virus infection: role of programmed neuronal death. Proc Natl Acad Sci USA 92: 3411-3415.
  • Gosztonyi G, Borchers K, Ludwig H (2009) Pathogenesis of equine herpesvirus-1 infection in the mouse model. APMIS 117: 10-21.
  • Jones C (2003) Herpes simplex virus type 1 and bovine herpesvirus 1 latency. Clin Microbiol Rev 16: 79-95.
  • Marshall KR, Field HJ (1997) Demonstration of equine herpesvirus-1 neuronal latency in murine olfactory bulbs rusing a novel combined in situ PCR and protein synthesis metod. Virology 229: 279-282.
  • Nugent J, Birch-Machin I, Smith KC, Mumford JA, Swann Z, Newton JR, Bowden RJ, Allen GP, Davis-Poynter N (2006) Analysis of equid herpesvirus 1 strain variation reveals a point mutation of the DNA polymerase strongly associated with neuropathogenic versus nonneuropathogenic disease outbreaks. J Virol 80: 4047-4060.
  • Perkins GA, Goodman LB, Tsujimura K, Van de Walle GR, Kim SG, Dubovi EJ, Osterrieder N (2009) Investigation of the prevalence of neurologic equine herpes virus type 1 (EHV-1) in a 23-year retrospective analysis (1984-2007). Vet Microbiol 139: 375-378.
  • Perng GC, Jones C, Ciacci-Zanella J, Stone M, Henderson G, Yukht A, Slanina SM, Hofman FM, Ghiasi H, Nesburn AB, Wechsler SL (2000) Virus-induced neuronal apoptosis blocked by the herpes simplex virus latency-associated transcript. Science. 287: 1500-1503.
  • de Regge N, Favoreel HW, Geenen K, Nauwynck HJ (2006) A homologous in vitro model to study interactions between alphaherpesviruses and trigeminal ganglion neurons. Vet Microbiol 113: 251-255.
  • Rola J, Żmudziński J (1997) Equine herpesvirus type 1 (EHV-1) a cause of mare’s abortions in Poland. Med Weter 53: 268-269.
  • Sauerbrei A, Wutzler P (2002) Laboratory diagnosis of central nervous system infections caused by herpesvirises. J Clinic Virol 25: 45-51.
  • Slater JD, Borchers K, Thackray AM, Field HJ (1994) The trigeminal ganglion is a location for equine herpesvirus-1 latency and reactivation in the horse. J Gen Virol 75: 2007-2016.
  • Smith KL, Allen GP, Branscum AJ, Cook RF, Vickers ML, Timoney PJ, Balasuriya UBR (2010) The increased prevalence of neuropathogenic strains of EHV-1 in equine abortion. Vet Microbiol 141: 5-11.
  • Vissani MA, Becerra ML, Olgutn Perglione C, Tordoya MS, Miño S, Barrandeguy M (2009) Neuropathogenic and non-neuropathogenic genotypes of Equid Herpesvirus type 1 in Argentina. Vet Microbiol 139: 361-364.
  • Walker C, Love DN, Whalley JM (1999) Comparison of the pathogenesis of acute equine herpesvirus 1 (EHV-1) infection in the horse and the mouse model: a review. Vet Microbiol 68: 3-13.
  • Woyciechowska S (1960) Adaptacja krajowego wirusa zakaźnego ronienia klaczy, szczep Rac-Heraldia do chomików syryjskich. Med Dośw Mikrobiol XII (3): 255-263.
  • Yamada S, Matsumura T, Tsujimura K, Yamaguchi T, Ohya K, Fukushi H (2008) Comparison of the growth kinetics of neuropathogenic and nonneuropathogenic equid herpesvirus type 1 (EHV-1) strains in cultured murine neuronal cells and the relevance of the D/N752 coding change in DNA polymerase gene (ORF30). J Vet Med Sci 70: 505-511.

Typ dokumentu

Bibliografia

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