Skip to main content
Journal of Virology logoLink to Journal of Virology
. 1993 Mar;67(3):1424–1432. doi: 10.1128/jvi.67.3.1424-1432.1993

Adult mouse kidneys become permissive to acute polyomavirus infection and reactivate persistent infections in response to cellular damage and regeneration.

I A Atencio 1, F F Shadan 1, X J Zhou 1, N D Vaziri 1, L P Villarreal 1
PMCID: PMC237512  PMID: 8382304

Abstract

Kidneys of newborn (but not adult) mice are normally high permissive for polyomavirus (Py) infection and readily establish persistent infections. We have proposed that ongoing cellular differentiation, which occurs in newborn mice, may be necessary for a high level of in vivo Py replication (R. Rochford, J. P. Moreno, M. L. Peake, and L. P. Villarreal, J. Virol. 66:3287-3297, 1992). This cellular differentiation requirement may also be necessary for the reactivation of a persistent Py kidney infection and could provide an alternative to the accepted view that reactivation results from immunosuppression. To examine this proposal, the ability of adult BALB/c mouse kidneys to support primary acute Py infection or to reactivate previously established persistent Py infections after kidney-specific damage was investigated. Kidney damage was induced by both chemical (glycerol, cisplatin, or methotrexate) and mechanical (through renal artery clamping to produce unilateral renal ischemia) treatments. We also examined the effects of epidermal growth factor (EGF), which enhances the rate of kidney regeneration, on Py replication. Using histopathologic techniques, in situ hybridization for Py DNA, and immunofluorescence for Py VP1 production, we established that both chemical damage and damage through renal artery clamping of adult kidneys promoted high levels of primary Py replication in these normally nonpermissive cells. This damage also promoted the efficient reactivation of Py replication from persistently infected kidneys, in the absence of immunosuppression. EGF treatment significantly increased acute Py replication and also reactivation in damaged kidneys. These results support the view that ongoing cellular division and differentiation may be needed both for high levels of acute Py replication and for reactivation of persistent infections in vivo.

Full text

PDF
1425

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arthur R. R., Shah K. V., Baust S. J., Santos G. W., Saral R. Association of BK viruria with hemorrhagic cystitis in recipients of bone marrow transplants. N Engl J Med. 1986 Jul 24;315(4):230–234. doi: 10.1056/NEJM198607243150405. [DOI] [PubMed] [Google Scholar]
  2. Arthur R. R., Shah K. V., Charache P., Saral R. BK and JC virus infections in recipients of bone marrow transplants. J Infect Dis. 1988 Sep;158(3):563–569. doi: 10.1093/infdis/158.3.563. [DOI] [PubMed] [Google Scholar]
  3. Bautch V. L., Toda S., Hassell J. A., Hanahan D. Endothelial cell tumors develop in transgenic mice carrying polyoma virus middle T oncogene. Cell. 1987 Nov 20;51(4):529–537. doi: 10.1016/0092-8674(87)90122-x. [DOI] [PubMed] [Google Scholar]
  4. Bautch V. L., Toda S., Hassell J. A., Hanahan D. Tissue specificity of oncogene action: endothelial cell tumours in polyoma middle T transgenic mice. IARC Sci Publ. 1989;(96):255–266. [PubMed] [Google Scholar]
  5. Bedell M. A., Hudson J. B., Golub T. R., Turyk M. E., Hosken M., Wilbanks G. D., Laimins L. A. Amplification of human papillomavirus genomes in vitro is dependent on epithelial differentiation. J Virol. 1991 May;65(5):2254–2260. doi: 10.1128/jvi.65.5.2254-2260.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bertrand L., Brière N., Ferrari J. Comparison between mouse kidneys of pre- and postnatal ages maturing in vivo and in serum-free organ culture. Comp Biochem Physiol B. 1988;91(4):763–769. doi: 10.1016/0305-0491(88)90205-2. [DOI] [PubMed] [Google Scholar]
  7. Brière N., Bertrand L., Ferrari J. Developmental profile of DNA synthesis and hydrolase activities in human fetal kidney. Clin Biochem. 1989 Oct;22(5):385–388. doi: 10.1016/s0009-9120(89)80037-2. [DOI] [PubMed] [Google Scholar]
  8. Chesters P. M., Heritage J., McCance D. J. Persistence of DNA sequences of BK virus and JC virus in normal human tissues and in diseased tissues. J Infect Dis. 1983 Apr;147(4):676–684. doi: 10.1093/infdis/147.4.676. [DOI] [PubMed] [Google Scholar]
  9. Coleman D. V., Field A. M., Gardner S. D., Porter K. A., Starzl T. E. Virus-induced obstruction of the ureteric and cystic duct in allograft recipients. Transplant Proc. 1973 Mar;5(1):95–98. [PubMed] [Google Scholar]
  10. Coleman D. V., Mackenzie E. F., Gardner S. D., Poulding J. M., Amer B., Russell W. J. Human polyomavirus (BK) infection and ureteric stenosis in renal allograft recipients. J Clin Pathol. 1978 Apr;31(4):338–347. doi: 10.1136/jcp.31.4.338. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Coleman D. V., Wolfendale M. R., Daniel R. A., Dhanjal N. K., Gardner S. D., Gibson P. E., Field A. M. A prospective study of human polyomavirus infection in pregnancy. J Infect Dis. 1980 Jul;142(1):1–8. doi: 10.1093/infdis/142.1.1. [DOI] [PubMed] [Google Scholar]
  12. DULBECCO R., HARTWELL L. H., VOGT M. INDUCTION OF CELLULAR DNA SYNTHESIS BY POLYOMA VIRUS. Proc Natl Acad Sci U S A. 1965 Feb;53:403–410. doi: 10.1073/pnas.53.2.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. De Simone V., Amati P. Replicative cis-advantage of polyomavirus regulatory region mutants in different murine cell lines. J Virol. 1987 May;61(5):1615–1620. doi: 10.1128/jvi.61.5.1615-1620.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Demengeot J., Jacquemier J., Torrente M., Blangy D., Berebbi M. Pattern of polyomavirus replication from infection until tumor formation in the organs of athymic nu/nu mice. J Virol. 1990 Nov;64(11):5633–5639. doi: 10.1128/jvi.64.11.5633-5639.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Dubeau L., Jones P. A. Growth of normal and neoplastic urothelium and response to epidermal growth factor in a defined serum-free medium. Cancer Res. 1987 Apr 15;47(8):2107–2112. [PubMed] [Google Scholar]
  16. Dubensky T. W., Freund R., Dawe C. J., Benjamin T. L. Polyomavirus replication in mice: influences of VP1 type and route of inoculation. J Virol. 1991 Jan;65(1):342–349. doi: 10.1128/jvi.65.1.342-349.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Dubensky T. W., Villarreal L. P. The primary site of replication alters the eventual site of persistent infection by polyomavirus in mice. J Virol. 1984 May;50(2):541–546. doi: 10.1128/jvi.50.2.541-546.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Dénes L., Szende B., Hajós G., Szporny L., Lapis K. Selective restoration of immunosuppressive effect of cytotoxic agents by thymopoietin fragments. Cancer Immunol Immunother. 1990;32(1):51–54. doi: 10.1007/BF01741724. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Felsani A., Maione R., Ricci L., Amati P. Coordinate expression of myogenic functions and polyoma virus replication. Cold Spring Harb Symp Quant Biol. 1985;50:753–757. doi: 10.1101/sqb.1985.050.01.093. [DOI] [PubMed] [Google Scholar]
  20. Fiala M., Mosca J. D., Barry P., Luciw P. A., Vinters H. V. Multi-step pathogenesis of AIDS--role of cytomegalovirus. Res Immunol. 1991 Feb;142(2):87–95. doi: 10.1016/0923-2494(91)90016-c. [DOI] [PubMed] [Google Scholar]
  21. Gardner S. D., Field A. M., Coleman D. V., Hulme B. New human papovavirus (B.K.) isolated from urine after renal transplantation. Lancet. 1971 Jun 19;1(7712):1253–1257. doi: 10.1016/s0140-6736(71)91776-4. [DOI] [PubMed] [Google Scholar]
  22. Gardner S. D., MacKenzie E. F., Smith C., Porter A. A. Prospective study of the human polyomaviruses BK and JC and cytomegalovirus in renal transplant recipients. J Clin Pathol. 1984 May;37(5):578–586. doi: 10.1136/jcp.37.5.578. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Gattone V. H., 2nd, Andrews G. K., Niu F. W., Chadwick L. J., Klein R. M., Calvet J. P. Defective epidermal growth factor gene expression in mice with polycystic kidney disease. Dev Biol. 1990 Mar;138(1):225–230. doi: 10.1016/0012-1606(90)90192-l. [DOI] [PubMed] [Google Scholar]
  24. Gattone V. H., 2nd, Calvet J. P., Cowley B. D., Jr, Evan A. P., Shaver T. S., Helmstadter K., Grantham J. J. Autosomal recessive polycystic kidney disease in a murine model. A gross and microscopic description. Lab Invest. 1988 Aug;59(2):231–238. [PubMed] [Google Scholar]
  25. Gershon D., Hausen P., Sachs L., Winocour E. On the mechanism of polyoma virus-induced synthesis of cellular DNA. Proc Natl Acad Sci U S A. 1965 Dec;54(6):1584–1592. doi: 10.1073/pnas.54.6.1584. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Griep A. E., Kuwabara T., Lee E. J., Westphal H. Perturbed development of the mouse lens by polyomavirus large T antigen does not lead to tumor formation. Genes Dev. 1989 Jul;3(7):1075–1085. doi: 10.1101/gad.3.7.1075. [DOI] [PubMed] [Google Scholar]
  27. Hall W. W., Farmer P. M., Takahashi H., Tanaka S., Furuta Y., Nagashima K. Pathological features of virus infections of the central nervous system (CNS) in the acquired immunodeficiency syndrome (AIDS). Acta Pathol Jpn. 1991 Mar;41(3):172–181. doi: 10.1111/j.1440-1827.1991.tb01644.x. [DOI] [PubMed] [Google Scholar]
  28. Hogan T. F., Borden E. C., McBain J. A., Padgett B. L., Walker D. L. Human polyomavirus infections with JC virus and BK virus in renal transplant patients. Ann Intern Med. 1980 Mar;92(3):373–378. doi: 10.7326/0003-4819-92-3-373. [DOI] [PubMed] [Google Scholar]
  29. Humes H. D., Cieslinski D. A., Coimbra T. M., Messana J. M., Galvao C. Epidermal growth factor enhances renal tubule cell regeneration and repair and accelerates the recovery of renal function in postischemic acute renal failure. J Clin Invest. 1989 Dec;84(6):1757–1761. doi: 10.1172/JCI114359. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Jones T. W., Chopra S., Kaufman J. S., Flamenbaum W., Trump B. F. Cis-diamminedichloroplatinum (II)-induced acute renal failure in the rat. Correlation of structural and functional alterations. Lab Invest. 1985 Apr;52(4):363–374. [PubMed] [Google Scholar]
  31. Kellett R., Bowmer C. J., Collis M. G., Yates M. S. Amelioration of glycerol-induced acute renal failure in the rat with 8-cyclopentyl-1,3-dipropylxanthine. Br J Pharmacol. 1989 Nov;98(3):1066–1074. doi: 10.1111/j.1476-5381.1989.tb14639.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Kryszke M. H., Piette J., Yaniv M. Induction of a factor that binds to the polyoma virus A enhancer on differentiation of embryonal carcinoma cells. Nature. 1987 Jul 16;328(6127):254–256. doi: 10.1038/328254a0. [DOI] [PubMed] [Google Scholar]
  33. Lian J. B., Stein G. S. Concepts of osteoblast growth and differentiation: basis for modulation of bone cell development and tissue formation. Crit Rev Oral Biol Med. 1992;3(3):269–305. doi: 10.1177/10454411920030030501. [DOI] [PubMed] [Google Scholar]
  34. Maione R., Felsani A., Pozzi L., Caruso M., Amati P. Polyomavirus genome and polyomavirus enhancer-driven gene expression during myogenesis. J Virol. 1989 Nov;63(11):4890–4897. doi: 10.1128/jvi.63.11.4890-4897.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Manteuffel-Cymborowska M., Chmurzyńska W., Grzelakowska-Sztabert B. Ornithine decarboxylase induction in mouse kidney as indicator of renal damage. Differential nephrotoxic effect of anticancer antifolate drugs. Cancer Lett. 1991 Sep;59(3):237–241. doi: 10.1016/0304-3835(91)90147-a. [DOI] [PubMed] [Google Scholar]
  36. Markowitz R. B., Eaton B. A., Kubik M. F., Latorra D., McGregor J. A., Dynan W. S. BK virus and JC virus shed during pregnancy have predominantly archetypal regulatory regions. J Virol. 1991 Aug;65(8):4515–4519. doi: 10.1128/jvi.65.8.4515-4519.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. McCall C. A., Cohen J. J. Programmed cell death in terminally differentiating keratinocytes: role of endogenous endonuclease. J Invest Dermatol. 1991 Jul;97(1):111–114. doi: 10.1111/1523-1747.ep12478519. [DOI] [PubMed] [Google Scholar]
  38. Moreno J. P., Villarreal L. P. Analysis of cellular DNA synthesis during polyoma virus infection of mice: acute infection fails to induce cellular DNA synthesis. Virology. 1992 Feb;186(2):463–474. doi: 10.1016/0042-6822(92)90011-d. [DOI] [PubMed] [Google Scholar]
  39. Ornitz D. M., Palmiter R. D., Messing A., Hammer R. E., Pinkert C. A., Brinster R. L. Elastase I promoter directs expression of human growth hormone and SV40 T antigen genes to pancreatic acinar cells in transgenic mice. Cold Spring Harb Symp Quant Biol. 1985;50:399–409. doi: 10.1101/sqb.1985.050.01.050. [DOI] [PubMed] [Google Scholar]
  40. Pepose J. S. External ocular herpesvirus infections in immunodeficiency. Curr Eye Res. 1991;10 (Suppl):87–95. doi: 10.3109/02713689109020363. [DOI] [PubMed] [Google Scholar]
  41. Rochford R., Campbell B. A., Villarreal L. P. A pancreas specificity results from the combination of polyomavirus and Moloney murine leukemia virus enhancer. Proc Natl Acad Sci U S A. 1987 Jan;84(2):449–453. doi: 10.1073/pnas.84.2.449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Rochford R., Campbell B. A., Villarreal L. P. Genetic analysis of the enhancer requirements for polyomavirus DNA replication in mice. J Virol. 1990 Feb;64(2):476–485. doi: 10.1128/jvi.64.2.476-485.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Rochford R., Moreno J. P., Peake M. L., Villarreal L. P. Enhancer dependence of polyomavirus persistence in mouse kidneys. J Virol. 1992 Jun;66(6):3287–3297. doi: 10.1128/jvi.66.6.3287-3297.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Rochford R., Villarreal L. P. Polyomavirus DNA replication in the pancreas and in a transformed pancreas cell line has distinct enhancer requirements. J Virol. 1991 Apr;65(4):2108–2112. doi: 10.1128/jvi.65.4.2108-2112.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Singh G. A possible cellular mechanism of cisplatin-induced nephrotoxicity. Toxicology. 1989 Sep;58(1):71–80. doi: 10.1016/0300-483x(89)90105-4. [DOI] [PubMed] [Google Scholar]
  46. Stein J. H., Lifschitz M. D., Barnes L. D. Current concepts on the pathophysiology of acute renal failure. Am J Physiol. 1978 Mar;234(3):F171–F181. doi: 10.1152/ajprenal.1978.234.3.F171. [DOI] [PubMed] [Google Scholar]
  47. Stoner G. L., Ryschkewitsch C. F., Walker D. L., Webster H. D. JC papovavirus large tumor (T)-antigen expression in brain tissue of acquired immune deficiency syndrome (AIDS) and non-AIDS patients with progressive multifocal leukoencephalopathy. Proc Natl Acad Sci U S A. 1986 Apr;83(7):2271–2275. doi: 10.1073/pnas.83.7.2271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Strange R., Li F., Saurer S., Burkhardt A., Friis R. R. Apoptotic cell death and tissue remodelling during mouse mammary gland involution. Development. 1992 May;115(1):49–58. doi: 10.1242/dev.115.1.49. [DOI] [PubMed] [Google Scholar]
  49. Sugimoto C., Hara K., Taguchi F., Yogo Y. Growth efficiency of naturally occurring BK virus variants in vivo and in vitro. J Virol. 1989 Jul;63(7):3195–3199. doi: 10.1128/jvi.63.7.3195-3199.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Swartzendruber D. E., Lehman J. M. Neoplastic differentiation: interaction of simian virus 40 and polyoma virus with murine teratocarcinoma cells in vitro. J Cell Physiol. 1975 Apr;85(2 Pt 1):179–187. doi: 10.1002/jcp.1040850204. [DOI] [PubMed] [Google Scholar]
  51. Villarreal L. P. Relationship of eukaryotic DNA replication to committed gene expression: general theory for gene control. Microbiol Rev. 1991 Sep;55(3):512–542. doi: 10.1128/mr.55.3.512-542.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Weil R. Viral 'tumor antigens': A novel type of mammalian regulator protein. Biochim Biophys Acta. 1978 Nov 17;516(3):301–388. doi: 10.1016/0304-419x(78)90012-4. [DOI] [PubMed] [Google Scholar]
  53. Williams K. J., Landgraf B. E., Whiting N. L., Zurlo J. Correlation between the induction of heat shock protein 70 and enhanced viral reactivation in mammalian cells treated with ultraviolet light and heat shock. Cancer Res. 1989 May 15;49(10):2735–2742. [PubMed] [Google Scholar]
  54. Wirth J. J., Amalfitano A., Gross R., Oldstone M. B., Fluck M. M. Organ- and age-specific replication of polyomavirus in mice. J Virol. 1992 Jun;66(6):3278–3286. doi: 10.1128/jvi.66.6.3278-3286.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Virology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES