August 1990
Volume 31, Issue 8
Free
Articles  |   August 1990
The pathogenesis of murine cytomegalovirus ocular infection. Anterior chamber inoculation.
Author Affiliations
  • J F Bale, Jr
    Department of Pediatrics, University of Iowa College of Medicine, Iowa City.
  • M E O'Neil
    Department of Pediatrics, University of Iowa College of Medicine, Iowa City.
  • B Lyon
    Department of Pediatrics, University of Iowa College of Medicine, Iowa City.
  • S Perlman
    Department of Pediatrics, University of Iowa College of Medicine, Iowa City.
Investigative Ophthalmology & Visual Science August 1990, Vol.31, 1575-1581. doi:
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      J F Bale, M E O'Neil, B Lyon, S Perlman; The pathogenesis of murine cytomegalovirus ocular infection. Anterior chamber inoculation.. Invest. Ophthalmol. Vis. Sci. 1990;31(8):1575-1581.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

To investigate the pathogenesis of ocular cytomegalovirus infections, 3-week-old BALB/c mice were inoculated with 10(4) plaque-forming units of murine cytomegalovirus (MCMV) by the right anterior chamber and studied sequentially with the use of virus assays and in situ nucleic acid hybridization methods. During acute infection, MCMV was recovered from the right vitreous, lens, cornea, retina/choroid, and optic nerve. Titers of MCMV exceeded 10(3) per ml of homogenate on days 4 and 7 after inoculation. With the use of biotinylated MCMV DNA probes, MCMV nucleic acids were detected in and adjacent to cells of the iris and ciliary body and occasionally within inflammatory lesions of the cornea. During chronic infection, MCMV was recovered, with the use of co-cultivation or explant methods, from ocular tissues of occasional mice inoculated with MCMV 1 yr earlier. Infectious MCMV was also recovered from the ocular homogenates of a group of mice immunosuppressed with antilymphocyte serum and cortisone. These studies indicate that cells of the uveal tract are permissive for MCMV and suggest that intrinsic persistence or latency of cytomegalovirus in ocular tissues could contribute to the pathogenesis of ocular infections in immunosuppressed hosts.

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