Abstract
Brains of macaques inoculated with macrophage-tropic, neuroviralent virus 7F, with lymphocyte-tropic SIVmac239, or with dual-tropic SIVmac239/17E, were examined for microglial activation, astrocyte activation, apoptosis and neuron loss. The brain of one animal inoculated with neurovirulent virus 7F showed massive microglial activation as assessed by expression of the major histocompatibility complex class II (MHC-II). In this animal very numerous, large microglial nodules expressing MHC-II were concentrated in the basal pons and internal capsule. These microglial nodules contained cells undergoing apoptosis detected by in situ end labeling of fragmented DNA. In this animal, neuron loss was apparent near the microglial nodules. In the animals inoculated with SIVmac239 or SIVmac239/17E, pathologic changes such as perivascular cuffing and formation of microglial nodules were absent. However, increased expression of MHC-II by microglial cells was also concentrated in white matter of the basal pons, midbrain and internal capsule. These results indicate that microglial activation in SIV-infected macaques follows a ventral to dorsal gradient regardless of viral tropism. These results also show that the type and severity of neuropathological changes in SIV-infected macaques is highly dependent on the tropism of the inoculated virus.
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