1 1 ntranuclear inclusion bodies in the renal epithelium of I domestic animals are usually caused by heavy metal toxicosis or viruses.' Intranuclear inclusions of unknown aetiology and apparently of no clinical significance have been reported in the renal epithelium of the common brushtailed possum(Trichosurus vulpecula).? Here we describe the appearance of idiopathic intranuclear inclusions, similar to those in the brushtail possum, in the renal tubular epithelium of several species of macropods and differentiate them from intranuclear inclusion bodies caused by viruses and lead toxicity. Sections of kidney from diagnostic necropsies on 169 macropods of 16 species from north Queensland and Papua New Guinea were available for examination. Species and number of specimens examined were rufous bettong (Aepyptymnus rujscens) (4), Lumholtz tree kangaroo (Dendrolagus lumholtzi) (2), Dorcopsulus vanheurni (2), musky rat kangaroo (Hypsiprymnodon moschatus) (I), spectacled hare wallaby (Lagorchestes conspicillatus) (6), agile wallaby (Macropus agilis) (37), antelopine kangaroo ( M antilopinus) (I), black stripe wallaby ( M dorsalis) (7), eastern grey kangaroo ( M giganteus) (48), pretty face wallaby (Mparryr) (4), eastern wallaroo ( M robustus) (5), red kangaroo ( M rufis) (12), bridled nail-tail wallaby (Onychogalea fiaenatu) (4), northern nail-tail wallaby ( 0 ungu;fera) ( lo), Palm Island rock wallaby (Petrogale assirnilis) (2), unadorned rock wallaby ( P inornata) (8), purple neck rock wallaby ( P purpuriecollis) (3), red-legged pademelon ( Thylogale stigmatila) (I), swamp wallaby (Wallabia bicolor) (9, and species of macropod not recorded (7). Macropods were both captive and wild, ranging in age from pouch young to mature adults. The kidneys were fixed in 10% buffered neutral formalin and embedded in paraffin. Sections were cut at 5 p m and stained with haematoxylin and eosin. Sections from a M dorsalis with typical lesions were also stained using Ziehl-Neelsen, von Kossa technique and periodic acid Schiff (PAS) methods for light microscopy.' Sections of formalin fixed kidney from the same M dorsalis were removed from the paraffin block and prepared for electron microscopy and X-ray dispersion analysis. The tissue was hydrated, given additional fixation in 2% paraformaldehyde and 2.5% glutaraldehyde in 0.1M sodium cacodylate buffer for 2 h, then 1% osmium, dehydrated and embedded in Spurr's resin. Sections of 200 nm thickness were stained in methanol uranyl acetate for 10 min. The sections were carbon-coated to 20 nm on copper grids and X-ray dispersion analysis was conducted at 80 kV. Dimensions of nuclei and inclusion bodies in haematoxylin and eosin stained sections from seven macropods were measured aCurrent address: Department of Public Health and Tropical Medicine bPrevious address: Graduate School of Tropical Veterinary Science CDepartment of Biomedical and Tropical Veterinary Science using a calibrated eyepiece graticule. Statistical analyses were performed using Statistix" program ( N H Analytical Software) ...