Barley yellow dwarf virus strain PAV (BYDV-PAV) RNA and the 17-kDa protein were localized in BYDV-PAV-infected oat cells using in situ hybridization and in situ immunolocalization assays, respectively. The in situ hybridization assay showed labeling of filamentous material in the nucleus, cytoplasm, and virus-induced vesicles with both sense and antisense nucleic acid probes, suggesting that the filamentous material found in BYDV-PAV-infected cells contains viral RNA. BYDV-PAV negative-strand RNA was detected before virus particles were observed, which indicates that RNA replication is initiated before synthesis of viral coat protein in the cytoplasm. The 17-kDa protein was associated with filamentous material in the cytoplasm, nucleus, and virus-induced vesicles. The labeling densities observed using antibodies against the 17-kDa protein were similar in the nucleus and cytoplasm. No labeling of the 17-kDa protein was observed in plasmodesmata, but filaments in the nuclear pores occasionally were labeled. Since BYDV-PAV RNA and 17-kDa protein colocalized within infected cells, it is possible that single-stranded viral RNA is always associated with the 17-kDa protein in vivo. The 17-kDa protein may be required for viral nucleic acid filaments to traverse the nuclear membrane or other membrane systems.
Epiphyses of the femura from 8-week-old broiler chicks were examined for morphology using scanning electron microscopy and for elemental composition using energy dispersive x-ray microanalysis. Birds between the ages of 4 and 8 weeks were subjected to either 25 or 35 C environments and given tap or carbonated drinking water. The morphological appearance of the epiphyses was affected by the kind of drinking water but not the thermal environment. Elemental constituents, however, were affected by both environmental temperature and drinking water.
SYNOPSIS
Ultrastructural analysis was performed on freeze‐thawed and heat inactivated Plasmodium berghei NK65 sporozoite preparations, which in parallel studies served as the immunogens against a malarial infection in A/J mice. Sporozoites in the freeze‐thawed sample appeared severely damaged with most of their cytoplasmic contents lost. The heat inactivated sporozoites remained intact and closely resembled the untreated controls.
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