Alterations in the ultrastructure of in vitro cultured larval salivary glands of Drosophila melanogaster in response to the steroid hormone ecdysone were studied in relation to complex changes in puffing patterns. We found that the changes in the fine structure of cultured glands reflected progression of the puffing pattern, and they paralleled those seen in vivo. We observed that glue secretion by exocytosis, the main function of salivary glands, took place between puff stage 5 (PS5) and PS7. Glue could not be expectorated under culture conditions but was slowly released from the lumen through a duct into the medium. After the cultured glands reached PS13/PS14, further progress of puffing and fine structural alterations required that the ecdysteroid titer be transiently extremely low or absent. Under in vitro conditions we did not observe the putative new secretory program(s) described for glands in vivo after PS12. However, ultrastructural changes which unambiguously indicated that an autohistolytic process had begun in vitro started to appear after PS17. Many salivary gland cells developed numerous features of progressive self-degradation between PS18 and PS21. Actual degradation of salivary glands in vivo seemed to be rapid, but in vitro degradation was never completed, probably due to a lack of exogenous factors from the hemolymph. Manipulations of ecdysone titer in vitro in the culture medium, known during the larval puffing cycle to cause premature induction of developmentally specific puffing patterns, did not affect the normal development of ultrastructural features of the cytoplasm and nucleus.

Treatment of Drosophila larval salivary glands with juvenile hormone or its analogues leads to ultrastructural changes of mitochondria that mimic those seen after application of uncouplers of oxidative phosphorylation. This alteration of mitochondria, also known as swelling, is manifested in strong dilatation of their intercristae space. The mitochondrial response of salivary glands to juvenile hormone is restricted to collum cells that are known to be ultrastructurally and functionally different from transitional and corpus cells and may reflect their specialization in energy metabolism and water/ion balance. Morphological change of mitochondria and about a fivefold increase in cytochrome c oxidase activity in response to juvenile hormone appear to be a consequence of uncoupling of oxidative phosphorylation. We have noticed no significant difference of the responses in Methoprene, the juvenile hormone resistant mutant, suggesting that this action of juvenile hormone may be mediated via a mechanism different from that using nuclear transcription factors. The "uncoupling" effect is caused also by juvenile hormone analogues which are considered inactive in producing morphogenetic effects in Drosophila. Mitochondrial response is independent of transcription and translation, as revealed by the use of RNA and protein synthesis inhibitors. Given these data together, we reasoned that the protonophoric/uncoupling effect of juvenile hormone is a cell type specific nongenomic response to this lipophilic ligand and contrasts with widely accepted notions about nuclear action of juvenile hormone.

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Rickettsiella phytoseiuli naturally occurring in Phytoseiulus persimilis mites was cultivated in adult female Dermacentor reticulatus ticks. It demonstrates all six known developmental stages: dense, intermediate, bacterial, giant, crystal-forming and small dark particles. These stages of rickettsiae were found in salivary glands, Malpighian tubules, synganglion, ovaries, tracheal complex, haemolymph, fat body and alimentary tract. Rickettsiella phytoseiuli did not infect the Gené's organ. It multiplied in female ticks in a manner similar to that in the typical host mite, P. persimilis.

Endocytobionts (ECBs) were detected in the ovaries of Dermacentor reticulatus. Their developmental cycle is directly related to the developmental stages of tick oocytes. Two basic forms of ECBs occur in tick cells, i.e. dense forms, occurring singly or in aggregates situated free in the cytoplasm of host cells, and the light forms which are larger, pleomorphic and always situated inside vacuoles of host cells. The light forms occur together with dense forms in all oocytes. The dense forms occur freely and independently in funicular cells of the oocyte, the epithelial cells of oviducts, and additionally in the cells of the Malpighian tubules. A probable function of ECBs in the tick host is discussed.

Treatment of Drosophila larval salivary glands with juvenile hormone or its analogues leads to ultrastructural changes of mitochondria that mimic those seen after application of uncouplers of oxidative phosphorylation. This alteration of mitochondria, also known as swelling, is manifested in strong dilatation of their intercristae space. The mitochondrial response of salivary glands to juvenile hormone is restricted to collum cells that are known to be ultrastructurally and functionally different from transitional and corpus cells and may reflect their specialization in energy metabolism and water/ion balance. Morphological change of mitochondria and about a fivefold increase in cytochrome c oxidase activity in response to juvenile hormone appear to be a consequence of uncoupling of oxidative phosphorylation. We have noticed no significant difference of the responses in Methoprene, the juvenile hormone resistant mutant, suggesting that this action of juvenile hormone may be mediated via a mechanism different from that using nuclear transcription factors. The "uncoupling" effect is caused also by juvenile hormone analogues which are considered inactive in producing morphogenetic effects in Drosophila. Mitochondrial response is independent of transcription and translation, as revealed by the use of RNA and protein synthesis inhibitors. Given these data together, we reasoned that the protonophoric/uncoupling effect of juvenile hormone is a cell type specific nongenomic response to this lipophilic ligand and contrasts with widely accepted notions about nuclear action of juvenile hormone.

The endocytobionts from ovaries of partially engorged female Dermacentor reticulatus ticks, inoculated introcoelomally into females of three tick species, D. reticulatus, Ixodes ricinus and Haemaphysalis inermis, caused considerable morphological alterations in the examined cells and tissues of the synganglion, fat body, tracheal complex and ovary of these recipients.