Synthesis and localization of Japanese encephalitis virus RNAs in the infected cells

Synthesis and localization of virus-specific RNA in cells infected with Japanese encephalitis virus (JEV) were examined. To prepare specific RNA probes, we constructed four kinds of plasmids which contained DNA fragments corresponding to JEV genomic RNA. Minus probes, JT18V and JT19III, transcribed by T7 RNA polymerase were able to recognize a negative strand of JEV-specific RNA synthesized in cells as early as 6 hr postinfection (p.i.). In the experiments using a plus-strand probe JT19V to hybridize the 3' end of JEV-RNA, not only full-length 42S(+) RNA but also 10S(+) RNA were detected in the infected cells at 24 hr p.i. The positive-strand 42S RNA was found in much greater abundance in the membrane fraction than in the supernatant fraction of the infected cells. In contrast, larger amounts of the negative-strand RNAs existed in the supernatant fraction. It is suggested from the data that the JEV-specific negative- and positive-strand RNAs accumulate at different sites in the infected cells.     

Circulating immune complexes in the serum of diabetes mellitus in childhood by a modified 125I-C1q binding test.

The 125I-C1q binding test for the detection of soluble immune complexes in native unheated human serum was applied to the study of sera from 52 patients with diabetes mellitus in childhood. This radiolabeled C1q binding test is more sensitive and reproducible among the various methods proposed for the detection of immune complexes. The 125I-C1q binding activity in 52 sera from diabetes mellitus in childhood was 9.47 +/- 0.36% compared to 6.94 +/- 0.74% in normal controls. 125I-C1q binding values in diabetes mellitus in childhood were significantly higher than normal controls. Slight high values were seen in 3 patients with positive anti-DNA-antibodies in diabetes mellitus in childhood. 125I-C1q binding was not significantly increased in patients with positive antithyroid antibodies and insulin antibodies. There was no significant correlation between the duration of diabetes and 125I-C1q binding activity.     

Studies on the behavior of meiotic protoplasts

Meiotic protoplasts obtained from lily microsporocytes in late prophase to telophase I were cultured in an enzyme solution which prevents formation of a cell wall around the protoplsts. The removal of the surface wall interfered with nuclear and cell division when the wall was removed prior to metaphase. The main effects were non-segregation of chromosomes and aberrant cytokinesis. In contrast, the absence of a cell wall during the later periods in which actual segregation of the nucleus and cytoplasm takes place did not interfere with the spindle function. The regular process was accomplished through the formation of a cell plate or septum, and 2 hemispheric daughter protoplasts were formed. After that, a furrow was usually formed at the septum in the absence of a surrounding cell wall, and the protoplasts became dumbbell shaped. Some abnormal behavior was also observed using the time lapse technique.