Sterol utilization and metabolism by Heliothis zea

Lipids ◽  
1997 ◽  
Vol 32 (12) ◽  
pp. 1317-1323 ◽  
Author(s):  
W. David Nes ◽  
Monica Lopez ◽  
Wen Zhou ◽  
De-an Guo ◽  
Patrick F. Dowd ◽  
...  
Keyword(s):  
1987 ◽  
Vol 16 (5) ◽  
pp. 1148-1151 ◽  
Author(s):  
W. H. Hendrix ◽  
T. F. Mueller ◽  
J. R. Phillips ◽  
O. K. Davis

1977 ◽  
Vol 6 (5) ◽  
pp. 627-628 ◽  
Author(s):  
Jerry H. Young ◽  
R. G. Price
Keyword(s):  

1968 ◽  
Vol 57 (4) ◽  
pp. 553-558
Author(s):  
R. L. Ridgway ◽  
L. A. Bariola ◽  
S. L. Jones ◽  
W. L. Lowry

Laboratory and field-cage studies were conducted in Texas in 1965 to evaluate treatments of the systemic insecticides, Azodrin (3-hydroxy-N-methyl-cis-crotonamide dimethyl phosphate), Bidrin (3-hydroxy-N, N dimethyl-cis-crotonamide dimethyl phosphate), American Cyanamid CL-47031 (cyclic ethylene (diethoxy-phosphinyl) dithioimidocarbonate) and Temik (2-methyl-2-(methylthio) propion-aldehyde O-(methylcarbamoyl) oxime), applied incorporated in lanolin to the stems of cotton plants against Heliothis zea (Boddie) and H. virescens (F.). Reductions in numbers of developing larvae of H. zea were substantial on individual plants the stems of which had been treated with Azodrin or CL-47031 and which were artificially infested with eggs. When first-instar larvae of H. zea or H. virescens were caged on plants 3, 7 or 14 days after stem treatment with 2.5, 5.0 or 100 mg. Azodrin, Bidrin or CL-47031 per plant, net mortalities ranged from 21 to 80 per cent after three days. The mortality of adults of H. zea provided with sucrose solutions containing 1 p.p.m. of the systemic insecticides indicated that Azodrin and Bidrin were about equally toxic and much more so than CL-47031 and Temik, and that of adults caged on individual plants in flower that had been treated with Azodrin or CL-47031 suggested that the moths may be killed by the systemic action of these insecticides translocated to the nectar. When adults of H. virescens were released on plants each treated with Azodrin at 25 or 30 mg. in large field cages, reductions in the numbers of eggs deposited, attributed to the effect on the moths of the insecticide in the nectar, and in the numbers of developing larvae, were substantial. Azodrin was the most consistently effective of the four insecticides evaluated.


1978 ◽  
Vol 71 (2) ◽  
pp. 165-168 ◽  
Author(s):  
C. M. Ignoffo ◽  
D. L. Hostetter ◽  
K. D. Biever ◽  
C. Garcia ◽  
G. D. Thomas ◽  
...  
Keyword(s):  

2009 ◽  
Vol 84 (2) ◽  
pp. 1057-1065 ◽  
Author(s):  
Yueh-Lung Wu ◽  
Carol P. Wu ◽  
Song-Tay Lee ◽  
Han Tang ◽  
Chi-Hua Chang ◽  
...  

ABSTRACT Heliothis zea nudivirus 1 (HzNV-1), previously known as Hz-1 virus, is an insect virus able to establish both productive and latent infections in several lepidopteran insect cells. Here, we have cloned and characterized one of the HzNV-1 early genes, hhi1, which maps to the HindIII-I fragment of the viral genome. During the productive viral infection, a 6.2-kb hhi1 transcript was detectable as early as 0.5 h postinfection (hpi). The level of transcript reached a maximum at 2 hpi and gradually decreased after 4 hpi. The transcript was not detectable during the latent phase of viral infection. Upon cycloheximide treatment, much higher levels of hhi1 transcript were detected throughout the productive viral infection cycle, suggesting that newly synthesized proteins are not needed for the expression of hhi1. Nevertheless, viral coinfection can further stimulate the expression of transfected hhi1 promoter in a plasmid. Transient hhi1 expression in latently infected cells resulted in a significant increase in virus titer and viral DNA propagation, suggesting that hhi1 plays a critical role in viral reactivation. Additional experiments showed that six early genes, which possibly function in transcription or DNA replication, were activated in the latent cells upon hhi1 transfection. Among these six genes, orf90 and orf121 expression could be induced by hhi1 alone without the need for other viral genes. Our discovery should be useful for future mechanistic study of the switches of latent/productive HzNV-1 viral infections.


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