Trends in the use of pesticides and pestiside residues on Queensland wool

Objective To determine the amounts of organophosphorous and synthetic pyrethroid residues on Queensland wool sampled between 1995 and 1997, and to study if pesticide use changed during the period.
Design Estimated amounts of residues were obtained from a survey of Queensland wool clips, and information on pesticide use was obtained from a trace-back postal survey of flock managers.
Procedure Trends in amounts of residues over time were assessed using analysis of variance and simple linear regression models, and changes in pesticide use was assessed using x² tests.
Results Significant linear reductions in organophosphorous (P = 0.0012), synthetic pyrethroid (P = 0.0044) and total (P = 0.0002) residues were detected. The proportion of woolgrowers treating for louse infestation (P = 0.0046) treating twice or more (P = 0.0006) and treating more than 4 months after shearing (P = 0.0001) decreased between 1994 and 1997. However, the proportion of growers who treated for blowfly strike (P = 0.0124) and used insect growth regulator pesticides increased (P < 0.0001). The use of handjetting to apply pesticides for blowfly strike control increased and the use of dips decreased (P < 0.0001).
Conclusion Residues of organophosphorous compounds and synthetic pyrethroids reduced in Queensland wool between 1994 and 1997. Although woolgrowers treated for louse infestation less, pesticide use to control blowfly strike increased. The increasing use of insect growth regulators in the industry needs to be monitored.     

Can the Genetic Origin Affect Rabbit Seminal Plasma Protein Profile along the Year?

The study was designed to evaluate the influence of genetic origin on rabbit seminal plasma protein profile variation along the year. Seminal plasma of rabbits from line A (maternal line) and R (paternal line) collected during a natural year was subjected to polyacrylamide gel electrophoresis (SDS‐PAGE). The electrophoretic profile of rabbit seminal plasma resulted in multiple protein bands of different intensity ranging from 9 to 240 kDa. Results showed that seven protein bands were significantly different between genetic lines, and among these, three protein bands were significantly different between seasons. The differentially expressed proteins were identified by MALDI‐TOF/TOF or LC‐MS/MS analysis and were the following ones: FAM115E‐like (220, 113 and 59 kDa), ectonucleoside triphosphate diphosphohydrolase 3 isoform X2 (72 kDa), annexin A5 (32 kDa), lipocalin allergen Ory c 4 precursor (19 kDa), and haemoglobin subunit zetalike (13 kDa) between genetic lines and FAM115E‐like (113 kDa), haemoglobin subunit zetalike (13 kDa) and β‐nerve growth factor (12 kDa) between seasons. These results indicate that proteins from rabbit seminal plasma are under both seasonal control and genetic control. Furthermore, the differential presence of these proteins could be one of the causes explaining the differences observed in fertility and seminal parameters between these two lines in earlier studies.     

Mechanistic target of rapamycin is activated in bovine granulosa cells after LH surge but is not essential for ovulation

The LH surge induces functional and morphological changes in granulosa cells. Mechanistic target of rapamycin (mTOR) is an integrator of signalling pathways in multiple cell types. We hypothesized that mTOR kinase activity integrates and modulates molecular pathways induced by LH in granulosa cells during the preovulatory period. Cows were ovariectomized and granulosa cells collected at 0, 3, 6, 12 and 24 hr after GnRH injection. While RHEB mRNA levels increased at 3 and 6 hr, returning to basal levels by 12 hr after GnRH treatment, RHOA mRNA levels increased at 6 hr and remained high thereafter. Western blot analyses revealed increased S6K phosphorylation at 3 and 6 hr after GnRH injection. Similarly, mRNA levels of ERK1/2, STAR and EGR‐1 were higher 3 hr after GnRH treatment. Rapamycin treatment inhibited mTOR activity and increased AKT activity, but did not alter ERK1/2 phosphorylation and EGR1 protein levels in cultured bovine granulosa cells. Rapamycin also inhibited LH‐induced increase in EREG mRNA abundance in granulosa cells in vitro. However, intrafollicular injection of rapamycin did not suppress ovulation. These findings suggest that mTOR is involved in the control of EREG expression in cattle, which may be triggered by LH surge stimulating RHEB and S6K activity.