ENZYMES IN SALIVA FROM 4 PARASITIC ARTHROPODS

被引:56
作者
KERLIN, RL
HUGHES, S
机构
[1] C.S.I.R.O. Division of Tropical Animal Production, Long Pocket Laboratories, Brisbane, Queensland
关键词
AEDES-AEGYPTI; BOOPHILUS-MICROPLUS; HAEMATOBIA-IRRITANS-EXIGUA; LUCILIA-CUPRINA; ENZYMES; API-ZYME; APYRASE; SALIVA; PARASITE; ELECTROPHORESIS;
D O I
10.1111/j.1365-2915.1992.tb00587.x
中图分类号
Q96 [昆虫学];
学科分类号
摘要
Enzyme assays and SDS polyacrylamide gel electrophoresis were carried out on saliva and in some cases homogenates of salivary gland and gut from four parasitic arthropods (the cattle tick, Boophilus microplus (Canestrini); the mosquito, Aedes aegypti (L.); non-parasitic adult and parasitic larval blowfly of sheep, Lucilia cuprina (Wiedemann); the buffalo fly, Haematobia irritans exigua de Meijere). Saliva from all species showed large differences in the number and molecular weight of components, as judged by electrophoresis. Enzyme profiles, however, showed similar enzyme activities (phosphatase, esterase/lipase) in saliva from species with dissimilar feeding behaviours. There were obvious differences in the enzyme profiles of saliva and gut tissues from the different species that reflected feeding strategies. These differences were mainly in the type and levels of glycosidase and protease activities. It was concluded that many of the components of saliva from different species had similar functions, although a small number of them may be specifically adapted to the mode of feeding for each parasite.
引用
收藏
页码:121 / 126
页数:6
相关论文
共 20 条
[1]  
Bergmeyer H.U., Methods of enzymatic analysis, Enzymes 3: Peptidases, Proteinases and their inhibitors, Vol. V, pp. 119-129, (1984)
[2]  
Binnington K.C., Sequential changes in salivary gland structure during attachment and feeding of the cattle tick, Boophilus microplus, International Journal of Parasitology, 8, pp. 97-115, (1978)
[3]  
Boorman J., Induction of salivation in biting midges and mosquitoes, and demonstration of virus in the saliva of infected insects, Medical and Veterinary Entomology, 1, pp. 211-214, (1987)
[4]  
Bousquet J., Marty G.P., Clauss C., Michel F.B., Enzymes of bee venom, sac and whole body, Annals of Allergy, 43, pp. 110-114, (1979)
[5]  
Bowles V.M., Carnegie P.R., Sandeman R.M., Characterization of proteolytic and collagenolytic enzymes from the larvae of Lucilia cuprina, the sheep blowfly, Australian Journal of Biological Research, 41, pp. 269-278, (1988)
[6]  
Davey M.G., Lander H., Effect of adenosine diphosphate on circulating platelets in man, Nature, 201, pp. 1037-1039, (1964)
[7]  
Forbush B., Assay of Na, K‐ATPase in plasma membrane preparations: increasing the permeability of membrane vesicles using sodium dodecyl sulfate buffered with bovine serum albumin, Analytical Biochemistry, 128, pp. 159-163, (1983)
[8]  
Hansen-Bay C., The control of enzyme secretion from fly salivary glands, Journal of Physiology, 274, pp. 421-435, (1978)
[9]  
Hori K., Atalay R., Araki S., Digestive enzymes in the gut and salivary gland of the adult horn fly Haematobia ir‐ritans (Diptera: Museidac), Applied Entomology and Zoology, 16, pp. 16-23, (1981)
[10]  
Kolodny G.M., An improved method for increasing the resolution and sensitivity of silver staining of nucleic acid bands in polyacrylamide gels, Analytical Biochemistry, 138, pp. 66-67, (1984)