Densitometric Thin-Layer Chromatographic Analyses of Free Sterols in Echinostoma revolutum (Trematoda) Adults and Their Excretory-Secretory Products

1983 ◽  
Vol 69 (4) ◽  
pp. 789 ◽  
Author(s):  
Susan Bennett ◽  
Bernard Fried
Parasitology ◽  
1982 ◽  
Vol 84 (2) ◽  
pp. 375-380 ◽  
Author(s):  
B. Fried ◽  
D. A. Leiby

SUMMARYIntraspecific pairing of Haematoloechus medioplexus and Echinostoma revolutum adults and interspecific pairing of H. medioplexus and E. revoltum adults were studied in vitro at 21 ± 1 °C and 30 ± 1 °C in Petri-dish cultures containing an agar substrate and a Locke's 1:1 solution overlay. Salinity and temperature tolerance tests showed that both species survived for 24 h in a Locke's 1:1 solution at 21 ± 1 °C and 30 ±1 °C. For behaviour studies, worms were placed 2 cm apart and then observed at various intervals from 5 min to 4 h. H. medioplexus and E. revolutum showed significant intraspecific pairing at 30±1 °C, whereas only H. medioplexus paired significantly at 21±1°C. Significant interspecific pairing of H. medioplexus and E. revolutum occurred at 21 ±1 °C and 30 ±1 °C. Thin-layer chromatographic analysis showed that H. medioplexus adults released mainly free sterol, along with traces of triacylglycerols and free fatty acids into a non-nutrient medium.


Parasitology ◽  
1969 ◽  
Vol 59 (4) ◽  
pp. 973-989 ◽  
Author(s):  
J. A. Clegg

An artificial skin of hardened gelatine was used to examine the factors affecting penetration of skin by cercariae of the bird schistosome, Austrobilharzia terrigalensis.The percentage of cercariae able to penetrate through a gelatine membrane was increased by a factor of 3–4 by coating the membrane with a thin layer of lipid collected from the surface of chicken skin.The free sterol fraction, isolated from chicken skin surface lipid by thin-layer chromatography, stimulated penetration to the same extent as whole skin lipid.Cholesterol was detected in the sterol fraction by mass spectrometry and pure cholesterol had the full stimulating effect on cercarial penetration.Skin lipid, from which free sterols had been removed, lost the stimulatory effect on cercariae, but full activity was recovered by adding cholesterol to the sterol-free lipid. Fractions of skin lipid containing free fatty acids or triglycerides, wax esters and sterol esters similarly failed to stimulate penetration.These results establish that penetration of A. terrigalensis cercariae is greatly stimulated by the free sterols present in the surface lipid of chicken skin but cholesterol may not be the only active sterol. Cholestanol and the plant sterols campesterol and β-sitosterol were also detected in chicken skin surface lipid. These sterols were not tested for activity on cercariae because samples free from cholesterol could not be obtained.Some cercariae were able to penetrate plain gelatine membranes not coated with cholesterol but small amounts of free sterol were detected in the gelatine itself. This sterol could not be completely removed by prolonged solvent extraction and consequently it is not known whether any cercariae are able to penetrate in the complete absence of sterols.Temperature had a marked effect on penetration of cercariae; lowering the temperature from 40 to 25 °C reduced the number of successful penetrants by a factor of 4.I am grateful to Miss V. Bowen for excellent technical assistance and to Dr J. McLeod of the Research School of Chemistry, Australian National University, who performed and interpreted the mass spectrometry. This investigation was partly supported by a research grant from the World Health Organization.


Parasitology ◽  
1981 ◽  
Vol 82 (2) ◽  
pp. 225-229 ◽  
Author(s):  
B. Fried ◽  
G. A. Robinson

SUMMARYHistochemical and thin-layer chromatographic (t.l.c.) analyses were made on neutral lipids in the free (unencysted) metacercariae of Amblosoma suwaense (Brachylaimidae). As determined by t.l.c. the major neutral lipid fractions in metacercariae removed directly from Campeloma decisum snails were free sterols and sterol esters. Metacercariae incubated for 1 h at 37±1° C in sterile Locke's solution released mainly sterol esters and a lesser amount of free sterols into the medium. As determined by Oil Red O (ORO) staining, metacercariae accumulated neutral lipid in the intestinal caeca during incubation and the excretory system was ORO negative. Behavioural studies showed that metacereariae paired and aggregated in vitro and were attracted to lipophilic but not to hydrophilic worm products. Following t.l.c. preparative analysis it was demonstrated that metacercariae were attracted to sterol ester worm products but not to free sterol products.


1965 ◽  
Vol 20 ◽  
pp. 354-357 ◽  
Author(s):  
N.W. Ditullio ◽  
C.S. Jacobs ◽  
W.L. Holmes

1966 ◽  
Vol 44 (1) ◽  
pp. 119-128 ◽  
Author(s):  
H. L. Haust ◽  
A. Kuksis ◽  
J. M. R. Beveridge

Conditions are described for the quantitative precipitation of nine 3β-hydroxysterols with digitonin. After removal of excess reagent, the sterol and digitonin moieties are dissolved in a known volume of dry pyridine. An aliquot of the pyridine solution is processed to give a measure of total 3β-hydroxysterol by estimating the digitonin moiety with the use of anthrone. From another aliquot, the free sterols may be regenerated for differential-photometric and gas–liquid or thin-layer chromatographic analysis.Recoveries for each sterol at three levels of concentration were as follows: β-sitosterol, 98.6 ± 1.8% (mean and S.D.); campesterol, 99.1 ± 1.9%; stigmasterol, 98.9 ± 1.7%; stigmastanol, 99.1 ± 1.9%; cholesterol, 100.1 ± 1.5%; cholestanol, 100.8 ± 1.3%; coprostanol, 93.6 ± 1.6%; Δ7-cholestenol, 98.5 ± 1.8%; and 7-dehydrocholesterol, 91.9 ± 1.8%.


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