Penetration of Mouse and Rat Skin by "Schistosoma mansoni" cercariae

AIBS Bulletin ◽  
1963 ◽  
Vol 13 (6) ◽  
pp. 27
Author(s):  
D. R. Lincicome ◽  
E. U. Eni
Keyword(s):  
1972 ◽  
Vol 31 (2) ◽  
pp. 217-224 ◽  
Author(s):  
F.G. Austin ◽  
M.A. Stirewalt ◽  
R.E. Danziger

Parasitology ◽  
1972 ◽  
Vol 64 (2) ◽  
pp. 333-339 ◽  
Author(s):  
B. Gilbert ◽  
Marlene N. Da Rosa ◽  
R. Borojević ◽  
J. Pellegrino

The transformation of cercariae ofSchistosoma mansoniinto schistosomula has previously been achieved by passage through membranes of biological origin. This transformation has now been effected in the absence of a membrane. Chemical stimulus for transformation results from contact with human or rat skin lipid and fractionation of the latter led to localization of the active component in a fraction containing phospholipids. The series of processes involved in transformation was subsequently found to be set in motion by the action of egg lecithin-water mixtures on an aqueous suspension of cercariae and yields of 90% of live schistosomula may be obtained reproducibly with crude egg lecithin-water in the ratio 1:50. The juvenile worms were found, by accepted criteria, to be identical to those produced by the normal penetration procedure. Purified lecithin does not produce the same stimulus and the effect of the physical state and of possible impurities present in crude egg lecithin is discussed.This work was supported by the Conselho Nacional de Pesquisas (Brazil), the Banco Nacional de Desenvolvimento Econâmico FUNTEC contracts nos. 99 and 110 (Brazil), U.S. Army Grants nos. DAHC-19-70-G-0017 (to B.G.) and DAHC-19-70-G-0070 (to J.P.) and by the FORGE Foundation. Contribution no. 18 from the Schistosomiasis Research Unit, Institute of Biological Sciences, Federal University of Minas Gerais, Brazil.


Parasitology ◽  
1968 ◽  
Vol 58 (1) ◽  
pp. 111-128 ◽  
Author(s):  
J. A. Clegg ◽  
S. R. Smithers

A large percentage of the cercariae ofSchistosoma mansonidie while penetrating the abdominal skin of rats or mice but relatively few cercariae die in the skin of hamsters.Comparison of hamsters and mice infected from the same pool of cercariae showed that the higher percentage of cercariae recovered as adult worms from hamsters than from mice was due to the lower percentage of cercariae which died during penetration of hamster skin.In similar comparisons of rats with mice the lower percentage of adult worms recovered from rats was not entirely accounted for by the higher percentage of cercariae which died in rat skin. Losses of schistosomula at later stages of development are apparently higher in rats than in mice.Cercariae die within 10 min after beginning to penetrate the skin of mice. At this stage the cercariae, which are now termed schistosomula, are attempting to penetrate the Malpighian layer of the epidermis. Five minutes later many schistosomula have entered the dermis.The cause of death of cercariae has not been determined. It is not related to the development of sensitivity to water which accompanies the transition from cercaria to schistosomulum. Sensitivity to water appears much sooner after penetration in some cercariae than in others; even after 30 min in the skin some cercariae can tolerate a return to water.In rats, hyper-immunized by a series of infections with cercariae through the abdominal skin, the percentage of challenging cercariae which die in the abdominal skin shows a slight increase over controls. No further mortality of schistosomula occurs during the next 24 h.Age resistance to infection withS. mansonicould not be demonstrated in comparisons of young mice (1 month) with old mice (1 year) of the Parkes and CBA strain.We should like to thank Dr F. Hawking for performing the skin biopsies on the dogs and Mrs P. Clark and Miss J. Marsh for their excellent technical assistance.


Author(s):  
Betty Ruth Jones ◽  
Steve Chi-Tang Pan

INTRODUCTION: Schistosomiasis has been described as “one of the most devastating diseases of mankind, second only to malaria in its deleterious effects on the social and economic development of populations in many warm areas of the world.” The disease is worldwide and is probably spreading faster and becoming more intense than the overall research efforts designed to provide the basis for countering it. Moreover, there are indications that the development of water resources and the demands for increasing cultivation and food in developing countries may prevent adequate control of the disease and thus the number of infections are increasing.Our knowledge of the basic biology of the parasites causing the disease is far from adequate. Such knowledge is essential if we are to develop a rational approach to the effective control of human schistosomiasis. The miracidium is the first infective stage in the complex life cycle of schistosomes. The future of the entire life cycle depends on the capacity and ability of this organism to locate and enter a suitable snail host for further development, Little is known about the nervous system of the miracidium of Schistosoma mansoni and of other trematodes. Studies indicate that miracidia contain a well developed and complex nervous system that may aid the larvae in locating and entering a susceptible snail host (Wilson, 1970; Brooker, 1972; Chernin, 1974; Pan, 1980; Mehlhorn, 1988; and Jones, 1987-1988).


2008 ◽  
Vol 46 (09) ◽  
Author(s):  
P Bodammer ◽  
G Waitz ◽  
M Löbermann ◽  
EC Reisinger ◽  
J Emmrich
Keyword(s):  

Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
AIO Salloum ◽  
R Lucarini ◽  
MG Tozatti ◽  
J Medeiros ◽  
MLA Silva ◽  
...  

1973 ◽  
Vol 30 (02) ◽  
pp. 363-370
Author(s):  
D Thilo ◽  
E Böhm

SummaryExperiments with injury of the abdominal rat skin were carried out to examine the haemostatic system mechanism in vivo after zero to 30 seconds bleeding time. In the bleeding area only a few platelet aggregates could be found with no primary platelet thrombus. After 3.5 second bleeding time the first fibrin strands have been observed at the site of injury. The hypothesis is put forward that there is a very fast reacting haemostatic mechanism which results in the fibrin formation already at 3.5 seconds.


2019 ◽  
Author(s):  
M Roderfeld ◽  
J Lichtenberger ◽  
F Wolters ◽  
T Quack ◽  
CG Grevelding ◽  
...  
Keyword(s):  

2020 ◽  
Author(s):  
SM Gindner ◽  
V von Bülow ◽  
L Hehr ◽  
N Buß ◽  
G Schramm ◽  
...  
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