ライフサイエンスコーパス: cercariae

1 ) were infected with 500 Schistosoma mansoni cercariae.

2 in humans from nonspecific skin-penetrating cercariae.

3 in vivo early postinfection with S. mansoni cercariae.

4 ties of infected snails and human-infectious cercariae.

5 t rhesus macaques were exposed to S. mansoni cercariae.

6 -/-) mice were also infected with S. mansoni cercariae.

7 animals were exposed to Schistosoma mansoni cercariae.

8 mph nodes of mice vaccinated with irradiated cercariae.

9 as associated with the presence of trematode cercariae.

10 ercariae tentatively identified as virgulate cercariae.

11 ted, with the highest concentration found in cercariae.

12 animals previously immunized with irradiated cercariae.

13 various times postinfection with schistosome cercariae.

14 ors did not, however, enhance infectivity of cercariae.

15 sistently 50 to 80% carried a combination of cercariae and sporocysts of digenetic virgulate trematod

16 ral selection should favour the evolution of cercariae-avoidance behaviours.

17 Extracts of Schistosoma mansoni cercariae caused increased vascular permeability and ede

18 o repeated doses (4x) of Schistosoma mansoni cercariae, compared to a single dose (1x), results in CD

19 Schistosoma mansoni cercariae display specific behavioral responses to abiot

20 aling reduces a minnows' risk of exposure to cercariae, either directly via detection of cercariae in

21 Cercariae exposed to various light/temperature regimens

22 of an artificial shoal reduced their risk of cercariae exposure compared with those along peripheral

23 were percutaneously infected with S. mansoni cercariae, followed by i.v. injection of eggs.

24 Given that infected snails release cercariae for 3-4 months a year, the pond trematode comm

25 Minnows distinguished infective cercariae from other potential aquatic threats and respo

26 t after a single vaccination with irradiated cercariae in double cytokine-deficient vs wild-type mice

27 ansform rapidly from free-swimming infective cercariae in freshwater to endoparasitic schistosomules.

28 of such stimulants on signaling pathways of cercariae in relation to host finding and invasion.

29 cercariae, either directly via detection of cercariae in the water column followed by behavioural av

30 oma mansoni sporocysts capable of generating cercariae in vitro.

31 ed between 14 and 1660 free-swimming larvae (cercariae) infected snail(-1) 24 h(-1) in mid-summer.

32 he transformation of free-living, infectious cercariae into schistosomula and coincides with the appe

33 Pacific treefrogs (Hyla regilla) exposed to cercariae of a trematode parasite (Ribeiroia sp.).

34 ole of NO in mice vaccinated with irradiated cercariae of S. mansoni.

35 vaccinated with 15- or 50-kilorad-irradiated cercariae of S. mansoni.

36 Mice immunized with radiation-attenuated cercariae of Schistosoma mansoni display resistance to c

37 ficant quantities of PGE(2) were produced by cercariae of Schistosoma mansoni following incubation wi

38 C57BL/6 mice vaccinated once with irradiated cercariae of Schistosoma mansoni, is mediated by CD4+ T

39 ice vaccinated a single time with attenuated cercariae of Schistosoma mansoni, the protection induced

40 Aquatic larvae (cercariae) of the trematode parasite Schistosoma mansoni

41 oaling in fathead minnows exposed to larvae (cercariae) of two of their most common species of tremat

42 , and adult worms, but is not present in the cercariae or ciliated miracidia.

43 Percutaneous infection with cercariae over the skin site at which cercarial homogena

44 -IG) predators that only consume free-living cercariae (parasitic trematodes) reduced metacercarial i

45 (IgE deficient), were infected by S. mansoni cercariae percutaneously.

46 ory products released by Schistosoma mansoni cercariae rapidly produce IL-10 as a result of MyD88-med

47 occupational exposure to Schistosoma mansoni cercariae revealed that some individuals develop resista

48 each schistosome life stage examined (eggs, cercariae, schistosomula, adult males and females).

49 Post-treatment cercariae-specific responses were also more proinflammat

50 e 22 degrees C the snails released trematode cercariae tentatively identified as virgulate cercariae.

51 developmental stages (eggs, sporocysts, and cercariae) that do not possess the specialized double me

52 cages in outdoor mesocosms, exposed them to cercariae, then compared mean worm numbers in grouped vs

53 e S. japonicum life cycle, especially during cercariae transformation, which enables parasites to sur

54 tral issue by using the radiation-attenuated cercariae vaccine in mice genetically engineered to exhi

55 We conclude that in the irradiated-cercariae vaccine model, C57BL/6J and CBA/J mice produce

56 The process of skin invasion by Schistosoma cercariae was reviewed in a recent Trends Research Updat

57 ollowing three immunizations with irradiated cercariae was similar in the two groups.

58 tive sera of mice vaccinated with irradiated cercariae were shown to recognize carbohydrate epitopes

59 atedly vaccinated with 15-kilorad-irradiated cercariae, which also achieve the highest levels of prot