ライフサイエンスコーパス: raccoon

1 n epidemic of rabies virus in North American raccoons.

2 tectable in nontumor tissue or in unaffected raccoons.

3 ntified in neuroglial tumors of free-ranging raccoons.

4 th 100% of neuroglial tumors in free-ranging raccoons.

5 ore than 20 years and including 35,387 rabid raccoons.

6 ct of potential behavioural changes in rabid raccoons.

7 lates induced pathological findings of AD in raccoons.

8 ts; 88 (4%) to rodents/rabbits; 10 (0.5%) to raccoons; 5 (0.2%) to bats; and 24 (1.2%) to other anima

9 .7%) received RPEP after dog (95), cat (21), raccoon (8), bat (4), or other animal (8) exposures.

10 nine parvovirus (CPV) variants isolated from raccoons-a newly recognized CPV host-to different carniv

11 (GABA) in the somatosensory thalamus of the raccoon and to compare these features to those of other

12 sily observed and/or common mammals, such as raccoons and bobcats, bode poorly for species of conserv

13 nd control within terrestrial mammals (e.g., raccoons and foxes).

14 uences from puma, coyote, gray wolf, bobcat, raccoon, and striped skunk revealed two major groups rel

15 infections with Baylisascaris procyonis, the raccoon ascarid, have been increasingly recognized in do

16 -2a strains, suggesting that passage through raccoons assisted in the evolution of CPV-2a.

17 e that selection favors oral transmission to raccoons but classical stercorarian transmission to wood

18 These results indicated that raccoons can become infected with ADV and may have a rol

19 n this study, we investigated the effects of raccoon contact patterns on rabies spread using network

20 ng detailed data describing the variation in raccoon contact rates into a network modelling approach,

21 t capsid (VP2) position 300 in the prototype raccoon CPV allows dog cell infection.

22 within raccoon populations, suggesting that raccoons develop little or no rabies immune class.

23 Although viruses from raccoons do not efficiently bind the dog transferrin rec

24 h related middle- and late-phase epidemic or raccoon dog strains.

25 o found serological evidence of infection in raccoon dogs (Nyctereutes procuyoinboides).

26 Himalayan palm civets (Paguma larvata), and raccoon dogs (Nyctereutes procyonoides), sold in exotic

27 hina and spread to humans via civet cats and raccoon dogs in the wet markets before spreading to 37 c

28 of zoonotic strains found in palm civets and raccoon dogs, as well as isolates spanning the early, mi

29 Trios of raccoons experimentally inoculated with ADV-TR and ADV-U

30 duced in Aleutian and non-Aleutian mink, but raccoons failed to show serological or pathological evid

31 s measured in seawater and in gull, cat, and raccoon feces.

32 iant virus that has circulated undetected in raccoons for at least 24 years, with transfers to and fr

33 The innervation of the digits on the raccoon forepaw was examined by using immunochemistry fo

34 Sylvatic carnivores, such as raccoons, have recently been recognized as important hos

35 orks incorporated the number and duration of raccoon interactions.

36 neurons in the somatosensory thalamus of the raccoon is less than that in the cat and monkey, but the

37 preparation of ADV-TR prepared from infected raccoon lymph nodes was inoculated into mink and raccoon

38 Raccoons may display different behaviours when infectiou

39 om fecal samples collected from anesthetized raccoons (n = 738) trapped in six Pennsylvania counties

40 umented a 99.3% decrease in the frequency of raccoon observations, decreases of 98.9% and 87.5% for o

41 s identified by PCR in samples from mink and raccoons on commercial ranches during an outbreak of Ale

42 rent trade-off scenarios in cycles involving raccoons or woodrats, including a proper three-way trade

43 Raccoon polyomavirus (RacPyV) is associated with 100% of

44 Recently, raccoon polyomavirus (RacPyV) was identified in neurogli

45 proximity logging collars on a wild suburban raccoon population and then simulated rabies spread acro

46 monstrate that when rabies enters a suburban raccoon population, the likelihood of a disease outbreak

47 of dumb and furious behaviours in the rabid raccoon population, there are similar outbreak sizes and

48 provide new insights into rabies dynamics in raccoon populations and have important implications for

49 approach, we were able to show that suburban raccoon populations are highly susceptible to rabies out

50 t patterns influence the spread of rabies in raccoon populations in order to design effective control

51 assumed low levels of immunity (1-5%) within raccoon populations, suggesting that raccoons develop li

52 A recombinant raccoon poxvirus, expressing the F1 antigen of Y. pestis

53 Raccoons (Procyon lotor) play an important role in the m

54 ites in outbred, free-ranging populations of raccoons (Procyon lotor).

55 ticks (Ixodes texanus; n=718) collected from raccoons (Procyon lotor; n=91) and genotyped at 11 micro

56 Comparison of raccoon pulsed-field gel electrophoresis (PFGE) pulse ty

57 e epizoology of rabies with the expansion of raccoon rabies from a small pocket around northern Virgi

58 Based on data for epidemic raccoon rabies in Connecticut, we developed a stochastic

59 An epizootic of raccoon rabies that began in the mid-Atlantic region of

60 ed kidney recipient were consistent with the raccoon rabies virus variant and were more than 99.9% id

61 exposed, infectious, and recovered model of raccoon rabies.

62 each host species but, with the exception of raccoons, relatively little evidence for onward transmis

63 e rabies virus outbreak among North American raccoons reveals the long lasting effect of the initial

64 DV, but only a single ADV-Pullman-inoculated raccoon showed evidence of infection.

65 ibutions of PV+ and CaBP+ cell bodies in the raccoon somatosensory thalamus are very similar to those

66 terozygote deficits (HDs) at the CP scale in raccoon ticks (Ixodes texanus; n=718) collected from rac

67 n the transmission of virus to mink but that raccoon-to-raccoon transmission of ADV is unlikely.

68 mission of virus to mink but that raccoon-to-raccoon transmission of ADV is unlikely.

69 Two of 3 raccoons trapped in the vicinity had positive hemocultur

70 nic tumor antigen genes, we cultured primary raccoon tumor cells and passaged them in mice, confirmin

71 oon lymph nodes was inoculated into mink and raccoons, typical AD was induced in Aleutian and non-Ale

72 Raccoon virus capsids showed little binding to the canin

73 y, in capsid protein (VP2) phylogenies, most raccoon viruses fell as evolutionary intermediates betwe

74 , and periodicity of rabies epizootics among raccoons were compared with predictions derived from a s

75 protein of ADV, indicated that both mink and raccoons were infected by a new isolate of ADV, designat