ライフサイエンスコーパス: white-tailed deer

1 their ability to reduce SARS-CoV-2 spread in white-tailed deer.

2 ological samples and polymorphic variants in white-tailed deer.

3 ing HD surveillance to hunter-harvested wild white-tailed deer.

4 duced, became enzootic, and co-circulated in white-tailed deer.

5 able for many common research objectives for white-tailed deer.

6 t competitive interactions between moose and white-tailed deer.

7 he spread among and between captive and wild white-tailed deer.

8 e animals and a single wildlife species, the white-tailed deer.

9 y of CWD infection in natural populations of white-tailed deer.

10 ed saliva and urine samples from CWD-exposed white-tailed deer.

11 d States after the hunters had field-dressed white-tailed deer.

12 in sheep, elk, and small numbers of mule and white-tailed deer.

13 s an alternative natural reservoir, possibly white-tailed deer.

14 major population cycles over large areas in white-tailed deer.

15 described malignant catarrhal fever virus of white-tailed deer.

16 oir system consisting of lone star ticks and white-tailed deer.

17 as found to be under purifying selection for white-tailed deer.

18 tect CWD infections in asymptomatic mule and white-tailed deer.

19 tropharyngeal lymph nodes (RPLNs) from Texas white-tailed deer.

20 ew, non-classical, MHC II gene (MHC-DOB) for white-tailed deer.

21 High white-tailed deer abundance in the United States represe

22 8,830 respiratory samples from free-ranging white-tailed deer across Washington, D.C. and 26 states

23 ly related species (Anaplasma marginale, the white-tailed deer agent, and additional E. chaffeensis-p

24 assay for anaplasma matched sequences of the white-tailed deer agent.

25 ) PrP(c) We demonstrate that the presence of white-tailed deer and bovine NTDs hindered seeded conver

26 cascading effect of population expansion of white-tailed deer and I. scapularis populations likely f

27 ent cervid species, including North American white-tailed deer and muntjac, and European reindeer and

28 nce for sustained evolution of SARS-CoV-2 in white-tailed deer and of deer-to-human transmission.

29 As a result, a confirmed 1,000 white-tailed deer and pronghorn antelope died over the c

30 We used bioassay studies of native white-tailed deer and transgenic cervidized mice to dete

31 found seasonal patterns in selection by the white-tailed deer and were able to link use of conifer f

32 of North American cervids, i.e., mule deer, white-tailed deer, and elk (wapiti).

33 Therefore, CWD isolates from mule deer, white-tailed deer, and elk were inoculated intracerebral

34 Overall, generalist mesocarnivores, white-tailed deer, and giant anteater were more likely t

35 Brain samples from CWD-positive elk, white-tailed deer, and mule deer produced disease in Tg(

36 hether third eyelids from naturally infected white-tailed deer are a reliable tissue for detecting CW

37 imal host range of SARS-CoV-2 and identifies white-tailed deer as a susceptible wild animal species t

38 a highly divergent lineage of SARS-CoV-2 in white-tailed deer (B.1.641).

39 and three cases of potential spillover from white-tailed deer back to humans.

40 data show that upon intranasal inoculation, white-tailed deer became subclinically infected and shed

41 from chronic wasting disease (CWD)-infected white-tailed deer brain homogenates and found that lipid

42 amples from naturally infected, pre-clinical white-tailed deer by comparing protocols aiming to conce

43 ove the maximum ambient temperature in which white-tailed deer can be detected increased in 72, 10, 1

44 ove the maximum ambient temperature in which white-tailed deer can be detected will increase in 32, 1

45 est that CWD prions from elk, mule deer, and white-tailed deer can be readily transmitted among these

46 mosquito-transmitted virus in North American white-tailed deer, causes several cases of severe neurol

47 Thirty-five white-tailed deer collected from three Amblyomma america

48 evolution is not only three-times faster in white-tailed deer compared to the rate observed in human

49 In the white-tailed deer examples, a recently developed index f

50 e and Fisheries Captive Facility where adult white-tailed deer females and their fawns were administe

51 The first examination of MHC-DOB in white-tailed deer found significantly less polymorphism

52 luated the occurrence of HD in wild Illinois white-tailed deer from 1982 to 2019.

53 We also identified several white-tailed deer from South Carolina with anti-SARS-CoV

54 ting disease (CWD) and from 210 free-ranging white-tailed deer harvested from an area in Wisconsin wh

55 and from EDTA-blood specimens obtained from white-tailed deer in Maryland.

56 ctly from I. scapularis ticks collected from white-tailed deer in Minnesota and represent the first i

57 These data suggest white-tailed deer in the populations assessed have been

58 phagocytophilum-like organisms obtained from white-tailed deer in the United States.

59 rsection) and genetic relatedness for female white-tailed deer in Wisconsin's area of highest CWD pre

60 in all mule deer sampled but was absent from white-tailed deer, indicating that this virus originally

61 isfolded prion proteins from tissues of wild white-tailed deer infected with chronic wasting disease

62 laris, is a vector of the HGE agent, and the white-tailed deer is the primary host for adult Ixodes t

63 the native ungulate Odocoileus virginianus (white-tailed deer) is overabundant and Alliaria petiolat

64 This virus, which causes classical MCF in white-tailed deer, is a newly recognized agent belonging

65 uding marine water, Siberian permafrost, and white-tailed deer lung tissues with the latter showcasin

66 hough A. phagocytophilum-like organisms from white-tailed deer may be closely related to A. phagocyto

67 gene region in ruminants, and suggests that white-tailed deer may have a recombination hotspot betwe

68 omestic and nondomestic cats, domestic dogs, white-tailed deer, mink, and golden hamsters, among othe

69 SARS-CoV-2 transmission from animals (e.g., white-tailed deer, mink, domestic cats, and others) back

70 t SARS-CoV-2 was introduced from humans into white-tailed deer more than 30 times in Ohio, USA during

71 ,243 retropharyngeal lymph node samples from white-tailed deer, mule deer, and moose, collected in th

72 Importantly, all of the white-tailed deer (n = 63) were independently tested usi

73 ush samples collected antemortem from farmed white-tailed deer (n= 409).

74 142 mule deer (Odocoileus hemionus), and 90 white-tailed deer (O. virginianus) collected from 2017 t

75 We examined how white-tailed deer Odocoileus virginianus fawn spatiotemp

76 of habitat use that varied seasonally for a white-tailed deer (Odocoileus virginianus) and coyote (C

77 traspecific encounter data from two species: white-tailed deer (Odocoileus virginianus) and elk (Cerv

78 We demonstrated that white-tailed deer (Odocoileus virginianus) and elk (Cerv

79 strongylus tenuis) between two prey species [white-tailed deer (Odocoileus virginianus) and moose (Al

80 wo lines of Tg mice expressing PrP common to white-tailed deer (Odocoileus virginianus) and mule deer

81 on-detection data of moose (Alces alces) and white-tailed deer (Odocoileus virginianus) and parasite

82 Here we document that free-ranging white-tailed deer (Odocoileus virginianus) are highly su

83 e N. caninum oocysts in their feces and that white-tailed deer (Odocoileus virginianus) are natural i

84 d fecal samples from farmed and free-ranging white-tailed deer (Odocoileus virginianus) around the Mi

85 eld and experimental studies have implicated white-tailed deer (Odocoileus virginianus) as probable r

86 vement behaviour and resource utilization by white-tailed deer (Odocoileus virginianus) determines bl

87 to an empirical telemetry data set of three white-tailed deer (Odocoileus virginianus) dyads.

88 We targeted white-tailed deer (Odocoileus virginianus) for serosurve

89 omes isolated from mink (Neovison vison) and white-tailed deer (Odocoileus virginianus) for which mul

90 ollected from healthy-appearing free-ranging white-tailed deer (Odocoileus virginianus) from multiple

91 High prevalence of SARS-CoV-2 infection in white-tailed deer (Odocoileus virginianus) has been repo

92 White-tailed deer (Odocoileus virginianus) have emerged

93 county using CWD surveillance data depicting white-tailed deer (Odocoileus virginianus) in 16 eastern

94 linical signs and lesions in five out of six white-tailed deer (Odocoileus virginianus) in a North Am

95 wild boar (Sus scrofa) in Spain, as well as white-tailed deer (Odocoileus virginianus) in the United

96 ecade, abnormalities have been documented in white-tailed deer (Odocoileus virginianus) in west-centr

97 Populations of white-tailed deer (Odocoileus virginianus) on islands of

98 on of SARS-CoV-2 from humans to free-ranging white-tailed deer (Odocoileus virginianus) poses a uniqu

99 me coronavirus 2 (SARS-CoV-2) from humans to white-tailed deer (Odocoileus virginianus) through unkno

100 studies to identify microsatellite loci for white-tailed deer (Odocoileus virginianus) with the pote

101 The white-tailed deer (Odocoileus virginianus), a popular ru

102 Louis, Missouri region, we found that white-tailed deer (Odocoileus virginianus), a preeminent

103 ot traffic data with hourly GPS data from 38 white-tailed deer (Odocoileus virginianus), a species li

104 Here we demonstrated that white-tailed deer (Odocoileus virginianus), an animal sp

105 llus), gray squirrel (Sciurus carolinensis), white-tailed deer (Odocoileus virginianus), and guinea p

106 evaluate the detection and classification of white-tailed deer (Odocoileus virginianus), domestic cow

107 To evaluate the effect of vaccinating white-tailed deer (Odocoileus virginianus), in combinati

108 transmission in wildlife hosts, particularly white-tailed deer (Odocoileus virginianus), remain poorl

109 ribution of activity across a diel cycle) of white-tailed deer (Odocoileus virginianus), with four pr

110 swabs, and ocular fluid were collected from white-tailed deer (Odocoileus virginianus).

111 plant availability or increased browsing by white-tailed deer (Odocoileus virginianus).

112 the prevalence of chronic wasting disease in white-tailed deer (Odocoileus virginianus).

113 vement in analyses of first-passage time for white-tailed deer (Odocoileus virginianus).

114 a sable antelope (Hippotragus niger), and a white-tailed deer (Odocoileus virginianus).

115 , were characterized for E. chaffeensis from white-tailed deer (Odocoileus virginianus).

116 rufus), black bears (Ursus americanus), and white-tailed deer (Odocoileus virginianus).

117 n Florida panthers (Puma concolor coryi) and white-tailed deer (Odocoileus virginianus).

118 ys would detect a commonly studied ungulate (white-tailed deer [Odocoileus virginianus]) during sunny

119 pulverized and inoculated intranasally into white-tailed deer once a week for 6 weeks.

120 Samples from heterozygous (G(96)/S(96)) white-tailed deer orally dosed with CWD from homozygous

121 ges were observed in our animal models using white-tailed deer origin viruses.

122 (IIb) on the MiSeq platform from an enclosed white-tailed deer population located in Alabama.

123 n dynamics of SARS-CoV-2 in wild and captive white-tailed deer populations across various simulated s

124 mitigate persistent SARS-CoV-2 outbreaks in white-tailed deer populations and potential spillback to

125 Still, SARS-CoV-2 has transmitted in white-tailed deer populations for a relatively short dur

126 As SARS-CoV-2 circulates within free-ranging white-tailed deer populations, there is the risk of tran

127 opagated within gestational fetal tissues of white-tailed deer populations.

128 (c), hinders seeded conversion of bovine and white-tailed deer PrP(c)s to the prion forms, but it fac

129 examined RAMALT collected postmortem from 76 white-tailed deer removed from a farm in Wisconsin known

130 more efficient seed for feline rPrP than for white-tailed deer rPrP; (iii) conversely, FSE more effic

131 er frequency in SARS-CoV-2 found in mink and white-tailed deer, suggesting that sustained transmissio

132 andemic cats and postpandemic South Carolina white-tailed deer that are specific for that SARS-CoV RB

133 blood from codon 96 glycine/glycine, captive white-tailed deer that were analyzed for prion infection

134 White-tailed deer, the predominant cervid in North Ameri

135 f choice for use for the diagnosis of CWD in white-tailed deer, the results of the present study furt

136 White-tailed deer tissues used to validate MN-QuIC inclu

137 gs the total number of documented alleles in white-tailed deer to 30 for MHC-DRB exon 2.

138 ge gap in early CWD pathogenesis, we exposed white-tailed deer to CWD prions by mucosal routes and pe

139 he obex and lymph nodes of naturally exposed white-tailed deer to identify potential biochemical stra

140 -2 from several mammals - primarily mink and white-tailed deer - to humans have raised concerns for t

141 Evolutionary analyses showed these white-tailed deer viruses originated from at least 109 i

142 from the sambar deer, the waterbuck, and the white-tailed deer were collected during winter dysentery

143 een 1998 and 2001, tissues from four captive white-tailed deer were observed to have histologic lesio

144 rate that imidacloprid has direct effects on white-tailed deer when administered at field-relevant do

145 For white-tailed deer, which were typically cryptic against

146 and mammals are large herbivores such as the white-tailed deer, wild boar, and African elephant.

147 and orally infected preclinical and infected white-tailed deer with clinical chronic wasting disease

148 Viruses repeatedly adapted to white-tailed deer with recurring amino acid substitution

149 e a bacterium previously referred to as the "white-tailed deer (WTD) agent" from two captive fawns in

150 me coronavirus 2 (SARS-CoV-2) from humans to white-tailed deer (WTD) and its ability to transmit from

151 Domestic cats and white-tailed deer (WTD) are particularly susceptible to

152 of CWD prions in naturally-infected, farmed white-tailed deer (WTD) fetal tissues using the Protein

153 conducted to determine the susceptibility of white-tailed deer (WTD) to the classic scrapie agent.

154 focused on the processing and consumption of white-tailed deer (WTD) venison are particularly vulnera

155 tected in blood of pre-clinical CWD-infected white-tailed deer (WTD) with high sensitivity and specif