ライフサイエンスコーパス: prairie dog

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1 of seven samples from patients and from the prairie dog.

2 issues or isolates from six patients and the prairie dog.

3 amples for analysis from 11 patients and one prairie dog.

4 m of transmission cannot drive epizootics in prairie dogs.

5 portant than competition among kin for young prairie dogs.

6 of the antiorthopoxvirus compound ST-246 in prairie dogs against a monkeypox virus challenge of 65 t

7 imilarities between the vaccine responses in prairie dogs and humans that enhance the value of the pr

8 lpox vaccine-induced responses in humans and prairie dogs and identify several differences.

9 infectious diseases: plague transmission in prairie dogs and lyssavirus dynamics in American and Afr

10 ents reported having direct contact with ill prairie dogs before experiencing a febrile illness with

11 an epidemic resulted from cross-infection of prairie dogs by imported African rodents.

12 suggest that other small mammals, infectious prairie dog carcasses, fleas that transmit plague withou

13 biology, we find that plague can persist in prairie-dog colonies for prolonged periods, because host

14 ge studies have established the black-tailed prairie dog (Cynomys ludovicianus) as a model of human s

15 radically erupts in epizootics that decimate prairie dog (Cynomys ludovicianus) colonies, yet the cau

16 field studies of plague in the black-tailed prairie dog (Cynomys ludovicianus).

17 alatable bait and offered to 18 black-tailed prairie dogs (Cynomys ludovicianus) for voluntary consum

18 Prairie dogs (Cynomys spp.) are highly susceptible to Ye

19 uirrel family (black-tailed and white-tailed prairie dogs) for which audiograms are available.

20 idemiologic investigation suggested that the prairie dogs had been exposed to at least one species of

21 breaks by increasing the connectivity of the prairie dog hosts and therefore, permitting percolation

22 y studies demonstrated that the black-tailed prairie dog is susceptible to MPXV infection and that th

23 ogs and humans that enhance the value of the prairie dog model system as an OPV vaccination model and

24 ct as a mechanism of transmission within the prairie dog MPXV animal model.

25 Previous studies have shown that the prairie dog MPXV model is a functional animal model for

26 ited States who had had contact with ill pet prairie dogs obtained through a common distributor.

27 sed on the results of this study, we believe prairie dogs offer a novel and potentially useful small

28 (e.g., invasive bite or scratch from an ill prairie dog plus potential noninvasive exposure), and as

29 us to non-African captive species, including prairie dogs, preceded human disease.

30 induction of humoral immunity in humans and prairie dogs receiving Dryvax, Acam2000, or Imvamune vac

31 pox virus intranasal infection of vaccinated prairie dogs resulted in a significant boost in humoral

32 prediction, but research over 31 years with prairie dogs reveals the opposite pattern: Young females

33 reservoirs have the potential to affect the prairie dog system.

34 was associated with direct contact with ill prairie dogs that were being kept or sold as pets.

35 , elapsed time from first exposure to an ill prairie dog through various benchmarks of illness) were

36 The prairie dog, using monkeypox virus as a challenge virus,

37 Prairie dogs were fed standard (n = 18) or 1.2% choleste

38 Adult female prairie dogs were randomly assigned to receive subcutane

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