Literature DB >> 24502719

The innate immune response may be important for surviving plague in wild Gunnison's prairie dogs.

Joseph D Busch1, Roger Van Andel, Nathan E Stone, Kacy R Cobble, Roxanne Nottingham, Judy Lee, Michael VerSteeg, Jeff Corcoran, Jennifer Cordova, William Van Pelt, Megan M Shuey, Jeffrey T Foster, James M Schupp, Stephen Beckstrom-Sternberg, James Beckstrom-Sternberg, Paul Keim, Susan Smith, Julia Rodriguez-Ramos, Judy L Williamson, Tonie E Rocke, David M Wagner.   

Abstract

Prairie dogs (Cynomys spp.) are highly susceptible to Yersinia pestis, with ≥99% mortality reported from multiple studies of plague epizootics. A colony of Gunnison's prairie dogs (Cynomys gunnisoni) in the Aubrey Valley (AV) of northern Arizona appears to have survived several regional epizootics of plague, whereas nearby colonies have been severely affected by Y. pestis. To examine potential mechanisms accounting for survival in the AV colony, we conducted a laboratory Y. pestis challenge experiment on 60 wild-caught prairie dogs from AV and from a nearby, large colony with frequent past outbreaks of plague, Espee (n = 30 per colony). Test animals were challenged subcutaneously with the fully virulent Y. pestis strain CO92 at three doses: 50, 5,000, and 50,000 colony-forming units (cfu); this range is lethal in black-tailed prairie dogs (Cynomys ludovicianus). Contrary to our expectations, only 40% of the animals died. Although mortality trended higher in the Espee colony (50%) compared with AV (30%), the differences among infectious doses were not statistically significant. Only 39% of the survivors developed moderate to high antibody levels to Y. pestis, indicating that mechanisms other than humoral immunity are important in resistance to plague. The ratio of neutrophils to lymphocytes was not correlated with plague survival in this study. However, several immune proteins with roles in innate immunity (VCAM-1, CXCL-1, and vWF) were upregulated during plague infection and warrant further inquiry into their role for protection against this disease. These results suggest plague resistance exists in wild populations of the Gunnison's prairie dog and provide important directions for future studies.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 24502719     DOI: 10.7589/2012-08-209

Source DB:  PubMed          Journal:  J Wildl Dis        ISSN: 0090-3558            Impact factor:   1.535


  6 in total

Review 1.  Evaluation of Yersinia pestis Transmission Pathways for Sylvatic Plague in Prairie Dog Populations in the Western U.S.

Authors:  Katherine L D Richgels; Robin E Russell; Gebbiena M Bron; Tonie E Rocke
Journal:  Ecohealth       Date:  2016-05-27       Impact factor: 3.184

2.  Reevaluation of the Role of Blocked Oropsylla hirsuta Prairie Dog Fleas (Siphonaptera: Ceratophyllidae) in Yersinia pestis (Enterobacterales: Enterobacteriaceae) Transmission.

Authors:  Adélaïde Miarinjara; David A Eads; David M Bland; Marc R Matchett; Dean E Biggins; B Joseph Hinnebusch
Journal:  J Med Entomol       Date:  2022-05-11       Impact factor: 2.435

3.  First Genome Sequence of the Gunnison's Prairie Dog (Cynomys gunnisoni), a Keystone Species and Player in the Transmission of Sylvatic Plague.

Authors:  Mirian T N Tsuchiya; Rebecca B Dikow; Loren Cassin-Sackett
Journal:  Genome Biol Evol       Date:  2020-05-01       Impact factor: 3.416

4.  Differential plague susceptibility in species and populations of prairie dogs.

Authors:  Robin E Russell; Daniel W Tripp; Tonie E Rocke
Journal:  Ecol Evol       Date:  2019-10-02       Impact factor: 2.912

5.  Genetic variation at the MHC DRB1 locus is similar across Gunnison's prairie dog (Cynomys gunnisoni) colonies regardless of plague history.

Authors:  Kacy R Cobble; Katy J Califf; Nathan E Stone; Megan M Shuey; Dawn N Birdsell; Rebecca E Colman; James M Schupp; Maliha Aziz; Roger Van Andel; Tonie E Rocke; David M Wagner; Joseph D Busch
Journal:  Ecol Evol       Date:  2016-03-16       Impact factor: 2.912

6.  The Genome of the Great Gerbil Reveals Species-Specific Duplication of an MHCII Gene.

Authors:  Pernille Nilsson; Monica H Solbakken; Boris V Schmid; Russell J S Orr; Ruichen Lv; Yujun Cui; Yajun Song; Yujiang Zhang; Helle T Baalsrud; Ole K Tørresen; Nils Chr Stenseth; Ruifu Yang; Kjetill S Jakobsen; William Ryan Easterday; Sissel Jentoft
Journal:  Genome Biol Evol       Date:  2020-02-01       Impact factor: 3.416

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.