Analyze Diet
Animals : an open access journal from MDPI2020; 10(6); 1086; doi: 10.3390/ani10061086

Survey of Serum Amyloid A and Bacterial and Viral Frequency Using qPCR Levels in Recently Captured Feral Donkeys from Death Valley National Park (California).

Abstract: Feral donkey removal from state land has raised concerns in terms of disease transmission between equine species. Disease outbreaks may occur as a result of the relocation of animals to new environments. Virus and bacteria DNA load and serum amyloid A derived from the pathogenic processes that they involve were measured in recently captured donkeys. Blood and nasal swabs were collected from 85 donkeys (Death Valley National Park, Shoshone, California); 24 were retested after 30/60 days in the Scenic (Arizona) long-term holding facility co-mingled with feral donkeys from Arizona and Utah. Quantitative Real-Time PCR (qPCR) was performed to detect viral and bacterial genomic material (equine influenza A [EIV], equine rhinitis A and B viruses, AHV-2, AHV-3, AHV-5 and EHV-1, EHV-4, subspecies and ,). Significant relations between behavior, body condition score, nasal discharge, and coughing were found in donkeys for which AHV-2 and DNA was detected. Higher SAA concentrations were found in foals. AHV-2 and DNA concentrations significantly differed between sampling moments ( < 0.05). In conclusion, donkeys do not appear to be a substantial risk for disease transmission to horses but could be if they carried strangles or other processes in which AHV-2 and were involved.
Publication Date: 2020-06-23 PubMed ID: 32585994PubMed Central: PMC7341296DOI: 10.3390/ani10061086Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research study analyzes the potential for disease transmission from feral donkeys to horses, using blood and nasal samples to measure bacteria and virus loads in recently captured donkeys. The results concluded that the donkeys did not pose a significant risk to horses unless certain conditions like strangles existed.

Introduction and Methodology

  • Considering the relevance of disease transmission between equine species and the potential disease outbreaks that can occur when animals are relocated to new environments, researchers conducted this study with the aim of determining the prevalence and type of viral and bacterial diseases present in feral donkeys.
  • They used blood, and nasal swabs from a sample of 85 donkeys recently captured from Death Valley National Park in Shoshone, California. 24 of these donkeys were retested after 30 and 60 days of being held in co-mingle with feral donkeys from Arizona and Utah at the Scenic long-term holding facility in Arizona.
  • A quantitative real-time polymerase chain reaction (qPCR) was employed to detect the viral and bacterial genomic material in the samples collected.

Results

  • The study found significant correlations between certain behaviors, such as nasal discharge and coughing, and the detection of AHV-2 and Streptococcus equi bacterial DNA. This implies that these symptoms may be indicative of the presence of these bacteria.
  • Additionally, higher levels of Serum Amyloid A (SAA), which is a protein that increases in the body’s response to inflammation or infection, were found in foals, or young donkeys.
  • The concentrations of AHV-2 and bacterial DNA significantly varied between the times the samples were taken, suggesting changes in the bacterial load over time.

Conclusion

  • The study concludes that feral donkeys do not appear to present a substantial risk for disease transmission to horses. However, there remains a potential risk if the donkeys carry ‘strangles’ (a bacterial infection in horses caused by Streptococcus equi) or are involved with other processes that implicate AHV-2 and Streptococcus equi.

Cite This Article

APA
Jerele S, Davis E, Mapes S, Pusterla N, Navas González FJ, Iglesias Pastrana C, Abdelfattah EM, McLean A. (2020). Survey of Serum Amyloid A and Bacterial and Viral Frequency Using qPCR Levels in Recently Captured Feral Donkeys from Death Valley National Park (California). Animals (Basel), 10(6), 1086. https://doi.org/10.3390/ani10061086

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 10
Issue: 6
PII: 1086

Researcher Affiliations

Jerele, Sara
  • International Animal Welfare Training Institute, School of Veterinary Medicine, University of California Davis, Davis, CA 95617, USA.
Davis, Eric
  • International Animal Welfare Training Institute, School of Veterinary Medicine, University of California Davis, Davis, CA 95617, USA.
Mapes, Samantha
  • Equine Viral Disease Laboratory, Department of Pathology, Microbiology, and Immunology, School of Veterinary Medicine, University of California Davis, Davis, CA 95617, USA.
Pusterla, Nicola
  • Equine Viral Disease Laboratory, Department of Pathology, Microbiology, and Immunology, School of Veterinary Medicine, University of California Davis, Davis, CA 95617, USA.
Navas González, Francisco Javier
  • Department of Genetics, Faculty of Veterinary Sciences, University of Córdoba, 14071 Córdoba, Spain.
  • The Worldwide Donkey Breeds Project, Faculty of Veterinary Sciences, University of Córdoba, 14071 Córdoba, Spain.
Iglesias Pastrana, Carlos
  • Department of Genetics, Faculty of Veterinary Sciences, University of Córdoba, 14071 Córdoba, Spain.
  • The Worldwide Donkey Breeds Project, Faculty of Veterinary Sciences, University of Córdoba, 14071 Córdoba, Spain.
Abdelfattah, Essam Mahmoud
  • Department of Animal Hygiene, and Veterinary Management, Faculty of Veterinary Medicine, Benha University, Qalubiya Governorate 13511, Egypt.
McLean, Amy
  • The Worldwide Donkey Breeds Project, Faculty of Veterinary Sciences, University of Córdoba, 14071 Córdoba, Spain.
  • Department of Animal Science, University of California Davis, Davis, CA 95616, USA.

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 45 references
  1. Tiller B. Feral Burro Populations: Distribution and Damage Assessment. Pacific Northwest National Laboratory; Richland, WA, USA: 1997.
  2. Weaver RA. Feral burros and wildlife. Proceedings of the 6th Vertebrate Pest Conference Anaheim, CA, USA. 5–7 March 1974.
  3. National Research Council. Using Science to Improve the BLM Wild Horse and Burro Program: A Way Forward. National Academies Press; Washington, DC, USA: 2013.
  4. National Research Council/Commission on Natural Resources/National Research Council, Committee on Wild, Free-Roaming Horses Burros. Wild and Free-Roaming Horses and Burros: Current Knowledge and Recommended Research. National Academies Press; Washington, DC, USA: 1980.
  5. Satué K, Calvo A, Gardón JC. Factors influencing serum amyloid type A (SAA) concentrations in horses. Open J Vet Med 2013;3:58.
    doi: 10.4236/ojvm.2013.31010google scholar: lookup
  6. Nolen-Walston R. How to interpret serum amyloid A concentrations. Proceedings of the 65th Annual American Association of Equine Practitioners (AAEP) Denver, CO, USA. 7–11 December 2019; pp. 130–137.
  7. Kay G, Tligui N, Semmate N, Azrib R, González FJN, Brizgys L, McLean A. Determining factors and interspecific modeling for serum amyloid a concentrations in working horses, donkeys, and mules.. Res Vet Sci 2019 Aug;125:256-265.
    doi: 10.1016/j.rvsc.2019.07.004pubmed: 31325640google scholar: lookup
  8. Jacobsen S, Andersen PH. The acute phase protein serum amyloid A (SAA) as a marker of inflammation in horses. Equine Vet Educ 2007;19:38–46.
  9. Pusterla N, Kass PH, Mapes S, Johnson C, Barnett DC, Vaala W, Gutierrez C, McDaniel R, Whitehead B, Manning J. Surveillance programme for important equine infectious respiratory pathogens in the USA.. Vet Rec 2011 Jul 2;169(1):12.
    doi: 10.1136/vr.d2157pubmed: 21676986google scholar: lookup
  10. Timoney JF. The pathogenic equine streptococci.. Vet Res 2004 Jul-Aug;35(4):397-409.
    doi: 10.1051/vetres:2004025pubmed: 15236673google scholar: lookup
  11. Wilson WD. Equine herpesvirus 1 myeloencephalopathy.. Vet Clin North Am Equine Pract 1997 Apr;13(1):53-72.
    doi: 10.1016/S0749-0739(17)30255-9pubmed: 9106343google scholar: lookup
  12. van Maanen C. Equine herpesvirus 1 and 4 infections: an update.. Vet Q 2002 Jun;24(2):58-78.
    doi: 10.1080/01652176.2002.9695126pubmed: 12095082google scholar: lookup
  13. Allen G, Kydd J, Slater J, Smith K. Recent advances in understanding the pathogenesis, epidemiology, and immunological control of equid herpesvirus-1 (EHV-1) abortion. J Equine Vet Sci 1999;8:129–146.
  14. Reed SM, Toribio RE. Equine herpesvirus 1 and 4.. Vet Clin North Am Equine Pract 2004 Dec;20(3):631-42.
    doi: 10.1016/j.cveq.2004.09.001pubmed: 15519823google scholar: lookup
  15. Ostlund EN. The equine herpesviruses.. Vet Clin North Am Equine Pract 1993 Aug;9(2):283-94.
    doi: 10.1016/S0749-0739(17)30396-6pubmed: 8395324google scholar: lookup
  16. Fortier G, van Erck E, Pronost S, Lekeux P, Thiry E. Equine gammaherpesviruses: pathogenesis, epidemiology and diagnosis.. Vet J 2010 Nov;186(2):148-56.
    doi: 10.1016/j.tvjl.2009.08.017pubmed: 19766026google scholar: lookup
  17. Ficorilli N, Studdert MJ, Crabb BS. The nucleotide sequence of asinine herpesvirus 3 glycoprotein G indicates that the donkey virus is closely related to equine herpesvirus 1.. Arch Virol 1995;140(9):1653-62.
    doi: 10.1007/BF01322539pubmed: 7487497google scholar: lookup
  18. Bell SA, Pusterla N, Balasuriya UB, Mapes SM, Nyberg NL, MacLachlan NJ. Isolation of a gammaherpesvirus similar to asinine herpesvirus-2 (AHV-2) from a mule and a survey of mules and donkeys for AHV-2 infection by real-time PCR.. Vet Microbiol 2008 Jul 27;130(1-2):176-83.
    doi: 10.1016/j.vetmic.2007.12.013pubmed: 18280676google scholar: lookup
  19. Kleiboeker SB, Schommer SK, Johnson PJ, Ehlers B, Turnquist SE, Boucher M, Kreeger JM. Association of two newly recognized herpesviruses with interstitial pneumonia in donkeys (Equus asinus).. J Vet Diagn Invest 2002 Jul;14(4):273-80.
    doi: 10.1177/104063870201400401pubmed: 12152805google scholar: lookup
  20. Kleiboeker SB, Turnquist SE, Johnson PJ, Kreeger JM. Detection and nucleotide sequencing of a DNA-packaging protein gene of equine gammaherpesviruses.. J Vet Diagn Invest 2004 Jan;16(1):67-74.
    doi: 10.1177/104063870401600112pubmed: 14974850google scholar: lookup
  21. Thiemann A. Respiratory disease in the donkey. Equine Vet Educ 2012;24:469–478.
  22. Vengust M, Wen X, Bienzle D. Herpesvirus-associated neurological disease in a donkey.. J Vet Diagn Invest 2008 Nov;20(6):820-3.
    doi: 10.1177/104063870802000620pubmed: 18987238google scholar: lookup
  23. Browning GF, Ficorilli N, Studdert MJ. Asinine herpesvirus genomes: comparison with those of the equine herpesviruses.. Arch Virol 1988;101(3-4):183-90.
    doi: 10.1007/BF01310999pubmed: 2845891google scholar: lookup
  24. Goodrich EL, Behling-Kelly E. Clinical Pathology of Donkeys and Mules.. Vet Clin North Am Equine Pract 2019 Dec;35(3):433-455.
    doi: 10.1016/j.cveq.2019.08.002pubmed: 31672198google scholar: lookup
  25. Valle E, Raspa F, Giribaldi M, Barbero R, Bergagna S, Antoniazzi S, Mc Lean AK, Minero M, Cavallarin L. A functional approach to the body condition assessment of lactating donkeys as a tool for welfare evaluation.. PeerJ 2017;5:e3001.
    doi: 10.7717/peerj.3001pmc: PMC5372837pubmed: 28367363google scholar: lookup
  26. Polidori P, Vincenzetti S. Chapter 4. Farm management and feeding strategies for donkey milk production. In: Mandhatri P.G.S., editor. Agricultural Research Updates. Nova Science Publishers, Inc.; Hauppauge, NY, USA: 2017. p. 93.
  27. Navas González FJ, Jordana Vidal J, León Jurado JM, Arando Arbulu A, McLean AK, Delgado Bermejo JV. Genetic parameter and breeding value estimation of donkeys' problem-focused coping styles.. Behav Processes 2018 Aug;153:66-76.
    doi: 10.1016/j.beproc.2018.05.008pubmed: 29763646google scholar: lookup
  28. Veterinary Medicine PCR Laboratory, UCDavis. q-PCR diagnostic submission packet. Veterinary Medicine PCR Laboratory, UCDavis [(accessed on 15 March 2020)]; Available online: https://pcrlab.vetmed.ucdavis.edu/sites/g/files/dgvnsk6571/files/inline-files/DiagnosticPacket08.2019.pdf.
  29. Derrick B, Toher D, White P. How to compare the means of two samples that include paired observations and independent observations: A companion to Derrick, Russ, Toher and White (2017). Tutor Quant Methods Psychol 2017;13:120–126.
    doi: 10.20982/tqmp.13.2.p120google scholar: lookup
  30. Moder K. Alternatives to F-test in one way ANOVA in case of heterogeneity of variances (a simulation study). Psychol Test Assess Model 2010;52:343–353.
  31. Rasch D, Kubinger KD, Moder K. The two-sample t test: Pre-testing its assumptions does not pay off. Stat Pap 2011;52:219–231.
    doi: 10.1007/s00362-009-0224-xgoogle scholar: lookup
  32. IBM Corp. IBM SPSS Statistics for Windows. IBM Corp; Armonk, NY, USA: 2017. 25.0.
  33. Derrick B. The Partially Overlapping Samples t-test. Package ‘Partiallyoverlapping’ for RStudio. [(accessed on 4 May 2020)]; Available online: https://cran.r-project.org/web/packages/Partiallyoverlapping/index.html.
  34. RStudio Team. RStudio 1.1.463. RStudio: Integrated Development for R. RStudio, Inc.; Boston, MA, USA: 2016.
  35. Oliveira FG, Cook RF, Naves JHF, Oliveira CHS, Diniz RS, Freitas FJC, Lima JM, Sakamoto SM, Leite RC, Issel CJ, Reis JKP. Equine infectious anemia prevalence in feral donkeys from Northeast Brazil.. Prev Vet Med 2017 May 1;140:30-37.
  36. Hartley CA, Dynon KJ, Mekuria ZH, El-Hage CM, Holloway SA, Gilkerson JR. Equine gammaherpesviruses: perfect parasites?. Vet Microbiol 2013 Nov 29;167(1-2):86-92.
    doi: 10.1016/j.vetmic.2013.05.031pubmed: 23845734google scholar: lookup
  37. Barrandeguy ME, Carossino M. Infectious diseases in donkeys and mules: An overview and update. J Equine Vet Sci 2018;65:98–105.
  38. Edington N, Bridges CG, Huckle A. Experimental reactivation of equid herpesvirus 1 (EHV 1) following the administration of corticosteroids.. Equine Vet J 1985 Sep;17(5):369-72.
  39. Osterrieder K. Herpesvirales. In: MacLachlan NJ, Dubovi EJ, editors. Fenner’s Veterinary Virology. 5th ed. Academic Press; Boston, MA, USA: 2015. pp. 189–216.
  40. Rushton JO, Kolodziejek J, Nell B, Nowotny N. Prevalence of asinine herpesvirus type 5 (AsHV-5) infection in clinically normal Lipizzaner horses.. Vet J 2014 Apr;200(1):200-3.
    doi: 10.1016/j.tvjl.2013.10.035pubmed: 24709517google scholar: lookup
  41. Fortier G, van Erck E, Fortier C, Richard E, Pottier D, Pronost S, Miszczak F, Thiry E, Lekeux P. Herpesviruses in respiratory liquids of horses: putative implication in airway inflammation and association with cytological features.. Vet Microbiol 2009 Oct 20;139(1-2):34-41.
    doi: 10.1016/j.vetmic.2009.04.021pubmed: 19427139google scholar: lookup
  42. Goehring LS. Donkeys. In: Sprayberry KA, Robinson NE, editors. Robinson’s Current Therapy in Equine Medicine. 1st ed. Elsevier; Philadelphia, PA, USA: 2015. pp. 155–157.
  43. Rickards KJ, Thiemann AK. Respiratory Disorders of the Donkey.. Vet Clin North Am Equine Pract 2019 Dec;35(3):561-573.
    doi: 10.1016/j.cveq.2019.08.009pubmed: 31587971google scholar: lookup
  44. Laus F, Preziuso S, Spaterna A, Beribè F, Tesei B, Cuteri V. Clinical and epidemiological investigation of chronic upper respiratory diseases caused by beta-haemolytic Streptococci in horses.. Comp Immunol Microbiol Infect Dis 2007 Jul;30(4):247-60.
    doi: 10.1016/j.cimid.2007.02.003pubmed: 17433441google scholar: lookup
  45. Dong J, Gao N, Waller AS, Cook FR, Fan S, Yuan D, Du Y, Li F, Norimine J, Zhu W. An outbreak of strangles associated with a novel genotype of Streptococcus equi subspecies equi in donkeys in China during 2018.. Equine Vet J 2019 Nov;51(6):743-748.
    doi: 10.1111/evj.13114pubmed: 30900775google scholar: lookup

Citations

This article has been cited 6 times.
  1. Bazzano M, Bonfili L, Eleuteri AM, Serri E, Scollo C, Yaosen Y, Tesei B, Laus F. Assessment of serum amyloid A concentrations and biochemical profiles in lactating jennies and newborn Ragusano donkey foals around parturition and one month after foaling in Sicily.. Reprod Domest Anim 2022 Mar;57(3):262-268.
    doi: 10.1111/rda.14048pubmed: 34816505google scholar: lookup
  2. Scheurer L, Bachofen C, Hardmeier I, Lechmann J, Schoster A. Prevalence of Nasal Shedding of Equid Gammaherpesviruses in Healthy Swiss Horses.. Viruses 2021 Aug 25;13(9).
    doi: 10.3390/v13091686pubmed: 34578268google scholar: lookup
  3. Pinto M, Navas González FJ, Heleski C, McLean A. Judgement Bias in Miniature Donkeys: Conditioning Factors and Personality Links.. Animals (Basel) 2021 Sep 19;11(9).
    doi: 10.3390/ani11092737pubmed: 34573703google scholar: lookup
  4. Mira F, Canuti M, Di Bella S, Puleio R, Lavazza A, Lelli D, Vicari D, Purpari G, Cannella V, Chiaramonte G, Schirò G, Castronovo C, Guercio A. Detection and Molecular Characterization of Two Gammaherpesviruses from Pantesco Breed Donkeys during an Outbreak of Mild Respiratory Disease.. Viruses 2021 Aug 2;13(8).
    doi: 10.3390/v13081527pubmed: 34452391google scholar: lookup
  5. Perez-Ecija A, Buzon-Cuevas A, Aguilera-Aguilera R, Gonzalez-De Cara C, Mendoza Garcia FJ. Reference intervals of acute phase proteins in healthy Andalusian donkeys and response to experimentally induced endotoxemia.. J Vet Intern Med 2021 Jan;35(1):580-589.
    doi: 10.1111/jvim.16015pubmed: 33336874google scholar: lookup
  6. Goodrich EL, McLean A, Guarino C. A Pilot Serosurvey for Selected Pathogens in Feral Donkeys (Equus asinus).. Animals (Basel) 2020 Oct 2;10(10).
    doi: 10.3390/ani10101796pubmed: 33023217google scholar: lookup