Natural Association Between Bovine Leukemia Virus and Reproductive Infectious Diseases
DOI:
https://doi.org/10.22456/1679-9216.129251Abstract
Background: Enzootic bovine leukosis (EBL) is a widespread infectious disease caused by the bovine leukemia virus (BLV), which results in immune system dysfunction. The resulting immunosuppression may lead to an increased prevalence of other diseases. Dairy cows infected have altered immune function associated with decreased milk production and shortened lifespan and decreased immune response to immunization. BLV infection, however, is often asymptomatic, so any connection between subclinical infection and common reproductive diseases remains unknown. This study aimed to
describe the relationship between naturally occurring subclinical BLV and infectious reproductive diseases seroconversion in the field.
Materials, Methods & Results: The diseases investigated included Bovine viral diarrhoea (BVD), Bovine alfaherpesvirus 1 (BoHV-1), Bovine gammaherpesvirus 4 (BoHV-4), Chlamydiosis, Leptospirosis, Brucellosis and Neosporosis in dairy cattle. Six hundred fifty-five sera samples from the northern and south-central regions of Uruguay, from asymptomatic female Holstein and Holstein crosses without a history of vaccination against reproductive diseases were processed using reference diagnostic methods (Seronautalization, ELISA, MAT, Rose Bengal Plate test). The seroprevalence of BLV was 20.0%. Seroprevalence of reproductive diseases BVD, BoHV-1 and BoHV-4 were 99.3%, 41.2% and 27.3% of the populations, respectively, and the total seroprevalence of Leptospirosis, bovine Neospora caninum and Chlamydiosis
were 19.8%, 29.8% and 33.0% respectively. The results revealed positive associations between naturally contracted BLV and the presence of antibodies against BoHV-1 (P = 0.002), as well as between naturally contracted BLV and presence of
antibodies against Leptospira spp. (P = 0.028).
Discussion: BLV infection can impact innate and adaptive immune system cells and alter the proper functioning of uninfected cells. BLV infection may also induce changes in the complex balance of cytokine expression, cell proliferation,
and programmed cell death in T- and B-lymphocytes, which is critical for immune competence and effective response to
infectious challenges. The progression of BLV infection has a substantial effect on host defense mechanisms. Indeed, lowmagnitude serologic responses to a commercial foot-and-mouth disease vaccine and a J5 Escherichia coli vaccine have been observed. These results are supported by recent trial studies showing a reduced immune response to vaccination against BoHV-1 and Leptospira spp. in asymptomatic animals infected with BLV. These are 2 of the most prevalent infectious reproductive diseases in cattle worldwide, and our results provide evidence that a link between BLV and susceptibility to these diseases may exist. Although there is evidence of the co-occurrence of these diseases, it remains unknown whether there is a direct or indirect effect of BLV on infertility, embryonic loss, or abortion. Another possibility is that natural infection with these reproductive pathogens (BoHV-1, Leptospira, or others) promotes BLV expression, negatively affecting the farms where these pathogens are endemic. Considering the high seroprevalence of BLV in dairy herds in North and South America where the infection is endemic, it was explored BLV’s role as an immunosuppressant by quantifying its co-occurrence with diseases that affect reproductive performance in breeding herds. Future work should clarify the role of BLV and the co-occurring pathogens in causing infertility or abortions.
Keywords: BLV, herpesvirus, Infectious Bovine Rhinotracheitis (IBR), Leptospirosis, reproductive performance.
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References
Alton G., Jones L. & Pietz D.E. 1975. Serological methods In: Laboratory Techniques in Brucellosis. 2nd edn. Geneva:
World Health Organization, pp.64-124.
Anziliero D., Martins M. Weiss M., Monteiro F.L., Ataide C.F., Weiblen R. & Flores E.F. 2014. Resposta sorológica aos herpesvirus bovino tipos 1 e 5 e vírus da diarreia viral bovina induzida por vacinas comerciais. Ciência Rural. 45(1): 58-63. DOI: 10.1590/0103-8478cr20130167 DOI: https://doi.org/10.1590/0103-8478cr20130167
Bartlett P.C., Sordillo L.M., Byrem T.M., Norby B., Grooms D.L., Swenson C.L., Zalucha J. & Erskine R.J. 2014. Options for the control of bovine leukemia virus in dairy cattle. Journal of the American Veterinary Medical Association. 244(8): 914-922. DOI: 10.2460/javma.244.8.914 DOI: https://doi.org/10.2460/javma.244.8.914
Erskine R.J., Bartlett P.C., Sabo K.M. &Sordillo L.M. 2011. Bovine leukemia virus infection in dairy cattle: Effect on serological response to immunization against J5 Escherichia coli Bacterin. Veterinary Medicine International. 2011: 915747. DOI: 10.4061/2011/915747 DOI: https://doi.org/10.4061/2011/915747
Frie M.C., Sporer K.R., Wallace J.C., Maes R.K., Sordillo L.M., Bartlett P.C. & Coussens P.M. 2016. Reduced humoral immunity and atypical cell-mediated immunity in response to vaccination in cows naturally infected with bovine leukemia virus. Veterinary Immunology and Immunopathology. 182: 125-135. DOI 10.1016/j.vetimm.2016.10.013 DOI: https://doi.org/10.1016/j.vetimm.2016.10.013
Kabeya H., Ohashi K. & Onuma M. 2001. Host Immune Responses in the Course of Bovine Leukemia Virus Infection. DOI: https://doi.org/10.1292/jvms.63.703
Journal of Veterinary Medical Science. 63(7): 703-708.
Meirom R., Moss S. & Brenner J. 1997. Bovine leukemia virus-gp51 antigen expression is associated with CD5 and IgM markers on infected lymphocytes. Veterinary Immunology and Immunopathology. 59(1-2): 113-119. DOI: 10.1292/jvms.63.703 DOI: https://doi.org/10.1016/S0165-2427(97)00056-1
Puentes R., De Brun L., Algorta A., Álvarez J.P., Sacco G., Oliveira M. & Llambi S. 2016. Horizontal Transmission
Dynamics of Bovine Leukemia Virus (Blv) and Negative Effect on Reproductive Performance in Naturally Infected
Holstein Heifers. Science And Animal Health. 4(3): 294. DOI:10.15210/SAH.V4I3.8295 DOI: https://doi.org/10.15210/sah.v4i3.8295
Puentes R., De Brun L., Algorta A., Da Silva V., Mansilla F., Sacco G., Llambí S. & Capozzo A.V. 2016. Evaluation of serological response to foot-and-mouth disease vaccination in BLV infected cows. BMC Veterinary Research. 12(1): 196. DOI: 10.1186/s12917-016-0749-x DOI: https://doi.org/10.1186/s12917-016-0749-x
Pyeon D., Diaz F.J. & Splitter G.A. 2000. Prostaglandin E2 Increases Bovine Leukemia Virustax and pol mRNA Levels via Cyclooxygenase 2: Regulation by Interleukin-2, Interleukin-10, and Bovine Leukemia Virus. Journal of Virology. 74(12): 5740-5745. DOI: 10.1128/jvi.74.12.5740-5745.2000 DOI: https://doi.org/10.1128/JVI.74.12.5740-5745.2000
Vanleeuwen J.A., Haddad J.P., Dohoo I.R., Keefe G.P., Tiwari A. & Tremblay R. 2010. Associations between reproductive performance and seropositivity for bovine leukemia virus, bovine viral-diarrhea virus, Mycobacterium avium subspecies paratuberculosis, and Neospora caninum in Canadian dairy cows. Preventive Veterinary Medicine. 94(1-2): 54-64. DOI: 10.1016/j.prevetmed.2009.11.012 DOI: https://doi.org/10.1016/j.prevetmed.2009.11.012
World Organization for Animal Health (OIE). 2018. Diarrea viral bovina. In: Manual of Diagnostic Tests and Vaccines
for Terrestrial Animals. Chap. 2.4.8. Paris: OIE, pp.1-22. https://www.woah.org/fileadmin/Home/esp/Health_standards/
tahm/3.04.07_BVD.pdf
World Organization for Animal Health (OIE). 2021. Leptospirosis: Manual of Diagnostic Tests and Vaccines for Terrestrial Animals. Chap. 3.1.12 Paris: OIE, pp.1-14. https://www.woah.org/fileadmin/Home/esp/Health_standards/
tahm/3.01.12_Leptospirosis.pdf
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