Cerebral Babesiosis: Transplacental Infection by Babesia bovis in a Calf

Authors

DOI:

https://doi.org/10.22456/1679-9216.132031

Keywords:

ENGLISH

Abstract

Background: Cerebral babesiosis is a significant cause of mortality in calves, as it can be transmitted through the placenta during gestation and presents with hemolytic and/or neurological symptoms. However, the role of this agent as a cause of abortion is still poorly understood. In endemic areas, the disease primarily affects cattle between the ages of 1 and 12 months and occasionally neonates. This study aimed to describe the epidemiological, clinical, anatomopathological, molecular, and differential diagnostic aspects of a naturally infected newborn Nelore calf.

Case: A newborn Nelore calf from Mato Grosso do Sul was discovered dead 1 h after birth and was subjected to necropsy, cytopathological and histopathological examinations by the Pathological Anatomy Laboratory (LAP) at the Federal University of Mato Grosso do Sul (UFMS), as well as complementary in situ hybridization (ISH) and polymerase chain reaction (PCR) tests. Hemoparasite research yielded negative results in all cows within the herd, including the mother of the necropsied calf, which were all clinically healthy. The clinical and hematological examination results of the cows were normal. At necropsy, the calf appeared thin, with a moderately jaundiced carcass and multiple petechiae on the pleural and pericardial surfaces. The lung was inflated until the opening of the thoracic cavity and floated when immersed in formalin, indicating that the calf was born alive and breathing. The spleen and liver were moderately enlarged with rounded edges, and the liver appeared slightly orange. The gray matter of the brain was significantly cherry red. Histologically, the central nervous system capillaries were slightly congested, with numerous punctiform and basophilic structures observed in the erythrocytes obliterating these vessels, either alone or in pairs, measuring 1 to 2 µm in diameter, which were morphologically consistent with Babesia bovis. In the cytological evaluation of the imprint slides of the brain cortex, blood capillaries filled with erythrocytes parasitized by solitary or paired punctiform basophilic structures, approximately 1 μm in diameter, morphologically compatible with B. bovis, were detected. Positive labeling for Babesia spp. was observed in the ISH examination, while the PCR identified B. bovis and B. bigemina in were identified in the brain fragments. The macroscopic findings, including pale or icteric mucous membranes, yellow and enlarged liver, and splenomegaly observed in cases of anaplasmosis, may be confused with those of cerebral babesiosis when the latter does not present with hemoglobinuria. Brain congestion indicates B. bovis infection but does not rule out co-infection with Anaplasma marginale in this case, although this rickettsia was not identified in the blood smear.

Discussion: The diagnosis of Babesia bovis infection was based on epidemiological and histological data, as well as the identification of the protozoan in spleen and brain smears and through PCR and ISH exams, which are highly sensitive and can aid in the diagnosis of B. bovis in cases of perinatal deaths. In situ hybridization is effective in cases where the material has autolysis, as the technique allows the genetic material of the agent to be associated with the lesion, even with tissue alterations caused by fixation in formalin. The findings of this study highlight the importance of considering this disease as a differential diagnosis among those that cause abortions or neonatal losses in cattle and emphasize the importance of conducting anatomopathological exams for definitive diagnosis.

Keywords: Cerebral babesiosis, Babesia bovis, pathology, transplacental transmission, intrauterine infection, in situ hybridization.

Downloads

Download data is not yet available.

References

Agrawal V., Jayraw A., Shakya M., Jatav G., Jamra N., Singh N. & Jain R. 2020. Transplacental transmission of Babesiosis in six week old Holestein Freisien Calf. Journal of Entomology and Zoology Studies. 8(5): 04-06. DOI: 10.22271/j.ento.2020.v8.i5a.7500 DOI: https://doi.org/10.22271/j.ento.2020.v8.i5a.7500

Anderson M.L. 2007. Infectious causes of bovine abortion during mid- to late-gestation. Theriogenology. 68(3): 474-486. DOI: 10.1016/j.theriogenology.2007.04.001 DOI: https://doi.org/10.1016/j.theriogenology.2007.04.001

Atif F.A., Hussain K., Qamar M.F., Sajid M.S., Zaman M.A. & Rafiq M.K. 2021. First Report on Transplacental Transmission of Anaplasma marginale in Neonatal Dairy Calves from District Jhang, Punjab, Pakistan. International Journal of Agriculture and Biology. 25(03): 541-546. DOI: 10.17957/IJAB/15.1699 DOI: https://doi.org/10.17957/IJAB/15.1699

Bastos C.V. 2020. Clinical description of transplacental anaplasmosis and the importance of congenital transmission in the epidemiology of cattle tick fever. Research Square. 11p. DOI:10.21203/rs.3.rs-65071/v1

Bock R., Jackson L., De Vos A. & Jorgensen W. 2004. Babesiosis of cattle. Parasitology. 129(S1): S247-S269. DOI: 10.1017/S0031182004005190 DOI: https://doi.org/10.1017/S0031182004005190

Buling A., Criado-Fornelio A., Asenzo G., Benitez D., Barba-Carretero J.C. & Florin-Christensen M. 2007. A quantitative PCR assay for the detection and quantification of Babesia bovis and B. bigemina. Veterinary Parasitology. 147(1-2): 16-25. DOI:10.1016/j.vetpar.2007.03.031 DOI: https://doi.org/10.1016/j.vetpar.2007.03.031

Buxton D., McAllister M.M. & Dubey J.P. 2002. The comparative pathogenesis of neosporosis. Trends in Parasitology. 18(12): 546-552. DOI: 10.1016/s1471-4922(02)02414-5 DOI: https://doi.org/10.1016/S1471-4922(02)02414-5

Chauvin A., Moreau E., Bonnet S., Plantard O. & Malandrin L. 2009. Babesia and its hosts: adaptation to long-lasting interactions as a way to achieve efficient transmission. Veterinary Research. 40(2): 37. DOI: 10.1051/vetres/2009020 DOI: https://doi.org/10.1051/vetres/2009020

Costa S.C.L., Magalhães V.C.S., Oliveira U.V., Carvalho F.S., Almeida C.P., Machado R.Z. & Munhoz A.D. 2016. Transplacental transmission of bovine tick-borne pathogens: Frequency, co-infections and fatal neonatal anaplasmosis in a region of enzootic stability in the northeast of Brazil. Ticks and Tick-Borne Diseases. 7(2): 270-275. DOI: http://dx.doi.org/10.1016/j.ttbdis.2015.11.001 DOI: https://doi.org/10.1016/j.ttbdis.2015.11.001

Farias N.A. 2023. Tristeza Parasitária Bovina. In: Riet-Correa F., Schild A.L., Lemos R.A.A., Borges J.R.J., Mendonça F.S. & Machado M. (Eds). Doenças de Ruminantes e Equídeos. 4.ed. São Paulo: MedVet, pp.563-570.

Georgieva D., Prelezov P.N. & Koinarski V.T. 2006. Neospora caninum and neosporosis in animals a review. Bulgarian Journal of Veterinary Medicine. 9(1): 1-26.

Grau H.E.G., Cunha Filho N.A., Pappen F.G. & Farias N.A.R. 2013. Transplacental transmission of Anaplasma marginale in beef cattle chronically infected in southern Brazil. Revista Brasileira de Parasitologia Veterinária. 22(2): 189-193. DOI:10.1590/S1984-29612013000200038 DOI: https://doi.org/10.1590/S1984-29612013000200038

Grooms D.L. 2006. Reproductive losses caused by bovine viral diarrhea virus and leptospirosis. Theriogenology. 66(3): 624-628. DOI:10.1016/j.theriogenology.2006.04.016 DOI: https://doi.org/10.1016/j.theriogenology.2006.04.016

Henker L.C., Lorenzett M.P., Fagundes-Moreira R., Dalto A.G.C., Sonne L., Driemeier D., Soares J.F. & Pavarini S.P. 2020. Bovine abortion, stillbirth and neonatal death associated with Babesia bovis and Anaplasma sp. infections in southern Brazil. Ticks and Tick-Borne Diseases. 11(4): 101443. DOI:10.1016/j.ttbdis.2020.101443 DOI: https://doi.org/10.1016/j.ttbdis.2020.101443

Henker L.C., Lorenzett M.P. & Pavarini S.P. 2021. Bovine congenital babesiosis. Brazilian Journal of Veterinary Pathology. 14(1): 70-74. DOI: 10.24070/bjvp.1983-0246.v14i1p70-74 DOI: https://doi.org/10.24070/bjvp.1983-0246.v14i1p70-74

Hülskötter K., Pfankuche V.M., van Dyck L., Höltershinken M., Springer A., Lienhart F., Ermel S., Rehage J., Hoedemarker M., Strube C., Hirzmann J., Bauer C., Baumgärtner W., Lehmbecker A. & Wohlsein P. 2020. Bovine Babesiosis Diagnosed in Formalin-Fixed, Paraffin-Embedded Tissues by Using In Situ Hybridization. Veterinary Pathology. 57(6): 812-820. DOI: 10.1177/0300985820948816 DOI: https://doi.org/10.1177/0300985820948816

Kessler R.H. 2001. Considerações sobre a transmissão de Anaplasma marginale. Pesquisa Veterinária Brasileira. 21(4): 177-179. DOI:10.1590/S0100-736X2001000400009 DOI: https://doi.org/10.1590/S0100-736X2001000400009

Leblanc S. 2010. Health in the transition period and reproductive performance. Western Canadian Dairy Seminar. 22: 97-110.

Mee J.F. 2020. Investigation of bovine abortion and stillbirth/perinatal mortality - similar diagnostic challenges, different approaches. Irish Veterinary Journal. 73(1): 20. DOI:10.1186/s13620-020-00172-0 DOI: https://doi.org/10.1186/s13620-020-00172-0

Orlando D.R., Costa R.C., Abreu R.V.S., Abreu C.C., Nakagaki K.Y.R., Wouters A.T.B., Raymundo D.L. & Varaschin M.S. 2014. Caracterização morfológica e imuno-histoquímica de lesões em casos de aborto bovino bacteriano e viral no sul de Minas Gerais. Pesquisa Veterinária Brasileira. 34(10): 974-980. DOI: 10.1590/S0100-736X2014001000009 DOI: https://doi.org/10.1590/S0100-736X2014001000009

Pupin R.C., Guizelini C.C., Lemos R.A.A., Martins T.B., Borges F.A., Borges D.G.L. & Gomes D.C. 2019. Retrospective study of epidemiological, clinical and pathological findings of bovine babesiosis in Mato Grosso do Sul, Brazil (1995-2017). Ticks and Tick-Borne Diseases. 10(1): 36-42. DOI: 10.1016/j.ttbdis.2018.08.015 DOI: https://doi.org/10.1016/j.ttbdis.2018.08.015

Reichel M.P., Wahl L.C. & Hill F.I. 2018. Review of Diagnostic Procedures and Approaches to Infectious Causes of Reproductive Failures of Cattle in Australia and New Zealand. Frontiers in Veterinary Science. 5: 222. DOI: 10.3389/fvets.2018.00222 DOI: https://doi.org/10.3389/fvets.2018.00222

Reynolds L.P., Borowicz P.P., Vonnahme K.A., Johnson M.L., Grazul-Bilska A.T., Redmer D.A & Caton J.S. 2005. Placental angiogenesis in sheep models of compromised pregnancy. The Journal of Physiology. 565(1): 43-58. DOI: 10.1113/jphysiol.2004.081745 DOI: https://doi.org/10.1113/jphysiol.2004.081745

Schild A.L., Ruas J.L., Farias N.A., Grecco F.B. & Soares M.P. 2008. Aspectos epidemiológicos de um surto de babesiose cerebral em bovinos em zona livre de carrapato. Ciência Rural. 38(9): 2646-2649. DOI:10.1590/S0103-84782008005000010 DOI: https://doi.org/10.1590/S0103-84782008005000010

Silva J.B. & Fonseca A.H. 2014. Risk factors for anaplasmosis in dairy cows during the peripartum. Tropical Animal Health and Production 46: 461-465. DOI: 10.1007/s11250-013-0514-0 DOI: https://doi.org/10.1007/s11250-013-0514-0

Spickler A.R. 2018. Bovine Babesiosis. Iastate, 10p. Disponível em: <http://www.cfsph.iastate.edu/DiseaseInfo/ factsheets.php.>

Trindade H.I., Almeida K.S. & Freitas F.L.C. 2011. Tristeza parasitária bovina – revisão de literatura. Revista Científica Eletrônica de Medicina Veterinária. 16: 1-21.

Wooding F.B.P. & Burton G. 2008. Synepitheliochorial Placentation: Ruminants (Ewe and Cow). In: Comparative Placentation: Structures, Functions and Evolution. Berlin: Springer, pp.133-138. DOI: https://doi.org/10.1007/978-3-540-78797-6_6

Yeruham I., Avidar Y., Aroch I. & Hadani A. 2003. Intra-uterine Infection with Babesia bovis in a 2-day-old Calf. Journal of Veterinary Medicine Series B. 50(2): 60-62. DOI: 10.1046/j.1439-0450.2003.00597.x. DOI: https://doi.org/10.1046/j.1439-0450.2003.00597.x

Zaugg J.L. & Watson J.L. 2015. Diseases of the hematopoietic and hemolymphatic systems. In: Smith B.P. (Ed). Large Animal Internal Medicine. 5th edn. Saint louis: Elsevier, pp.1056-1058.

Additional Files

Published

2023-11-20

How to Cite

Caldas Bonato, G., Lobeiro de Souza, L., Xavier e Silva, T., Fernandes da Fonseca, H. C., Zhang, J., Nascimento Ramos, C. A., Castro Guizelini, C., & Amaral de Lemos, R. A. (2023). Cerebral Babesiosis: Transplacental Infection by Babesia bovis in a Calf. Acta Scientiae Veterinariae, 51. https://doi.org/10.22456/1679-9216.132031