Campylobacter fetus in Abomasal Fluid from Spontaneously Aborted Bovine and Ovine Fetuses

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DOI:

https://doi.org/10.22456/1679-9216.117643

Abstract

Background: Pregnancy losses are a major concern in livestock industry due to their economic impact on producers. Campylobacter fetus subspecies fetus (Cff) and C. fetus subspecies venerealis (Cfv) are directly related to reproductive failures in ruminants. Cff colonizes the gastrointestinal tract of a wide range of hosts leading to abortion, while Cfv is restricted to genital tract being generally associated to infertility in bovine. Considering the great economic losses related to campylobacteriosis in cattle and ovine herds, this study aims to investigate the occurrence of C. fetus, considering Cff and Cfv subspecies, in bovine and ovine spontaneously aborted fetuses in state of Rio Grande do Sul, Brazil.

Materials, Methods & Results: In this study, samples of abomasal fluid collected from 30 spontaneously aborted bovine (n = 18) and ovine (n = 12) fetuses were investigated for the detection of Campylobacter fetus throughout conventional PCR. Positive fetuses for C. fetus presence were further analyzed by molecular assays for Cff and Cfv detection, in order to determine subspecies identification. When available, samples of the main organs of the thoracic and abdominal cavities, as well as the brain, skeletal muscle, eyelid, skin, and placenta were collected for further histopathological analyses and bacterial culture, aiming to assess the presence of infection lesions and pathogens in those sites, respectively. Additionally, RT-qPCR assays were also performed for the detection of ruminant pestivirus, in order to detect bovine viral diarrhea cases. Throughout the present methodology, C. fetus was detected in the abomasal fluid samples of 2 bovine fetuses, being both identified as Cfv subspecies by PCR. Histopathological analyses demonstrated that macroscopic and microscopic changes found in the Cfv-positive animals were not either specific or directly related to Campylobacter infections. Moreover, no significant bacterial growth was observed in microbiological culture from the collected tissues, and both fetuses were negative for ruminant pestivirus. Differently, there was no detection of C. fetus in any of the analyzed ovine fetuses.

DiscussionConsidering that abortion diagnosis rates reported in cattle and sheep industry are highly variable among the published studies, and that abortion diagnoses are commonly inconclusive due to difficulties in sampling methodology and inadequate identification of the pathogen involved, it is important to investigate the etiological causes of abortion the herds for better understanding the causes of pregnancy issues and monitoring their occurrence. In addition, the absence of pathognomonic lesions in the tissues investigated in the histopathological analyses observed in this study strongly suggests that well-known etiological agents commonly associated to abortion, such as Leptospira spp., Toxoplasma spp., Chlamydia spp. and Neospora caninum, are unlikely to be the cause of infection of the analyzed fetuses. Taking this into account, the presence of C. fetus in the abomasal fluid samples from two bovine fetuses demonstrated in the present study suggests the possible association of Cfv not only with infertility, but also with cases of bovine abortion, highlighting the importance of investigating unusual causal agents of abortions in sheep and cattle. Overall, an adequate diagnosis is essential for establishing better prevention strategies to avoid the circulation of abortion-related infectious agents in the herds.

Keywords: campylobacteriosis, molecular diagnosis, venereal disease, abortion, reproductive disease.

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References

Abril C., Vilei E.M., Brodard I., Burnens A., Frey J. & Miserez R. 2007. Discovery of insertion element ISCfe1: a new tool for Campylobacter fetus subspecies differentiation. Clinical Microbiology and Infection. 13(10): 993-1000. DOI: 10.1111/j.1469-0691.2007.01787.x

Barkallah M., Gharbi Y., Hassena A.B., Slima A.B., Mallek Z., Gautier M., Greub G., Gdoura R. & Fendri I. 2014. Survey of infectious etiologies of bovine abortion during mid- to late gestation in dairy herds. PloS One. 9(3): e91549. DOI: 10.1371/journal.pone.0091549

Campero C.M., Anderson M.L., Walker R.L., Blanchard P.C., Barbano L., Chiu P., Martínez A., Combessies G., Bardon J.C. & Cordeviola J. 2005. Immunohistochemical identification of Campylobacter fetus in natural cases of bovine and ovine abortions. Journal of Veterinary Medicine. B, Infectious Diseases and Veterinary Public Health. 52(3): 138-141. DOI: 10.1111/j.1439-0450.2005.00834.x

Clothier K. & Anderson M. 2016. Evaluation of bovine abortion cases and tissue suitability for identification of infectious agents in California diagnostic laboratory cases from 2007 to 2012. Theriogenology. 85(5): 933-938. DOI: 10.1016/j.theriogenology.2015.11.001

De Carli S., Saggin B., Dias M.E., Lopes C.E., Dalto A.G.C., Rolim V.M., Zucco R., Pastre G., Borges J.B. & Siqueira F.M. 2020. Frozen bovine preputial mucus as a suitable sample for the direct molecular diagnosis of Campylobacter fetus subsp. venerealis. Journal of Microbiological Methods. 179: 106101. DOI: 10.1016/j.mimet.2020.106101

Dorsch M.A., Casaux M.L., Calleros L., Aráoz V., Caffarena R.D., Monesiglio C., Barcellos M., Da Silva Silveira C., Perdomo Y., Banchero G., Uzal F.A., Fraga M. & Giannitti F. 2021. Placentitis and abortion caused by a multidrug resistant strain of Campylobacter fetus subspecies fetus in a sheep in Uruguay. Revista Argentina de Microbiologia. DOI: 10.1016/j.ram.2021.02.005

Fiorentino M.A., Stazionati M., Hecker Y., Morsella C., Cantón G, Harry H.R., Velilla A.V., Vaulet L.G., Fermepin M.R. & Bedotti D.O. 2017. Campylobacter fetus subsp. fetus ovine abortion outbreak in Argentina. Revista Electrónica Veterinaria. 18(11): 1-11.

Givens M.D. & Marley M.S.D. 2008. Infectious causes of embryonic and fetal mortality. Theriogenology. 70(3): 270-285. DOI: 10.1016/j.theriogenology.2008.04.018

Gressler L.T., Kirinus J.K., Machado G., Libardoni F. & Vargas A.C. 2012. Campylobacter fetus subespécie fetus: abortamento e natimortalidade em ovinos. Ciência Rural. 42: 697-700. DOI: 10.1590/S0103-84782012000400020

Hosseinzadeh S., Kafi M. & Pour-Teimouri M. 2013. PCR detection of Campylobacter fetus subspecies venerealis in smegma samples collected from dairy cattle in Fars, Iran. Veterinary Research Forum. 4(4): 227-231.

Hum S., Quinn K., Brunner J. & On S.L.W. 1997. Evaluation of a PCR assay for identification and differentiation of Campylobacter fetus subspecies. Australian Veterinary Journal. 75: 827-831. DOI: 10.1111/j.1751-0813.1997.tb15665.x

Kirkbride C.A. 1993. Diagnoses in 1,784 ovine abortions and stillbirths. Journal of Veterinary Diagnostic Investigation. 5(3): 398-402. DOI: 10.1177/104063879300500316

Lindsay D.S. & Dubey J.P. 2020. Neosporosis, Toxoplasmosis, and Sarcocystosis in Ruminants: An Update. The Veterinary Clinics of North America. Food Animal Practice. 36: 205-222. DOI: 10.1016/j.cvfa.2019.11.004

Lúcio E.C, Borges J.M., Batista Filho A.F.B., Gouveia G.V., Costa M.M., Mota R.A. & Pinheiro Junior J.W. 2018. Ocorrência de ovinos portadores da infecção por Campylobacter spp. no estado de Pernambuco. Pesquisa Veterinária Brasileira. 38(2): 262-270. DOI: 10.1590/1678-5150-PVB-4895

Macías-Rioseco M., Silveira C., Fraga M., Casaux L., Cabrera A. & Francia M.E. 2020. Causes of abortion in dairy cows in Uruguay. Pesquisa Veterinária Brasileira. 40(5): 325-332. DOI: 10.1590/1678-5150-PVB-6550

Molina L.L., Angón E., García A., Caballero-Villalobos J., Giorgis A.O., Moralejo R.H. & Perea J. 2018. A retrospective epidemiological analysis of shared risk factors for bovine trichomoniasis and bovine genital campylobacteriosis in La Pampa province (Argentina). Preventive Veterinary Medicine. 161: 109-114. DOI: 10.1016/j.prevetmed.2018.10.022

Morrell E.L., Barbeito C.G., Odeón C.A., Gimeno E.J. & Campero C.M. 2011. Histopathological, immunohistochemical, lectinhistochemical and molecular findings in spontaneous bovine abortions by Campylobacter fetus. Reproduction in Domestic Animals. 46(2): 309-315. DOI: 10.1111/j.1439-0531.2010.01668.x

Morrell E.L., Campero C.M., Cantón G.J., Odeón A.C., Moore D.P., Odriozola E., Paolicchi F. & Fiorentino M.A. 2019. Current trends in bovine abortion in Argentina. Pesquisa Veterinária Brasileira. 39(1): 12-19. DOI: 10.1590/1678-5150-PVB-5668

Sanhueza J.M., Heuer C., Jackson R., Hughes P., Anderson P., Kelly K. & Walker G. 2014. Pregnancy rates of beef cattle are not affected by Campylobacter fetus subsp. venerealis real-time PCR-positive breeding sires in New Zealand. New Zealand Veterinary Journal. 62(5): 237-243. DOI: 10.1080/00480169.2014.898202

Silveira C.S., Fraga M., Giannitti F., Macías-Rioseco M. & Riet-Correa F. 2018. Diagnosis of bovine genital campylobacteriosis in South America. Frontiers in Veterinary Science. 5: 321. DOI: 10.3389/fvets.2018.00321

Skirrow M.B. 1994. Diseases due to Campylobacter, Helicobacter and related bacteria. Journal of Comparative Pathology. 111(2): 113-149. DOI: 10.1016/s0021-9975(05)80046-5.

Uaboi-Egbenni P.O., Bessong P.O., Samie A. & Obi C.L. 2010. Campylobacteriosis in sheep in farm settlements in the Vhembe district of South Africa. African Journal of Microbiology Research. 4(20): 2109-2117. DOI: 10.5897/AJMR.9000139

van Bergen M.A., Dingle K.E., Maiden M.C., Newell D.G., van der Graaf-van Bloois L., van Putten J.P. & Wagenaar J.A. 2005. Clonal nature of Campylobacter fetus as defined by multilocus sequence typing. Journal of Clinical Microbiology. 43(12): 5888-5898. DOI: 10.1128/JCM.43.12.5888-5898.2005

van der Graaf-van Bloois L., van Bergen M.A.P., van der Wal F.J., Boer A.G., Duim B., Schmidt T. & Wagenaar J.A. 2013. Evaluation of molecular assays for identification Campylobacter fetus species and subspecies and development of a C. fetus specific real-time PCR assay. Journal of Microbiological Methods. 95(1): 93-97. DOI: DOI: 10.1016/j.mimet.2013.06.005

Wagenaar J.A., van Bergen M.A.P., Blaser M.J., Tauxe R.V., Newell D.G. & van Putten J.P.M. 2014. Campylobacter fetus infections in humans: exposure and disease. Clinical Infectious Diseases. 58(11): 1579-1586. DOI: 10.1093/cid/ciu085

Weber M.N., Mósena A.C., Simões S.V., Almeida L.L., Pessoa C.R., Budaszewski R.F., Silva T.R., Ridpath J.F., Riet-Correa F., Driemeier D. & Canal C.W. 2016. Clinical Presentation Resembling Mucosal Disease Associated with 'HoBi'-like Pestivirus in a Field Outbreak. Transboundary and Emerging Diseases. 63(1): 92-100. DOI: 10.1111/tbed.12223

Williams E.J. & O’Donovan J. 2009. Ovine abortion: an overview. Irish Veterinary Journal. 62(5): 342-346.

Ziech R.E., Machado G., Kirinus J.K., Libardoni F., Kessler J.D., Pötter L. & Vargas A.C. 2014. Campylobacter fetus in cattle from Rio Grande do Sul State, Brazil. Ciência Rural. 44(1): 141-146. DOI: 10.1590/S0103-84782014000100023

Published

2021-01-01

How to Cite

Merker Breyer, G., Dias, M. E., Henker, L. C., Lorenzett, M. P., Ferreira Baumbach, L., Canal, C. W., Petinatti Pavarini, S., & Maboni Siqueira, F. (2021). Campylobacter fetus in Abomasal Fluid from Spontaneously Aborted Bovine and Ovine Fetuses. Acta Scientiae Veterinariae, 49. https://doi.org/10.22456/1679-9216.117643

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