Seroprevalence and risk factors of the parainfluenza virus (VPI-3) in cattle from Colombia

Authors

  • M. A. Fernández Universidad Pedagógica y Tecnológica de Colombia, Grupo de Investigación en Medicina Veterinaria y Zootecnia, Boyacá, Colombia.
  • D. M. Bulla Universidad Pedagógica y Tecnológica de Colombia, Grupo de Investigación en Medicina Veterinaria y Zootecnia, Boyacá, Colombia.
  • A. M. Díaz Universidad Pedagógica y Tecnológica de Colombia, Grupo de Investigación en Medicina Veterinaria y Zootecnia, Boyacá, Colombia.
  • M. O. Pulido Universidad Pedagógica y Tecnológica de Colombia, Grupo de Investigación en Medicina Veterinaria y Zootecnia, Boyacá, Colombia.

DOI:

https://doi.org/10.30972/vet.3124737

Keywords:

bovine, parainfluenza virus type, enzyme-linked immune-sorbent assay, prevalence, Colombia

Abstract

Bovine parainfluenza virus type 3 (IPV-3) is considered one of the most important pathogens associated with bovine respiratory diseases. It is considered as a part of the bovine respiratory complex, since it is a multifactorial disease associated with the manifestation of different etiological agents that cause pneumonia or upper respiratory tract infections in all cattle ages. It is widely distributed worldwide and is characterized by causing symptoms such as severe bronchopneumonia, cough, anorexia, pyrexia, nasal and eye secretions, dyspnea and sometimes diarrhea. The objective was to determine the seroprevalence and risk factors of parainfluenzavirus (IPV-3) in cattle from the Oicatá (Boyacá, Colombia). Blood samples were collected from 360 bovine females, which were processed in the Veterinary Parasitology Laboratory of the Colombia University through the implementation of the ELISA Primacheck (Agrolabo, Spain). The seroprevalence of IPV-3 in the municipality of Oicatá was 31%, however, no statistical association was found with the breed and age of the individuals evaluated. The seroprevalence of the disease is high in this municipality, which directly affects the productivity and profitability of productions, for this reason it is necessary to implement control and prevention plans for this pathology.

Downloads

Download data is not yet available.

References

Alcaldía Municipal de Oicatá. 2019. Nuestro municipio [Internet], disponible en http://www.oicata-boyaca.gov.co.

Ali H, Ali AA, Atta MS, Cepica A. 2012. Common, emerging, vector-borne and infrequent abortogenic virus infections of cattle. Transbound Emerg Dis 59: 11-25.

Andrade OS, Chicaiza G. 2015. Prevalencia de anticuerpos a parainfluenza bovina (PI-3) en ganaderías lecheras de Cuenca, Ecuador. Maskana 8: 209-210.

Angen O et al. 2009. Respiratory disease in calves: microbiological investigations on trans-tracheally aspirated bronchoalveolar fluid and acute phase protein response. Vet Microbiol 137: 165-171.

Betancur HC, Orrego UA, González TM. 2010. Estudio seroepidemiológico del virus de parainfluenza-3 en bovinos de Montería (Colombia) con trastornos reproductivos. Rev Med Vet 20: 63-70.

Cabello RK, Quispe CR, Rivera GH. 2006. Frecuencia de los virus parainfluenza-3, respiratorio sincitial y diarrea viral bovina en un rebaño mixto de una comunidad campesina de Cusco. Rev Investig Vet Peru 17: 167-172.

Czuprynski CJ et al. 2004. Complexities of the pathogenesis of Mannheimia haemolytica and Haemophilus somnus infections: challenges and potential opportunities for prevention? Anim Heal Res Rev 5: 277-282.

Ellis JA. 2010. Bovine parainfluenza-3 virus. In: Veterinary Clinics of North America - Food Animal Practice, Elsevier Ltd, p. 575-593.

Gálvis GT, Bautista AH, Vásquez MC. 2016. Prevalencia de anticuerpos contra diarrea viral bovina, virus sincitial bovino, rinotraqueitis infecciosa bovina, leucosis bovina, neospora caninum, parainfluenza bovina (PI3) y paratuberculosis, en ganadería bovina de fincas ubicadas en Aguachica. Rev Fac Ciencias Salud 3: 36.

Givens DM, Marley MS. 2008. Infectious causes of embryonic and fetal mortality. Theriogenology 70: 270-285.

ICA: Censo Pecuario Nacional. 2019. Disponible en:

https://www.ica.gov.co/areas/ pecuaria/servicios/epidemiologia-veterinaria/censos-2016/censo-2018.

Karle BM et al. 2019. Regional management practices and

prevalence of bovine respiratory disease in California’s preweaned dairy calves. J Dairy Sci 102: 7583-7596.

Karron RA, Collins PL. 2013. Parainfluenza viruses. In: Fields Virology, Knipe DM & Howley PM editors, 6th ed., Philadelphia, p. 996-1023.

Krzysiak MK et al. 2018. Seroprevalence and risk factors

for selected respiratory and reproductive tract pathogen

exposure in european bison (Bison bonasus) in Poland. Vet Microbiol 215: 57-65.

Lv L, Zhao G, Wang H, He H. 2019. Cholesterol 25-hydroxylase inhibits bovine parainfluenza virus type 3 replication through enzyme activity-dependent and independent ways. Vet Microbiol 239: 108456.

Maidana SS et al. 2012. Isolation and characterization of

bovine parainfluenza virus type 3 from water buffaloes (Bubalus bubalis) in Argentina. Vet Res 8: 83-91.

Murray GM et al. 2017. Evolving views on bovine respiratory disease: An appraisal of selected key pathogens. Vet J 217: 95-102.

Murray GM et al. 2016. Pathogens, patterns of pneumonia, and epidemiologic risk factors associated with respiratory disease in recently weaned cattle in Ireland. J Vet Diagn Investig 29: 20-34.

Neill JD, Ridpath JF, Valayudhan BT. 2015. Identification and genome characterization of genotype B and genotype C bovine parainfluenza type 3 viruses isolated in the United States. BMC Vet Res 11: 1-6.

Pansri P et al. 2020. Evaluation of novel multiplex qPCR assays for diagnosis of pathogens associated with the bovine respiratory disease. Vet J 256: 105425.

Pourhoseingholi MA, Vahedi M, Rahimzadeh M. 2013. Sample size calculation in medical studies. Gastroenterol Hepatol from Bed to Bench 6: 14-17.

Sobhy NM et al. 2017. Surveillance, isolation and complete genome sequence of bovine parainfluenza virus type 3 in Egyptian cattle. Int J Vet Sci Med 5:8-13.

Solís JJ, Segura JC, Aguilar F, Segura VM. 2007. Detection of antibodies and risk factors for infection with bovine respiratory syncytial virus and parainfluenza virus-3 in beef cattle of Yucatan, Mexico. Prev Vet Med 82: 102-110.

Sudaryatma PE et al. 2018. Bovine respiratory syncytial virus infection enhances P. multocida adherence on respiratory epithelial cells. Vet Microbiol 220: 33-38.

Sudaryatma PE et al. 2019. Co-infection of epithelial cells established from the upper and lower bovine respiratory tract with bovine respiratory syncytial virus and bacteria. Vet Microbiol 235: 80-85.

Thanthrige DN et al. 2018. A novel multiplex PCR-electronic microarray assay for rapid and simultaneous detection of bovine respiratory and enteric pathogens. J Virol Methods 261: 51-62.

Wathes DC, Oguejiofor CF, Thomas C, Cheng Z. 2020. Importance of viral disease in dairy cow fertility. Engineering 6: 26-33.

Zhao G et al. 2018. Development of a recombinase polymerase amplification combined with a lateral flow dipstick assay for rapid detection of the Mycoplasma bovis. BMC Vet Res 14: 1-10.

Zhao G, Wang H, Hou P, Xia X, He H. 2018. A lateral flow dipstick combined with reverse transcription recombinase polymerase amplification for rapid and visual detection of the bovine respirovirus 3. Mol Cell Probes 41: 22-26.

Zhao G, He H, Wang H. 2019. Use of a recombinase polymerase amplification commercial kit for rapid visual detection of P. multocida. BMC Vet Res 15: 1-8.

Published

2021-04-07

How to Cite

Fernández, M. A., Bulla, D. M., Díaz, A. M., & Pulido, M. O. (2021). Seroprevalence and risk factors of the parainfluenza virus (VPI-3) in cattle from Colombia. Revista Veterinaria, 31(2), 155–159. https://doi.org/10.30972/vet.3124737

Issue

Section

Trabajos de Investigación