Journal of Community Medicine & Public Health Care Category: Medical Type: Short Communication

Zika Virus-Bovine Viral Diarrhea Virus Potential Interaction in the Etiopathology of Birth Defects in Brazil, a One Health Issue?

Massimo Giangaspero1* and Ion De Andrade2
1 Faculty of veterinary medicine, Teramo, Italy
2 Medical school, Health State Secretariat, Potiguar University, Rio Grande do Norte, Brazil

*Corresponding Author(s):
Massimo Giangaspero
Faculty Of Veterinary Medicine, Teramo, Italy
Tel:+33 450392875,

Received Date: Oct 31, 2018
Accepted Date: Jan 17, 2019
Published Date: Jan 31, 2019


In 2015, Brazil has lived an unprecedented epidemic of microcephaly that has not yet been fully explained. Also cases of Guillain-Barré syndrome increased dramatically. Preliminary observations suggested involvement of cofactors in the etiopathology of Zika virus associated microcephaly in Brazil. Research teams identified Bovine Viral Diarrhea Virus (BVDV) in fetal samples with microcephaly, originating in the state of Paraíba, and two virus sequences, obtained from the amniotic fluid collected from mothers with babies affected by Zika and microcephaly, have been characterized as sub genotype BVDV-1b1, of cosmopolitan diffusion, and BVDV-2b, typical genotype circulating in South America, showing unreported variants in the Internal Ribosome Entry Site (IRES). Further studies established a statistical association between microcephaly and cattle breeding in the north-eastern Brazilian states of Rio Grande do Norte, Paraíba and Ceará. The expanded epidemiological analysis throughout Brazil showed that the association between cattle breeding rural areas and microcephaly was confirmed for the entire Brazil, against typical arbovirus diffusion patterns.


Bovine viral diarrhea virus; Microcephaly; Zika virus

Short Communication

The “One Health” concept, based on the evidence that human health and animal health are inter-dependent and bound to the health of the ecosystems in which they exist, was introduced at the beginning of the 2000’s, envisaged and implemented by the World Organization for Animal Health (Office International des Epizooties - OIE) to strengthen the fight against transmissible diseases from living animals to humans. Taking into account that 60% of existing human infectious diseases are zoonotic, at least 75% of emerging diseases of humans have an animal origin, and 3 of 5 new human diseases which appear every year are of animal origin [1], it is therefore necessary a close collaboration between medical and veterinary sanitary professionals. Investigation of potential interaction among human and animal pathogens is also a topic of interest in the framework of a collaborative global approach to understanding risks and roles in the human animal ecosystems interface.

In 2015, epidemic in South America revealed unprecedently described severe sanitary impact of Zika virus infection. About 150 countries have been notified at risk of Zika virus, and 31 countries and territories have reported cases of microcephaly and other Central Nervous System (CNS) malformations associated with Zika virus infection, particularly since 2015 in the Americas [2]. Brazil was the most affected country, where 3,071 confirmed cases of affected infants and 2,869 suspected cases, still under investigation, have been reported [3]. Most observations referred to in particular the north-eastern states of Ceará, Paraíba, Pernambuco and Rio Grande do Norte. Relation was also suspected with neurological disorders, mainly Guillain-Barré syndrome, in adults. Zika virus was rapidly declared a public health emergency of international concern by the World Health Organization (WHO), in February 2016, because of the potential association with serious fetal cerebral anomalies. In November 2016, WHO announced that the Zika virus was not anymore a worldwide emergency? The decision taken by the WHO crisis committee to withdraw the emergency status was motivated on the base of International Health Regulations, while Zika virus and its consequences remain persistent and important public health challenge that has not yet been fully explained.

Given the new epidemic-pathological traits, from a previously relatively neglected disease, Zika became a global long term important problem. At present, despite progress toward discovery of Zika virus vaccines and therapeutics [4], no preventive or curative measures are available; therefore, it is important to improve our understanding on epidemiology and etiopathogenesis of the disease. Zika virus is known since 1947 and never previously reported as a danger for fetus in man. Comparison of Zika virus deposited sequences with those recently detected in Brazil did not reveal relevant differences or mutations supporting hypothetical acquisition of higher virulence due to genetic changes. Therefore, other co-factors can be suspected and should be reasonably identified and evaluated.

The similarity of Zika related birth defects with Bovine Viral Diarrhea Virus (BVDV) prenatal infection, pathological outcomes in cattle and, previous reports indicating circulation of BVDV in man [5-7] and suspected correlation to Central Nervous System (CNS) fetal damage including microcephaly in man [8,9] induced some researchers to investigate in this direction.

Research teams from the Federal University of Rio de Janeiro and Instituto de Pesquisa Professor Joaquim Amorim Neto, Campina Grande, identified Bovine Viral Diarrhea Virus (BVDV) in fetal samples with microcephaly, originating in the state of Paraíba. Using mass spectrometry proteomics to analyze protein extracts from three Zika positive brains of deceased babies with severe brain lesions and arthrogryposis, Nogueira and others detected the presence of peptides from the poly-protein of a Bovine-like viral diarrhea virus, suggesting that Zika virus may not be the only etiological agent responsible for microcephaly [10]. Melo and her team sug¬gested that Zika infection might facilitate BVDV to cross placenta barrier and cause fetal infections; however, they haven’t ruled out the possibility that their findings might be due to contamination [11]. In addition to the proteomics analysis in the brain tissue of fetuses bearing microcephaly, during the outbreak in Paraíba State, Brazil, in 2015, BVDV RNA was also found in the amniotic fluid collected from four mothers with babies affected by Zika and microcephaly. Two 5’-Untranslated Region (UTR) RNA genomic sequences, obtained by PCR and sequencing, respectively related to BVDV-1b and BVDV-2, have been provided by Professor Tanuri, Federal University of Rio de Janeiro, for further secondary structure analysis based on palindromic nucleotide substitutions method for Pestivirus genotyping [12,13]. The analysis was focused on the Internal Ribosomal Entry Site (IRES) that form specific secondary stem loop sequence structures in the 5’-UTR, recognized strategic genomic region for virus biology [14]. The BVDV-1 isolate 12p belonged to a genotype of cosmopolitan diffusion, the 1b, sub genotype 1, the only group within the heterogeneous BVDV-1 species which includes hypervirulent strains responsible of hemorrhagic syndrome in European cattle [15,16]. The highest homology (99%) was observable only with the bovine strain UEL9-BR/11 (Rodrigues et al., unpublished) collected in 2011 in the Southern Brazilian State of Paraná about 10 years later than the three other closely genetically related strains 133/02, 4092/00 and 3310/01 [17], previously identified in Spain in 2002, but showing a divergence at the stem of V2 locus in the IRES. The human strain 12p showed also homology (98% nucleotide identity) with four contaminant strains isolated in Mexico in 2012, the BVDV-1b1 NGR2, NGR3, NGR11 and NGR12 (Gomez-Romero et al., unpublished). The BVDV-2 strain 4P sequence showed high homology (96%) only with two previously deposited Brazilian bovine isolates LV Patol 0209 (Silveira et al., unpublished) and LV 56-10/13 [18], collected in 2009 and 2010, respectively. These sequences belonged to BVDV-2b, typical genotype circulating in South America, but the bovine isolates diverged from the human sequence at the level of V1 locus stem and V3 locus loop of the IRES. The fact that both detected sequences showed not previously described nucleotide base pair combinations in particularly important and strategic genomic site (e.g., IRES) and they were related with Brazilian circulating strains, corroborates that they are unlikely contaminants, and may reflects evolutionary history of the species in this geographic area and eventual involvement with human pathology. The only strain previously reported in humans belonged to genotype BVDV-1c [7], another Pestivirus cluster with cosmopolitan diffusion.

Another interesting aspect suggesting an existing link between Zika associated microcephaly and animal pathogens was the distribution of cases in the affected areas: the prevalence in large cities was low, being exponentially higher in small towns, close to farmers [19]. In addition, in Rio Grande do Norte state, the cases of microcephaly overlapped the river basins, regions surrounded by livestock, avoiding others ones where Zika vector Aedes mosquitoes infestation rates were higher. Furthermore, a significant association was found between the density of farm animals in the territory and the prevalence of microcephaly calculated by live births. Starting from an initial evaluation on three north-eastern Brazilian states of Rio Grande do Norte, Paraíba and Ceará (144 counties and 234 cases of microcephaly), an expanded analysis, considering all the 725 Brazilian counties where the totality of the confirmed cases of microcephaly have been reported under the national monitoring plan [20], showed stronger and statistically significant associations between cattle density and the prevalence of microcephaly in the entire Brazilian territory [21]. This epidemiological profile was similar even considering the different chronological stages of the disease evolution in the first affected areas as well as in the more recently affected ones. Relation with cattle density was observable in both regions affected by high and low microcephaly prevalence. Un-clarified to date, the higher prevalence in the north-east of Brazil, in low-income families and in small counties might be explained by the imbrication of animals and humans so frequent in the poor rural areas of this Brazilian region [22].

Despite there is general consensus on the correlation of Zika virus with microcephaly [23], no direct experimental causal evidence confirms that the Zika virus is the sole etiological agent responsible for the development of brain malformations in human fetuses during pregnancy [10]. The zoonotic potential of BVDV, its ability to cross species barrier, to cross hemato-placental barrier, the high tropism for CNS in animal fetuses, as well as the synergistic action with other pathogens trough the virus induced transient but severe immune-depression, suggest this virus as cofactor candidate for eventual interaction with Zika virus in the etiopathogenesis of CNS lesions induced in human in epidemic areas of South America.

Subsequent to these preliminary observations, a research protocol has been elaborated under the patronage of the State Secretariat of Public Health of the Rio Grande do Norte and approved by the Brazilian National Council of Ethics in Research, with the aim to clarify existence of cofactors through serological and antigenic investigations for animal pathogens as BVDV among mothers of infants with microcephaly. Meanwhile, the Brazilian Ministry of Health made available to the Brazilian public health laboratories the serological test for the Zika virus for the confirmation of presumed diagnosis for all cases of mothers of infants with microcephaly. All these further multi-disciplinary investigations on samples associated to microcephaly and Guillain-Barré syndrome, collected since the epidemic in 2015 until current cases, will provide lights on the epidemiology of priority health risks, and they will clarify role of suspected pathogens of animal origin, in the respect of the One Health Principle.


  1. World Organization for Animal Health (2018) One Health. World Organisation for Animal Health, Paris, France.
  2. World Health Organization (2017) Situation report: Zika virus, microcephaly, Guillain-Barré syndrome. WHO, Geneva, Switzerland.
  3. Ministério da Saúde (2018) Boletim Epidemiológico. Ministério da Saúde, Brazil.
  4. World Health Organization (2018) Progress toward discovery of Zika virus vaccines and therapeutics. WHO, Geneva, Switzerland.
  5. Giangaspero M, Vacirca G, Morgan D, Baboo KS, Luo NP, et al. (1993) Anti-bovine viral diarrhoea virus antibodies in adult Zambian patients infected with the human immunodeficiency virus. Int J STD AIDS 4: 300-302.
  6. Giangaspero M, Vacirca G, Buettner M, Wolf G, Vanopdenbosch E, et al. (1993) Serological and antigenical findings indicating pestivirus in man. Arch Virol Suppl 7: 53-62.
  7. Giangaspero M, Harasawa R, Verhulst A (1997) Genotypic analysis of the 5'-untranslated region of a pestivirus strain isolated from human leucocytes. Microbiol Immunol 41: 829-834.
  8. Potts BJ, Sever JL, Tzan NR, Huddleston D, Elder GA (1987) Possible role of pestiviruses in microcephaly. Lancet 1: 972-973.
  9. Yolken RH, Petric M, Collett M, Fuller TE (1993) Pestivirus infection in identical twins discordant for schizophrenia. Proceedings of the IXth Congress of Virology, Glasgow, England 148.
  10. Nogueira FCS, Velasquez E, Melo ASO, Domont GB (2016) Zika virus may not be alone: proteomics associates a bovine-like viral diarrhea virus to microcephaly. bioRxiv preprint.
  11. Butler D (2016) Brazil asks whether Zika acts alone to cause birth defects. Nature 535: 475-476.
  12. Harasawa R, Giangaspero M (1998) A novel method for Pestivirus genotyping based on palindromic nucleotide substitutions in the 5'-untranslated region. J Virol Methods 70: 225-230.
  13. Giangaspero M, Harasawa R (2007) Numerical taxonomy of genus Pestivirus based on palindromic nucleotide substitutions in the 5’ untranslated region. J Virol Methods 146: 375-388.
  14. Deng R, Brock KV (1992) Molecular cloning and nucleotide sequence of the pestivirus genome, noncytopathic bovine viral diarrhea virus strain SD-1. Virology 191: 867-869.
  15. Broes A, Wellemans G, Dheedene J (1992) Syndrome hémorrhagique chez des bovins infectés par le virus de la diarrhée virale bovine (BVD/MD). Ann Méd Vét 137: 33-38.
  16. Lecomte C, Navetat H, Hamers C, Lambot M, Schelcher F, et al. (1996) Isolement du virus de la diarrhée virale bovine de deux cas de syndromes hémorragiques, chez des bovins de race charolaise. Ann Méd Vet 140: 435-438.
  17. Hurtado A, García-Pérez AL, Aduriz G, Juste RA (2003) Genetic diversity of ruminant pestiviruses from Spain. Virus Res 92: 67-73.
  18. Weber MN, Silveira S, Machado G, Groff FH, Mósena AC, et al. (2014) High frequency of bovine viral diarrhea virus type 2 in Southern Brazil. Virus Res 191: 117-124.
  19. de Andrade IG (2016) Livestock and microcephaly, traces of an association? bioRxiv. Pg no: 1-15.
  20. Ministério da Saúde (2017) Sala de apoio à Gestão Estratégica, Ministério da Saúde, Brazil.
  21. de Andrade I, Giangaspero M (2017) Epidemiology of Zika Virus Associated Microcephaly in Brazil Suggesting Cofactor Involvement. SF J Virol 1: 1-6.
  22. Doshi P (2016) Convicting Zika. BMJ 353: i1847.
  23. World Health Organization (2017) Zika virus. WHO, Geneva, Switzerland.

Citation: Giangaspero M, de Andrade I (2019) Zika Virus-Bovine Viral Diarrhea Virus Potential Interaction in the Etiopathology of Birth Defects in Brazil, a One Health issue? J Community Med Public Health Care 6: 040.

Copyright: © 2019  Massimo Giangaspero, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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