Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 16, Number 12—December 2010

Transmission of Ovine Herpesvirus 2 from Asymptomatic Boars to Sows

On This Page
Article Metrics
citations of this article
EID Journal Metrics on Scopus

Cite This Article

To the Editor: Malignant catarrhal fever (MCF) is an often lethal viral disease of susceptible biungulates from the Bovidae, Cervidae, and Suidae subfamilies. MCF in pigs has been associated with direct or indirect contact with sheep, which are the main reservoir of ovine herpesvirus 2 (OvHV-2) (1). A recent report detected infected but asymptomatic swine in the absence of known exposure to sheep or goats (2). Porcine MCF is difficult to diagnose because of its nonspecific clinical signs and sporadic nature; however, an outbreak involving 41 swine has been described (3). Pigs are terminal hosts and are not believed to spread the virus. Here we describe OvHV-2 DNA in the blood and semen of asymptomatic boars and from the brain of symptomatic sows and gilts with MCF that was probably transmitted by artificial insemination.

The MCF cases occurred on two 3-site commercial farms with 2,700 and 1,670 sows in 2 different counties in southwestern Brazil. No MCF losses previously had been recorded in the region, and the animals had no known direct or indirect contact with sheep. The 2 farms had high biosecurity. The first case was recorded in September 2004, and the number of cases increased in July 2006. Twenty-eight sows and gilts, 20 of them pregnant and at >25 days’ gestation, died during January 2007–March 2008, when the last case was observed.

Clinical features in sows and gilts were depression followed by abortion, fever (41°C), and anorexia. After the onset of clinical signs, neurologic symptoms developed such as ataxia, tremors, convulsions, and aggressive behavior. Animals that survived longer showed forelimb paralysis, stood in a dog-sit position, and gnawed with abundant salivation on pen bars.


Thumbnail of Brainstem of a sow with vasculitis that was associated with ovine herpesvirus 2, showing edema, necrosis (fibrinoid necrosis), and infiltration of lymphocytes in the adventitia of the artery. Severe perivascular (Virchow-Robin space) lymphocytic cuffing was observed. Hematoxylin and eosin stain; scale bar = 50 μm.

Figure. Brainstem of a sow with vasculitis that was associated with ovine herpesvirus 2, showing edema, necrosis (fibrinoid necrosis), and infiltration of lymphocytes in the adventitia of the artery. Severe perivascular (Virchow-Robin...

Specimens from randomly selected dead sows and gilts from the outbreaks during 2004–2008 were obtained for histopathologic examination, immunofluorescence testing for rabies virus, viral and bacterial isolation, and PCR. No bacterial or viral growth was detected, and direct immunofluorescence for rabies virus was negative. Microscopic examination showed high-grade nonpurulent meningoencephalitis characterized by lymphocytic cuffings with vasculitis in the brain hemisphere, the brainstem, the spinal cord, and, to a lesser extent, the cerebellum. Multifocal areas of edema, fibrinoid necrosis, and lymphocytic infiltration also were observed (Figure). OvHV-2 DNA was detected by using a specific PCR (4) in 5 of 7 paraffinized sections of the brainstem (5). To analyze the possible presence of other porcine lymphotropic herpesviruses in samples that reacted positively for OvHV-2, a nested PCR with degenerate primers (6,7) was applied. None of the OvHV-2–positive samples reacted positively for porcine lymphotropic herpesviruses. To confirm that the virus was a member of the MCFV group, we purified 1 amplicon and submitted it for automated sequencing. This nucleotide sequence was deposited in GenBank under accession no. HQ223415, and it showed 99% identity with previously deposited OvHV-2 sequences.

To find possible carriers of the virus, blood samples were collected from 9 pregnant sows, 10 nonpregnant sows, and 30 breeding boars and analyzed for OvHV-2 DNA. Samples from 3 boars were positive. Nasal swabs and semen samples were collected from these infected boars to investigate the potential mode of OvHV-2 transmission, and OvHV-2 DNA was detected only in semen samples. Two of the 3 semen samples had >350 copies/2 µg of total DNA, suggesting that these animals shed virus (8,9). During this period, all infected boars remained clinically healthy.

In Brazil, porcine MCF has been found primarily in pregnant sows and gilts. Our findings of OvHV-2 DNA in the semen of asymptomatic boars suggest that the OvHV-2 in the sows and gilts originated from asymptomatic boars that were responsible for maintaining the virus in the herd. Whether virus shedding in the semen was temporary or lasted for a long period is not known.

Emergence of OvHV-2 in boars that had no known contact with sheep was surprising, especially given the possibility of venereal transmission through contaminated semen. The occurrence of OvHV-2 infection in other specific pathogen–free farms is unknown, and it is not possible to suggest a strategy to guarantee OvHV-2-free herds.



Financial support was provided by Fundação de Amparo à Pesquisa do Estado de Minas Gerais, Conselho Nacional de Desenvolvimento Científico e Tecnológico, and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.


Érica Azevedo Costa, Aline de Marco Viott, Glauber de Souza Machado, Maria Rosa Quaresma Bomfim, Fabiana Magalhães Coelho, Zélia Inês Portela Lobato, Mauricio Resende, and Roberto Mauricio Carvalho GuedesComments to Author 

Author affiliations: Author affiliations: Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil (É. Azevedo Costa, G. de Souza Machado, M.R. Quaresma Bomfim, F. Magalhães Coelho, Z.I. Portela Lobato, M. Resende, R.M. Carvalho Guedes); Universidade Federal do Paraná, Palotina, Paraná, Brazil (A. de Marco Viott)



  1. Loken  T, Aleksandersen  M, Reid  HW, Pow  I. Malignant catarrhal fever caused by ovine herpesvirus-2 in pigs in Norway. Vet Rec. 1998;143:4647. DOIPubMed
  2. Loken  T, Bosman  A-M, Van Vuuren  M. Infection with ovine herpesvirus 2 in Norwegian herds with a history of previous outbreaks of malignant catarrhal fever. J Vet Diagn Invest. 2009;21:25761. DOIPubMed
  3. Gauger  PC, Patterson  AR, Kim  WI, Stecker  KA. An outbreak of porcine malignant catarrhal fever in a farrow-to-finish swine farm in the United States. J. Swine Health Prod. 2010;18:2448.
  4. Baxter  SIF, Pow  I, Bridgen  A, Reid  HW. PCR detection of the sheep-associated agent of malignant catarrhal fever. Arch Virol. 1993;132:14559. DOIPubMed
  5. Mesquita  RA, Anzai  EK, Oliveira  RN, Nunes  FD. Evaluation of 3 methods of DNA extraction from paraffin-embedded material for the amplification of genomic DNA using PCR [in Portuguese]. Pesqui Odontol Bras. 2001;15:3149.PubMed
  6. Van Devanter  DR, Warremer  P, Bennett  L, Schultz  ER, Coulter  S, Garber  RL, Detection and analysis of diverse herpesviral species by consensus primer PCR. J Clin Microbiol. 1996;34:166671.PubMed
  7. Ehlers  B, Ulrich  S, Goltz  M. Detection of two novel porcine herpesvirus with high simularity to gammaherpesvirus. J Gen Virol. 1999;80:9718.PubMed
  8. Albini  S, Zimmermann  W, Neff  F, Ehlers  B, Hani  H, Li  H, Identification and quantification of ovine gammaherpesvirus 2 DNA in fresh and stored tissues of pigs with symptoms of porcine malignant catarrhal fever. J Clin Microbiol. 2003;41:9004. DOIPubMed
  9. Hüssy  D, Janett  F, Albini  S, Staüber  N, Thun  R, Ackermann  M. Analysis of the pathogenetic basis for shedding and transmission of ovine gamma herpesvirus 2. J Clin Microbiol. 2002;40:47004. DOIPubMed




Cite This Article

DOI: 10.3201/eid1612.101453

Related Links


Table of Contents – Volume 16, Number 12—December 2010


Please use the form below to submit correspondence to the authors or contact them at the following address:

Roberto Mauricio Carvalho Guedes, Departamento de Clínica e Cirurgia Veterinárias, Escola de Veterinária, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Bairro Pampulha, CEP 31270-901, Belo Horizonte, MG, Brazil

Send To

character(s) remaining.

Comment submitted successfully, thank you for your feedback.


Page created: August 29, 2011
Page updated: August 29, 2011
Page reviewed: August 29, 2011
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.