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Volume 21, Number 12—December 2015
Letter

Alternative Routes of Zoonotic Vaccinia Virus Transmission, Brazil

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To the Editor: Vaccinia virus (VACV) causes exanthematous disease (bovine vaccinia) in Brazil. Outbreaks of this disease in humans have been reported since the late 1990s and have spread throughout Brazil (1). Natural human infections with VACV occur by close contact with infected cattle during milking. Lesions can spread to secondary body sites (forearms, arms, and face). Thus, person-to-person transmission occurs (1).

Moreover, virus can persist in household environments, remain infectious, and be transmitted by fomites (2). Although raw milk and cheese are potential sources of infection, no clinical cases have been associated with this transmission route (3,4). Data for person-to-person transmission in Brazil are scarce, but person-to-person transmission was recently reported (5). We report a possible case of person-to-person transmission of VACV.

This study was approved by the Research Ethics Committee of Universidade Federal de Minas Gerais (registration protocol FR-413704). In September 2012, during a serologic survey in a rural area of Serro City (18°36′17″S, 43°22′46″W), Minas Gerais, Brazil (Technical Appendix Figure, panel A), blood samples were obtained from a family of 5 persons (father, mother, and 3 daughters). The father and mother were 48 and 53 years of age, respectively, and had been vaccinated against smallpox. They reported contact with cows and horses (Technical Appendix Table 1). Only the father had milked cows. The 3 daughters (13, 13, and 14 years of age) did not engage in any exposure activity. However, all family members had consumed raw milk and cheese.

Bovine vaccinia lesions were observed on the hand of the father (Technical Appendix Figure, panel B). In 2011, he had vesicular disease (no laboratory diagnosis) with clinical and epidemiologic features (lesions) suggestive of bovine vaccinia on his hands and forearms and systemic symptoms (fever, headache, malaise, myalgia, lymphadenopathy, and abdominal pain). His symptoms were mild and without any systemic clinical features. Two lesions developed on his hands and dried swab samples were collected from both lesions. Swab samples were processed as described (2) and used for virus isolation and molecular diagnosis.

On the basis of previous studies that detected viral DNA in clinical samples from persons with bovine vaccinia (1), we used a quantitative PCR to amplify the vgf and ha genes of VACV (35), a standard PCR to detect the ha gene (35), and a seminested PCR to detect the ati gene (F.L. Assis, unpub. data). Serum samples were used for detection of virus-neutralizing antibodies (orthopoxvirus 50% plaque-reduction neutralization test) and molecular diagnostic studies (1). Virus isolation was attempted in Vero cells and chorioallantoic membrane. All results were negative.

The 50% plaque-reduction neutralization test showed that the father, mother, and 14-year-old daughter had neutralizing antibodies against orthopoxvirus (titers 800, 3,200, and 800 neutralizing units/mL, respectively). All family members had positive results by molecular diagnostic test for >1 virus gene (Technical Appendix Table 1). To rule out infection with parapopoxvirus, a complementary PCR (6) was also performed, and all family members had negative results.

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Thumbnail of A) Nucleotide sequence of vaccinia virus (VACV) hemagglutinin gene and homologous sequences of several orthopoxviruses, Brazil. Dots indicate sequence identity; dashes indicate deletions. VARV, variola virus; MPXV, monkeypox virus; CPXV, cowpox virus. B) Consensus phylogenetic tree based on nucleotide sequences of orthopoxvirus hemagglutinin genes. Tree was constructed with hemagglutinin gene sequences by using the neighbor-joining method with 1,000 bootstrap replicates and the Tamu

Figure. A) Nucleotide sequence of vaccinia virus (VACV) hemagglutinin gene and homologous sequences of several orthopoxviruses, Brazil. Dots indicate sequence identity; dashes indicate deletions. VARV, variola virus; MPXV, monkeypox virus; CPXV, cowpox...

Quantitative PCR products for the ha gene from 3 virus-positive samples were sequenced in both directions in triplicate (Mega BACE Sequencer; GE Healthcare, Little Chalfont, UK). Sequences were aligned by using ClustalW (http://www.genome.jp/tools/clustalw/) and MEGA4.1 (http://www.megasoftware.net/) and showed 100% identity with each other (Figure). A phylogenetic tree was constructed by using the neighbor-joining method and 1,000-bootstrap replicates in the Tamura-3 parameter model (MEGA4.1). Sequences were grouped with VACV group 2 isolates. Sequences obtained were deposited in GenBank under accession nos. KP889223–5).

In Brazil, outbreaks of bovine vaccinia are associated with rural environments. However, some clinical and epidemiologic aspects remain unclear. The infection of the father was associated with direct contact with cattle. Immunity conferred by smallpox vaccination did not prevent infection; this lack of immune response has been demonstrated in other studies in Brazil (7). Long-term protection might require multiple virus exposures, and severity of poxvirus infections might be influenced by the immunologic state of the host and virulence of virus strains (1,8,9).

The mother and 2 daughters with virus DNA in blood samples and the 14-year-old daughter with high titers of virus-neutralizing antibodies suggest that alternative routes (other than milking) for VACV infection of humans should be considered. These alternative routes can include person-to-person or environmental transmission because the 2 daughters did not report any exposure activities related to milking or contact with cattle (Technical Appendix Tables 1, 2). Persistence of VACV in household environments has been reported (2,10). The family also consumed raw milk and cheese, a common practice in the region. Therefore, infection with VACV through raw milk and cheese consumption should also be considered. The patients did not report oral lesions or a history of skin/mucosal lesions.

In conclusion, person-to-person transmission of VACV in these cases might have been caused by direct contact between the father and family members, contact with virus in the home, or consumption of unpasteurized milk and cheese. Additional studies are necessary to elucidate the role of these transmission pathways in spread of VACV in Brazil.

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Acknowledgments

We thank João Rodrigues dos Santos and colleagues for excellent technical support and the Instituto Mineiro de Agropecuária for assistance.

This study was supported by Conselho Nacional de Desenvolvimento Científico e Tecnológico, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Fundação de Amparo à Pesquisa do Estado de Minas Gerais, and Pró-Reitoria de Pesquisa/Universidade Federal de Minas Gerais. G.S.T., P.C.P.F., and E.G.K. are researchers of the Conselho Nacional de Desenvolvimento Científico e Tecnológico.

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Galileu B. Costa, Iara A. Borges, Pedro A. Alves, Júlia B. Miranda, Ana Paula M.F. Luiz, Paulo C.P. Ferreira, Jônatas S. Abrahão, Elizabeth C. Moreno, Erna G. Kroon, and Giliane de Souza TrindadeComments to Author 

Author affiliations: Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil (G.B. Costa, I.A. Borges, P.A. Alves, J.B. Miranda, A.P.M.F. Luiz, P.C.P. Ferreira, J.S. Abrahão, E.G. Kroon, G. de Souza Trindade); Fundação Hemominas. Belo Horizonte (E.C. Moreno)

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References

  1. Kroon  EG, Mota  BE, Abrahão  JS, da Fonseca  FG, de Souza Trindade  G. Zoonotic Brazilian vaccinia virus: from field to therapy. Antiviral Res. 2011;92:15063. DOIPubMed
  2. Assis  FL, Borges  IA, Mesquita  VS, Ferreira  PC, Trindade  GS, Kroon  EG, Vaccinia virus in household environment during bovine vaccinia outbreak, Brazil. Emerg Infect Dis. 2013;19:20457 .PubMed
  3. Abrahão  JS, Oliveira  TM, Campos  RK, Madureira  MC, Kroon  EG, Lobato  ZI. Bovine vaccinia outbreaks: detection and isolation of vaccinia virus in milk samples. Foodborne Pathog Dis. 2009;6:11416. DOIPubMed
  4. de Oliveira  TM, Rehfeld  IS, Siqueira  JM, Abrahão  JS, Campos  RK, dos Santos  AK, Vaccinia virus is not inactivated after thermal treatment and cheese production using experimentally contaminated milk. Foodborne Pathog Dis. 2010;7:14916. DOIPubMed
  5. Pereira Oliveira  G, Tavares Silva Fernandes  A, Lopes de Assis  F, Augusto Alves  P, Moreira Franco Luiz  AP, Barcelos Figueiredo  L, Intrafamilial transmission of vaccinia virus during a bovine vaccinia outbreak in Brazil: a new insight in viral transmission chain. Am J Trop Med Hyg. 2014;90:10213. DOIPubMed
  6. Inoshima  Y, Morooka  A, Sentsui  H. Detection and diagnosis of parapoxvirus by the polymerase chain reaction. J Virol Methods. 2000;84:2018. DOIPubMed
  7. Silva-Fernandes  AT, Travassos  CE, Ferreira  JM, Abrahão  JS, Rocha  ES, Viana-Ferreira  F, Natural human infections with Vaccinia virus during bovine vaccínia outbreaks. J Clin Virol. 2009;44:30813. DOIPubMed
  8. Gallwitz  S, Schutzbank  T, Heberling  RL, Kalter  SS, Galpin  JE. Smallpox: residual antibody after vaccination. J Clin Microbiol. 2003;41:406870. DOIPubMed
  9. Hammarlund  E, Lewis  MW, Hansen  SG, Strelow  LI, Nelson  JA, Sexton  GJ, Duration of antiviral immunity after smallpox vaccination. Nat Med. 2003;9:11317. DOIPubMed
  10. Lederman  E, Miramontes  R, Openshaw  J, Olson  VA, Karem  KL, Marcinak  J, Eczema vaccinatum resulting from the transmission of vaccinia virus from a smallpox vaccinee: an investigation of potential fomites in the home environment. Vaccine. 2009;27:3757. DOIPubMed

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DOI: 10.3201/eid2112.141249

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Table of Contents – Volume 21, Number 12—December 2015

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Giliane de Souza Trindade, Departamento de Microbiologia, Laboratório de Vírus, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Brazil. Av Antônio Carlos, no. 6627, Pampulha, Belo Horizonte, Minais Gerais CEP: 31270-901, Brazil

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Page created: November 17, 2015
Page updated: November 17, 2015
Page reviewed: November 17, 2015
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.
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