Parapoxviruses

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Parapoxviruses

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Poxviridae are a family of oval or brick-shaped, quite large, double-stranded DNA viruses that can infect both humans and animals. The genus Parapoxvirus is included among these viruses; these viruses measure 260 X 160-nm and possess a unique spiral coat that distinguishes them from the other poxviruses. Parapoxvirus species are enzootic to hoofed animals (ungulates) throughout the world. Three similar parapoxviruses (orf virus, pseudocowpox virus, and bovine papular stomatitis virus) commonly cause infection in humans; transmission is through direct or indirect contact with infected animals. The zoonotic hosts of these parapoxviruses are sheep and goats (orf, ie, ecthyma contagiosum virus) and cattle (pseudocowpox virus [ie, milker’s nodule virus or paravaccinia virus] and bovine papular stomatitis virus).

Other parapoxviruses have been recognized in New Zealand red deer, [1] Finnish reindeer, [2] Japanese serows, [3] European musk oxen, [4] red squirrels in the United Kingdom, [5] harbor seals in the North Sea, [6] and California sea lions. [7] A novel parapoxvirus from white-tailed deer in the United States has caused cases of human infection. [8]

Parapoxvirus infections manifest as pathologic lesions on the animal’s oral mucosa (eg, lips, nostrils, eyes) or the moist hairless areas of the skin (eg, udders, groin). The virus may be contacted even in the absence of obvious lesions on the animal. [9]

Incidence of deer-associated parapoxvirus infections may rise as the deer population in the United States continues to increase. [8]

Clinical cutaneous manifestations of infection with the parapoxviruses are identical; therefore, some authors propose the term “farmyard pox” for any of the 3 common parapoxvirus infections. [10]

Go to Poxviruses, Orf, and Milker’s Nodules for complete information on these topics. 

Parapoxvirus infection results in solitary or multiple, relatively painless, cutaneous lesions that heal slowly, usually without complications. Occasionally, the lymphatic system is involved. Even in immunocompromised hosts, little evidence suggests spread of infection outside external surfaces.

Lasting immunity to parapoxviruses does not seem to occur, and reinfection has been reported. [11]

United States

Orf, milker’s nodule, and bovine papular stomatitis are viral illnesses enzootic to sheep, goats, and cattle throughout the world. No reports contain data specific to the United States.

International

Data from England and Wales for 1990-1995 indicate an annual mean of 15 human cases of parapoxvirus infections, significantly less than the reported annual mean of 46 cases between 1978 and 1986. Sheep were a more frequent source of infection than other ungulates. [12]

Among high-risk populations, such as animal caretakers or meat handlers, [13] the typical clinical appearance and the benign nature of the infection may be well known. As a result, infected individuals may not seek medical attention and many authors believe that the infection is much more common than actually reported.

Parapoxvirus lesions generally heal without treatment, albeit slowly. Scarring is typically absent. Immunocompromised patients and those with atopic dermatitis are at risk for progressive or disseminated disease. One case reported described blindness resulting from ocular involvement; no cases resulting in death have been reported. [14]

Race is often not specified in the existing literature, but the infection occurs throughout the world.

Most cases occur in males, reflecting the male predominance in the occupations or activities of the infected patients, which include veterinarians, veterinary students, farmers, shepherds, and other animal caretakers. Women are susceptible to infection if they have close contact with animals.

Most cases occur in young to middle-aged adults, although school-aged children also are infected. Parapoxviruses do not appear to have a predilection for any particular age group. Children may be at higher risk due to behavioral reasons that cause them to sustain more animal bites, to have poorer adherence to good hand hygiene and personal protective measures, and to engage in high-risk behaviors such as nuzzling a sick animal. [15] A recent analysis of an orf outbreak found that age less than 20 years was an independent risk factor for infection. [16]

Horner GW, Robinson AJ, Hunter R, Cox BT, Smith R. Parapoxvirus infections in New Zealand farmed red deer (Cervus elaphus). N Z Vet J. 1987 Apr. 35(4):41-5. [Medline].

Tikkanen MK, McInnes CJ, Mercer AA, Büttner M, Tuimala J, Hirvelä-Koski V. Recent isolates of parapoxvirus of Finnish reindeer (Rangifer tarandus tarandus) are closely related to bovine pseudocowpox virus. J Gen Virol. 2004 Jun. 85(Pt 6):1413-8. [Medline].

Inoshima Y, Yamamoto Y, Takahashi T, Shino M, Katsumi A, Shimizu S. Serological survey of parapoxvirus infection in wild ruminants in Japan in 1996-9. Epidemiol Infect. 2001 Feb. 126(1):153-6. [Medline].

Falk ES. Parapoxvirus infections of reindeer and musk ox associated with unusual human infections. Br J Dermatol. 1978 Dec. 99(6):647-54. [Medline].

Tompkins DM, Sainsbury AW, Nettleton P. Parapoxvirus causes a deleterious disease in red squirrels associated with UK population declines. Proc Biol Sci. 2002. 269:529-33.

Hicks BD, Worthy GA. Sealpox in captive grey seals (Halichoerus grypus) and their handlers. J Wildl Dis. 1987 Jan. 23(1):1-6. [Medline].

Nollens HH, Jacobson ER, Gulland FM, Beusse DO, Bossart GD, Hernandez JA. Pathology and preliminary characterization of a parapoxvirus isolated from a California sea lion (Zalophus californianus). J Wildl Dis. 2006 Jan. 42(1):23-32. [Medline].

Roess AA, Galan A, Kitces E, Li Y, Zhao H, Paddock CD. Novel deer-associated parapoxvirus infection in deer hunters. N Engl J Med. 2010 Dec 30. 363(27):2621-7. [Medline].

Bowman KF, Barbery RT, Swango LJ, Schnurrenberger PR. Cutaneous form of bovine papular stomatitis in man. JAMA. 1981 Dec 18. 246(24):2813-8. [Medline].

Shelley WB, Shelley ED. Farmyard pox: parapox virus infection in man. Br J Dermatol. 1983 Jun. 108(6):725-7. [Medline].

Groves RW, Wilson-Jones E, MacDonald DM. Human orf and milkers” nodule: a clinicopathologic study. J Am Acad Dermatol. 1991 Oct. 25(4):706-11. [Medline].

Baxby D, Bennett M. Poxvirus zoonoses. J Med Microbiol. 1997 Jan. 46(1):17-20, 28-33. [Medline].

Robinson AJ, Petersen GV. Orf virus infection of workers in the meat industry. N Z Med J. 1983 Feb 9. 96(725):81-5. [Medline].

Lewis-Jones S. Zoonotic poxvirus infections in humans. Curr Opin Infect Dis. 2004 Apr. 17(2):81-9. [Medline].

Lederman ER, Austin C, Trevino I, Reynolds MG, Swanson H, Cherry B. ORF virus infection in children: clinical characteristics, transmission, diagnostic methods, and future therapeutics. Pediatr Infect Dis J. 2007 Aug. 26(8):740-4. [Medline].

Bayindir Y, Bayraktar M, Karadag N, Ozcan H, Kayabas U, Otlu B, et al. Investigation and analysis of a human orf outbreak among people living on the same farm. New Microbiol. 2011 Jan. 34(1):37-43. [Medline].

Mendez B, Burnett JW. Orf. Cutis. 1989 Oct. 44(4):286-7. [Medline].

Villadsen LS, Zachariae CO. Unusual presentation of ORF in an otherwise healthy individual. Acta Derm Venereol. 2008. 88(3):277-8. [Medline].

Leavell UW Jr, McNamara MJ, Muelling R, et al. Orf. Report of 19 human cases with clinical and pathological observations. JAMA. 1968 May 20. 203(8):657-64. [Medline].

Centers for Disease Control and Prevention. Orf virus infection in humans–New York, Illinois, California, and Tennessee, 2004-2005. MMWR Morb Mortal Wkly Rep. 2006 Jan 27. 55(3):65-8. [Medline].

Venkatesan G, Balamurugan V, Bhanuprakash V. Multiplex PCR for simultaneous detection and differentiation of sheeppox, goatpox and orf viruses from clinical samples of sheep and goats. J Virol Methods. 2014 Jan. 195:1-8. [Medline].

Mast J, Demeestere L. Electron tomography of negatively stained complex viruses: application in their diagnosis. Diagn Pathol. 2009 Feb 10. 4:5. [Medline].

Töndury B, Kühne A, Kutzner H, Palmedo G, Lautenschlager S, Borelli S. Molecular diagnostics of parapox virus infections. J Dtsch Dermatol Ges. 2010 Sep. 8(9):681-4. [Medline].

Zabawski EJ Jr. A review of topical and intralesional cidofovir. Dermatol Online J. 2000 Sep. 6(1):3. [Medline].

McCabe D, Weston B, Storch G. Treatment of orf poxvirus lesion with cidofovir cream. Pediatr Infect Dis J. 2003 Nov. 22(11):1027-8. [Medline].

Ara M, Zaballos P, Sánchez M, Querol I, Zubiri ML, Simal E. Giant and recurrent orf virus infection in a renal transplant recipient treated with imiquimod. J Am Acad Dermatol. 2008 Feb. 58(2 Suppl):S39-40. [Medline].

Gallina L, Scagliarini A. Virucidal efficacy of common disinfectants against orf virus. Vet Rec. 2010 Jun 5. 166(23):725-6. [Medline].

Schmidt E, Weissbrich B, Brocker EB. Orf followed by erythema multiforme. Eur Acad Dermatol Venereol. 2006. 20:612-3.

Slattery WR, Juckett M, Agger WA. Milkers’ nodules complicated by erythema multiforme and graft-versus-host after allogenic hematopoietic stem cell transplantation for multiple myeloma. Clin Infect Dis. 2005. 40:e63-6.

Murphy JK, Ralfs IG. Bullous pemphigoid complicating human orf. Br J Dermatol. 1996 May. 134(5):929-30. [Medline].

White KP, Zedek DC, White WL, Simpson EL, Hester E, Morrison L. Orf-induced immunobullous disease: A distinct autoimmune blistering disorder. J Am Acad Dermatol. 2008 Jan. 58(1):49-55. [Medline].

de la Torre C. Gianotti-Crosti syndrome following milkers” nodules. Cutis. 2004 Nov. 74(5):316-8. [Medline].

Luke Bloomquist, MD Combat Aviation Brigade Surgeon, 1st Armored Division, Fort Bliss, Texas

Luke Bloomquist, MD is a member of the following medical societies: American Academy of Family Physicians, Society of US Army Flight Surgeons

Disclosure: Nothing to disclose.

Gary P Holmes, MD, FSHEA, FIDSA Joint Professor, Department of Epidemiology and Biostatistics, Texas A&M University School of Rural Public Health

Gary P Holmes, MD, FSHEA, FIDSA is a member of the following medical societies: American Society for Microbiology, Armed Forces Infectious Diseases Society, Infectious Diseases Society of America, Society for Healthcare Epidemiology of America

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

Thomas M Kerkering, MD Chief of Infectious Diseases, Virginia Tech Carilion School of Medicine

Thomas M Kerkering, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Physicians, American Public Health Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Medical Society of Virginia, Wilderness Medical Society

Disclosure: Nothing to disclose.

Mark R Wallace, MD, FACP, FIDSA Clinical Professor of Medicine, Florida State University College of Medicine; Clinical Professor of Medicine, University of Central Florida College of Medicine

Mark R Wallace, MD, FACP, FIDSA is a member of the following medical societies: American College of Physicians, American Medical Association, American Society for Microbiology, Infectious Diseases Society of America, International AIDS Society, Florida Infectious Diseases Society

Disclosure: Nothing to disclose.

Pranatharthi Haran Chandrasekar, MBBS, MD Professor, Chief of Infectious Disease, Department of Internal Medicine, Wayne State University School of Medicine

Pranatharthi Haran Chandrasekar, MBBS, MD is a member of the following medical societies: American College of Physicians, American Society for Microbiology, International Immunocompromised Host Society, Infectious Diseases Society of America

Disclosure: Nothing to disclose.

The authors and editors of Medscape Reference gratefully acknowledge the contributions of previous authors Larry I Lutwick, MD, and Adam M Rotunda, MD, to the development and writing of this article.

Parapoxviruses

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