Sheep Pox and Goat Pox (SGP)
Last updated June 24, 2003
Agent
Hosts
Epidemiology
SGP As a Biological Weapon
Clinical Features
Differential Diagnosis
Laboratory Diagnosis
Treatment
Prevention
Outbreak Control
Public Health Issues
References
Agent
Sheep pox and goat pox (collectively known as SGP) were recognized in the second century AD. However, they were not recognized as contagious diseases until 1673. SGP is a viral disease that causes the formation of generalized pox lesions and systemic illness in affected sheep and goats. Characteristics of SPG virus (SPGV) include:
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Family: Poxviridae
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Genus: Capripoxvirus
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Cannot be serologically distinguished from the virus that causes lumpy skin disease
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Has only one serotype but numerous strains that affect sheep only, goats only, or both
Environmental Survival of SGPV
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Resistant to desiccation and to acidic and alkaline conditions (see References: VEIN)
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Can survive for years in dried scabs; remains viable in wool for 2 months and on environmental surfaces for 6 months (see References: OIE: Technical disease card database)
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Hosts
As the name implies, the primary hosts of SGP are sheep and goats. The virus can replicate in cattle but does not cause clinical disease. It has not yet been detected in wild ungulates, and there has been no evidence that SGP is infectious to humans (see References: House 1998).
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Epidemiology
Transmission
SGP is transmitted through direct contact and can be passed between sheep and goats. Routes of transmission include:
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Inhalation of aerosols from acutely infected animals
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Inhalation of aerosols from dust contaminated by pox scabs in barns and night holding areas
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Contact through skin abrasions by fomites or direct contact with a pox lesion or scab
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Insect transmission (less likely)
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Intravenous, intradermal, intranasal, or subcutaneous inoculation (experimental only) (see References: House 1998)
Sources
The main source of the virus is skin lesions (see References: VEIN).
Occurrence
SGP is endemic in Africa, the Middle East, the Indian subcontinent, and much of Asia. A similar disease was reported in the western United States, but it was not proven to be SGP (see References: House 1998). SPG has recently made frequent appearances in southern Europe (see References: OIE: Manual of standards). A few of the recent outbreaks are listed below:
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In September 2002, an outbreak occurred in eastern Russia. There were 391 cases reported, with 66 deaths and 325 animals slaughtered (see References: OIE: Sheep pox and goat pox in Russia).
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In December 2001, there were seven outbreaks of sheep pox reported in Morocco. Fifty cases were reported, with 42 deaths (see References: OIE: Sheep pox in Morocco).
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SGP As a Biological Weapon
Characteristics that make SGP a potential biological weapon include:
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High morbidity and extremely high mortality in young animals
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Significant economic losses in terms of reduced productivity and lower quality of wool and leather (see References: Rao 2000).
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Can be spread by many routes, including aerosol and fomite transmission
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Clinical Features
SGP is an acute to chronic disease of sheep and goats that can manifest in a papulovesicular or nodular form. The severity of disease varies with age of the animal. Lambs and kids under 1 month of age suffer from a very severe generalized form of SGP. In older animals, clinical signs may be less severe and mortality is lower. Clinical features are outlined in the table below.
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Clinical Features of Sheep Pox and Goat Pox
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Feature
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Characteristics
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Incubation period
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4 to 8 days; can be up to 3 wk
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General clinical signs
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Fever within 3-5 days after inoculation Depression Conjunctivitis Lacrimation Rhinitis Photophobia Generalized pox lesions throughout skin and mucous membranes within 2 days; most easily observed on hairless parts of body (perineum, inguinal area, scrotum, udder, axilla, muzzle) (see FAO figure) More severe skin lesions with more severe illness Lymphadenitis Focal viral pneumonia with lesions distributed uniformly throughout lungs (see FAO figure) Respiratory rate of up to 90/min Anorexia and emaciation Nervous signs Swollen muzzle Nares and oral mucosa may have extensive lesions Secondary bacterial infection (may interfere with healing) Disease may last 4-6 wk Full recovery after 3 mo Abortion rare Death caused by infection of internal organs, especially lungs Morbidity rate up to 80%, mortality up tp 50%
(adults) Morbidity rate up to 100%, and mortality up to 95% (lambs and kids under 1 mo) Mortality rate increases to 50%-90% with peste des petits ruminants coinfection
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Papulovesicular form
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White-grey papules that dessicate and form easily removable crusts Papules may transform into vesicles Vesicle rupture leaves thick crust over lesion
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Nodular form ("stone pox")
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Nodules arise from papules Involves all layers of skin and subcutaneous tissue Necrosis and sloughing of nodules leaves hairless scar
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The lesions in SGP involve the entire epidermis and dermis and penetrate into the subcutaneous tissue; they follow a regular development pattern (see References: House 1998):
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First appears as an erythematous area (macula)
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Progresses to a raised, slightly blanched erythematous lesion with edema in the central part of the lesion (papula)
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If palpated, lesions feel thick
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A transudate may form during the vesicular stage of the lesion
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Vesicles are rarely found on the skin
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Center of the lesion becomes necrotic, appearing depressed and gray, and is surrounded by an area of hyperemia
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2 to 4 weeks after the first signs, a scab forms
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With severe lesions, scars may form after healing
In some cases, the lesions on the eyes may be so severe that the inflammation causes the eyes to close. Lesions may also be found in the pharynx, epiglottis, trachea, vulva, prepuce, testicles, udder, teats, and the epithelium of the rumen and omasum. The lesions in the lungs may be severe, extensive, and uniformly distributed throughout owing to hematogenous infection.
The mortality rate of SGP is worsened by poor nutrition, heavy parasitism, and severe climatic conditions.
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Differential Diagnosis
The following conditions should be considered in the diagnosis of SGP (see References: House 1998; VEIN):
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Contagious ecthyma (contagious pustular dermatitis)
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Bluetongue
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Peste des petits ruminants
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Photosensitization
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Dermatophilosis
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Sheep scab (psoroptic mange)
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Insect bites
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Parasitic pneumonia
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Caseous lymphadenitis
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Streptothricosis (Dermatophilus congolensis infection)
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Mange
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Laboratory Diagnosis
Samples for laboratory diagnosis should be obtained from both acute and chronic cases. The samples needed include the following (see References: House 1998):
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Skin biopsies of early lesions
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Aspirates from enlarged lymph nodes
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Necropsy samples, including a full set of tissue samples, especially from gross lesions of the lungs, trachea, and rumen
The samples should be shipped under wet ice if they will arrive in less than 2 days and under dry ice if delivery will take longer. Samples for histopathology should be preserved in 10% buffered formalin (see References: House 1998).
The following tests can be used to identify the agent (see References: OIE: Manual of standards):
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Immunofluorescence staining of intracytoplasmic inclusion bodies
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Antigen detection enzyme-linked immunosorbent assay (ELISA)
Serologic tests include:
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Virus neutralization
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Indirect fluorescent antibody test
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Western blot analysis
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Agar gel immunodiffusion (AGID)
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ELISA
AGID is not recommended for the diagnosis of capripox because of a cross-reaction with antibody to contagious pustular dermatitis virus (the main consideration in differential diagnosis).
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Treatment
There is currently no treatment for SGP.
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Prevention
Vaccination
Two effective vaccines are available for SGP. The Romanian strain has been used for many years and is the most widely used. The Kenya O 180 strain is thought to have the best safety record and highest efficacy. All known strains of capripoxvirus share a neutralization site and will therefore cross-protect (see References: OIE: Manual of standards).
Killed vaccines are also available, but they have proven impractical in the field because they fail to provide lasting immunity (see References: House 1998). There is also a new recombinant vaccine that provides protection against capripox, rinderpest, and peste des petits ruminants.
Other measures
Additional methods of prevention include:
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Restrictions on movement of sheep and goats between infected and noninfected areas
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Restrictions on movement of animal products
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Decontamination of animal products before allowing entry into nonendemic areas
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Outbreak Control
Control procedures depend on how much the disease has spread.
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Before extensive spread:
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Quarantine area for at least 45 days after recovery (see References: OIE: Technical disease card database).
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Slaughter infected and exposed animals.
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Clean and disinfect premises.
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Vaccinate animals on surrounding premises.
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After the disease has spread:
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Vaccinate to control losses.
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Consider elimination of infected and exposed flocks via slaughter.
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Dispose of dead/slaughtered animals and contaminated materials.
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Clean and disinfect contaminated premises, equipment, and facilities (see References: House 1998).
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Public Health Issues
SGP does not cause infection in humans; therefore, there are no public health issues to be considered.
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References
FAO (Food and Agriculture Organization of the United Nations). In: Specific diseases of sheep and goat. Chap 5 [Web page]
House JA. Sheep and goat pox. In: US Animal Health Association, Committee on Foreign Animal Disease. Foreign animal diseases: the gray book. Ed 6. Part IV. Richmond, VA: US Animal Health Assoc, 1998 [Full text]
OIE (Office International des Epizooties/World Organization for Animal Health). Sheep and goat pox. In: Manual of standards for diagnostic tests and vaccines 2000. Chap 2.1.10 [Full text]
OIE (Office International des Epizooties/World Organization for Animal Health). Sheep pox and goat pox in Russia. Outbreak report, Sep 2002 [Full text]
OIE (Office International des Epizooties/World Organization for Animal Health). Sheep pox in Morocco. Outbreak report, Dec 2001 [Full text]
OIE (Office International des Epizooties/World Organization for Animal Health). Sheep pox and goat pox. Technical disease card database [Web page]
Parker MT, Collier LH. Topley and Wilson's principles of bacteriology, virology, and immunity. Vol 1. Kent, England: Edward Arnold, Hodder & Sloughton, 1990: 567-8
Rao TV, Bandyopadhyay SK. A comprehensive review of goat pox and sheep pox and their diagnosis. Anim Health Res Rev 2000 Dec; 1(2): 127-36 [Abstract]
VEIN (Veterinary Education and Information Network). Dermatological diseases: sheep pox [Web page]
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