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Fowlpox in Chickens and Turkeys

By

Deoki N. Tripathy

, DVM, MS, PhD, DACVM, DACPV, Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Illinois

Last full review/revision Jul 2019 | Content last modified Jul 2019
Topic Resources

Fowlpox is a worldwide viral infection of chickens and turkeys. Nodular lesions on unfeathered skin are common in the cutaneous form. In the diphtheritic form, which affects the upper GI and respiratory tracts, lesions occur from the mouth to the esophagus and on the trachea. Diagnosis is by observing characteristic gross and microscopic lesions and PCR. Vaccination can prevent the disease and limit spread in affected flocks.

Fowlpox is a slow-spreading viral infection of chickens and turkeys characterized by proliferative lesions in the skin that progress to thick scabs (cutaneous form) and by lesions in the upper GI and respiratory tracts (diphtheritic form). Virulent strains may cause lesions in the internal organs (systemic form). Fowlpox is seen worldwide.

Etiology and Epidemiology of Fowlpox

The large DNA virus (an avipoxvirus in the Poxviridae family) is resistant and may survive in the environment for extended periods in dried scabs. Photolyase and A-type inclusion body protein genes in the genome of fowlpox virus appear to protect the virus from environmental insults. Field strains associated with outbreaks and vaccine strains show differences in their genomic profiles, although the strains can be differentiated to some extent by restriction endonuclease analysis, nucleotide analysis of specific genes, and immunoblotting. Molecular analyses of vaccine and field strains of fowlpox viruses have shown significant differences.

The virus is present in large numbers in the lesions and is usually transmitted by contact through abrasions of the skin. Skin lesions (scabs) shed from recovering birds in poultry houses can become a source of aerosol infection. Mosquitoes and other biting insects may serve as mechanical vectors. Transmission within a susceptible flock is rapid when mosquitoes are plentiful. The disease tends to persist for extended periods in multiple-age poultry complexes because of slow spread of the virus and availability of susceptible birds.

Clinical Findings of Fowlpox

The cutaneous form of fowlpox is characterized by nodular lesions on various parts of the unfeathered skin of chickens and on the head and upper neck of turkeys. Generalized lesions of feathered skin may also be seen. In some cases, lesions are limited chiefly to the feet and legs. The lesion is initially a raised, blanched, nodular area that enlarges, becomes yellowish, and progresses to a thick, dark scab. Multiple lesions usually develop and often coalesce. Lesions in various stages of development may be found on the same bird. Localization around the nostrils may cause nasal discharge. Cutaneous lesions on the eyelids may cause complete closure of one or both eyes. Only a few birds develop cutaneous lesions at one time. Lesions are prominent in some birds and may significantly decrease flock performance.

In the diphtheritic form of fowlpox, lesions develop on the mucous membranes of the mouth, esophagus, pharynx, larynx, and trachea (wetpox or fowl diphtheria). Occasionally, lesions are seen almost exclusively in one or more of these sites. Caseous patches firmly adherent to the mucosa of the larynx and mouth or proliferative masses may develop. Mouth lesions interfere with feeding. Tracheal lesions cause difficulty in respiration. Laryngeal and tracheal lesions in chickens must be differentiated from those of infectious laryngotracheitis, which is caused by a herpesvirus that produces intranuclear inclusions. In cases of systemic infection caused by virulent fowlpox virus strains, lesions may be seen in internal organs. More than one form of the disease, ie, cutaneous, diphtheritic, and/or systemic, may be seen in a single bird.

Often, the course of the disease in a flock is protracted. Extensive infection in a layer flock results in decreased egg production. Cutaneous infections alone ordinarily cause low or moderate mortality, and these flocks generally return to normal production after recovery. Mortality is usually high in diphtheritic or systemic infections.

Diagnosis of Fowlpox

  • Characteristic gross and microscopic lesions and PCR

Cutaneous infections usually produce characteristic gross and microscopic lesions. When only small cutaneous lesions are present, it is often difficult to distinguish them from abrasions caused by fighting. Microscopic examination of affected tissues stained with H&E reveals eosinophilic cytoplasmic inclusion bodies. This is the most commonly used method in diagnostic laboratories. Cytoplasmic inclusions are also detectable by fluorescent antibody and immunohistochemical methods (using antibodies against fowlpox virus antigens). The elementary bodies in the inclusion bodies can be detected in smears from lesions stained by the Gimenez method. Viral particles with typical poxvirus morphology can be demonstrated by negative-staining electron microscopy as well as in ultrathin sections of the lesions. The virus can be isolated by inoculating chorioallantoic membrane of developing chicken embryos, susceptible birds, or cell cultures of avian origin. Chicken embryos (9–12 days old) from an SPF flock are the preferred and convenient host for virus isolation.

The genomic profiles of field isolates and vaccine strains of fowlpox virus can be compared by restriction fragment length polymorphism. Detailed genetic analysis reveals differences between vaccine strains and field strains responsible for outbreaks of fowlpox in previously vaccinated chicken flocks. Whereas vaccine strains of fowlpox virus contain remnants of long terminal repeats of reticuloendotheliosis virus (REV), most field strains contain full-length REV in their genome.

Although nucleic acid probes derived from cloned genomic fragments of fowlpox virus have been used for differentiation of the diphtheritic form of fowlpox (involving the trachea) from infectious laryngotracheitis, PCR amplification of virus-specific genomic fragments is becoming more convenient where facilities are available.

PCR can be used to amplify genomic DNA sequences of various sizes using specific primers. This procedure is useful when an extremely small amount of viral DNA is present in the sample. PCR has been used effectively to differentiate field and vaccine strains of the virus, whether full-length REV is present in those strains that are associated with outbreaks in vaccinated birds. In this regard, DNA isolated from the formalin-fixed tissue sections of birds that are histologically positive for fowlpox can be used for PCR amplification of genomic fragments using specific primers. Because most outbreaks of fowlpox in previously vaccinated chickens are caused by strains with a genome that contains full-length REV, use of REV envelope-specific primers to determine the presence of full-length REV is helpful in such cases.

Two monoclonal antibodies that recognized different fowlpox virus antigens were developed. These monoclonal antibodies were useful for strain differentiation by immunoblotting.

The complete nucleotide sequence of the genome of fowlpox virus, canarypox virus, and some other avianpox viruses have been determined. This information is useful to compare the sequences of selected genes of other avian poxviruses as well as in their phylogenic analysis.

Naturally infected or vaccinated birds develop both humoral and cell-mediated immune responses. Humoral immune response can be measured by ELISA, agar gel precipitation (AGP), or virus neutralization tests. AGP is a very simple and convenient test, but its sensitivity is low compared with ELISA.

Prevention and Treatment of Fowlpox

  • Vaccination effectively prevents the disease and may limit spread within actively infected flocks.

Where fowlpox is prevalent, chickens and turkeys should be vaccinated with a live-embryo or cell-culture-propagated virus vaccine. The most widely used vaccines are attenuated fowlpox virus and pigeonpox virus isolates of high immunogenicity and low pathogenicity. In high-risk areas, vaccination with an attenuated vaccine of cell-culture origin in the first few weeks of life and revaccination at 12–16 weeks is often sufficient. Health of birds, extent of exposure, and type of operation determine the timing of vaccinations. Because the infection spreads slowly, vaccination is often useful to limit spread in affected flocks if administered when <20% of the birds have lesions. Passive immunity may interfere with multiplication of vaccine virus; progeny from recently vaccinated or recently infected flocks should be vaccinated only after passive immunity has declined.

Vaccinated birds should be examined 1 week later for swelling and scab formation (“take”) at the site of vaccination. Absence of “take” indicates lack of potency of vaccine, passive or acquired immunity, or improper vaccination. Revaccination with another serial lot of vaccine may be indicated.

Zoonotic Risk of Fowlpox

There is no zoonotic risk associated with fowlpox virus. Avian poxviruses cause a productive infection in avian species but a nonproductive infection in mammalian hosts. Consequently, avianpox viruses have been used as vectors for expression of genes from mammalian pathogens in the development of safe recombinant vaccines.

Key Points

  • Fowlpox is a disease of economic importance in chickens and turkeys.

  • Histopathology of infected tissue is commonly used for diagnosis.

  • Live vaccines are available for prevention.

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