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ARS Home » Research » Publications at this Location » Publication #271710

Title: Newcastle disease: An in-depth review including epidemiology and molecular diagnostics

item Miller, Patti

Submitted to: Meeting Abstract
Publication Type: Abstract Only
Publication Acceptance Date: 9/5/2011
Publication Date: N/A
Citation: N/A

Interpretive Summary:

Technical Abstract: Infections of birds with strains of avian paramyxovirus serotype 1 (APMV-1), (synonyms: Newcastle disease virus (NDV), pigeon PMV-1 (PPMV-1)) are associated with two clinical outcomes: 1) Newcastle disease (ND) results from infections with virulent APMV-1, and is also called Exotic ND (END) in U. S. Code of Federal Regulations, or virulent NDV (vNDV). Virulent forms of the disease are reportable to regulatory agencies because of the potential of rapid spread and devastating losses. ND in poultry impacts international trade. 2) Lentogenic Newcastle disease virus infections are typically the cause of mild or inapparent clinical forms unless exacerbated by complicating infections. Virus shed from respiratory and intestinal tract of infected birds is transmitted by aerosol and/or ingestion. Species and the breed of the infected host have some affect on clinical disease observed. Chickens are most the most susceptible species, turkeys more resistant, and generally waterfowl are believed to be quite resistant although there were severe outbreaks of ND in geese in Israel and China. Gross lesions are usually unremarkable except in birds infected with viscerotropic velogenic viruses which may have eyelid edema, perithymic hemorrhage and occasionally edema, splenic necrosis, and necrohemorrhagic lesions localized at the sites of lymphoid aggregation. The primary lesions of neurotropic velogenic ND are neuronal degeneration and variable disruption of heart muscle. Gross lesions of the viscerotropic strains are similar to lesions of highly pathogenic avian influenza and are only suggestive of a possible diagnosis. Definitive diagnosis requires virus isolation, most often from oropharyngeal and/or cloacal swabs from live birds, or tissue samples from necropsied birds. Detection of hemagglutination in culture fluids and inhibition of that hemagglutination with NDV specific antiserum confirms the diagnosis of an APMV-1 infection. Characterization of the virulence of an isolate usually requires chicken inoculation but a presumptive indication of virulence potential may be accomplished by noting the time to death of inoculated embryos (more rapid death usually indicates a more virulent virus) and by determining the deduced amino acid sequence of the fusion protein cleavage site from nucleotide sequence analysis of reverse transcriptase polymerase chain reaction (RT-PCR) product of fusion gene. Real time RT-PCR procedures were developed and validated to detect most NDV strains and within that broad grouping the END virus in swab samples during the outbreak in California. The genes of NDV and the proteins for which they code are: NP – nucleocapsid protein; P - phosphoprotein; M – matrix protein; F – fusion glycoprotein; HN – hemagglutinin-neuraminidase glycoprotein; L – polymerase protein. The two NDV surface glycoproteins are critical to establish a cellular infection. The HN protein provides the initial virus attachment and the F protein functions to fuse virus and cell membranes for entry of the virus nucleocapsid into the cell. Biosecurity is a critical component of any disease control program even when there are efficacious vaccines available as is the case with ND. A complete program includes for example limiting visitors to any production facility, rodent and free-flying bird control to prevent entry into bird housing, preventing feed contamination, and avoiding use of shared equipment as well as use of vaccines where appropriate and providing surveillance for all diseases of concern. Low virulence strains of NDV, B1, La Sota and VG/GA, are used in live vaccines and in the preparation of inactivated whole virus vaccines prepared as oil emulsions. Both live and inactivated vaccines are used widely in chicken and turkey flocks. These vaccines are protective against disease but not against infection therefore use of vacc