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Newcastle disease
1.
Newcastle
Importance Newcastle disease is a viral disease of birds with a wide range of clinical signs Disease from mild to severe. This disease is caused by a diverse group of viruses; the milder strains are endemic in the United States, while highly virulent strains are exotic. The Avian Paramyxovirus-1Infection, highly virulent form of Newcastle disease is one of the most important poultry dis- eases worldwide. Chickens are particularly susceptible, and may experience morbid- Goose Paramyxovirus Infection ity and mortality rates up to 100%. Outbreaks of virulent Newcastle disease have a tremendous impact on backyard chickens in developing countries, where these birds are a significant source of protein and this disease is endemic. In developed countries, Last Updated: July 14, 2008 where the more virulent forms of the virus have been eradicated, trade embargoes and restrictions cause significant economic losses during outbreaks. In the United States, one epidemic in 2002-2003 resulted in the death of more than three million birds and caused industry losses estimated at $5 billion. Low pathogenicity isolates, which are common in poultry worldwide, can decrease productivity but have no impact on in- ternational trade. Although the most significant impact of Newcastle disease is on chickens, other species can also be affected. Some pet and zoo birds become ill after infection, while other species can carry and shed virulent viruses asymptomatically. These birds, par- ticularly illegally imported psittacines, can introduce Newcastle disease viruses to dis- ease-free countries. Newcastle disease is also an important cause of death during the first three months of life in cormorant colonies. Since the late 1990s, novel strains have caused outbreaks among geese (a species that is usually resistant to disease) in China. Etiology Newcastle disease is caused by viruses in the serotype avian paramyxovirus type 1 (APMV-1). These viruses, which are called either APMV-1 or Newcastle disease viruses (NDV), are members of the genus Avulavirus in the family Paramyxoviridae. APMV-1 strains maintained in pigeon populations have some antigenic differences from other NDV isolates, and are sometimes called pigeon paramyxovirus type 1 (PPMV-1). APMV-1 strains are classified into three pathotypes based on their virulence in chickens. Lentogenic strains are the least virulent, mesogenic strains are moderately virulent, and velogenic strains are the most virulent. Most strains cluster toward the two extremes of virulence, and are either lentogenic or velogenic. Velogenic viruses can be subdivided into a neurotropic form, which is typically associated with respira- tory and neurologic signs, and a viscerotropic form with hemorrhagic intestinal le- sions. These clinical forms overlap and are rarely clear-cut, even in specific pathogen free (SPF) chickens. Several tests can be used to assess the virulence of an APMV-1 strain, and coun- tries may use different criteria to define Newcastle disease. The OIE defines Newcas- tle disease as an infection caused by a highly virulent APMV-1 virus – an isolate that has either 1) an intracerebral pathogenicity index (ICPI) of at least 0.7 in day-old chicks, or 2) an amino acid sequence that resembles those seen in highly virulent vi- ruses (multiple basic amino acids at the C-terminus of the F2 protein and phenyla- lanine at residue 117 of the F1 protein). Such viruses must be reported to the OIE and have severe repercussions for international trade. The U.S. defines “exotic Newcastle disease” (END) as the disease caused by velogenic viscerotropic strains. APMV-1 isolates can also be separated into two clades, called class I and class II, based on the genetic relationship between viruses. The vast majority of APMV-1 strains belong to class II, which is divided into at least nine genotypes (I to IX). Class I isolates have been found mainly in wild waterfowl, and are usually of low pathogenicity. Species Affected Newcastle disease primarily affects birds. Some avian species become ill, while others carry these viruses asymptomatically. Infections also occur in humans, but have not been reported in other species of mammals. NEWC_A2008 © 2005 CFSPH page 1 of 7
2.
Newcastle Disease
APMV-1 viruses are known to infect more than 250 1 for only 1-2 weeks, but psittacine birds often shed these species of birds in 27 orders; other avian species may also viruses for several months. Some species of psittacine be susceptible. Wild birds, particularly waterfowl (order birds can excrete virus for more than a year. Prolonged Anseriformes), tend to carry these viruses asymptomati- shedding has also been reported in some members of cally. Most of the viruses found in wild birds are lento- other orders, including owls (more than four months) and genic; however, virulent APMV-1 has become established cormorants (one month). Shedding can be sporadic. in some cormorant populations (Phalacrocorax sp.; order APMV-1 is present in all parts of the carcass, and some Pelecaniformes) and causes disease in juvenile birds. outbreaks in raptors have been linked to eating infected Susceptibility to illness varies widely among poultry chicken, pigeon or quails. When the temperature is just and pet birds. Members of the order Phasianiformes (gal- above freezing (1-2ºC [34-35ºF]), this virus is reported to linaceous birds), particularly chickens, are highly suscep- survive on chicken skin for up to 160 days and in bone tible to disease. Turkeys are less likely to develop severe marrow for nearly 200 days. The importance of aerosols symptoms, and the susceptibility of game birds (pheas- in long distance transmission is controversial. In one ants, partridges, quail and guinea fowl) varies with the study, APMV-1 was found 64 meters but not 165 meters species. Ducks and geese usually have inapparent infec- downwind of an infected farm. The survival of aerosol- tions, but some isolates (in genotypes VII and VI) have ized virus is probably dependent on humidity and other caused outbreaks among geese in China since the 1990s. environmental factors, as well as the concentration of Clinical cases have been also been described occasionally infected poultry. Some isolates can be transmitted through in ducks. Outbreaks have been reported in ostriches (order the egg to hatching chicks. Egg-associated transmission of Struthioniformes). Pigeons (order Columbiformes) are highly virulent isolates is possible but uncommon, as the susceptible to disease, and lentogenic or mesogenic embryo usually dies unless the viral titer in the egg is low. APMV-1 viruses (PPMV-1) are endemic in pigeon popu- Other sources of virus for newly hatched chicks are feces- lations. Susceptibility to disease varies widely in psit- contaminated eggshells and cracked or broken eggs. tacine birds (order Psittaciformes); cockatiels often die or APMV-1 is readily transmitted on fomites. Survival develop neurological signs, but some species tend to carry is prolonged on eggshells and especially in feces, com- velogenic viruses subclinically. pared to an inorganic surface (filter paper). Published Some birds found in the wild or in zoos also become information on virus survival is highly variable, probably ill. Penguins (order Sphenisciformes) are highly suscepti- because it is affected by the humidity, temperature, sus- ble to Newcastle disease, and birds often die acutely. Fa- pending agent and exposure to light. One study reported tal or severe disease has been reported in some raptors that APMV-1 survived in contaminated, uncleaned poul- (order Falconiformes) including a bearded vulture try houses for up to 7 days in summer, as long as 14 days (Gypaetus barbatus), some species of falcons, a captive in the spring, and 30 days during the winter. Another white-tailed sea eagle (Haliaeetus albicilla) and a wild group reported virus isolation up to 16 days after depopu- osprey (Pandion haliaetus). Other raptors tend to be resis- lation of an unvaccinated flock. However, one study tant to disease. Illness has also been reported in gulls (or- found that APMV-1 remained viable for up to 255 days in der Charadriiformes) owls (order Strigiformes) pelicans a henhouse, at ambient temperatures of –11ºC (12ºF) to (order Pelecaniformes) and a Northern gannet (Morus 36ºC (97ºF). At 23-29ºC (73-84ºF), APMV-1 is reported bassanus; order Pelecaniformes). Susceptibility varies to survive in contaminated litter for 10 to 14 days, and at among passerine birds (order Passeriformes), with some 20ºC (68ºF) in soil for 22 days. Virus has also been re- species excreting virus subclinically and others develop- covered from earthworms for 4 to 18 days, and from ex- ing severe clinical signs. Occasional deaths have also perimentally contaminated lake water for 11 to 19 days. been reported in Corvidae (crows and ravens). Flies might be able to transmit APMV-1 mechanically, but it is still uncertain whether insects can carry enough Geographic Distribution virus to infect poultry. The importance of arthropod-borne Velogenic APMV-1 is endemic in Asia, the Middle transmission may vary with the type of housing and flock East, Africa, Central and South America, and parts of management. Mexico. Virulent strains are endemic in wild cormorants The epidemiology of APMV-1 is incompletely un- in the U.S. and Canada, but commercial poultry are free derstood; however, wild birds, particularly waterfowl, of velogenic isolates. Lentogenic isolates are found in may be the reservoir hosts for lentogenic viruses. These poultry throughout the world, including the U.S. Mesog- viruses could become more virulent after becoming estab- enic strains may also be found, but are less common. lished in poultry. Some recent outbreaks were apparently caused by velogenic viruses that emerged from local, low Transmission pathogenic isolates. Acquisition of virulence has also APMV-1 can be transmitted by inhalation or inges- been reported in experimentally infected birds. Psittacine tion (fecal/ oral route). Birds shed virus in both feces and birds have introduced APMV-1 to poultry flocks in some respiratory secretions. Gallinaceous birds excrete APMV- outbreaks. Although early reports suggested that virulent Last Updated: July 2008 © 2008 CFSPH page 2 of 7
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be endemic in wild psittacine populations, In psittacine birds, Newcastle disease may be acute, these birds are now thought to become infected after cap- subacute, chronic or inapparent. The clinical signs are ture. Cormorants could transmit velogenic viruses to poul- highly variable, but may include respiratory and/or neu- try; gulls associated with cormorant colonies could also rologic signs, as well as diarrhea and sudden death. Respi- be a source of virus, and are more likely to visit farms. ratory signs tend to predominate in ostriches and emus, Lentogenic or mesogenic APMV-1 viruses are endemic in and these birds are usually less severely affected than pigeon populations, and can become more virulent if they chickens. Diarrhea, polydipsia, conjunctivitis and neuro- enter and cycle in poultry flocks. logical signs are generally seen in pigeons and doves. Neurological signs, particularly talon convulsions and the Incubation period inability to coordinate flight, are prominent in raptors. The incubation period in poultry varies from 2 to 15 Sudden death may also occur. Geese and ducks are usu- days depending on the virulence of the strain and the sus- ally infected subclinically (with most strains), but illness ceptibility of the population. In chickens infected with is occasionally reported. Neurological signs, diarrhea, velogenic isolates, an incubation period of 2 to 6 days is anorexia and sudden death may be seen in these birds. common. Incubation periods up to 25 days have been Respiratory symptoms appear to be rare in waterfowl. reported in some avian species. In cormorant colonies, Newcastle disease is usually Clinical signs characterized by neurological signs, and illness is almost always limited to juveniles. Affected birds may be weak, The clinical signs vary with the pathogenicity of the with paresis or paralysis of one or both legs and/or wings, isolate and the species of bird. In chickens, lentogenic incoordination, tremors, torticollis and/or drooping of the strains usually cause subclinical infections or mild respi- head. Sick or dead birds can be found in the same nest as ratory disease with coughing, gasping, sneezing and rales. apparently normal nestmates. Older fledged cormorants Mesogenic strains can cause acute respiratory disease and may be seen trying to walk, fly, swim or dive. Sick or dead neurologic signs in some chickens, but the mortality rate gulls and juvenile white pelicans have been seen near af- is usually low. Lentogenic or mesogenic strains can pro- fected cormorant colonies. Sick pelicans had neurological duce more severe symptoms if the flock is co-infected signs similar to cormorants, such as unilateral or bilateral with other pathogens. wing and or leg paralysis/ paresis, drooping neck, and an Velogenic strains cause severe, often fatal, disease in inability or reluctance to move; however, it has not been chickens. The clinical signs are highly variable. Most proven that these symptoms were caused by APMV-1. In birds are lethargic and inappetent, and the feathers may be addition to increased mortality, the only clinical signs re- ruffled. Conjunctival reddening and edema may be an ported in gulls were wing and/or leg paralysis or paresis. early sign. Some birds develop watery, greenish or white diarrhea, respiratory signs (including cyanosis) or swell- Post Mortem Lesions Click to view images ing of the tissues of the head and neck. Neurologic signs Significant gross lesions are usually found only in including tremors, clonic spasms, paresis or paralysis of birds infected with velogenic strains. The head or perior- the wings and/or legs, torticollis (twisted neck) and cir- bital region may be swollen, and the interstitial tissue of cling may also be seen. Nervous signs can occur concur- the neck can be edematous, especially near the thoracic rently with other symptoms but are generally seen later in inlet. Congestion or hemorrhages may be found in the the course of disease. Egg laying often declines dramati- caudal pharynx and tracheal mucosa, and diphtheritic cally, and eggs may be misshapen, abnormally colored, membranes sometimes occur in the oropharynx, trachea and rough or thin-shelled, with watery albumen. Sudden and esophagus. Petechiae and small ecchymoses may be death, with few or no symptoms, is also common. Birds seen in the mucosa of the proventriculus. Hemorrhages, that survive for two weeks usually live but may have ulcers, edema and/or necrosis often occur in the cecal permanent neurological damage and/or a permanent de- tonsils and lymphoid tissues of the intestinal wall (includ- crease in egg production.. The symptoms may be less ing Peyer’s patches); this lesion is particularly suggestive severe in vaccinated birds. of Newcastle disease. Thymic and bursal hemorrhages Similar clinical signs are seen in other species of birds; may also be present, but can be difficult to see in older however, either neurological signs or respiratory signs can birds. The spleen may be enlarged, friable and dark red or predominate in some species. Newcastle disease is gener- mottled. Pancreatic necrosis and pulmonary edema can be ally milder in turkeys than chickens, but some strains may found in some birds. The ovaries are often edematous or cause significant disease. Severe clinical signs can some- degenerated, and may contain hemorrhages. Some birds, times be seen in game birds, particularly pheasants. Respi- particularly those that die suddenly, have few or no gross ratory signs have been reported in some but not all out- lesions. Similar lesions have been reported in geese, tur- breaks in pheasants. Guinea fowl sometimes become ill, keys, pheasants and other species infected with virulent but they can also carry velogenic isolates subclinically. strains. In experimentally infected guinea fowl, the only Last Updated: July 2008 © 2008 CFSPH page 3 of 7
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Newcastle Disease significant lesions
were hemorrhages at the tip of the high, and the symptoms could be consistent with this dis- glands of the proventriculus and in the cecal tonsil. ease. Unexpected deaths are sometimes the first sign. In chickens infected with less virulent strains, the le- There are no pathognomonic gross lesions; however, sions may be limited to congestion and mucoid exudates some lesions may be suggestive, particularly when several in the respiratory tract, and opacity and thickening of the carcasses are examined. air sacs. More severe lesions can be seen in birds with Differential diagnosis secondary bacterial infections. The differential diagnosis for velogenic Newcastle Morbidity and Mortality disease includes other causes of septicemia, enteritis, res- Morbidity and mortality rates vary greatly depending piratory disease and/or neurologic signs. In poultry, these on the virulence of the strain and susceptibility of the host. diseases include fowl cholera, highly pathogenic avian Lentogenic and mesogenic viruses usually kill few birds; in influenza, laryngotracheitis, the diphtheritic form of fowl poultry, the mortality rate is approximately 10% for pox, psittacosis, mycoplasmosis, infectious bronchitis, mesogenic strains and negligible with lentogenic strains. aspergillosis, and management problems such as depriva- Concurrent illnesses may increase the severity of illness tion of water or feed, and poor ventilation. In pet birds, and result in a higher death rate. In contrast, velogenic iso- diseases to consider include psittacosis, Pacheco’s dis- lates have morbidity and mortality rates up to 100% in un- ease, salmonellosis, adenovirus, and nutritional deficien- vaccinated chickens. The onset of disease is usually rapid, cies, as well as other paramyxovirus infections. In cormo- and the virus often spreads quickly, particularly in group- rants, botulism, fowl cholera and traumatic skeletal ab- housed flocks. Some isolates can affect young birds more normalities are among the differentials. severely. Vaccinated poultry tend to have milder infections. Laboratory tests In one epidemic mainly affecting vaccinated chickens, Newcastle disease can be diagnosed by isolating flock mortality rates were 30% to 90%. APMV-1 from affected birds. This virus is usually recov- Other species of birds are usually affected less se- ered by inoculating samples into 9-11 day old embryo- verely than chickens. Velogenic isolates can kill up to nated chicken eggs. Chorioallantoic fluid from the eggs is 100% of experimentally infected pheasants, but some tested for hemagglutinating activity, and any agents that individual birds may be resistant to disease, and the mor- hemagglutinate are examined for hemagglutination inhibi- tality rate reported during outbreaks is highly variable. tion (HI) with a monospecific antiserum to APMV-1. From 22% to 77% of the pheasants in affected flocks died Some HI tests that use monoclonal antibodies can identify during one epizootic in Denmark, but in another outbreak particular strains of APMV-1. APMV-1 can cross-react in the U.K., the mortality rate was less than 3% even in with some other avian paramyxoviruses, particularly the most severely affected pen. In guinea fowl, the mor- APMV-3 and APMV-7, in the HI test. tality rate was 21% during one outbreak, and 8-100% in The pathogenicity of the isolate can be quantified by 1) experimental infected birds (depending on the strain of the mean death time (MDT) in chicken embryos, 2) the the virus). Mortality rates as high as 28% have been re- intracerebral pathogenicity index (ICPI) in 1-day old ported in ostriches in some outbreaks, but few birds died chicks, or 3) the intravenous pathogenicity index (IVPI) in in others. Newcastle disease is rarely severe in waterfowl; 6-week old chickens. In the MDT assay, velogenic isolates however, some velogenic strains circulating in China have have an MDT of less than 60 hours, mesogenic strains have an average morbidity rate of 17.5% and an average mor- an MDT of 60-89 hours, and lentogenic viruses have an tality rate of 9% in geese. MDT greater than 90 hours. The ICPI and IVPI tests are APMV-1 (PPMV-1) is endemic in pigeons and doves scoring systems that evaluate illness or death in chickens. in many countries. In these birds, highly virulent strains The values in the ICPI test range from 0 to 2.0; the most have morbidity rates as high as 70% and mortality rates virulent viruses approach 2.0, while lentogenic strains are that approach 40%. Velogenic strains are endemic in usually close to 0.0. The values in the IVPI test are from 0 cormorants, but adult birds do not appear to develop clini- to 3.0; the IVPI for velogenic strains approach 3.0, while cal signs or die. The estimated mortality during several lentogenic strains and some mesogenic strains have IVPI outbreaks in juvenile cormorants ranged from less than values of zero. However, some viruses that can produce 1% to 92%. Up to 90% of juvenile white pelicans near severe disease have IVPI values of zero; the ICPI test is these colonies have died in some outbreaks; however, it generally preferred for this reason. Other variations of these has not been proven that the disease in pelicans was tests are also used; some can distinguish viscerotropic (ve- caused by APMV-1. logenic) from neurotropic strains. Diagnosis Reverse-transcription polymerase chain reaction (RT- PCR), gene sequencing, restriction enzyme analysis and Clinical other molecular techniques are also used to identify Newcastle disease should be considered, especially in APMV-1 in eggs or clinical specimens. Some of these chicken flocks, when the morbidity and mortality rates are tests can also determine the virus’s pathotype. Most iso- Last Updated: July 2008 © 2008 CFSPH page 4 of 7
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Newcastle Disease lates that
are highly virulent for chickens have a particular Control sequence, 112R/K-R-Q-K/R-R116 (multiple basic amino Good biosecurity can help prevent Newcastle disease acids) at the C-terminus of the F2 protein and phenyla- in poultry flocks. Flocks should not be allowed to contact lanine at residue 117 of the F1 protein. The presence of domesticated poultry of unknown health status, any pet this genetic sequence is enough to classify an isolate as birds (particularly psittacines), and wild or feral birds highly virulent for the purposes of international trade. If (particularly cormorants, gulls and pigeons). Whenever this pattern is not present, the pathogenicity of the virus possible, workers should avoid contact with birds outside must be determined in the ICPI or other test. Rapid diag- the farm. Biosecurity measures include bird-proofing nostic tests, as well as tests using monoclonal antibodies, houses, feed and water supplies, minimizing travel on and are optimized for more virulent viruses, and may not iden- off the facility, and disinfecting vehicles and equipment tify some lentogenic viruses (particularly Class I isolates). that enter the farm. Pests such as insects and mice should Serological assays may be useful in some circum- also be controlled. If possible, employees should shower stances. Hemagglutination inhibition is the most com- and change into dedicated clothing for work. All in/ all monly used serological test. Other tests include virus neu- out breeding (one age group per farm), with disinfection tralization, hemagglutination and enzyme-linked immu- between groups, is also advisable. More detailed biosecu- nosorbent assays (ELISA). Vaccination can interfere with rity guidelines can be found in the Internet Resources serologic testing. In some species, immunohistochemistry section of this factsheet. may be used to detect antigens in tissues; this test is not Similar biosecurity measures can protect birds kept in performed routinely for diagnosis in chickens. zoos or aviaries, or as pets (see Internet Resources). Estab- Samples to collect lishing an effective biosecurity program can decrease the Before collecting or sending any samples from ani- risk that hobby or pet birds would be euthanized during a mals with a suspected foreign animal disease, the Newcastle disease outbreak. Pet birds should be bought proper authorities should be contacted. Samples should only from suppliers who can certify that the birds have only be sent under secure conditions and to authorized been imported legally or bred in the U.S., and are healthy. laboratories to prevent the spread of the disease. New- Legally imported pet birds have been quarantined and castle disease is zoonotic; samples should be collected tested for velogenic strains of APMV-1. Domestically and handled with all appropriate precautions. raised birds are usually closed-banded. Some species such as Amazon parrots are difficult to raise domestically; ven- Tracheal and cloacal swabs should be taken from live dors who are selling large numbers of young birds of these birds for virus isolation. If cloacal swabs might harm the species (particularly when they are bargain-priced) without bird, fresh feces may be collected instead. Whenever pos- adequate documentation should be viewed with caution. sible, samples should be taken in the early stages of dis- Newly acquired birds should be isolated or quarantined for ease. At necropsy, samples should be collected from the at least 30 days, and they should be monitored closely for spleen, trachea, lung, intestines (particularly the cecal signs of illness. Avian carcasses (of any species) that could tonsil), intestinal contents, liver, kidneys, heart and brain. be infected with velogenic Newcastle disease should never Oronasal swabs should also be taken. Samples for virus be fed to raptors, chickens or other birds. Illegally imported isolation should be collected from recently dead birds or psittacines should be reported, because many of them may moribund birds after euthanasia. Tissues may be collected be carrying velogenic APMV-1. separately or pooled; intestinal samples are generally processed separately. These samples should be kept cold Vaccines are used in chickens, pheasants and other (e.g. on wet ice), and swabs should be sent to the labora- species. In addition, birds in aviaries, breeding farms and tory in transport medium. Similar tissues and feces are zoos are often vaccinated. Vaccination can protect birds collected for RT-PCR and other molecular assays. Clotted from clinical signs but does not necessarily prevent virus blood or serum samples can be submitted for serology. replication and shedding. Sentinel chickens are sometimes used to monitor vaccinated flocks. Recommended actions if highly virulent Outbreaks are eradicated with quarantines and Newcastle disease is suspected movement controls, depopulation of all infected and ex- posed birds, and thorough cleaning and disinfection of the Notification of authorities premises. Effective disinfectants include chlorhexidine, State and federal veterinarians should be informed sodium hypochlorite (6%), phenolic disinfectants and immediately of any suspected cases of highly virulent oxidizing agents (e.g. Virkon®). APMV-1 can also be (velogenic) Newcastle disease. inactivated by heat (56°C [133°F] for 3 hours or 60°C Federal: Area Veterinarians in Charge (AVIC): [140°F] for 30 min), acid (pH 3), ether and formalin; the http://www.aphis.usda.gov/animal_health/area_offices/ efficacy of formalin varies with the temperature. Whether State Veterinarians: flies are competent vectors for APMV-1 is still uncertain, http://www.aphis.usda.gov/vs/sregs/official.html but fly control is prudent on and near infected farms. Be- fore eradication begins, the facilities should be treated Last Updated: July 2008 © 2008 CFSPH page 5 of 7
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Newcastle Disease with insecticides
that can kill adult flies. Insect control References should be continued until disinfection is complete. Farms must generally remain empty for a few weeks before re- Aldous EW, Alexander DJ. Newcastle disease in pheasants stocking; the specific time may vary with the climate, (Phasianus colchicus): a review. Vet J. 2008 ;175:181-5. season and other factors. During some eradication pro- Alexander DJ. Newcastle disease. Br Poult Sci. 2001; 42:5-22. grams, government agencies may collect and test birds California Department of Food and Agriculture [CDFA]. that die suddenly in any facility. This measure can be Biosecurity guidelines to prevent the spread of exotic helpful in recognizing new cases. Newcastle disease. Information for bird owners [online]. Public Health CDFA; 2002. Available at: http://www.cdfa.ca.gov/ahfss/Animal_Health/pdfs/Biose Velogenic strains of APMV-1 can cause conjunctivi- cu_long_Dec_%202002.pdf. Accessed 18 Jul 2008. tis in humans, usually when the person has been exposed Chakrabarti S, King DJ, Afonso C, Swayne D, Cardona CJ, to large quantities of virus. Laboratory workers and vac- cination crews are affected most often. Poultry workers Kuney DR, Gerry AC. Detection and isolation of exotic are rarely infected, and handling or consuming poultry Newcastle disease virus from field-collected flies. J Med Entomol. 2007;44:840-4. products does not appear to be a risk. The conjunctivitis usually resolves rapidly without treatment, but APMV-1 Chen JP, Wang CH. Clinical epidemiologic and experimen- is shed in the ocular discharges for 4 to 7 days. All direct tal evidence for the transmission of Newcastle disease vi- or indirect contact with birds should be avoided during rus through eggs. Avian Dis. 2002;46:461-5. this time. Falcon M. Exotic Newcastle disease. Semin Avian and Exot Mild, self-limiting influenza-like disease with fever, Pet Med. 2004;13 79-85. headache and malaise has also been reported in humans; Garner G, Saville P, Fediaevsky A. Manual for the recogni- in some cases, it is uncertain whether the illness was tion of exotic diseases of livestock: A reference guide for caused by APMV-1 or misdiagnosed by cross-reactions in animal health staff [online]. Food and Agriculture Or- serologic tests. A recent report, confirmed by virus isola- ganization of the United Nations [FAO]; 2004. Newcas- tion, suggests that APMV-1 could cause serious opportun- tle disease. Available at: http://www.spc.int/rahs/. Ac- istic infections in people who are immunosuppressed. A cessed 5 Jul 2008. patient developed fatal pneumonia 18 days after receiving Gerlach H. Paramyxovirus. In: Harrison GJ, Harrison LR., a peripheral blood stem cell transplant. There was no his- editors. Clinical avian medicine and surgery. Philadel- tory of contact with poultry, and the isolate was most phia: WB Saunders; 1986. p. 421-426. closely related to APMV-1 viruses from pigeons. Glaser LC, Barker IK, Weseloh DV, Ludwig J, Windingstad RM, Key DW, Bollinger TK. The 1992 epizootic of Internet Resources Newcastle disease in double-crested cormorants in North America. J Wildl Dis. 1999;35:319-30. California Department of Food and Agriculture. Goebel SJ, Taylor J, Barr BC, Kiehn TE, Castro-Malaspina Newcastle Disease Information HR, Hedvat CV, Rush-Wilson KA, Kelly CD, Davis http://www.cdfa.ca.gov/ahfss/Animal_Health/Newcastle SW, Samsonoff WA, Hurst KR, Behr MJ, Masters PS. _Disease_Info.html Isolation of avian paramyxovirus 1 from a patient with a The Merck Veterinary Manual lethal case of pneumonia. J Virol. 2007;81:12709-14. http://www.merckvetmanual.com/mvm/index.jsp Jørgensen PH, Herczeg J, Lomniczi B, Manvell RJ, Holm E, United States Animal Health Association. Alexander DJ. Isolation and characterization of avian pa- Foreign Animal Diseases ramyxovirus type 1 (Newcastle disease) viruses from a http://www.vet.uga.edu/vpp/gray_book02/fad/index.php flock of ostriches (Struthio camelus) and emus (Dro- United States Department of Agriculture (USDA). maius novaehollandiae) in Europe with inconsistent se- Biosecurity for the Birds rology. Avian Pathol. 1998;27:352-8. http://www.aphis.usda.gov/animal_health/birdbiosecurit Kahn CM, Line S, editors. The Merck veterinary manual y/ [online]. Whitehouse Station, NJ: Merck and Co; 2006. World Organization for Animal Health (OIE) Newcastle disease. Available at: http://www.oie.int http://www.merckvetmanual.com/mvm/index.jsp?cfile=h OIE Manual of Diagnostic Tests and Vaccines for tm/bc/203702.htm. Accessed 7 Jul 2008. Terrestrial Animals http://www.oie.int/eng/normes/mmanual/a_summry.htm OIE Terrestrial Animal Health Code http://www.oie.int/eng/normes/mcode/A_summry.htm Last Updated: July 2008 © 2008 CFSPH page 6 of 7
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King DJ, Curry PE, Suarez DL, Swayne DE, Wakamatsu N, King DJ, Kapczynski DR, Seal BS, Brown Stallknecht DE, Slemons RD, Pedersen JC, Senne DA, CC. Experimental pathogenesis for chickens, turkeys, Winker K, Afonso CL. Phylogenetic diversity among and pigeons of exotic Newcastle disease virus from an low-virulence newcastle disease viruses from waterfowl outbreak in California during 2002-2003. Vet Pathol. and shorebirds and comparison of genotype distributions 2006;43:925-33. to those of poultry-origin isolates. J Virol. Wan H, Chen L, Wu L, Liu X. Newcastle disease in geese: 2007;81:12641-53. natural occurrence and experimental infection. Avian Kinde H, Hullinger PJ, Charlton B, McFarland M, Hietala Pathol. 2004;33:216-21. SK, Velez V, Case JT, Garber L, Wainwright SH, Miko- Watson DW, Niño EL, Rochon K, Denning S, Smith L, Guy lon AB, Breitmeyer RE, Ardans AA. The isolation of JS. Experimental evaluation of Musca domestica (Dip- exotic Newcastle disease (END) virus from nonpoultry tera: Muscidae) as a vector of Newcastle disease virus. J avian species associated with the epidemic of END in Med Entomol. 2007;44:666-71. chickens in southern California: 2002-2003. Avian Dis. World Organization for Animal Health [OIE] .Animal dis- 2005;49:195-8. eases data [online]. Paris: OIE; 2002. Newcastle disease. Kinde H, Utterback W, Takeshita K, McFarland M. Survival Available at: http://www.oie.int/eng/maladies/fiches/ of exotic Newcastle disease virus in commercial poultry a_A160.htm. Accessed 7 Jul 2008. environment following removal of infected chickens. World Organization for Animal Health [OIE]. Manual of Avian Dis. 2004;48:669-74. diagnostic tests and vaccines for terrestrial animals King DJ. Newcastle disease. In: Foreign animal diseases. [online]. Paris: OIE; 2004. Newcastle disease. Available Boca Raton, FL: United States Animal Health Associa- at: http://www.oie.int/eng/normes/mmanual/ tion, 2008. p. 343-349. In: Foreign Animal Diseases. A_00038.htm. Accessed 7 Jul 2008. Richmond, VA: United States Animal Health Associa- World Organization for Animal Health (OIE). World animal tion; 1998. p. 396-405. health information database (WAHID) [database online]. Kuiken, T. 1999. Review of Newcastle disease in cormo- Newcastle disease: 2005 –2008. Paris:OIE;2007. Avail- rants. Waterbirds 22: 333-347. able at: http://www.oie.int/wahid-prod/public.php. Ac- Lublin A, Mechani S, Siman-Tov Y, Weisman Y, Horowitz cessed 7 Jul 2008. HI, Hatzofe O. Sudden death of a bearded vulture (Gypaetus barbatus) possibly caused by Newcastle dis- ease virus. Avian Dis. 2001;45:741-4. Mathivanan B, Kumanan K, Mahalinga Nainar A. Charac- terization of a Newcastle disease virus isolated from ap- parently normal guinea fowl (Numida melagridis). Vet Res Commun. 2004;28:171-7. Mishra S, Kataria JM, Sah RL, Verma KC, Mishra JP. Stud- ies on the pathogenicity of Newcastle disease virus iso- lates in guinea fowl. Trop Anim Health Prod. 2001;33:313-20. Olesiuk OM. Influence of environmental factors on viability of Newcastle disease virus. Am J Vet Res. 1951;12:152-5. Piacenti AM, King DJ, Seal BS, Zhang J, Brown CC. Pathogenesis of Newcastle disease in commercial and specific pathogen-free turkeys experimentally infected with isolates of different virulence. Vet Pathol. 2006;43:168-78. Roy P, Venugopalan AT, Manvell R. Characterization of Newcastle disease viruses isolated from chickens and ducks in Tamilnadu, India. Vet Res Commun. 2000;24:135-42. U.S. Department of Agriculture, Animal and Plant Health Inspection Service [USDA APHIS]. Exotic Newcastle disease. USDA APHIS; 2003 Jan. Available at: http://www.aphis.usda.gov/lpa/pubs/fsheet_faq_notice/fs _ahend.html. Accessed 14 Jul 2008. Last Updated: July 2008 © 2008 CFSPH page 7 of 7
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