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PubMed2006

A cross-sectional survey of Australian chicken farms to identify risk factors associated with seropositivity to Newcastle-disease virus.

Several outbreaks of virulent Newcastle-disease occurred in Australia in 1998-2000. We conducted a cross-sectional survey of 753 Australian chicken farms to identify risk factors associated with the seroprevalence of chicken flocks with Newcastle-disease virus (NDV). We had a 99.7% response rate to the survey and the overall prevalence of NDV seropositive farms was 39.8%. Associations were analysed for the layer, chicken-meat and breeder production sectors in sector-specific logistic-regression models using 187, 198 and 146 farms, respectively. In the layer sector, increased risk of seroprevalence was associated with increasing age of the chickens, and decreased risk when the nearest-neighbour poultry farm was >10 km distant (odds ratio (OR)=0.30). In the chicken-meat sector, increased risk of seroprevalence was associated with location in the Sydney basin (OR=13.67), eastern Victoria (OR=26.10) or western Victoria (OR=5.43), and decreased risk when the nearest-neighbour poultry farm was greater than 0.5 km distant (OR=0.34). In the breeder sector, increased risk of seroprevalence was associated with increasing age of the chickens, the presence of wild birds on the farm (OR=5.28) and location in eastern Victoria (OR=16.19). A conditional logistic-regression for 112 pairs of farms matched for age, survey region and production sector identified a distance of >1.0 km to the nearest-neighbour poultry farm (OR=0.24) and ownership by owner 2 (OR=0.02), owner 5 (OR=0.11) or owner 9 (OR=0.25) as significant in reducing the risk of NDV seroprevalence. Our survey found that high levels of biosecurity and hygiene practices had been adopted by most farms.

Age Factors↗
PubMed2000

Antigenetically unusual Newcastle disease virus from racing pigeons in India.

Newcastle disease virus isolated from an outbreak in racing pigeons in India was found to be velogenic, based on the mean time to death in 10-day-old embryonated hen's eggs, the intravenous pathogenicity index in 6-week-old chickens and the pathogenesis in chickens and pigeons. The virus induced disease in chickens without prior adaptation in chickens. The virus was antigenically unusual since it could not be grouped with the available panel of monoclonal antibodies at the World Reference Laboratory for Newcastle disease, UK. However, commercially available lentogenic and mesogenic vaccines provided 100% protection to chickens against this antigenically unusual NDV.

Animals↗
PubMed1978

The isolation and characterisation of a Newcastle disease virus from an exotic parrot.

A newcastle disease virus was isolated from a salmon-crested cockatoo (Cacatua moluccensis) illegally introduced into Australia, Viral-characterisation and chicken-transmission studies indicated that the isolate, G5320/1, was a lentogenic pathotype. It caused a severe respiratory disease in chickens exposed oronasally at 1-day old and in chickens housed at 1 day of age with chickens infected with Newcastle disease virus. No harmful effects were detected in 5-week old chickens inoculated intravenously or oranasally with the virus.

Animals↗
PubMed2005

Pathotyping of Newcastle disease virus isolates from pet birds.

Four Newcastle disease virus (NDV) isolates obtained from a pigeon, lory, parrot, and love bird were subjected to biological and molecular characterization. All the isolates were identified as velogenic with intracerebral pathogenicity indices (ICPI) of 1.9-2.0. All the isolates had a 112RRQKRF117 motif in the fusion protein cleavage site (FPCS), typical for pathogenic NDV. Phylogenetic analysis placed the isolates along with a velogenic Indian isolate of Cl group recovered during 1987.

Animals↗
PubMed1979

[Serological response and the viral carrier state in chickens infected with the pathogenic Newcastle disease virus].

Three groups of susceptible chickens were treated with Newcastle Disease vaccine, as follows: group I--orally, strain La Sota; group II--aerosole treatment, strain La Sota and group III--intramusculary, Komarov's vaccine. Varying HI antibody levels were observed following vaccine application. The average antibody titer of group I and II experimental chickens (40 in number for each group) was 25 days post vaccination respectively log2 = 3.47 and log2 = 6.2 while of group III (50 chickens) it was 14 days post vaccination log2 = 8.4. Aerosole challenge with velogenic viscerothropic strain of Newcastle Disease virus caused a sharp change in serum antibody titer. The low antibody titer in group I rose quickly post challenge while in groups II and III, on the contrary, it fell sharply. This characteristic dynamics is proposed for use as an indicator showing the presence of pathogenic virus in vaccinated birds. It was proven that pathogenic Newcastle Disease virus persisted in birds from group I for 40 days and 10% of them were in a state of latent infection (clinically healthy). The virus was isolated after method of organ cultures of tracheal explantates. It was established that the HI antibody level in the blood serum of virus carriers was higher as compared with that of the remaining birds in the group. The use of this fact as an indicator for beginning virusological investigations aiming to reveal latent Newcastle Disease infection is proposed.

Animals↗
PubMed1982

Newcastle disease virus in waterfowl in wisconsin.

Newcastle disease virus was isolated from the cloaca of 1-5% of live-trapped waterfowl in Wisconsin in the fall from 1978-1980. Antibody to NDV was detected in 8% of the birds tested, with no apparent difference between sex and age classes. Experimental infection resulted in persistence of virus shedding for months after exposure. Lack of detectable antibody in some of the experimentally infected birds suggests that reported antibody prevalence may not be indicative of the true prevalence of the infection. Isolation of NDV for the last 9 years as well as the detection of antibody in waterfowl over 25 years ago, suggests a well-adapted host-parasite relationship. Experimental evidence of virus persistence in individual mallards (Anas platyrhynchos) provides a mechanism for maintenance of the virus in the wild population.

Animal Population Groups↗
PubMed1995

Recent isolates of Newcastle disease virus in Australia.

Forty-five recently isolated strains of Newcastle disease virus and the V4 vaccine strain of Newcastle disease virus were used to infect experimental chickens. Neither V4 nor any of the new strains produced detectable clinical disease. All the viruses produced an antibody response and spread by contact. Some of the newly isolated viruses produced a more rapid serological response than V4 virus did. Dual or multiple infections with one of the new strains of Newcastle disease virus, infectious bronchitis virus and Escherichia coli did not enhance the pathogenicity of any of the agents.

Animals↗
PubMed1980

Transcriptional map for Newcastle disease virus.

A transcriptional map of Newcastle disease virus was determined by measuring the kinetics of UV inactivation of the transcription of individual genes and of viral infectivity. The inactivation of single genes was monitored by measuring the reduction in the accumulation of viral gene products in vivo and in vitro. In vivo, the accumulation of viral polypeptides in infected cells was measured after reversal of a cycloheximide treatment designed to inhibit secondary transcription. Actinomycin D and a hypertonic medium were used to decrease selectively the synthesis of host cell polypeptides in infected cells. In vitro, mRNA's synthesized by irradiated viruses were analyzed by translation in cell-free systems under conditions in which the amount of each polypeptide synthesized reflected the relative abundance of the corresponding mRNA. UV target sizes were obtained for the genes coding for the HN, F0, NP, M, L, and P polypeptides; the 47,000-dalton protein was not detected. A comparison of the UV target sizes with the corresponding gene sizes suggested that transcription of these genes initiated at a single promotor and proceeded in the order NP, P, (F0, M), HN, L. These experiments were performed with Newcastle disease virus strains Australia-Victoria and B1-Hitchner; for both strains, two forms of the P polypeptide which differed in electrophoretic mobility were detected. Proof that the P protein is virus specific was obtained. In addition, infection of chicken embryo cells with avirulent strain B1-Hitchner enhanced the accumulation of at least four polypeptides that appeared to be specified by the host cell rather than by the infecting virus.

Genes, Viral↗
PubMed1978

[Variability and the virulence of the Newcastle disease virus].

Six isolates of the Newcastle Disease virus (NDV), taken at different periods of time after provocation of immune birds with velogenous viscerotrophic strain, are used. It is shown that the virulence of the initial NDV challenge strain remains unchanges up the 46th day of persistence. The isolate, taken after 70 days of carriage, manifests a considerably decreased virulence. It is established that the reduced virulence is not genetically stable and reverts towards the initial one following passage through appropriate host organism. The latent infection with NDV is examined from ecological and practical aspects.

Animals↗
PubMed2001

Studies on the pathogenicity of Newcastle disease virus isolates in guinea fowl.

Newcastle disease viruses isolated from chickens and guinea fowl were characterized as viscerotropic, velogenic strains on the basis of their mean death time, intracerebral pathogenicity index, intravenous pathogenicity index and cloacal and conjunctival mean death time. The pathogenesis of the disease caused by both the strains was studied in 4-week-old guinea fowl. Both strains had an incubation period of 5 days and the birds showed dullness, depression, anorexia, diarrhoea and paralysis of the legs. They also exhibited nervous signs such as incoordination, muscle tremors and trembling of the neck at the advanced stage of the disease. Mortality reached 52% in the group infected with the chicken isolate but it was only 8% in the birds infected with the guinea fowl isolate. No specific changes were observed at post-mortem examination except haemorrhages at the tip of the glands of the proventriculus and in the caecal tonsil. Changes in the lymphoid organs and brain were always present in both the groups. Despite the low mortality, the guinea fowl isolated had multiplied in various organs in the birds. In both groups, the frequency of virus isolation increased from 5 to 10 days post infection.

Animals↗
PubMed1992

Characterisation of Newcastle disease viruses isolated in India.

Eleven Newcastle disease virus (NDV) isolates obtained from outbreaks of disease in chickens (9) and Japanese quail (2) in Tamil Nadu, India were characterised in pathogenicity tests, antigenically, using mouse monoclonal antibodies (MAbs), and other established tests devised to distinguish between different strains. All 11 isolates were shown to be highly virulent for chickens. In indirect immunoperoxidase tests used to assess the ability of a panel of 28 MAbs to bind to infected cell cultures, 10 of the isolates showed an identical reaction pattern, the other isolate (No. 4) failed to react with one MAb which bound to cells infected with the other isolates. Isolates 9 was unstable at pH 3 while the other 10 were stable. All other properties were shared by the 11 isolates.

Animals↗
PubMedDate not supplied

Isolation of Newcastle disease virus and Salmonella typhimurium from the brain of double-crested cormorants (Phalacrocorax auritus).

Avian paramyxovirus type 1 (Newcastle disease virus) and Salmonella typhimurium were isolated from the brain and lung tissues of double-crested cormorants (Phalacrocorax auritus) from Lac Canard, Alberta, Canada. More than 100 birds died during this outbreak in 1999. Affected birds presented signs of central nervous system disease characterized by unilateral wing and leg paralysis. Other geographic locations in the provinces of Alberta and Saskatchewan have reported cases of cormorants suffering from diseases with signs compatible with Newcastle disease. The virus isolated in the 1999 outbreak was characterized as mesogenic. These findings suggest that other pathogens, like S. typhimurium, may influence the clinical presentation of disease caused by mesogenic strains of Newcastle disease virus in cormorants.

Alberta↗
PubMed1975

Adequacy of commercial lentogenic vaccines against Canadian strains of viscerotropic Newcastle disease virus.

Three field strains of Newcastle Disease virus, designated S20, S21 and S23, isolated from chickens or turkeys in Ontario during the 1971-72 epizootic, were characterized as velogenic viscerotropic viruses. No significant antigenic differences were demonstrated among B1, LaSota and a field strain (S23) of velogenic vescerotropic virus by haemagglutination inhibition or protection tests. Primary water vaccination of chicks with commercial B1 and LaSota vaccines at five weeks of age and aerosol revaccination with the same strains four weeks later resulted in protection that lasted 16 weeks after revaccination against experimental challenge with strain S23. The differences in haemagglutination inhibition titres noted when the homologous or the heterologous viruses were used as haemagglutinating antigen were not statistically significant. The rates of decay of virus neutralizing and haemagglutination inhibition antibodies in vaccinated birds showed a divergence indicating the possible duality of antibodies measured in serum neutralization and haemagglutination inhibition tests.

Administration, Oral↗
PubMedDate not supplied

The preparation and efficacy of manually emulsified Newcastle disease oil-emulsion vaccines.

Experimental Newcastle disease oil-emulsion vaccines were prepared by manually shaking small quantities of antigen, surfactant, and mineral oil and compared with oil-emulsion vaccines made by the more conventional mechanical methods. Emulsion stability (prolonged emulsification of aqueous antigen) of the manually prepared vaccines was achieved by four different processes and tested for efficacy in broilers. White rock broilers were vaccinated at 3-5 weeks of age and bled at 1- to 2 week intervals thereafter for 8 weeks. Cumulative 8-week hemagglutination-inhibition (HI) mean titers (reciprocals) ranged from 15 to 250 for manually emulsified vaccines and from 18 to 240 for mechanically emulsified vaccines. Eight-week cumulative mean HI responses induced by manually emulsified vaccines were never significantly (P less than 0.05) lower than their specific mechanically emulsified comparison vaccines and were occasionally significantly higher. Highest HI titers were induced when hydrophile-lipophile balances of 7, 9, and 6 were used for the preparation of manually emulsified vaccines. In general, most of the vaccine emulsions were stable for more than 30 days. Vaccine efficacy, however, was not always diminished by poor emulsion stability. These results indicate that manual emulsification can be used for the production of oil-emulsion vaccines of high efficacy that can provide benefits over existing mechanical methods.

Animals↗
PubMed2002

[Sequence analysis of the fusion (F) protein genes of four Newcastle disease virus strains causing clinical disease in geese].

Four strains of Newcastle disease virus(NDV), which have proven to be responsible for the disease outbreaks in south and east China regions called "geese paramyxovirus infection" or "avian paramyxovirus infection of geese", were examined for the features of their fusion(F) protein genes. A 1700 nucleotides(nt) fragment of the F gene (1705 nt) of each of the 4 strains were sequenced, the results revealed that the NDV strains of goose origin share common transcriptional sequence and translational start position with the hitherto reported NDV, the F gene homologies among the 4 strains were 97.8%-98.9%, while the corresponding homologies between these strains and the standard challenge strain F48E8 were only 86.0-86.8%. The deduced amino acid sequences near cleavage site of F0 proteins showed a 112RRQKR/F117 motif, comforming well with that of the virulent strains. The cleavage sites distribution of 3 restriction enzymes(Hinf I, Basto I, Rsa I) in 75% region of the F gene(between 334-1682 nt), which is used to group NDV strains into different genotypes, were also analysed with the aid of computer program MegAlign, it is very interesting to find that the 4 strains showed a distinct distribution pattern from all the genotypes so far reported(genotype I-VIII), characterized by the simultaneously presence of a Bsto I site at 752 nt and two Rsa I sites at 872 nt and 973 nt. Additionally, 3 out of the 4 strains, despite their different geographical locations, showed a novel Rsa I site at position 1249 which is absent in all of the other genotypes. The 4 NDV strains of goose origin were essentially virulent ones, and probably belong to a new genotype.

Amino Acid Sequence↗
PubMedDate not supplied

Experimental infection of vaccinated slaughter ostriches in a natural, open-air feedlot facility with virulent Newcastle disease virus.

The presence of virulent Newcastle disease virus (NDV) since the 1993-94 epidemic in southern Africa holds major implications for the export of ostrich products from this region. A challenge experiment with this field strain was conducted in open-air feedlot facilities under strict biosecurity measures. The experiment was designed to follow vaccination and preslaughter quarantine regulations currently enforced in South African export ostrich facilities in order to determine the viremia period and immune response under these specific circumstances. One hundred forty-three slaughter ostriches were allocated into three test groups, according to the time period between pretrial vaccination and challenge (1-2 mo, 2-4 mo, 4-6 mo), and an unchallenged control group. All birds in the test groups were challenged by oral, tracheal, and ocular routes with a field isolate of NDV. They were slaughtered over the next 4 wk on nine separate occasions and bled on 12 occasions. Virus isolation was attempted from seven sets of pooled samples from each bird to determine the viremia period and the serum antibody concentrations were measured by hemagglutination inhibition (HI) and enzyme-linked immunosorbent assay (ELISA) methods to establish an immune response curve. NDV could be back-isolated only up to day 9 postinfection and from only six ostriches with poor immune response titers and corresponding to a rise in antibody levels above an indirect ELISA optical density reading of 0.33. Virus could be recovered only from brain and respiratory tract tissue. The HI test was less sensitive than the ELISA. Immune response curves did not differ significantly between the groups and peaked on day 14 post-infection. From these data, ELISA titers would appear to be a good indicator of the probability that an ostrich will be clinically infected after velogenic NDV challenge. These results also suggest that the current vaccination schedule enforced by the South African Veterinary Authorities results in protective immunity in up to 95% of slaughter ostriches from export approved facilities. The standard 30-day preslaughter quarantine period introduced as part of Crimean-Congo hemorrhagic fever virus control measures also appears sufficient to encompass the determined NDV viremia period of 9-11 days in slaughter ostriches.

Abattoirs↗
PubMed2004

Molecular epidemiology of Newcastle disease viruses isolated in South Korea using sequencing of the fusion protein cleavage site region and phylogenetic relationships.

The study, using sequence analysis and the phylogenetic relationship of the fusion protein gene, divided the Korean epizootic isolates of Newcastle disease virus (NDV) into several lineages to determine the molecular epidemiology of the virus. A 695 base pair fragment was amplified by polymerase chain reaction between matrix protein gene and fusion protein gene of 30 Korean NDV isolates, which were isolated from field outbreaks of Newcastle disease between 1949 and 2002. All isolates showed the amino acid sequence 112R-R-Q/R-K-R116 at the C-terminus of the F2 protein and phenylalanine (F) at the N-terminus of the F1 protein, residue 117. These amino acid sequences were identical to a known virulent motif. The region of the F gene between nucleotides 47 and 435 was compared by phylogenetic analysis. Based on nucleotide sequence, the Korean NDV isolates belonged to genotype III, V, VI and VII corresponding to isolates in 1949, 1982 to 1984, 1988 to 1997, and 1995 to 2002, respectively. These data showed that genotypes of five Korean Newcastle disease epizootics had replaced each other serially (III, V, VI and VII) in chronological order. Further, the five Korean Newcastle disease epizootics were closely related with the Newcastle disease panzootics or Newcastle disease epizootics in other countries. Present study showed that the Korean genotype V isolated before 1984 was related with European Newcastle disease epizootics in the 1970s, whereas the Korean genotypes VI and VII isolated after 1988 were more closely related with Far East Newcastle disease epizootics, especially Newcastle disease epizootics in Japan, Taiwan and China. Since 1988, the genotypes VI and VII of Far East origin were dominant in South Korea. That might be due to the increased trade of agricultural products including poultry among Far East Asian countries.

Animals↗