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PubMed1989

Persistence of the V4 strain of Newcastle disease virus in an open-range flock of chickens.

The V4 strain of Newcastle disease virus was introduced into a small open range flock of bantam chickens, by dosing half the birds directly into the crop. As indicated by rises in titres of haemagglutination inhibition antibody, the virus spread to the uninoculated birds and persisted in the flock for two years, infecting chickens that were introduced by natural brooding and rearing. All new clutches of chicks seroconverted by 80 days of age, and the titres of adult birds showed a concurrent rise, suggesting that the chicks were amplifying the virus. The modes of spread and of persistence of the virus were not determined; although cloacal swabs were taken regularly, only one yielded virus. Antibody titres of the inoculated birds remained above the presumptive protective level of 3 (log2) for over a year, whereas the titres of birds infected by contact were generally less than 3.

Animal Husbandry↗
PubMedDate not supplied

[Method of production of the dried highly dispersed vaccine of Newcastle disease virus].

Experimental batches of dried dust-like vaccine on the basis of Newcastle disease virus, strain La Sota, have been prepared. The technology of the preparation of the vaccine includes the lyophilization of the technical fluid of the culture under study, milling dried biomass and mixing the pulverized biomass with excipient. As revealed in the process of this work, lyophilization ensures high concentration of the virus in dried biomass and its pulverization, a high content of the target fraction of biomass particles in the vaccine preparation with the moderate inactivation of the bioagent. By mixing the pulverized biomass with excipient the required concentration of the viable virus in the finished product may be achieved. The viability of the bioagent during the storage of the dried vaccine under conditions, determined by optimum storage temperature and time, has been found satisfactory.

Aerosols↗
PubMedDate not supplied

Biological and molecular characterization of Newcastle disease virus isolates from surveillance of live bird markets in the northeastern United States.

Newcastle disease virus (NDV) is frequently recovered from surveillance samples collected by U.S. Department of Agriculture, Animal and Plant Health Inspection Service personnel in live bird markets. Six NDV isolates, five from chickens and one from a pheasant, were characterized for comparison with reference NDV isolates from poultry and other birds. All isolates tested were of low virulence for chickens. Four of the six isolates were similar to reference lentogens B1 and La Sota, but two isolates, one from a chicken and one from a pheasant, were different. The aberrant chicken isolate had a monoclonal antibody-binding profile like an unusual Canadian pigeon isolate. Sequence analysis of the matrix gene of this isolate demonstrated that it differed from all isolates included in the comparison and therefore may represent a third phylogenetic NDV group. The pheasant isolate had a monoclonal antibody-binding profile typical of other U.S. NDV lentogens but had a matrix gene sequence and hemagglutinin thermostability similar to strains Ulster and Queensland V4 (QV4), viruses originally isolated in Northern Ireland and Australia, respectively. The pheasant virus is the first lentogen isolated in the United States known to be closely related phylogenetically to Ulster and QV4. The unusual chicken and pheasant isolates were readily shed from the intestinal tract during chicken passage, whereas the other isolates were shed from the respiratory tract with little or no intestinal shedding. The frequency in live bird markets of viruses similar to those previously thought to be exotic to the United States in unknown.

Animals↗
PubMedDate not supplied

Comparison of three velogenic strains of Newcastle disease virus by RNA oligonucleotide fingerprinting.

The purified RNA from three velogenic strains of Newcastle disease virus (Ca-1083 [Fontana], Largo, and Texas GB) was analyzed by oligonucleotide fingerprinting. An image-processing system used to manipulate and rescale autoradiographs to uniform dimensions assisted the manual comparison of RNA fingerprints. Based on this analysis, the fingerprints of the Largo and Ca-1083 viscerotropic strains were more similar to each other than either virus was to the Texas GB neurotropic strain. By contrast, the Largo and Texas GB strains displayed more differences in the pattern of RNA fragment migration than other strain comparisons. Fingerprint comparisons were also performed between velogenic and previously reported lentogenic strains of NDV. No large RNA fragments were identified as NDV-specific or virulence-specific. This study evaluates the relationships among these NDV strains.

Animals↗
PubMed1975

Studies on the specificity of agglutinins against human erythrocytes modified by Newcastle disease virus.

The specificity of agglutinins in human sera against human erythrocytes modified by Newcastle disease virus (NDV-O agglutinins) was studied with agglutination and agglutination inhibition techniques. Virus grown in both embryonic eggs and tissue culture was used in the experiments. The findings were compatible with the existence of four specificities of agglutinins. In some sera, including those from subjects recently inoculated with vaccines prepared in eggs, the agglutinins were directed against a component of the allantoic fluid. In high-titred infectious mononucleosis (IM sera the agglutinins were directed against antigenic groupings present in the Vic strain but not the B1 strain of NDV, whereas in certain other sera they were directed against antigens present in both of them. Finally, in some sera the agglutinins probably reacted with a red cell antigen uncovered by the viral neuraminidase.

Agglutinins↗
PubMed1996

Preferential cytotoxic effect of Newcastle disease virus on lymphoma cells.

Susceptibility of lymphoma cells (Daudi, HD-Mar) to Newcastle disease virus toxicity was found to be higher than that of lymphoblastoid cells (Milstein) and of resting peripheral blood lymphocyte (PBL). Phytohemagglutinin- and/or pokeweed-mitogen-activated PBL however, exhibited, elevated sensitivity, similar to that of lymphoma cells. The level of cytotoxicity was monitored by cell viability, inhibition of DNA synthesis and release of 51Cr. When Daudi cells were mixed with PBL they were significantly more sensitive to the killing effect of the virus (70% mortality compared to 30% 30 h after infection, P < 0.05). The degree of sensitivity to viral cytotoxicity was unrelated to the efficacy of adsorption, which was similar for all cell lines as shown by immunofluorescent staining and flow cytometry. Also an influenza strain A/PR/8/34 (H1N1) adsorbed but did not affect the viability of any of the cells tested. Our results demonstrate that New-castle disease virus caused preferential damage to lymphoma cells as compared to non-cancerous normal cells.

Burkitt Lymphoma↗
PubMed1981

Comparative immune response from vaccinating chickens with lentogenic Newcastle disease virus strains.

The immune response of chickens to 11 isolates of LaSota strain Newcastle disease virus (NDV) and to 7 isolates of B1 strain NDV was studied in specific-pathogen-free chickens. Most of the vaccine strains were from commercial vaccine producers. Comparison of immunogenicity were made of these vaccines; five other lentogenic NDV strains, not used commercially, were also evaluated. From the criteria of hemagglutination inhibition (HI) and virus serum (VN) neutralizing titers, differences were observed with certain isolates within the LaSota and B1 vaccine groups. Whereas the majority of vaccine strains fell within a predictable range, some proved considerably less in their ability to engender expected titers. Two-to threefold differences in titers were observed with some of the strains compared. Two cloned LaSota NDV strains did not compare favorably, or with expected higher titers, with uncloned or conventional LaSota strain virus isolates. Similarly, certain B1 and LaSota strains passaged in chickens did not demonstrate a greater immunogenic potential over conventional, commercial vaccines of similar strain designation but not passaged in chickens. Whereas none of the NDV strains demonstrated evidence of neurotropism or lethality, postvaccination respiratory reactions were difficult, if not impossible, to evaluate in laboratory isolation units. The complexity of selecting ND vaccines for field use is discussed briefly.

Animals↗
PubMedDate not supplied

Pathogenesis of chicken-passaged Newcastle disease viruses isolated from chickens and wild and exotic birds.

The pathogenesis of six Newcastle disease virus (NDV) isolates recovered from chickens (Ckn-LBM and Ckn-Australia) and wild (Anhinga) and exotic (YN parrot, pheasant, and dove) birds was examined after the isolates had been passaged four times in domestic chickens. Groups of 10 4-wk-old specific-pathogen-free white leghorn chickens were inoculated intraconjunctivally with each one of the isolates. The infected birds were observed for clinical disease and were euthanatized and sampled at selected times from 12 hr to 14 days postinoculation or at death. Tissues were examined by histopathology, by immunohistochemistry (IHC) to detect viral nucleoprotein (IHC/NP), and by in situ hybridization to detect viral mRNA and were double labeled for apoptosis (terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling ([TUNEL] or IHC/caspase-3) and viral nucleoprorein (IHC/NP). Birds infected with the three low virulence viruses (Ckn-LBM, YN parrot, and Ckn-Australia) did not develop clinical disease. Microscopic lesions were observed only at the inoculation site and in organs of the respiratory system. The detection of viral nucleoprotein (N) was restricted to the inoculation site. The pheasant and dove isolates were highly virulent for chickens with marked tropism for lymphoid tissues, confirmed by the presence of large numbers of cells positive for viral N protein and viral mRNA. Viral N protein was detected early in the cytoplasm of cells in the center of the splenic ellipsoids. The apoptosis assays (TUNEL and IHC/caspase-3) showed increased apoptosis in the splenic ellipsoids as well. Apparently, apoptosis is an important mechanism in lymphoid depletion during NDV infection.

Air Sacs↗
PubMed1975

Effects of bile and gastrointestinal secretions on the infectivity of Newcastle disease virus.

Bile aspirated from chicken gall bladders was found to contain substances neutralizing Newcastle disease virus (NDV). Nonspecific factors were present in the bile, probably the bile acids, which caused a reduction in the infectivity of the virus. Specific anti-NDV activity was found in the bile of birds that had been vaccinated with a lentogenic strain, Ulster, and challenged with a velogenic, viscerotropic strain, California 1083. Immunoglobulins were also found in these secretions and demonstrated to include the immunoglobulin A class as well as immunoglobulin G. Variability in the neutralizing capacity of bile was found with two different plaque clones of strain 1083, indicating antigenic heterogeneity in the viral population. No difference was found between bile from uninfected birds and the bile from NDV-immune birds in their activities against influenza strain Turkey Ontario 7732, whereas activity existed against a non-viscerotropic strain of NDV, Texas GB. These findings suggest that the specific activity of the secretions was most probably due to the presence of secretory antibody. The importance of the antiviral substances present in the alimentary tract was discussed with respect to the protection of the chicken against the viscerotropic pathotype of NDV.

Animals↗
PubMed1981

Genetic and phenotypic correlations between immune response to Escherichia coli and to Newcastle disease virus vaccines.

Genetic and phenotypic variation and covariation in immune response to inactivated Newcastle disease virus (NDV) vaccine and to Escherichia coli vaccine were studied in commercial poultry strains. Within any given experiment there was no tendency for individual birds to respond in a correlated manner to NDV and E. coli vaccines. There were highly significant differences between sire families in immune response to NDV vaccine (57 sire families) and to E. coli vaccine (35 sire families). Heritabilities of immune response levels to NDV and to E. coli were .41 and .25, respectively. In both cases, additive genetic standard deviations were slightly over 1.0 titer unit. The correlation between sire-family means for response to NDV and sire-family means for response to E. coli (35 sire families) was .077 and statistically nonsignificant. Thus, the data provide evidence for the presence of significant genetic variation in immune response with respect to two endemic disease antigens, but they provide no evidence for a genetic correlation in response to the two antigens.

Animals↗
PubMed1992

Isolation and characterisation of Newcastle disease virus strain in a feral dove (Stigmatopelia senegalensis) in Nigeria.

An isolate of Newcastle disease virus (NDV) was obtained from a feral dove, (Stigmatopelia senegalensis). The isolate was shown to have a mean-death-time of 96 h and an intracerebral pathogenicity index of 0.10. It was immunogenic but not pathogenic for 6-week old chicks on experimental infection. Based on these observations the isolate was classified as a lentogenic strain. The role of such isolates of NDV from wild birds on the Nigerian poultry industry is discussed.

Animals↗
PubMedDate not supplied

Comparative efficacy of the B-1 and VG/GA vaccine strains against velogenic viscerotropic Newcastle disease virus in chickens.

Groups of eight 1-day-old white rock chickens were vaccinated with either B-1 or VG/GA strain of Newcastle disease virus (NDV) by eyedrop instillation. Some of the chickens were vaccinated a second time at 17 days of age. Eight groups of chickens vaccinated either once or twice were challenged with the California 1083 strain of velogenic viscerotropic Newcastle disease virus (VVNDV) at 30 days of age by either intramuscular injection or eyedrop instillation. One group of unvaccinated control chickens was challenged by eyedrop instillation. All eight unvaccinated controls, two of the 16 B-1 vaccinates, and none of the 16 VG/GA vaccinates died following challenge. There were no obvious differences in pre-challenge serum antibody levels among the vaccinates. Only the twice-vaccinated chickens that were challenged by eyedrop and the unchallenged vaccinates failed to show a marked rise in serum antibody titers. The VG/GA strain of NDV provided protection against the mortality associated with VVNDV challenge similar to that provided by the B-1 strain within the conditions of this experiment.

Animals↗
PubMedDate not supplied

[Role of intracellular proteinases and glycosidases in the degradation of the 'large glycoprotein' responsible for the neuraminidase and hemagglutinating activity of the Newcastle disease virus].

It was shown that the decrease in neuraminidase and hemagglutinin activities in Newcastle disease virus (NDV) infected cells, which was revealed in conditions of disturbed protein synthesis, could be significantly diminished by addition of an inhibitor or trypsin-like proteinases tosyl-lysil-chloromethyl keton. The same effect was caused by D-galactonolactone--inhibitor of some glycosidases. These data suggested that the action of intracellular proteinases and glycosidases are the cause of degradation of 'large glycoprotein', responsible for neuraminidase and hemagglutinin activities in NDV-infected cells.

Animals↗
PubMedDate not supplied

Identification of seven isolants of infectious bronchitis virus by interference with the B-1 isolant of Newcastle disease virus.

Seven isolants of infectious bronchitis virus (IBV) interfered with the development of hemagglutinins (HA) by the B-1 isolant of Newcaslte disease virus (NDV) in eggs previously inoculated with these IBV isolants. The I50 [defined as the minimum amount of IBV needed to produce, upon inoculation in embryonating chicken eggs (ECE), HA interference in 50% of these ECE reioculated 10 hr later with 10(2,41 EID50 (HA) of the B-1 strain of NDV] was less than 1 EID50. The interference was considered specific for IBV because if could be eliminated by addition of homologous anti-IBV serum. Furthermore, three other common poultry viruses (laryngotracheitis, fowlpox, and CELO viruses) did not interfere with NDV. In view of its sensitivity, specificity, and simplicity of performance, the IBV-NDV interference test appears to have considerable potential as a diagnostic test for IBV under field conditions.

Coronaviridae↗
PubMed1996

Ultrastructural changes in the cardiac muscle of chickens infected with the GB strain of Newcastle disease virus.

The changes in chicken cardiomyocytes resulting from infection with the GB strain of Newcastle disease virus were studied by electron microscopy. The virus infection caused shortening of the sarcomeres and generalized oedema in the perivascular region of the heart muscle, containing debris from degenerated mitochondria and myofilaments. Some of the cardiomyocytes had condensed chromatin, resembling that of apoptotic cells.

Animals↗