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Effect of bursectomy and depletion of immunoglobulin A on antibody production and resistance to respiratory challenge after local or systemic vaccination of chickens with Newcastle disease virus.

Surgical removal of the bursa of Fabricius from newly hatched chicks resulted in a depletion of immunoglobulin A (IgA) from serum and bile of 55 and 67% of the birds, respectively, up to 11 weeks of age. The occurrence of IgG and IgM in serum and IgG in bile was not affected by neonatal bursectomy (Bx). A slight compensatory increase in the occurrence of IgM in bile was noted in Bx birds. When exposed to a lentogenic strain of Newcastle disease virus by either intramuscular or intratracheal routes, the Bx group produced a level of serum hemagglutinating antibody and tracheal wash neutralizing antibody indistinguishable from that reached in the sham-Bx group. All of the vaccinated Bx birds challenged by intratracheal exposure to a velogenic strain of Newcastle disease virus remained healthy. These results suggest that IgA is not essential for the development of immunity in the chicken and that other locally produced immunoglobulins or transuded serum antibody may protect the tracheal mucosa in the absence of IgA.

Aerosols↗

Specificity of antibodies to Newcastle disease virus.

Specificity of antibodies to Victoria strain of Newcastle disease virus (NDV) found in infectious mononucleosis (IM) and other pathologic sera was investigated by agglutination of NDV-modified human O red blood cells, as well as by immunodiffusion and enzyme immunoassay with various preparations of the virus. These studies clearly demonstrated that the NDV antibodies are distinct from P-B or H-D antibodies. The unexpected observation that guinea pig kidney (GPK) tissues absorbed NDV antibodies allowed their classification into a group of 'GPK-positive' heterophile antibodies. The simultaneous occurrence of the NDV antibodies and H-D antibodies in IM and other diseases suggests the possibility that multiple new antigenic determinants, especially those of carbohydrate nature, may appear due to the alteration of self-antigens as a result of various pathologic processes.

Antibodies, Viral↗

Effect of multiplicity of infection on Newcastle disease virus-HeLa cell interaction.

The effects of a hundred-fold difference in virus/cell multiplicity on the interaction of Newcastle disease virus (NDV) with HeLa cells were studied, and various phases of the virus reproductive cycle were related to cellular consequences of infection. At both multiplicities used all cells were infected. The following events occurred 1 to 2 hours earlier in cells which were inoculated with the higher multiplicity: (a) first appearance of newly made virus antigen, and the amount present at any time during the period of rapid increase; (b) onset and time course of production of infective virus; (c) development by infected cells of hemadsorbing ability; (d) onset and time course of inhibition of mitosis; and (e) onset and time course of marked cell damage. Double infection of HeLa cells with NDV and NWS was demonstrated by the fluorescent antibody technique, and was used to show that the establishment of interference against NWS was also dependent upon the multiplicity of NDV. In cells inoculated at each multiplicity, newly made virus antigen appeared at the same time as the first infective virus particles. Infective virus rapidly reached a peak, and then declined. Viral antigen continued to increase for several hours after the decline in infective virus had begun. Thus, only a small fraction of the virus antigen produced was incorporated into new infective particles. The maximal yield of such particles was only 6 to 11 per HeLa cell. Over 95 per cent of new virus was cell-associated, but could be neutralized by treatment with antiserum before disruption of cells. Mitosis occurred in cells which had produced and released infective NDV. Progressive inhibition of mitotic activity in infected cells was correlated with continued production of viral antigen. Marked cytopathic changes developed after mitotic activity had decreased to low levels. The mechanism by which NDV inhibits mitosis in HeLa cells is discussed.

Animals↗

Protein organization in Newcastle disease virus as revealed by perturbant treatment.

Treatment of Newcastle disease virus with lithium diiodosalicylate differentially elutes the internally disposed proteins, M and NP, showing that these proteins are extrinsic, i.e., not associated with the lipid hydrophobic core. This selective elution requires disruption of the viral envelope, a process that is maximal at low temperature and influenced by the lipid composition of the virus envelope.

Electrophoresis, Polyacrylamide Gel↗

Rapid in vitro assessment of the virulence of Newcastle disease virus isolates using the ligase chain reaction.

The ligase chain reaction was used to assess the virulence of isolates of Newcastle disease virus. In the main study, 18/18 virulent isolates whose nucleotide sequences that code for the cleavage site and fusor peptide regions were known, successfully ligated oligonucleotides in a primer mix for virulent viruses termed VPM. Five of these isolates yielded a more intense ligated product with a second primer mix for virulent viruses called VPM1. No ligation was evident with eight avirulent isolates in tests with VPM or VPM1, however, each of these viruses did yield a strong ligated product with the primer mix for avirulent viruses (AVPM) as did one virulent isolate considered to be a mixture. Two virulent Australian isolates, 1238/1998 and 1248/1998, showed low but seemingly specific ligation with AVPM. In a blind study, 8/9 virulent isolates whose sequences were unknown ligated primers in VPM. Three avirulent and one virulent isolate, the latter again probably a mixture, ligated primers in AVPM. Ligation of oligonucleotides in VPM and AVPM was detectable in mixtures where virulent and avirulent isolates represented 0.1% and 0.01% by volume respectively of the viral population. The results indicate that LCR offers a potential in vitro alternative to current in vivo tests for virulence determination of Newcastle disease virus isolates.

Ligase Chain Reaction↗

Study of the influence of salt concentration on Newcastle disease virus matrix protein aggregation.

The aggregation process of Newcastle disease virus matrix protein (M protein) has been studied using light scattering. We observed that the aggregation of M protein is inversely correlated with ionic strength and that this process can be reversed by high salt concentrations. It was found that the oligomeric structure of NDV matrix protein is different from those described earlier for other matrix proteins of enveloped viruses.

Light↗

Induction potential of Sendai virus and Newcastle disease virus for human lymphoblastoid interferon production.

Sendai and Newcastle disease viruses were tested for their induction potential in the production of human lymphoblastoid interferon [HuIFN-alpha(Ly)] from Namalva cell cultures. Tests were performed at multiple induction levels, for two induction periods, and on primed and nonprimed cell cultures. Sendai virus proved statistically more effective overall; priming and induction period had no significant effect.

Burkitt Lymphoma↗

Pathogenicity and immunogenicity in chickens of Newcastle disease viruses isolated from wild ducks. Brief report.

Three Newcastle disease viruses (NDV) isolated from wild ducks in Japan were evaluated for their biological activities, pathogenicity and immunogenicity against one-day-old chickens. One isolate was of the mesogenic type and the other two were of the lentogenic type for chicken. The lentogenic isolates could induce enough immunity in chickens to protect them from challenge with a virulent strain of NDV.

Animals↗

A comparison between the haemagglutination inhibition and complement fixation tests for Newcastle disease.

The value of the complement fixation (CF) test as a means of assessing the immune response of fowls to Newcastle disease virus was examined using several strains of virus. A close degree of correlation was found between the CF test and the simpler haemagglutination-inhibition (HI) test. Like the HI test, the CF test only gave an indication of the immune status and was not a direct measurement of immunity.

Animals↗

Local antibody response in chickens: analysis of antibody synthesis to Newcastle disease virus by solid-phase radioimmunoassay and immunofluorescence with class-specific antibody for chicken immunoglobulins.

The antibody response to Newcastle disease virus was monitored in the sera and salivas of adult chickens immunized by two methods: (i) combined intratracheal-intranasal vaccination followed by intratracheal revaccination or (ii) intramuscular vaccination followed by intratracheal revaccination. By solid-phase radioimmunoassay, only immunoglobulin G (IgG) and IgA antibodies to Newcastle disease virus were detected in the salivas, whereas IgA and IgM antibodies were present in egg whites. The first method produced the highest antibody levels in both serum and saliva and, in addition, prevented detectable virus multiplication in the respiratory tracts upon revaccination 4 weeks later. Plasma cells of all three classes were distributed throughout the tissues lining the oral cavities. The highest densities of plasma cells were in the Harderian glands; IgG was the predominant class, whereas IgA and IgM plasma cells were present in almost equal but lower numbers. The Harderian plasma cells were the most likely source of the antibody found in saliva.

Animals↗

The fate of glutamate in different brain regions of the chick during Newcastle disease virus infection.

Alterations in the glutamate metabolism during Newcastle disease virus (NDV) infection were studied in different brain regions of chick. The glutamate dehydrogenase, the glutamine synthetase, the glutamic acid decarboxylase activities were decreased and the glutamine content was decreased in all brain regions of chick after 24 hr. and 72 hr. of NDV infection. The results obtained in the present study reveal that the glutamate metabolism and its conversion to GABA were operated in low profile during NDV infection.

Animals↗

Characterization of Newcastle disease viruses isolated from field cases in Japan.

Seven Newcastle disease viruses isolated in Japan from 1930 to 1984 were cloned on chicken embryo fibroblasts (CEFs) and characterized biologically. All seven produced two or more types of plaques on CEFs. The plaques were classified into four types. Plaque cloning was carried out five times, and 22 cloned viruses were established. The biological characters of the cloned viruses suggested that the strains contain different clones and that their clones are different even among close cases, such as G strain and H strain.

Animals↗

Isolation of Newcastle disease virus from teals (Anas crecca) in Iran.

Eight of 30 teals (Anas crecca) died several days following capture and Newcastle Disease Virus (NDV) was isolated from all eight. Brains from the dead birds were homogenized and inoculated into chicken embryos. The allantoic fluid from the embryos were inoculated into 10 domestic chickens susceptible to NDV and 10 chickens immunized against NDV. Eight of 10 (80%) susceptible chickens died, while the immunized chickens remained healthy. Anti-NDV serum showed complete homology against NDV and the eight isolates.

Animals↗

Serology-based potency test for inactivated Newcastle disease vaccines.

Twenty-seven inactivated oil-emulsion Newcastle disease vaccines were tested for potency in chickens. Serum samples from groups given 1/50 dose of vaccine were examined by the haemagglutination inhibition (HI) test and the indirect enzyme-linked immunosorbent assay (ELISA). Good correlations were observed between potency and HI titres and between potency and ELISA absorbance. It is recommended that a serology-based potency test replaces the challenge test, reserving challenge only for those batches of vaccines where a clear pass is not indicated.

Animals↗

Cytochalasin B changes the cytoskeletal organization in Newcastle disease virus-infected cells.

The microfilament structures of Newcastle disease virus (NDV)-infected BHK-21 cells were studied in the presence (5 micrograms/ml) or absence of cytochalasin B (CB) by means of phase contrast, indirect immunofluorescence and thin-section immunoelectron microscopy. The results indicated that CB treatment not only impaired virus infections titers and antiactin fluorescence strength but also disrupted cytoplasmic membrane and untagged ferritin-conjugated antibody on the surface of NDV specific antigens.

Actins↗

Phospholipids in Newcastle Disease Virus infected cells.

Infection of chicken cells with Newcastle Disease Virus modifies phosphatidylserine and phosphatidylcholine synthesis in the host cell. The virion contains cellular phospholipids synthesized both before and after infection. Relative concentration of various labeled phospholipids in the virus differ from those in the corresponding cells and their surface membranes. Late in infection, fragments of membranes with a distribution of labeled phospholipids similar but not identical to that of the virus can be found in the supernatant of infected cells. The significance of these findings is discussed in relation to the origin of viral phospholipids and the intervention of the host cell membrane in the assembly of the viral envelope.

Animals↗

[The immunization of pheasants against Newcastle disease].

ND-Adsorbatvakzine "Dessau" and Lasovak are well effective and tolerated in pheasants as immuno-prophylactic methods against Newcastle disease infection. Lasovak produces higher titres of antibodies and better rates of protection. The antibodies are created quicker too and reduced more slowly. There is no correlation between the average of antibody level and rate of protection after experimental infection. Even if antibodies are not demonstrable in hemagglutination inhibition test there is still existing a satisfactory protection. After two vaccinations in the age of chickens in 3 to 4 weeks interval and repetition after always 16 weeks pheasants can be protected effectively for the rearing and breeding seasons.

Animals↗

Observation on flock immunity to Newcastle disease after routine vaccination and experimental aerosol vaccination.

Serological responses in groups of chicks either routinely or experimentally vaccinated with Newcastle disease vaccines via various routes were compared by the micro method of HI test. The lowest serological response to vaccination was found in those groups which had been routinely vaccinated with LaSota strain in drinking water, but a better response was observed in the farm with improved environmental conditions and lower maternal antibody level. Antibody titers in experimentally vaccinated groups were higher than those of routinely vaccinated groups, and the highest antibody response was obtained by aerosol vaccination.

Administration, Oral↗