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Community assembly and invasion: an experimental test of neutral versus niche processes.

A species-addition experiment showed that prairie grasslands have a structured, nonneutral assembly process in which resident species inhibit, via resource consumption, the establishment and growth of species with similar resource use patterns and in which the success of invaders decreases as diversity increases. In our experiment, species in each of four functional guilds were introduced, as seed, into 147 prairie-grassland plots that previously had been established and maintained to have different compositions and diversities. Established species most strongly inhibited introduced species from their own functional guild. Introduced species attained lower abundances when functionally similar species were abundant and when established species left lower levels of resources unconsumed, which occurred at higher [corrected] species richness. Residents of the C4 grass functional guild, the dominant guild in nearby native grasslands, reduced the major limiting resource, soil nitrate, to the lowest levels in midsummer and exhibited the greatest inhibitory effect on introduced species. This simple mechanism of greater competitive inhibition of invaders that are similar to established abundant species could, in theory, explain many of the patterns observed in plant communities.

Biomass↗

A test of neutrality based on interlocus associations.

The evolutionary processes governing variability within genomic regions of low recombination have been the focus of many studies. Here, I investigate the statistical properties of a measure of interlocus genetic associations under the assumption that mutations are selectively neutral and sites are completely linked. This measure, denoted ZnS, is based on the squared correlation of allelic identity at pairs of polymorphic sites. Upper bounds for ZnS are determined by simulations. Various deviations from the neutral model, including several different forms of natural selection, will inflate the value of ZnS relative to its neutral theory expectations. Larger than expected values of ZnS are observed in genetic samples from the yellow-ac-scute and Adh regions of Drosophila melanogaster.

Alcohol Dehydrogenase↗

Application of the indirect enzyme-labeled antibody microtest to the detection and surveillance of animal diseases.

The rapid, indirect enzyme-labeled antibody (ELA) microplate test has been developed as a diagnostic and surveillance tool to aid in the control of animal disease. The test has been applied to viral (hog cholera), parasitic (trichinosis), and bacterial (brucellosis) diseases of animals. A correlation of greater than 95% was observed between the hog cholera ELA test and the serum neutralization test for hog cholera in greater than 2,000 field samples obtained during the 1976 epizootic in New Jersey. Serum samples from all of 56 swine naturally infected with Trichinella spiralis at a level considered dangerous to humans were ELA-positive, whereas only one of 360 packinghouse sera negative for T. spiralis was ELA-positive. Preliminary experiments with bovine brucellosis (Brucella abortus) indicate that the ELA test is more sensitive than other test methods currently in use. ELA procedures should soon become tests of choice for the detection of antibodies to animal disease agents.

Animals↗

Clinical, virological and serological findings after intranasal inoculation of pigs with bovine viral diarrhoea virus and subsequent intranasal challenge with hog cholera virus.

Five groups of weaner pigs were intranasally inoculated with constant doses of bovine viral diarrhoea virus (BVDV) strain OSLOSS/2482. Four weeks post primary inoculation (p.p.i.) the animals were intranasally challenged with decreasing doses of hog cholera virus (HCV) strain Alfort/187. Clinical signs were not observed apart from a short febrile period (2 days, > 40 degrees C) in one animal. Another animal died intercurrently without showing any pathological signs. Virus isolation from leucocyte samples taken regularly during one week post challenge detected HC viraemia in most animals that had received HCV doses > 100 TCID50 per animal. Using monoclonal antibody (mab) analysis all isolates obtained were proven to be HCV. Serological investigations using the virus neutralization test (VNT) yielded HC neutralizing antibodies in all groups with higher titres in those animals having received HCV doses > 100 TCID50. However, HCV specific neutralizing antibodies never exceeded the BVDV antibody titre. A complex trapping blocking (CTB) ELISA applying a HCV specific mab detected HCV specific antibodies in animals that had gone through HC viraemia while discriminating BVDV specific antibodies.

Animals↗

Cross-protection in hamsters immunized with group A arbovirus vaccines.

Cross-protection between Venezuelan, Eastern, and Western equine encephalomyelitis (VEE, EEE, WEE) viruses was studied in the hamster by using challenge responses and neutralizing antibody titers as indexes of protection. Formalin-inactivated vaccines induced only homologous protection regardless of the sequence of vaccination or the combination of vaccines employed. Use of attenuated VEE vaccine, singly, produced absolute homologous protection as well as 37 and 59% protection against WEE and EEE challenges, respectively. Neither deleterious nor enhancing interaction occurred when attenuated VEE and inactivated WEE and EEE vaccines were employed in various sequences of immunization and all possible combinations. The most rapid and simple immunization scheme eliciting excellent homologous protection consisted of a single dose of combined attenuated VEE and inactivated WEE and EEE vaccines. Studies with attenuated strains of VEE, EEE, and WEE viruses showed that all elicited excellent homologous protection when administered singly. However, use of these live strains in many combinations and sequences resulted in a significant (P < 0.05 to <0.001) decrease in the protective efficacy of the WEE or EEE strains. These results are discussed in relation to serum neutralization test data obtained on sera drawn pre- and postchallenge.

Animals↗

Infectivity titration of hemorrhagic fever with renal syndrome virus: use of immune adherence hemagglutination for detection of virus growth.

Serial dilutions of hemorrhagic fever with renal syndrome viruses were inoculated into Vero-E6 cells in microplates. After 2 weeks of incubation, infected cells were disrupted by freezing and thawing, and virus antigens were detected by immune adherence hemagglutination. The infectivity titers of the virus as determined by this method were in close agreement with those obtained by the immunofluorescent antigen endpoint method. Then, a neutralization method was established. Japanese hemorrhagic fever with renal syndrome isolates, strains SR-11 and TR-352, were found to be distinct from Hantaan virus, strain 76-118, by the neutralization test.

Animals↗

Simple and rapid differentiation of Mycobacterium tuberculosis H37Ra from M. tuberculosis clinical isolates through two cytochemical tests using neutral red and nile blue stains.

The attenuated Mycobacterium tuberculosis strain H37Ra is one of the most commonly used controls for M. tuberculosis identification in the clinical laboratory and is a source of false-positive results for M. tuberculosis as a consequence of cross-contamination. Therefore, the ability to discriminate between H37Ra and real clinical isolates has important public health implications. To date, differentiation of H37Ra from M. tuberculosis clinical isolates is possible only by IS6110 genotyping and spoligotyping. In the 1950s, some authors reported that the virulent strain H37Rv and M. tuberculosis clinical isolates were able to fix basic dyes in their anionic forms, while H37Ra was not. We have studied the different techniques described for M. tuberculosis cytochemical staining and have chosen the best of these, introducing certain modifications in order to increase their discriminative power and reproducibility. We describe cytochemical staining of M. tuberculosis cells with neutral red and Nile blue, which differentiates H37Ra from virulent strains. This method could be used as an easy laboratory tool for distinguishing between H37Ra and real M. tuberculosis clinical isolates.

Bacterial Typing Techniques↗

Evaluation of a solid phase radioimmunoassay (Ausria-125) for the detection of hepatitis B antigen (Australia antigen) in two clinical materials.

A solid-phase radioimmunoassay (Ausria-125) was compared to an immunoelectro-osmophoresis method in detecting hepatitis-B antigen (HBAg). The radioimmunoassay detected HBAg in approximately 230 times higher dilutions than the immunoelectroosmophoresis method. In cases of acute hepatitis HBAg could be detected for about 70% longer after the onset of jaundice using radioimmunoassay compared with immunoelectroosmophoresis. Of 138 patients with acute hepatitis, who were HBAg-negative by immunoelectroosmophoresis, 23 (17%) were positive by radioimmunoassay. The specificity of the positive results with this test was investigated by neutralization tests with human antiserum to HBAg.

Animals↗

Antibodies to snowshoe hare virus of the California group in the horse population in Nova Scotia.

A large number of North American equine samples were tested for the California group of arboviruses (CAL). Of 861 equine sera tested by hemagglutination inhibition using the snowshoe hare virus as an antigen, 106 (12.3%) were positive. Neutralization tests confirmed antibodies to this virus in 72 of the positive sera. This study provides evidence of CAL activity in the domestic animal population of Nova Scotia.

Animals↗

Testing the neutral theory of molecular evolution using genomic data: a comparison of the human and bovine transcriptome.

Despite growing evidence of rapid evolution in protein coding genes, the contribution of positive selection to intra- and interspecific differences in protein coding regions of the genome is unclear. We attempted to see if genes coding for secreted proteins and genes with narrow expression, specifically those preferentially expressed in the mammary gland, have diverged at a faster rate between domestic cattle (Bos taurus) and humans (Homo sapiens) than other genes and whether positive selection is responsible. Using a large data set, we identified groups of genes based on secretion and expression patterns and compared them for the rate of nonsynonymous (dN) and synonymous (dS) substitutions per site and the number of radical (Dr) and conservative (Dc) amino acid substitutions. We found evidence of rapid evolution in genes with narrow expression, especially for those expressed in the liver and mammary gland and for genes coding for secreted proteins. We compared common human polymorphism data with human-cattle divergence and found that genes with high evolutionary rates in human-cattle divergence also had a large number of common human polymorphisms. This argues against positive selection causing rapid divergence in these groups of genes. In most cases dN/dS ratios were lower in human-cattle divergence than in common human polymorphism presumably due to differences in the effectiveness of purifying selection between long-term divergence and short-term polymorphism.

Animals↗

Seroprevalence survey of Aino virus infection in dairy cattle of Fukuoka, Japan in 1990.

The seroprevalence and seroconversion to Aino virus infection were epidemiologically analyzed in Fukuoka Prefecture, by a cohort study, in 1990. Serum samples (872) were taken from 436 cattle of 128 farms in five different districts at twice sampling with four month-intervals and were tested by a serum neutralizing test with Aino virus. In the first sampling (May-July), 38.3% of sera and 40.6% of farms tested were positive and 33.3% of cattle and 40.6% of farms were sero-converted during the period of September-November in 1990. Significant differences were found in seroprevalence of farms and seroconversion of cattle/farms among five districts; there was, however, a highly significant correlation between seroprevalence and seroconversion of farm. Consequently, five districts of Fukuoka Prefecture were classified into four epidemic areas according to seroprevalence and seroconversion factors of a principal component analysis.

Animals↗