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Biomedical subjects

A A Pinto

Publications and source records attributed to A A Pinto.

At least 19 recordsLinked to original sources

Rapid coagglutination test for the detection and typing of foot and mouth disease virus.

Protein A containing Staphylococcus aureus was used to develop a coagglutination (COA) test for the detection and typing of foot and mouth disease virus (FMDV) O, A and C serotypes in infected cells and tissues. Different batches and amounts of guinea pig anti-FMDV sera were assessed to optimize the preparation of COA conjugates. The sensitivity and specificity of the COA Test for the detection of FMDV O, A and C serotypes and heterologous viruses was also characterized. Comparison between the COA Test and complement fixation test for the detection and typing of FMDV obtained from extracts of tongue epithelial tissues from infected cattle revealed high agreement in the results and indicated a potential application of the COA Test for the direct diagnosis of viruses.

Agglutination Tests

Serological diagnosis of brucellosis in water buffaloes (Bubalus bubalis): comparison among complement fixation, serum agglutination and rose bengal plate test.

The results of a comparative study among complement fixation (CFT), plate agglutination (PAT), tube agglutination (TAT) and Rose Bengal plate tests ( RBPT ) to the serodiagnosis of brucellosis in Indian buffaloes are reported. Sera from 212 buffaloes unvaccinated against brucellosis were examined and the CFT was able to reveal significant titres in sera with low agglutinating titres. From 109 sera which did not show agglutination titres in the PAT, four showed complement fixing titre greater than 1 in 200. All the positive sera to the RBPT gave complement fixing titre equal to or greater than 1 in 20. In sera that showed negative result to the RBPT the CFT was able to reveal relatively high titres. From 131 sera negative to the RBPT five showed complement fixing titres greater than 1 in 60.

Agglutination Tests

Comparative study among complement fixation, serum agglutination and Rose Bengal Plate tests in the serodiagnosis of bovine brucellosis.

The complement fixation test (CFT) based on the 50 per cent hemolytic end point technique was applied to the diagnosis of bovine brucellosis in a comparative study involving the plate agglutination test (PAT), the tube agglutination test (TAT) and the Rose Bengal plate test (RBPT). Among 180 bovine sera that were examined the CFT was able to reveal significant titres in sera that gave low agglutinating titres. Some sera with agglutinating titres between 1 in 50 and 1 in 100 did not given a titre in the CFT. The results show that the CFT is useful for bovine brucellosis diagnosis and may be used after sera screening with PAT and RBPT.

Agglutination Tests

Comparative study among complement fixation, serum agglutination and Rose Bengal plate tests in the serodiagnosis of bovine brucellosis.

The complement fixation test (CFT) based on the 50 per cent hemolytic end point technique was applied to the diagnosis of bovine brucellosis in a comparative study involving the plate agglutination test (PAT), the tube agglutination test (TAT) and the Rose Bengal plate test (RBPT). Among 180 bovine sera that were examined the CFT was able to reveal significant titres in sera that gave low agglutinating titres. Some sera with agglutinating titres between 1 in 50 and 1 in 100 did not give a titre in the CFT. The results show that the CFT is useful for bovine brucellosis diagnosis and may be used after sera screening with PAT and RBPT.

Agglutination Tests

Comparative study between microscopic agglutination and complement fixation tests in experimental canine leptospirosis.

In order to evaluate the antibody response to pathologic leptospira from both serovars icterohaemorrhagiae and canicola, dogs were experimentally inoculated with these leptospiras. Each of the serovar were inoculated in 15 dogs and the antibody response in the acute phase of infected was followed by microscopic agglutination and complement fixation tests. Complement fixing antibodies were detected in both groups at the 4th day post infection and agglutinins appeared in circulation at the 7th day post infection when homologous antigens were used. On the 63rd day post infection with serovar canicola and on 56th day post infection with serovar icterohaemorrhagiae, complement fixing antibodies could no longer be detected but, in both experimental groups, specific agglutinins were presented in significant titers.

Agglutination Tests

Immune response to virus-infection-associated (VIA) antigen in cattle repeatedly vaccinated with foot-and-mouth disease virus inactivated by formalin or acetylethyleneimine.

The results of experiments to investigate antibody to 'virus infection associated' (VIA) antigen in cattle repeatedly vaccinated with formalin- or acetylethyleneimine- (AEI) inactivated foot-and-mouth disease (FMD) vaccines under laboratory conditions are reported. Results are also presented from some vaccinated animals subsequently exposed to FMD infection. Antibody against VIA was not detected before and after the first vaccination with formalin or AEI-inactivated vaccine but did develop in all animals after the second formalin vaccination and persisted throughout the experiment. After the second AEI vaccination, 4 of 12 animals developed antibody which persisted for at least 37 days. This transient response in some cattle was repeated after successive vaccinations but, in general, more animals responded as the number of vaccinations increased. After exposure to infection a transient VIA antibody response was occasionally observed in immune AEI-vaccinated animals. Some immune repeatedly AEI-vaccinated cattle did not develop detectable VIA antibody after challenge despite the persistence of virus in oesophageal-pharyngeal (O/P) fluid. The presence of antibody to VIA antigen is not conclusive proof that vaccinated animals have been exposed to infection and field data must be interpreted with caution.

Animals

The detection of antibody to virus-infection associated (VIA) antigen in various species of African wildlife following natural and experimental infection with foot and mouth disease virus.

The double immuno-diffusion (DID) test has been applied to detect antibody to VIA antigen in sera from various species of African wild ungulates. In conjunction with the serum neutralisation (SN) test it can be used to decide the degree of risk of movement of animals to other countries free from foot and mouth disease (FMD). The value of the test in assessing the history of infection is limited by its relatively low sensitivity and specificity in respect of virus type.

Africa

[The complement-fixation test in rabies. I. Antibody titer of vaccinated dogs (author's transl)].

Complement-fixation test based in 50% hemolytic end point was applied to investigate the immune status to rabies of dogs vaccinated with heigh egg-passage Flury vaccine. The complement-fixation titer was compared with serum neutralization results. Twenty-five sera was employed and the complement fixation titer varied of 0 to 256. Three sera was anticomplementary. The results indicated a lack of quantitative correlation, but was found a qualitative correlation between the two methods.

Animals

[Foot-and-mouth disease in buffaloes (Bubalus bubalis, Linnaeus, 1758): search of antiantigen antibodies and isolation of the virus].

The immune response to virus-infection-associated (VIA) antigen was studied in 379 Indian buffalos (Bubalus bubalis). These animals were vaccinated three times a year with commercial acetylethyleneimine (AEI)--inactivated foot-and-mouth disease vaccines under field conditions. Two months after the last vaccination, antibody against virus-infection-associated (VIA) antigen was found in 23 per cent. Foot-and-mouth disease virus -- (FMDV) type C "Waldmann" was isolated from oesophageal/pharyngeal fluid of 7 samples buffalos.

Animals