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S Waghela

Publications and source records attributed to S Waghela.

15 recordsLinked to original sources
PubMed2005

Spatial distribution of antibodies to Salmonella enterica serovar Typhimurium O antigens in bulk milk from Texas dairy herds.

Environmental factors that enhance either the survivability or dispersion of Salmonella enterica serovar Typhimurium (S. Typhimurium) could result in a spatial pattern of disease risk. The objectives of this study were to: (1) describe herd status based on antibody response to Salmonella Typhimurium as estimated from bulk tank milk samples and (2) to describe the resulting geographical patterns found among Texas dairy herds. Eight hundred and fifty-two bulk milk samples were collected from georeferenced dairy farms and assayed by an indirect enzyme-linked immunosorbent assay (ELISA) using S. Typhimurium lipopolysaccharide (LPS). ELISA signal-to-noise ratios for each bulk tank milk sample were calculated and used for geostatistical analyses. Best-fit parameters for the exponential theoretical variogram included a range of 438.8 km, partial sill of 0.060 and nugget of 0.106. The partial sill is the classical geostatistical term for the variance that can be explained by the herd's location and the nugget is the spatially random component of the variance. We have identified a spatial process in bulk milk tank titers for S. Typhimurium in Texas dairy herds and present a map of the expected smoothed surface. Areas with higher expected titers should be targeted in further studies on controlling Salmonella infection with environmental modifications.

Animals↗
PubMed1992

Non-immunologic methods of diagnosis of babesiosis.

The diagnosis of tick-borne diseases such as babesiosis still depends on observing the parasite in the infected erythrocyte. Microscopic observation is tedious and often problematic in both early and carrier infections. Better diagnostic methods are needed to prevent clinical disease, especially when susceptible cattle are being moved into disease enzootic areas. This study evaluates two techniques for early diagnosis of Babesia bovis infections in cattle, DNA probes specific for the organism and fluorescent probes specific for nucleic acid. The radioisotopically labeled DNA probes are used in slot blot hybridizations with lysed blood samples, not purified DNA. Thusfar, the probe is specific for B. bovis and can detect as few as 1000 B. bovis parasites in 10 microliters of blood. The specificity of the fluorescent probe depends on the characteristic morphology of the babesia in whole blood samples, as determined microscopically. The fluorescent probe detects as few as 10,000 B. bovis parasites in 10 microliters os blood. The application of each method for laboratory and field use is discussed.

Animals↗
PubMed1988

The occurrence of infectious diseases in mixed farming of domesticated wild herbivores and livestock in Kenya. II. Bacterial diseases.

The prevalence of antibodies to Brucella spp., Mycobacterium paratuberculosis and the Mycoplasma spp. causing contagious bovine pleuropneumonia and contagious caprine pleuropneumonia was determined in various species of ruminants on a ranch in the semi-arid zone of southeastern Kenya. Antibody titers to Brucella spp. were found in eland (Taurotragus oryx), oryx (Oryx beisa) and camels (Camelus dromedarius). Reactors were not found in buffalo (Syncerus caffer), sheep (Ovis aries) and goats (Capra hircus). Brucella sp. was not isolated from eland and camels. Antibody titers to M. paratuberculosis were found only in camels and goats. Mycobacteria were not detected in feces of two serologically positive camels. Significant serum antibody titers to Mycoplasma mycoides mycoides were found only in camels. Antibody titers to Mycoplasma sp. (strain F38), which causes contagious caprine pleuropneumonia, were found in buffalo, cattle and camels but not in the other species. Attempts to isolate the Mycoplasma sp. from nasal secretion of the buffalo and camels failed. The possible occurrence of tuberculosis in camels is discussed. Under the conditions at the ranch, contagious bacterial diseases appear to be of minor importance in the domesticated wild herbivores. The introduced camels, however, might be a source of various infections such as brucellosis, mycoplasmosis and possibly tuberculosis for the other susceptible species.

Animals↗
PubMed1986

Antibodies to Brucella spp. among blue wildebeest and African buffalo in Kenya.

A serologic survey of blue wildebeest (Connochaetes taurinus Burchell) and African buffalo (Syncerus caffer Sparrman) in the Masai Mara area was conducted. Antibodies to Brucella spp. were found in 18% of the blue wildebeest and 30% of the African buffalo examined. There were titers in all age groups and in both sexes. Hygromata were seen in both species. The increase in numbers of blue wildebeest and African buffalo which share grazing and watering areas with cattle of the Masai people, makes the presence of infections by Brucella spp. in wildlife an important consideration in any program for control of brucellosis.

Age Factors↗
PubMed1984

Global survey of serological evidence of caprine arthritis-encephalitis virus infection.

Using caprine arthritis-encephalitis virus antigen in the agar gel immunodiffusion test, 3729 serum samples from goats in over 112 locations around the world were tested for precipitating antibodies. Over 90 per cent of the 1265 positive samples came from Canada, France, Norway, Switzerland and the USA, all of which had 65 per cent reactors or greater. Fiji, Great Britain, Kenya, Mexico, New Zealand and Peru had fewer than 10 per cent positive samples; the majority of these could be traced to importations of goats from countries where there was a high occurrence of precipitating antibody. Somalia, Sudan and South Africa had no reactors among 306 samples. No reactors were found among 1116 samples from domestic and indigenous goats which were known to have had no contact with imported goats from countries which had a high occurrence.

Africa↗
PubMed1983

Serological response of cattle, sheep and goats in Kenya vaccinated with killed Brucella melitensis strain H38 adjuvant vaccine.

The antibody responses of cattle, sheep and goats to the Brucella melitensis H38 adjuvant vaccine were monitored by serum (tube) agglutination, complement fixation and Rose Bengal plate tests. High and persisting antibody titres were induced by a single dose of this vaccine in all three species. It would be difficult to classify reactors by commonly used diagnostic tests in a control or an eradication programme using the H38 adjuvant vaccine.

Adjuvants, Immunologic↗
PubMed1980

Comparison of four serological tests in the diagnosis of caprine brucellosis.

Results from four serological tests for diagnosing brucellosis--serum tube agglutination (SAT), agar gel immunodiffusion (AGIT), Rose Bengal plate (RBPT) and complement fixation (CFT)--were compared using sera from goats from farms infected with Brucella melitensis. Ninety-two goats were negative and 29 positive to all four tests. The remaining 85 reacted to one or more tests. The RBPT was the most sensitive test and the AGIT the most specific, when compared with the CFT. The results suggest that the SAT adds little information when used with other tests but that RBPT and AGIT are useful for testing caprine brucellosis where facilities for the CFT are not available.

Agglutination Tests↗
PubMed1974

The rose bengal plate test in human brucellosis.

In Machakos Hospital, Kenya, the sera of 452 patients suspected of brucellosis were examined with the Rose Bengal Plate Test (RBPT), the complement fixation test (CFT) and the tube serum agglutination test (SAT). The percentage of false positive findings on the RBPT was 0.22% when compared with the SAT, 0.44% with the CFT. The percentage of false negative findings on the RBPT was 3% when compared with the SAT, 0.88% with the CFT. A good correlation between the RBPT and both the SAT and the CFT was also found by Morgan et al. (1969). The RBPT may be considered as a highly reliable test in the diagnosis of human brucellosis. The test is especially valuable in areas where laboratory facilities are not available and can be used as a screening test in areas with good laboratory facilities.

Agglutination Tests↗