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A total 13 800 cattle were examined serologically and 399 bacteriologically for leptospirosis. The samples of sera were tested by the microscopic agglutination test using 17 antigens from 16 serogroups of Leptospira spp. Specific antibodies were found in 29 per cent of animals. Most often there were recorded the titers against the antigens of serovars of the Sejroe serogroup (21%). The pathogens were isolated from 5 cows. The isolates were identified as belonging to the hardjo serovar.
In order to evaluate seroprevalence of leptospiral infection in the population of the European wild boar (Sus scrofa L.), 107 sera obtained from this species after hunting were tested. All sera were examined by microagglutination test (MAT) and passive hemagglutination test (PHT). The latter test detects only IgM antibodies and allows a differentiation between recent and past infections. A panel of 18 serowars (icterohaemorrhagiae, grippotyphosa, sejroe, tarassovi, pomona, canicola, australis, ballum, hebdomadis, patoc, poi, calledoni, zanoni, cynopteri, autumnalis, bataviae, hardjo, bratislava) from 16 serogroups was used in MAT. The screening dilution of sera was 1 in 100. A result of at least 50% agglutination of leptospires at 1:100 dilution or greater was considered positive. PHT was prepared from the strain of Perepelicin belonging to the Tarassovi serogroup. Altogether 25.2% positive results were obtained. 23 sera reacted in MAT. 12 serovars were recorded. The most prevalent was sejroe (6 positive results), then grippotyphosa and poi (4 positive results). Most of the positive sera reacted in MAT in a dilution of 1:100 (19 cases), in 6 cases in a dilution of 1:200, in 4 at 1:400 and 1 had an end point titre of 1:800. By using a passive hemagglutination test, positive reactions were recorded in 7 cases. In one case a doubtful result was obtained. 4 sera reacted only in PTH. The results indicate the wild boar as a potential source of pathogenic leptospires.
Leptospirosis can be an important problem and a cause of significant economic losses in swine herds. Because of a high susceptibility of leptospires to many factors, laboratory diagnosis of the disease (especially pathogen isolation and identification) is difficult and often based on serological methods. The aim of this study was to show the possible use of PCR for detection and partial identification of Leptospira spp. in clinical samples from swine. Four aborted fetuses and 2 serum samples from sows reared on a farm infected by the serovar Pomona and 4 fetuses from a farm infected by leptospires from the serogroup Sejroe were submitted for examination. Additionally, urine and serum samples from 8 aborting sows reared on 2 farms infected by the serogroup Sejroe were investigated. Serum samples were examined by the microagglutination test (MAT). Samples of urine and tissue samples from fetuses were examined by PCR with pairs of primers detecting DNA sequences specific to a) genus Leptospira, b) species L. borgpetersenii, c) two selected groups of serovars of the species L. interrogans, d) serogroup Sejroe. Serological findings showed in all examined sows the presence of titers to the serogroup Pomona or Sejroe, depending on the serogroup causing infection on a given farm. DNA of the genus Leptospira was detected in tissues of all fetuses from sows infected by the serovar Pomona, in 3 fetuses from the farm infected by the Sejroe serogroup, and in all urine samples. The presence of the DNA sequence specific for the group of L. interrogans serovars including the serovar Pomona was found in tissues of all 4 fetuses from dams presenting titers to the serogroup Pomona. DNA of the serogroup Sejroe was detected in 6 out of 8 urine samples examined, and DNA of the species L. borgpetersenii (including the serovar Sejroe) was found in 5 urine samples. No DNA of the species L. borgpetersenii or of the serogroup Sejroe was found in tissues of fetuses from the farm infected by the serogroup Sejroe. This study demonstrated the usefulness of PCR in confirming the presence of Leptospira spp. in clinical samples from swine. Furthermore, PCR confirmed the presence of the serovar Pomona in tissues of aborted fetuses and the presence of L. borgpetersenii and/or the Sejroe serogroup in samples of urine. A conclusive evaluation of the usefulness of PCR in identifying DNA of L. borgpetersenii and the serogroup Sejroe in tissue samples requires further investigations.
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