Using the competitive enzyme-linked immunosorbent assay for the seromonitoring of rinderpest in Saudi Arabia, antibodies were detected in 30% of the sera of 1,018 cattle slaughtered at Riyadh abattoir during June and July 1995. The correlation between the detection of antibodies and the origins of the slaughtered animals was analysed. All the culled dairy cows had detectable antibodies. The proportions of bulls giving serologically positive results were as follows: 57% for animals imported from rinderpest-free countries and vaccinated upon arrival in Saudi quarantine, 20% for native breeding animals and 17% for five- to ten-month-old bull calves born on commercial dairy farms and then raised on separate feedlot farms. In addition, of 105 native cattle sacrificed during the Hajj season in May 1994, 77% had antibodies against rinderpest virus. On the other hand, testing of 17 groups of dairy heifers (from 1 week to 24 months of age), born to immune dams and vaccinated against rinderpest at the ages of six and ten months, revealed the absence of detectable antibodies in the sera of some animals which were between two and ten months of age. Results are interpreted in relation to evaluation of the continuing vaccination programmes and their efficacy as an element of the national programme for the control of rinderpest.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.20506/rst.16.3.1069 | DOI Listing |
Arch Virol
July 2018
OIE Regional Representation for Africa, B.P. 2954, Bamako, Mali.
Peste des petits ruminants (PPR) is a contagious and economically important disease affecting production of small ruminants (i.e., sheep and goats).
View Article and Find Full Text PDFTrop Anim Health Prod
October 2008
Department of Veterinary Microbiology, Faculty of Veterinary Science, University of Agriculture, Street No. 2, Khalsa College, Faisalabad, Pakistan.
Monoclonal antibody-based competitive ELISA (C-ELISA) has been used for the specific measurement of antibodies to peste des petits ruminants (PPR) viruses in sheep, goats, cattle and buffalo. Serum samples from sheep (n = 232), goats (n = 428), cattle (n = 43), buffalo (n = 89) were tested. The animals had not been vaccinated against rinderpest or PPR.
View Article and Find Full Text PDFTrop Anim Health Prod
November 2002
FAO Consultant, Littlehampton, UK.
In January 1997, Tanzania requested international assistance against rinderpest on the grounds that the virus had probably entered the country from southern Kenya. Over the next few months, a variety of attempts were made to determine the extent of the incursion by searching for serological and clinical evidence of the whereabouts of the virus. At the clinical level, these attempts were hampered by the low virulence of the strain, and at the serological level by the lack of a baseline against which contemporary interpretations could be made.
View Article and Find Full Text PDFPrev Vet Med
January 2003
Livestock Health Research Institute (LIRI), P.O. Box 96, Tororo, Canada.
Based on passive and active data, we report on an epidemiological assessment of surveillance and control of rinderpest (RP) in Uganda between 1990 and 1998. Active data were collected by administration of questionnaires to animal health personnel and their auxiliaries and to stockowners in six selected districts of eastern and northeastern Uganda. Passive data were extracted from vaccination and seromonitoring reports, and from field and laboratory reports.
View Article and Find Full Text PDFVirology
July 2002
Project Directorate on Animal Disease Monitoring and Surveillance, Hebbal, Bangalore- 560 024, India.
Monoclonal antibodies (mAbs) against secreted hemagglutinin (H) protein of rinderpest virus (RPV) expressed by a recombinant baculovirus were generated to characterize the antigenic sites on H protein and regions of functional significance. Three of the mAbs displayed hemagglutination inhibition activity and these mAbs were unable to neutralize virus infectivity. Western immunoblot analysis of overlapping deletion mutants indicated that three mAbs recognize antigenic regions at the extreme carboxy terminus (between amino acids 569 and 609) and the fourth mAb between amino acids 512 and 568.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!