1995
DOI: 10.1016/0034-5288(95)90088-8
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Development of a competitive ELISA for detecting antibodies to the peste des petits ruminants virus using a recombinant nucleobrotein

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Cited by 233 publications
(192 citation statements)
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“…A confidence interval of 95%, a margin of error of 5%, an infinite population, an assumed true overall prevalence of 50% to obtain maximum sample size, and the sensitivity (94.5%) and specificity (99.4%) of the PPR competitive enzyme-linked immunosorbent assay (cELISA) [35] were used [36,37] in calculations of the sample size (PPR cELISA was used to calculate sample size as PPR was the main focus of the study). This gave the needed sample size of 435 samples for each of the two years when herds (containing sheep and/or goats) were visited.…”
Section: Methodsmentioning
confidence: 99%
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“…A confidence interval of 95%, a margin of error of 5%, an infinite population, an assumed true overall prevalence of 50% to obtain maximum sample size, and the sensitivity (94.5%) and specificity (99.4%) of the PPR competitive enzyme-linked immunosorbent assay (cELISA) [35] were used [36,37] in calculations of the sample size (PPR cELISA was used to calculate sample size as PPR was the main focus of the study). This gave the needed sample size of 435 samples for each of the two years when herds (containing sheep and/or goats) were visited.…”
Section: Methodsmentioning
confidence: 99%
“…Commercial enzyme-linked immunosorbent assay (ELISA) kits were used to analyse the presence of antibodies to the selected pathogens: ID screen PPR competition ELISA (detects anti-PPRV nucleoprotein antibodies [35], sensitivity 94.5%, specificity 99.4%; ID. Vet, Grabels, France), IDEXX CCPP Ab test (uses monoclonal antibody ‘4.52’ against Mycoplasma sp.…”
Section: Methodsmentioning
confidence: 99%
“…As a rapid, simple and sensitive assay, ELISA has been widely used in serological profiling of PPRV in mass screening of samples for sermonitoring/serosurveillance or clinical prevalence. Various workers have used MAb produced against PPRV and RPV for detection of antibodies and antigens in ELISA [2,83,117]. Saliki et al [118] and Anderson and Mckay [2], used neutralizing MAbs against H protein of PPRV for specific detection of PPRV antibodies in competitive ELISA (c-ELISA) and blocking ELISA (B-ELISA) [83,118,131,136] for antibody detection.…”
Section: Enzyme-linked Immunosorbent Assay (Elisa)mentioning
confidence: 99%
“…Various workers have used MAb produced against PPRV and RPV for detection of antibodies and antigens in ELISA [2,83,117]. Saliki et al [118] and Anderson and Mckay [2], used neutralizing MAbs against H protein of PPRV for specific detection of PPRV antibodies in competitive ELISA (c-ELISA) and blocking ELISA (B-ELISA) [83,118,131,136] for antibody detection. Use of the virus neutralising MAb was more advantageous as it produced better correlation between VNT and ELISA [83,117].…”
Section: Enzyme-linked Immunosorbent Assay (Elisa)mentioning
confidence: 99%
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