2010
DOI: 10.1128/cvi.00349-09
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Evaluation of a Caprine Arthritis-Encephalitis Virus/Maedi-Visna Virus Indirect Enzyme-Linked Immunosorbent Assay in the Serological Diagnosis of Ovine Progressive Pneumonia Virus in U.S. Sheep

Abstract: A caprine arthritis-encephalitis virus (CAEV)/maedi-visna virus (MVV) indirect enzyme-linked immunosorbent assay (iELISA) was validated with samples from U.S. sheep and by the use of radioimmunoprecipitation as the standard for comparison. The sensitivity and the specificity were 86.0% (؎5.8%) and 95.9% (؎2.9%), respectively. The iELISA format and phylogenetic differences based on the MVV gag sequence contribute to the reduced sensitivity.The diagnosis of small ruminant lentivirus (SRLV) infections in sheep an… Show more

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Cited by 17 publications
(12 citation statements)
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“…The tree was bootstrapped with 1000 pseudoalignments. Sequence representatives of SRLV subgroups 1 and 2 were included in the analyses, as were those of what we describe as subgroup 3, which infected a flock of sheep in the Western United States [29], and has not been tested for an association with TMEM154 genotypes.
Figure 1 Neighbor-Joining network of SRLV partial gag sequences. The sequences were either produced in this study or were available from GenBank, and with amplification primer sites excluded correspond to nucleotide positions 1290–1771 of reference sequence [GenBank:NC_001452].
…”
Section: Introduction Methods and Resultsmentioning
confidence: 99%
“…The tree was bootstrapped with 1000 pseudoalignments. Sequence representatives of SRLV subgroups 1 and 2 were included in the analyses, as were those of what we describe as subgroup 3, which infected a flock of sheep in the Western United States [29], and has not been tested for an association with TMEM154 genotypes.
Figure 1 Neighbor-Joining network of SRLV partial gag sequences. The sequences were either produced in this study or were available from GenBank, and with amplification primer sites excluded correspond to nucleotide positions 1290–1771 of reference sequence [GenBank:NC_001452].
…”
Section: Introduction Methods and Resultsmentioning
confidence: 99%
“…Competitive ELISA methods (cELISA CAEV of VMRD Inc. Pullman, WA) [184,185] using monoclonal antibodies to viral envelope protein (ENV-SU, gp135) epitopes have been developed [186] and indirect ELISAs have been frequently applied [187,188], although few of them have been compared internationally for both sheep and goats [189,190,191]. Currently available indirect standard ELISAs are used in different formats and designs.…”
Section: In Vitro Diagnosismentioning
confidence: 99%
“…Consequently, SRLVs are classified as a major infectious disease of small ruminants by the (Organisation Internationale des epizooties) OIE. In spite of OIE’s efforts and many eradication programs operating in various countries, SRLV still remains a challenge for farmers and health authorities due to the absence of an efficient vaccine or a diagnostic tool capable of detecting all SRLV subtypes [50,66]. …”
Section: Implications Of Srlv Genetic Diversity and Cross-species mentioning
confidence: 99%