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Title

Antibody-based diagnosis of small ruminant lentivirus infection in seminal fluid

AuthorsRamírez, Hugo ; San Román, Beatriz ; Glaria, Idoia ; Reina, Ramsés ; Hernández, Mirna M.; Andrés, Ximena de ; Crespo, Helena ; Hichou, B.; Cianca, Silvia; Grilló, María Jesús ; Andrés, Damián F. de ; Amorena Zabalza, Beatriz
KeywordsDiagnosis
Polymerase chain reaction
Semen
Small ruminant lentivirus
Antibody
Issue DateNov-2009
PublisherElsevier
CitationTheriogenology 72(8): 1085-1096 (2009)
AbstractAntibody-based diagnosis of small ruminant lentiviruses (SRLVs) has been efficiently achieved using serum and milk, but not semen, for which polymerase chain reaction (PCR) has been proposed as a confirmatory technique. This work, involving 296 ovine (Ovis aries) and caprine (Capra hircus) semen donors, investigates whether seminal fluid (SF) can be reliably used in antibody-based SRLV diagnosis. First, a gold standard was established to assess the infection status and determine the sensitivity and specificity of three commercial enzyme-linked immunosorbent assays (ELISAs) in serum testing using Western blot and PCR as confirmatory tests. For SF testing, both gold standard and serum testing results were used as reference. The performance of SF testing was affected not only by the ELISA assay sensitivity (related to antigen spectrum) compared with that of the gold standard (as it occurred in serum testing) but also by SF sample quality and SF working dilution. Nonturbid SF samples, commonly collected in artificial insemination centers (AICs), were required. Compared with serum, SF testing had a decreased sensitivity in two of the ELISA assays (with original serum working dilutions ≤1/20 in serum testing) but reached a similar sensitivity (and specificity) in the assay designed to work at the highest serum dilution (1/500). A SF concentration of about 1/2 (250-fold that used in serum testing) was found optimal in this assay, yielding highly repeatable results that were in almost perfect agreement with those of serum testing (κ ± SE, 0.91 ± 0.81). Thus, SF ELISA can be reliably applied in antibody-based SRLV diagnosis. This information may be useful to control infection in AICs and animal and semen trade programs requiring health-certified quality of semen donors. © 2009 Elsevier Inc. All rights reserved.
DescriptionRamírez, Hugo et al.
Publisher version (URL)http://dx.doi.org/10.1016/j.theriogenology.2009.06.028
URIhttp://hdl.handle.net/10261/114218
DOI10.1016/j.theriogenology.2009.06.028
Identifiersdoi: 10.1016/j.theriogenology.2009.06.028
issn: 0093-691X
Appears in Collections:(IDAB) Artículos
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