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Development and Field Testing of a Real-Time PCR Assay for Caprine Arthritis-Encephalitis-Virus (CAEV)

Caprine arthritis/encephalitis (CAE) of goats and occasionally sheep are persistent virus infections caused by a lentivirus (CAEV). This viral infection results in arthritis in adult animals and encephalitis in kids. Prognosis for the encephalitic form is normally poor, with substantial economic los...

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Autores principales: Brajon, Giovanni, Mandas, Daniela, Liciardi, Manuele, Taccori, Flavia, Meloni, Mauro, Corrias, Franco, Montaldo, Caterina, Coghe, Ferdinando, Casciari, Cristina, Giammarioli, Monica, Orrù, Germano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414719/
https://www.ncbi.nlm.nih.gov/pubmed/22888382
http://dx.doi.org/10.2174/1874357901206010082
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author Brajon, Giovanni
Mandas, Daniela
Liciardi, Manuele
Taccori, Flavia
Meloni, Mauro
Corrias, Franco
Montaldo, Caterina
Coghe, Ferdinando
Casciari, Cristina
Giammarioli, Monica
Orrù, Germano
author_facet Brajon, Giovanni
Mandas, Daniela
Liciardi, Manuele
Taccori, Flavia
Meloni, Mauro
Corrias, Franco
Montaldo, Caterina
Coghe, Ferdinando
Casciari, Cristina
Giammarioli, Monica
Orrù, Germano
author_sort Brajon, Giovanni
collection PubMed
description Caprine arthritis/encephalitis (CAE) of goats and occasionally sheep are persistent virus infections caused by a lentivirus (CAEV). This viral infection results in arthritis in adult animals and encephalitis in kids. Prognosis for the encephalitic form is normally poor, with substantial economic loss for the farm. In this context an early/fast laboratory diagnosis for CAEV infection could be useful for effective prophylactic action. In this work we performed a quantitative real time PCR designed on the CAEV env gene to detect/quantify in goat/sheep samples, viral RNA or proviral DNA forms of CAEV. This procedure was validated in 15 sheep, experimentally infected with CAEV or with a highly correlated lentivirus (visna maedi, MVV); in addition, a total of 37 clinical goat specimens recruited in CAEV positive herds were analyzed and compared using serological analysis (Elisa and AGID). All samples infected with MVV resulted negative. In sheep experimentally infected with CAEV, proviral DNA was detectable 15 days post infection, whereas the serological methods revealed an indicative positivity after 40-60 days.This method showed a sensitivity of 10(2) env fragments/PCR) with a linear dynamic range of quantitation from 10(3) to 10(7) env fragments/PCR; the R2 correlation coefficient was 0.98. All subjects with a clinical diagnosis for Caprine Arthritis-Encephalitis (CAE) resulted CAEV DNA positive.
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spelling pubmed-34147192012-08-10 Development and Field Testing of a Real-Time PCR Assay for Caprine Arthritis-Encephalitis-Virus (CAEV) Brajon, Giovanni Mandas, Daniela Liciardi, Manuele Taccori, Flavia Meloni, Mauro Corrias, Franco Montaldo, Caterina Coghe, Ferdinando Casciari, Cristina Giammarioli, Monica Orrù, Germano Open Virol J Article Caprine arthritis/encephalitis (CAE) of goats and occasionally sheep are persistent virus infections caused by a lentivirus (CAEV). This viral infection results in arthritis in adult animals and encephalitis in kids. Prognosis for the encephalitic form is normally poor, with substantial economic loss for the farm. In this context an early/fast laboratory diagnosis for CAEV infection could be useful for effective prophylactic action. In this work we performed a quantitative real time PCR designed on the CAEV env gene to detect/quantify in goat/sheep samples, viral RNA or proviral DNA forms of CAEV. This procedure was validated in 15 sheep, experimentally infected with CAEV or with a highly correlated lentivirus (visna maedi, MVV); in addition, a total of 37 clinical goat specimens recruited in CAEV positive herds were analyzed and compared using serological analysis (Elisa and AGID). All samples infected with MVV resulted negative. In sheep experimentally infected with CAEV, proviral DNA was detectable 15 days post infection, whereas the serological methods revealed an indicative positivity after 40-60 days.This method showed a sensitivity of 10(2) env fragments/PCR) with a linear dynamic range of quantitation from 10(3) to 10(7) env fragments/PCR; the R2 correlation coefficient was 0.98. All subjects with a clinical diagnosis for Caprine Arthritis-Encephalitis (CAE) resulted CAEV DNA positive. Bentham Open 2011-07-27 /pmc/articles/PMC3414719/ /pubmed/22888382 http://dx.doi.org/10.2174/1874357901206010082 Text en © Brajon et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http: //creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Brajon, Giovanni
Mandas, Daniela
Liciardi, Manuele
Taccori, Flavia
Meloni, Mauro
Corrias, Franco
Montaldo, Caterina
Coghe, Ferdinando
Casciari, Cristina
Giammarioli, Monica
Orrù, Germano
Development and Field Testing of a Real-Time PCR Assay for Caprine Arthritis-Encephalitis-Virus (CAEV)
title Development and Field Testing of a Real-Time PCR Assay for Caprine Arthritis-Encephalitis-Virus (CAEV)
title_full Development and Field Testing of a Real-Time PCR Assay for Caprine Arthritis-Encephalitis-Virus (CAEV)
title_fullStr Development and Field Testing of a Real-Time PCR Assay for Caprine Arthritis-Encephalitis-Virus (CAEV)
title_full_unstemmed Development and Field Testing of a Real-Time PCR Assay for Caprine Arthritis-Encephalitis-Virus (CAEV)
title_short Development and Field Testing of a Real-Time PCR Assay for Caprine Arthritis-Encephalitis-Virus (CAEV)
title_sort development and field testing of a real-time pcr assay for caprine arthritis-encephalitis-virus (caev)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414719/
https://www.ncbi.nlm.nih.gov/pubmed/22888382
http://dx.doi.org/10.2174/1874357901206010082
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