Molecular Epidemiology of Ovine Papillomavirus Infections Among Sheep in Southern Italy

Ovine papillomaviruses (OaPVs) were detected and quantified, for the first time, using droplet digital polymerase chain reaction (ddPCR) and real-time quantitative PCR (qPCR) via blood samples of 165 clinically healthy sheep. OaPV DNA was detected in 126 blood samples (~76.4%). DdPCR detected OaPV D...

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Autores principales: Francesca De Falco, Anna Cutarelli, Nicola D'Alessio, Pellegrino Cerino, Cornel Catoi, Sante Roperto
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:1db0feaee93b44f5b64c1f20776ebdc02021-11-22T04:39:01ZMolecular Epidemiology of Ovine Papillomavirus Infections Among Sheep in Southern Italy2297-176910.3389/fvets.2021.790392https://doaj.org/article/1db0feaee93b44f5b64c1f20776ebdc02021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fvets.2021.790392/fullhttps://doaj.org/toc/2297-1769Ovine papillomaviruses (OaPVs) were detected and quantified, for the first time, using droplet digital polymerase chain reaction (ddPCR) and real-time quantitative PCR (qPCR) via blood samples of 165 clinically healthy sheep. OaPV DNA was detected in 126 blood samples (~76.4%). DdPCR detected OaPV DNA in 124 samples; in only two additional samples positive for real-time qPCR, ddPCR failed to detect the presence of any OaPVs. In 70 of the positive samples (~55.6%), a single OaPV infection was observed, 12 of which were caused by OaPV1 (~17.1%) and 14 by OaPV2 (20%). OaPV3 was responsible for 19 single infections (~27.1%), and OaPV4 for 25 single infections (~35.7%). Multiple OaPV coinfections were observed in 56 (~44.4%) positive samples. OaPV coinfections caused by two genotypes were observed in 31 positive samples (~55.4%), with dual OaPV3/OaPV4 infection being the most prevalent as seen in 11 blood samples. In addition, five OaPV1/OaPV4, four OaPV1/OaPV2, four OaPV2/OaPV3, four OaPV1/OaPV3, and three OaPV2/OaPV4 dual coinfections were also detected. OaPV coinfections by triple and quadruple genotypes were detected in 24 (~42.8%) and only one (~1.8%) of coinfected blood samples, respectively. Multiple infections caused by OaPV1/OaPV3/OaPV4 genotypes were the most prevalent, as observed in 12 (50%) blood samples harboring triple OaPV infections. This study showed that ddPCR is the most sensitive and accurate assay for OaPV detection and quantification thus outperforming real-time qPCR in terms of sensitivity and specificity. Therefore, ddPCR may represent the molecular diagnostic tool of choice, ultimately providing useful insights into OaPV molecular epidemiology and field surveillance.Francesca De FalcoAnna CutarelliNicola D'AlessioPellegrino CerinoCornel CatoiSante RopertoFrontiers Media S.A.articledroplet digital polymerase chain reactionliquid biopsymolecular epidemiologyovine papillomavirusreal-time quantitative PCRVeterinary medicineSF600-1100ENFrontiers in Veterinary Science, Vol 8 (2021)
institution DOAJ
collection DOAJ
language EN
topic droplet digital polymerase chain reaction
liquid biopsy
molecular epidemiology
ovine papillomavirus
real-time quantitative PCR
Veterinary medicine
SF600-1100
spellingShingle droplet digital polymerase chain reaction
liquid biopsy
molecular epidemiology
ovine papillomavirus
real-time quantitative PCR
Veterinary medicine
SF600-1100
Francesca De Falco
Anna Cutarelli
Nicola D'Alessio
Pellegrino Cerino
Cornel Catoi
Sante Roperto
Molecular Epidemiology of Ovine Papillomavirus Infections Among Sheep in Southern Italy
description Ovine papillomaviruses (OaPVs) were detected and quantified, for the first time, using droplet digital polymerase chain reaction (ddPCR) and real-time quantitative PCR (qPCR) via blood samples of 165 clinically healthy sheep. OaPV DNA was detected in 126 blood samples (~76.4%). DdPCR detected OaPV DNA in 124 samples; in only two additional samples positive for real-time qPCR, ddPCR failed to detect the presence of any OaPVs. In 70 of the positive samples (~55.6%), a single OaPV infection was observed, 12 of which were caused by OaPV1 (~17.1%) and 14 by OaPV2 (20%). OaPV3 was responsible for 19 single infections (~27.1%), and OaPV4 for 25 single infections (~35.7%). Multiple OaPV coinfections were observed in 56 (~44.4%) positive samples. OaPV coinfections caused by two genotypes were observed in 31 positive samples (~55.4%), with dual OaPV3/OaPV4 infection being the most prevalent as seen in 11 blood samples. In addition, five OaPV1/OaPV4, four OaPV1/OaPV2, four OaPV2/OaPV3, four OaPV1/OaPV3, and three OaPV2/OaPV4 dual coinfections were also detected. OaPV coinfections by triple and quadruple genotypes were detected in 24 (~42.8%) and only one (~1.8%) of coinfected blood samples, respectively. Multiple infections caused by OaPV1/OaPV3/OaPV4 genotypes were the most prevalent, as observed in 12 (50%) blood samples harboring triple OaPV infections. This study showed that ddPCR is the most sensitive and accurate assay for OaPV detection and quantification thus outperforming real-time qPCR in terms of sensitivity and specificity. Therefore, ddPCR may represent the molecular diagnostic tool of choice, ultimately providing useful insights into OaPV molecular epidemiology and field surveillance.
format article
author Francesca De Falco
Anna Cutarelli
Nicola D'Alessio
Pellegrino Cerino
Cornel Catoi
Sante Roperto
author_facet Francesca De Falco
Anna Cutarelli
Nicola D'Alessio
Pellegrino Cerino
Cornel Catoi
Sante Roperto
author_sort Francesca De Falco
title Molecular Epidemiology of Ovine Papillomavirus Infections Among Sheep in Southern Italy
title_short Molecular Epidemiology of Ovine Papillomavirus Infections Among Sheep in Southern Italy
title_full Molecular Epidemiology of Ovine Papillomavirus Infections Among Sheep in Southern Italy
title_fullStr Molecular Epidemiology of Ovine Papillomavirus Infections Among Sheep in Southern Italy
title_full_unstemmed Molecular Epidemiology of Ovine Papillomavirus Infections Among Sheep in Southern Italy
title_sort molecular epidemiology of ovine papillomavirus infections among sheep in southern italy
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/1db0feaee93b44f5b64c1f20776ebdc0
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