Detection and quantification of bovine papillomavirus DNA by digital droplet PCR in sheep blood

Abstract Highly pathogenic bovine papillomaviruses (BPVs) were detected and quantified for the first time using digital droplet polymerase chain reaction (ddPCR) by liquid biopsy in 103 clinically healthy sheep. Overall, ddPCR detected BPVs in 68 blood samples (66%). BPV infection by a single genoty...

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Main Authors: Sante Roperto, Anna Cutarelli, Federica Corrado, Francesca De Falco, Canio Buonavoglia
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-89782-4
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spelling doaj-6b4e5c7a86a84baeabc52284f516c8592021-05-16T11:24:01ZengNature Publishing GroupScientific Reports2045-23222021-05-011111710.1038/s41598-021-89782-4Detection and quantification of bovine papillomavirus DNA by digital droplet PCR in sheep bloodSante Roperto0Anna Cutarelli1Federica Corrado2Francesca De Falco3Canio Buonavoglia4Dipartimento di Medicina Veterinaria e Produzioni Animali, Università degli Studi di Napoli Federico IIIstituto Zooprofilattico Sperimentale del MezzogiornoIstituto Zooprofilattico Sperimentale del MezzogiornoDipartimento di Medicina Veterinaria e Produzioni Animali, Università degli Studi di Napoli Federico IIDipartimento di Medicina Veterinaria, Università degli Studi di Bari “Aldo Moro”Abstract Highly pathogenic bovine papillomaviruses (BPVs) were detected and quantified for the first time using digital droplet polymerase chain reaction (ddPCR) by liquid biopsy in 103 clinically healthy sheep. Overall, ddPCR detected BPVs in 68 blood samples (66%). BPV infection by a single genotype was revealed in 61.8% of the blood samples, and BPV coinfection by double, triple or quadruple genotypes was observed in 38.2% of liquid biopsies. The BPV-2 genotype was most frequently seen in sheep, whereas BPV-1 was the least common. Furthermore, ddPCR was very useful for detection and quantification; the BPV-14 genotype was observed for the first time in ovine species, displaying the highest prevalence in some geographical areas (Apulia). In 42 of the positive samples (61.8%), a single BPV infection was observed, 26 of which were caused by BPV-2 (61.9%) and 7 by BPV-13 (16.7%). BPV-14 was responsible for 7 single infections (16.7%) and BPV-1 for 2 single infections (4.7%). Multiple BPV coinfections were observed in the remaining 26 positive samples (38.2%), with dual BPV-2/BPV-13 infection being the most prevalent (84.6%). BPV infection by triple and quadruple genotypes was also observed in 11.5% and 3.8% of cases, respectively. The present study showed that ddPCR, a biotechnological refinement of conventional PCR, is by far the most sensitive and accurate assay for BPV detection compared to conventional qPCR. Therefore, ddPCR displayed an essential diagnostic and epidemiological value very useful for the identification of otherwise undetectable BPV genotypes as well as their geographical distributions and suggesting that animal husbandry practices contribute to cross-species transmission of BPVs.https://doi.org/10.1038/s41598-021-89782-4
collection DOAJ
language English
format Article
sources DOAJ
author Sante Roperto
Anna Cutarelli
Federica Corrado
Francesca De Falco
Canio Buonavoglia
spellingShingle Sante Roperto
Anna Cutarelli
Federica Corrado
Francesca De Falco
Canio Buonavoglia
Detection and quantification of bovine papillomavirus DNA by digital droplet PCR in sheep blood
Scientific Reports
author_facet Sante Roperto
Anna Cutarelli
Federica Corrado
Francesca De Falco
Canio Buonavoglia
author_sort Sante Roperto
title Detection and quantification of bovine papillomavirus DNA by digital droplet PCR in sheep blood
title_short Detection and quantification of bovine papillomavirus DNA by digital droplet PCR in sheep blood
title_full Detection and quantification of bovine papillomavirus DNA by digital droplet PCR in sheep blood
title_fullStr Detection and quantification of bovine papillomavirus DNA by digital droplet PCR in sheep blood
title_full_unstemmed Detection and quantification of bovine papillomavirus DNA by digital droplet PCR in sheep blood
title_sort detection and quantification of bovine papillomavirus dna by digital droplet pcr in sheep blood
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-05-01
description Abstract Highly pathogenic bovine papillomaviruses (BPVs) were detected and quantified for the first time using digital droplet polymerase chain reaction (ddPCR) by liquid biopsy in 103 clinically healthy sheep. Overall, ddPCR detected BPVs in 68 blood samples (66%). BPV infection by a single genotype was revealed in 61.8% of the blood samples, and BPV coinfection by double, triple or quadruple genotypes was observed in 38.2% of liquid biopsies. The BPV-2 genotype was most frequently seen in sheep, whereas BPV-1 was the least common. Furthermore, ddPCR was very useful for detection and quantification; the BPV-14 genotype was observed for the first time in ovine species, displaying the highest prevalence in some geographical areas (Apulia). In 42 of the positive samples (61.8%), a single BPV infection was observed, 26 of which were caused by BPV-2 (61.9%) and 7 by BPV-13 (16.7%). BPV-14 was responsible for 7 single infections (16.7%) and BPV-1 for 2 single infections (4.7%). Multiple BPV coinfections were observed in the remaining 26 positive samples (38.2%), with dual BPV-2/BPV-13 infection being the most prevalent (84.6%). BPV infection by triple and quadruple genotypes was also observed in 11.5% and 3.8% of cases, respectively. The present study showed that ddPCR, a biotechnological refinement of conventional PCR, is by far the most sensitive and accurate assay for BPV detection compared to conventional qPCR. Therefore, ddPCR displayed an essential diagnostic and epidemiological value very useful for the identification of otherwise undetectable BPV genotypes as well as their geographical distributions and suggesting that animal husbandry practices contribute to cross-species transmission of BPVs.
url https://doi.org/10.1038/s41598-021-89782-4
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