Cutarelli Anna, De Falco Francesca, Cuccaro Bianca, Milićević Vesna, Kureljušić Branislav, Bojkovski Jovan, Cerino Pellegrino, Perillo Antonella, Marica Raluca, Catoi Cornel, Roperto Sante
Istituto Zooprofilattico Sperimentale del Mezzogiorno, Portici, Italy.
Dipartimento di Medicina Veterinaria e delle Produzioni Animali, Università degli Studi di Napoli Federico II, Napoli, Italy.
Front Vet Sci. 2023 Jun 15;10:1213150. doi: 10.3389/fvets.2023.1213150. eCollection 2023.
Caprine papillomaviruses (ChPVs, Capra hircus papillomaviruses) were detected and quantified for the first time using droplet digital polymerase chain reaction (ddPCR) blood samples of 374 clinically healthy goats from farms located in Italy, Romania, and Serbia. Overall, ddPCR revealed ChPV DNA in 78 of the 374 examined samples, indicating that 21% of the goats harbored circulating papillomavirus DNA. In particular, in Italian goat farms, ChPV genotypes were detected and quantified in 58 of 157 blood samples (37%), 11 of 117 samples from Serbian farms (9.4%), and 9 of 100 from Romanian blood samples (9%). Blood samples from Italian goat farms showed a high prevalence of ChPV1, which was detected in 45 samples (28.6%). The ChPV2 genotype was detected in 13 samples (8.3%). Therefore, significant differences in prevalence and genotype distributions were observed. On Serbian and Romanian farms, no significant differences were observed in the genotype prevalence of ChPVs. Molecular findings are consistent with ChPV prevalence, characterized by a territorial distribution similar to that of papillomaviruses in other mammalian species. Furthermore, this study showed that ddPCR is a very sensitive and accurate assay for ChPV detection and quantification. The ddPCR may be the molecular diagnostic tool of choice, ultimately providing useful insights into the molecular epidemiology and field surveillance of ChPV.
首次使用液滴数字聚合酶链反应(ddPCR)对来自意大利、罗马尼亚和塞尔维亚农场的374只临床健康山羊的血液样本进行检测和定量分析,以检测山羊乳头瘤病毒(ChPVs,山羊乳头瘤病毒)。总体而言,ddPCR在374份检测样本中的78份中检测到ChPV DNA,这表明约21%的山羊携带循环乳头瘤病毒DNA。具体而言,在意大利山羊养殖场,157份血液样本中的58份(约37%)检测到并定量了ChPV基因型,塞尔维亚养殖场117份样本中的11份(约9.4%),罗马尼亚血液样本100份中的9份(9%)。意大利山羊养殖场的血液样本显示ChPV1的高流行率,在45份样本中检测到(28.6%)。在13份样本中检测到ChPV2基因型(约8.3%)。因此,观察到流行率和基因型分布存在显著差异。在塞尔维亚和罗马尼亚的养殖场,ChPVs的基因型流行率未观察到显著差异。分子研究结果与ChPV流行情况一致,其特征是地域分布与其他哺乳动物物种的乳头瘤病毒相似。此外,本研究表明ddPCR是一种用于ChPV检测和定量的非常灵敏和准确的检测方法。ddPCR可能是首选的分子诊断工具,最终为ChPV的分子流行病学和现场监测提供有用的见解。