Verin Ranieri, Varuzza Paolo, Mazzei Maurizio, Poli Alessandro
1 Dipartimento di Scienze Veterinarie, Università di Pisa, Viale delle Piagge, 2 I-56124, Pisa, Italy.
J Wildl Dis. 2014 Jul;50(3):559-65. doi: 10.7589/2013-01-004. Epub 2014 May 21.
To investigate pseudorabies-virus (PrV) -antibody and viral-DNA prevalence, we collected blood, nasal and genital swabs, and tonsillar and lymph-node tissue samples from 139 wild boars (Sus scrofa; 39 piglets, 30 juveniles, and 70 adults), during the hunting season of 2010-2011 in Tuscany, Central Italy. We performed immunohistochemistry with anti-PrV monoclonal antibodies on selected tissue samples. Forty-three of 139 (30.9%) boars were PrV-antibody positive and a 1,954-base-pair PrV-specific product was amplified from nine nasal (6.5%) and 26 genital (18.7%) swabs. Sequence analysis of PrV-positive PCR products revealed identity scores of 99-100% with Suid herpesvirus 1 strain Becker (JF797219) and confirmed the identification of PrV DNA in tested swabs. There was significantly higher antibody prevalence in adults than in juveniles and in piglets than in juveniles. The prevalence of viral DNA was significantly higher in genital swabs than in nasal specimens. The percentage of positive nasal swabs did not differ among age classes. Piglets had a higher percentage of PCR-positive genital swabs than juvenile and adult subjects (30.8% vs. 13.3% and 14.3%, respectively). Results confirmed that PrV infection is widespread in the wild boar population in the study area. The presence of anti-PrV antibodies and of the PrV virus in piglets could be related to vertical transmission of the virus. This hypothesis was also supported by a higher presence of viral genome in genital swabs than in nasal swabs. This field study supports the importance of vertical transmission of PrV, and the high prevalence of virus in genital swabs supports venereal transmission in adult feral boars.
为调查伪狂犬病病毒(PrV)抗体和病毒DNA的流行情况,我们于2010 - 2011年狩猎季节期间,在意大利中部托斯卡纳地区采集了139头野猪(野猪;39头仔猪、30头幼猪和70头成年猪)的血液、鼻拭子和生殖器拭子,以及扁桃体和淋巴结组织样本。我们对选定的组织样本进行了抗PrV单克隆抗体免疫组织化学检测。139头野猪中有43头(30.9%)PrV抗体呈阳性,从9份鼻拭子(6.5%)和26份生殖器拭子(18.7%)中扩增出了一条1954个碱基对的PrV特异性产物。对PrV阳性PCR产物的序列分析显示,其与猪疱疹病毒1型贝克尔株(JF797219)的同一性分数为99 - 100%,并证实了在检测的拭子中鉴定出PrV DNA。成年猪的抗体流行率显著高于幼猪,仔猪的抗体流行率显著高于幼猪。生殖器拭子中病毒DNA的流行率显著高于鼻拭子。不同年龄组鼻拭子阳性百分比无差异。仔猪PCR阳性生殖器拭子的百分比高于幼猪和成年猪(分别为30.8%对13.3%和14.3%)。结果证实PrV感染在研究区域的野猪种群中广泛存在。仔猪中抗PrV抗体和PrV病毒的存在可能与病毒的垂直传播有关。这一假设也得到了生殖器拭子中病毒基因组比鼻拭子中更高存在率的支持。这项实地研究支持了PrV垂直传播的重要性,生殖器拭子中病毒的高流行率支持了成年野猪的性传播。