Elia Gabriella, Tarsitano Elvira, Camero Michele, Bellacicco Anna Lucia, Buonavoglia Domenico, Campolo Marco, Decaro Nicola, Thiry Julien, Tempesta Maria
Department of Animal Health and Well-being, Faculty of Veterinary Medicine, University of Bari, Sp Casamassima km. 3, 70010 Valenzano, Italy.
J Virol Methods. 2008 Mar;148(1-2):155-60. doi: 10.1016/j.jviromet.2007.10.021.
Caprine herpesvirus 1 (CpHV-1) is an alphaherpesvirus interfering with goat reproductive performances. The virus is associated with neonatal mortality in kids and reproductive failure in adults. A real-time PCR assay based on TaqMan technology and targeting the gene encoding for glycoprotein C (gC) was developed for detection and quantitation of CpHV-1 in samples collected from infected goats. The detection limit of the assay was 1 x 10(2) standard DNA copies, with a sensitivity of 1-2 logs higher than the conventional gel-based PCR assay targeting the same gene. The real-time PCR was reproducible, as shown by satisfactory low intra-assay and interassay coefficients of variation. The quantitative assay was validated on clinical samples, including genital swabs and various tissue samples collected from goats either infected naturally or experimentally with CpHV-1. The high sensitivity, simplicity and reproducibility of the CpHV-1 fluorogenic PCR assay, combined with its wide dynamic range and high throughput, make this method especially suitable for studies on the pathogenesis and for trials with experimental vaccines and antiviral drugs.
山羊疱疹病毒1型(CpHV-1)是一种干扰山羊繁殖性能的α疱疹病毒。该病毒与羔羊的新生儿死亡率和成年羊的繁殖失败有关。基于TaqMan技术并靶向编码糖蛋白C(gC)的基因开发了一种实时PCR检测方法,用于检测和定量从感染山羊采集的样本中的CpHV-1。该检测方法的检测限为1×10²个标准DNA拷贝,灵敏度比靶向同一基因的传统基于凝胶的PCR检测方法高1-2个对数。实时PCR具有可重复性,低批内和批间变异系数令人满意即表明了这一点。该定量检测方法在临床样本上得到了验证,这些临床样本包括从自然感染或实验感染CpHV-1的山羊采集的生殖器拭子和各种组织样本。CpHV-1荧光PCR检测方法的高灵敏度、简便性和可重复性,再加上其宽动态范围和高通量,使得该方法特别适用于发病机制研究以及实验疫苗和抗病毒药物试验。