Abdul-Careem Mohamed Faizal, Hunter Bruce D, Nagy Eva, Read Leah R, Sanei Babak, Spencer J Lloyd, Sharif Shayan
Department of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, Ont., Canada N1G 2W1.
J Virol Methods. 2006 Apr;133(1):34-40. doi: 10.1016/j.jviromet.2005.10.018. Epub 2005 Nov 18.
Feather follicles of birds infected with Marek's disease virus (MDV) serve as the sole source of infectious virus particles. The present study was aimed at developing a SYBR Green real-time PCR assay to detect and quantify MDV loads in feather tips targeting meq gene of the virus. The assay had a dynamic range of 8 logs, mean inter- and intra-assay coefficient variation (CV) of <5% and minimum detection limit of 15 MDV genome copies when plasmid DNA was used as the template. The sensitivity of the assay was compared with that of the conventional PCR technique and found to be 2.5-10 times more sensitive than the conventional PCR technique. The assay was validated using feather tip DNA preparations derived from chickens infected with 250 plaque forming units (PFU) of RB1B strain of MDV and sampled on days 7, 14, 21 and 28 post-infection (p.i.) along with uninfected chickens. MDV genome was quantifiable in feather tips of infected birds by day 7 p.i. and the number of MDV copies peaked by day 14 p.i., but then gradually decreased by day 28. This reliable real-time PCR assay may be used for monitoring MDV genome loads in tissues of experimentally or naturally infected birds.
感染马立克氏病病毒(MDV)的鸟类羽毛毛囊是传染性病毒颗粒的唯一来源。本研究旨在开发一种SYBR Green实时荧光定量PCR检测方法,以检测和定量针对该病毒meq基因的羽毛尖端中的MDV载量。当使用质粒DNA作为模板时,该检测方法的动态范围为8个对数,平均批间和批内变异系数(CV)<5%,最低检测限为15个MDV基因组拷贝。将该检测方法的灵敏度与传统PCR技术进行比较,发现其灵敏度比传统PCR技术高2.5至10倍。使用来自感染250个MDV RB1B株蚀斑形成单位(PFU)的鸡的羽毛尖端DNA制剂进行验证,并在感染后(p.i.)第7、14、21和28天以及未感染的鸡进行采样。在感染后第7天,感染鸟类的羽毛尖端可检测到MDV基因组,MDV拷贝数在感染后第14天达到峰值,但到第28天逐渐下降。这种可靠的实时荧光定量PCR检测方法可用于监测实验性或自然感染鸟类组织中的MDV基因组载量。