Valverde Estefania J, Borrego Juan J, Castro Dolores
Universidad de Málaga, Departamento de Microbiología, 29071 Málaga, Spain.
J Virol Methods. 2016 Dec;238:62-65. doi: 10.1016/j.jviromet.2016.09.016. Epub 2016 Oct 15.
The lymphocystis disease virus (LCDV), a member of the Iridoviridae family, infects a wide range of fish species including gilthead seabream (Sparus aurata L.), the most important species cultured in the Mediterranean. LCDV is difficult to propagate in cell culture and does not produce clear and consistent cytopathic effects (CPE), especially in samples collected from subclinically infected fish. An integrated cell culture reverse transcription-polymerase chain reaction (ICC-RT-PCR) assay, followed by dot-blot hybridization of the RT-PCR products, was developed to improve the detection of infectious LCDV. The sensitivity of the ICC-RT-PCR assay, which can be performed in 7 d, was at least 100-fold higher than viral diagnosis obtained by CPE development. The developed assay thus allows the determination of infectious titres in samples with low viral loads, including those from asymptomatic carrier fish, in which no CPE was recorded after a 14-d incubation period. The ICC-RT-PCR assay enables rapid, specific and sensitive detection and quantification of infectious LCDV, and may be a valuable tool in the study of aspects of LCDV infection including transmission or epizootiology.
淋巴囊肿病病毒(LCDV)是虹彩病毒科的一员,可感染多种鱼类,包括地中海养殖的最重要品种——金头鲷(Sparus aurata L.)。LCDV难以在细胞培养中增殖,且不会产生明显且一致的细胞病变效应(CPE),尤其是从亚临床感染鱼类采集的样本。为提高对感染性LCDV的检测能力,开发了一种整合细胞培养逆转录-聚合酶链反应(ICC-RT-PCR)检测方法,并对RT-PCR产物进行斑点杂交。ICC-RT-PCR检测方法可在7天内完成,其灵敏度比通过观察CPE进行病毒诊断至少高100倍。因此,所开发的检测方法能够测定病毒载量低的样本中的感染滴度,包括来自无症状携带鱼的样本,这些样本在14天的孵育期后未记录到CPE。ICC-RT-PCR检测方法能够快速、特异性且灵敏地检测和定量感染性LCDV,可能是研究LCDV感染的传播或流行病学等方面的宝贵工具。