Corbeil Serge, Faury Nicole, Segarra Amélie, Renault Tristan
Australian Animal Health Laboratory, CSIRO Animal Food Health Sciences, Geelong, Victoria 3220, Australia.
Ifremer, Unité Santé Génétique et Microbiologie des Mollusques (SG2M), Laboratoire de Génétique et Pathologie des Mollusques Marins (LGPMM), 17390 La Tremblade, France.
J Virol Methods. 2015 Jan;211:43-50. doi: 10.1016/j.jviromet.2014.10.007. Epub 2014 Oct 25.
An in situ hybridization protocol for detecting mRNAs of ostreid herpesvirus type 1 (OsHV-1) which infects Pacific oysters, Crassostrea gigas, was developed. Three RNA probes were synthesized by cloning three partial OsHV-1 genes into plasmids using three specific primer pairs, and performing a transcription in the presence of digoxigenin dUTP. The RNA probes were able to detect the virus mRNAs in paraffin sections of experimentally infected oysters 26 h post-injection. The in situ hybridization showed that the OsHV-1 mRNAs were mainly present in connective tissues in gills, mantle, adductor muscle, digestive gland and gonads. DNA detection by in situ hybridization using a DNA probe and viral DNA quantitation by real-time PCR were also performed and results were compared with those obtained using RNA probes.
开发了一种用于检测感染太平洋牡蛎(Crassostrea gigas)的1型牡蛎疱疹病毒(OsHV-1)mRNA的原位杂交方案。通过使用三对特异性引物对将三个OsHV-1部分基因克隆到质粒中,并在存在地高辛素dUTP的情况下进行转录,合成了三种RNA探针。这些RNA探针能够在注射后26小时检测实验感染牡蛎石蜡切片中的病毒mRNA。原位杂交显示,OsHV-1 mRNA主要存在于鳃、外套膜、闭壳肌、消化腺和性腺的结缔组织中。还使用DNA探针通过原位杂交进行DNA检测,并通过实时PCR进行病毒DNA定量,并将结果与使用RNA探针获得的结果进行比较。