Lee C-K, Kono K, Haas E, Kim K-S, Drescher K M, Chapman N M, Tracy S
Enterovirus Research Laboratory, Department of Pathology and Microbiology, University of Nebraska Medical Center, 986495 Nebraska Medical Center, Omaha, NE 68198, USA.
Department of Pathology and Microbiology, University of Nebraska Medical Center, 986495 Nebraska Medical Center, Omaha, NE 68198, USA.
J Gen Virol. 2005 Jan;86(Pt 1):197-210. doi: 10.1099/vir.0.80424-0.
Group B coxsackieviruses (CVB) cause numerous diseases, including myocarditis, pancreatitis, aseptic meningitis and possibly type 1 diabetes. To date, infectious cDNA copies of CVB type 3 (CVB3) genomes have all been derived from pathogenic virus strains. An infectious cDNA copy of the well-characterized, non-pathogenic CVB3 strain GA genome was cloned in order to facilitate mapping of the CVB genes that influence expression of a virulence phenotype. Comparison of the sequence of the parental CVB3/GA population, derived by direct RT-PCR-mediated sequence analysis, to that of the infectious CVB3/GA progeny genome demonstrated that an authentic copy was cloned; numerous differences were observed in coding and non-coding sequences relative to other CVB3 strains. Progeny CVB3/GA replicated similarly to the parental strain in three different cell cultures and was avirulent when inoculated into mice, causing neither pancreatitis nor myocarditis. Inoculation of mice with CVB3/GA protected mice completely against myocarditis and pancreatitis induced by cardiovirulent CVB3 challenge. The secondary structure predicted for the CVB3/GA domain II, a region within the 5' non-translated region that is implicated as a key site affecting the expression of a cardiovirulent phenotype, differs from those predicted for cardiovirulent and pancreovirulent CVB3 strains. This is the first report characterizing a cloned CVB3 genome from an avirulent strain.
B组柯萨奇病毒(CVB)可引发多种疾病,包括心肌炎、胰腺炎、无菌性脑膜炎,还可能与1型糖尿病有关。迄今为止,3型柯萨奇病毒(CVB3)基因组的感染性cDNA拷贝均来源于致病病毒株。为便于对影响毒力表型表达的CVB基因进行定位,克隆了特征明确的非致病性CVB3毒株GA基因组的感染性cDNA拷贝。通过直接RT-PCR介导的序列分析得出亲代CVB3/GA群体的序列,并将其与感染性CVB3/GA子代基因组的序列进行比较,结果表明克隆得到了一个真实拷贝;相对于其他CVB3毒株,在编码和非编码序列中观察到了许多差异。子代CVB3/GA在三种不同的细胞培养物中的复制情况与亲代毒株相似,接种到小鼠体内时无毒力,既不引起胰腺炎也不引起心肌炎。用CVB3/GA接种小鼠可使其完全免受心脏毒性CVB3攻击诱导的心肌炎和胰腺炎。预测的CVB3/GA结构域II的二级结构与心脏毒性和胰腺毒性CVB3毒株预测的二级结构不同,该结构域位于5'非翻译区内,被认为是影响心脏毒性表型表达的关键位点。这是首次报道对无毒力毒株的克隆CVB3基因组进行表征。