Kiang David, Kalra Ishmeet, Yagi Shigeo, Louie Janice K, Boushey Homer, Boothby John, Schnurr David P
Viral and Rickettsial Disease Laboratories, California State Department of Public Health, Richmond, California 94804, USA.
J Clin Microbiol. 2008 Nov;46(11):3736-45. doi: 10.1128/JCM.00674-08. Epub 2008 Aug 27.
Increasing recognition of the association of rhinovirus with severe lower respiratory tract illnesses has clarified the need to understand the relationship between specific serotypes of rhinovirus and their clinical consequences. To accomplish this, a specific and sensitive assay to detect and serotype rhinovirus directly from clinical specimens is needed. Traditional methods of serotyping using culture and serum neutralization are time-consuming, limited to certain reference laboratories, and complicated by the existence of over 100 serotypes of human rhinoviruses (HRVs). Accordingly, we have developed a sequence-based assay that targets a 390-bp fragment accounting for approximately two-thirds of the 5' noncoding region (NCR). Our goal was to develop an assay permitting amplification of target sequences directly from clinical specimens and distinction among all 101 prototype strains of rhinoviruses. We determined the sequences of all 101 prototype strains of HRV in this region to enable differentiation of virus genotypes in both viral isolates and clinical specimens. We evaluated this assay in a total of 101 clinical viral isolates and 24 clinical specimens and compared our findings to genotyping results using a different region of the HRV genome (the VP4-VP2 region). Five specimens associated with severe respiratory disease in children did not correlate with any known serotype of rhinovirus and were found to belong to a novel genogroup of rhinovirus, genogroup C. Isolates were also found that corresponded to the genogroup A2 variant identified in New York and Australia and two other novel group A clusters (GAC1 and GAC2).
对鼻病毒与严重下呼吸道疾病之间关联的认识不断增加,这明确了了解鼻病毒特定血清型与其临床后果之间关系的必要性。为实现这一目标,需要一种能够直接从临床标本中检测和血清型鉴定鼻病毒的特异性和灵敏性检测方法。使用培养和血清中和进行血清型鉴定的传统方法耗时较长,仅限于某些参考实验室,而且由于存在100多种人类鼻病毒(HRV)血清型而变得复杂。因此,我们开发了一种基于序列的检测方法,该方法靶向一个390碱基对的片段,约占5'非编码区(NCR)的三分之二。我们的目标是开发一种检测方法,能够直接从临床标本中扩增目标序列,并区分所有101种鼻病毒原型毒株。我们确定了该区域所有101种HRV原型毒株的序列,以便在病毒分离株和临床标本中区分病毒基因型。我们在总共101份临床病毒分离株和24份临床标本中评估了该检测方法,并将我们的发现与使用HRV基因组不同区域(VP4-VP2区域)的基因分型结果进行了比较。发现5份与儿童严重呼吸道疾病相关的标本与任何已知的鼻病毒血清型均不相关,并且属于一种新型鼻病毒基因组C。还发现了与在纽约和澳大利亚鉴定出的A2基因型变体以及另外两个新型A组簇(GAC1和GAC2)相对应的分离株。