McErlean Peter, Shackelton Laura A, Andrews Emily, Webster Dale R, Lambert Stephen B, Nissen Michael D, Sloots Theo P, Mackay Ian M
Queensland Paediatric Infectious Diseases Laboratory, Sir Albert Sakzewski Virus Research Centre, Royal Children's Hospital, Brisbane, Queensland, Australia.
PLoS One. 2008 Apr 2;3(4):e1847. doi: 10.1371/journal.pone.0001847.
Human rhinoviruses (HRVs) are the most frequently detected pathogens in acute respiratory tract infections (ARTIs) and yet little is known about the prevalence, recurrence, structure and clinical impact of individual members. During 2007, the complete coding sequences of six previously unknown and highly divergent HRV strains were reported. To catalogue the molecular and clinical features distinguishing the divergent HRV strains, we undertook, for the first time, in silico analyses of all available polyprotein sequences and performed retrospective reviews of the medical records of cases in which variants of the prototype strain, HRV-QPM, had been detected.
METHODOLOGY/PRINCIPLE FINDINGS: Genomic analyses revealed that the six divergent strains, residing within a clade we previously called HRV A2, had the shortest polyprotein of all picornaviruses investigated. Structure-based amino acid alignments identified conserved motifs shared among members of the genus Rhinovirus as well as substantive deletions and insertions unique to the divergent strains. Deletions mostly affected regions encoding proteins traditionally involved in antigenicity and serving as HRV and HEV receptor footprints. Because the HRV A2 strains cannot yet be cultured, we created homology models of predicted HRV-QPM structural proteins. In silico comparisons confirmed that HRV-QPM was most closely related to the major group HRVs. HRV-QPM was most frequently detected in infants with expiratory wheezing or persistent cough who had been admitted to hospital and required supplemental oxygen. It was the only virus detected in 65% of positive individuals. These observations contributed to an objective clinical impact ranging from mild to severe.
The divergent strains did not meet classification requirements for any existing species of the genus Rhinovirus or Enterovirus. HRV A2 strains should be partitioned into at least one new species, putatively called Human rhinovirus C, populated by members detected with high frequency, from individuals with respiratory symptoms requiring hospital admission.
人鼻病毒(HRV)是急性呼吸道感染(ARTI)中最常检测到的病原体,但对于各个成员的流行率、复发情况、结构及临床影响却知之甚少。2007年,报道了6种先前未知且高度分化的HRV毒株的完整编码序列。为了梳理区分这些分化的HRV毒株的分子和临床特征,我们首次对所有可用的多聚蛋白序列进行了计算机分析,并对检测到原型毒株HRV-QPM变体的病例的病历进行了回顾性分析。
方法/主要发现:基因组分析显示,这6种分化的毒株位于我们先前称为HRV A2的一个进化枝内,其多聚蛋白是所有所研究的小RNA病毒中最短的。基于结构的氨基酸比对确定了鼻病毒属成员共有的保守基序以及分化毒株特有的大量缺失和插入。缺失大多影响编码传统上参与抗原性并作为HRV和HEV受体足迹的蛋白质的区域。由于HRV A2毒株尚未能培养,我们构建了预测的HRV-QPM结构蛋白的同源模型。计算机比较证实HRV-QPM与主要组HRV关系最为密切。HRV-QPM最常于因呼气性喘息或持续性咳嗽入院并需要补充氧气的婴儿中检测到。它是65%的阳性个体中唯一检测到的病毒。这些观察结果导致了从轻度到重度的客观临床影响。
这些分化的毒株不符合鼻病毒属或肠道病毒属任何现有种的分类要求。HRV A2毒株应至少分为一个新种,假定称为人鼻病毒C,由从有呼吸道症状需要入院的个体中高频检测到的成员组成。