Zhu Ru-nan, Qian Yuan, Deng Jie, Wang Fang, Hu Ai-zhong, Lu Jing, Cao Li, Yuan Yi, Cheng Hui-zhong
Laboratory of Virology, Beijing Municipal Laboratory of Infection and Immunity, and Children's Hospital Affiliated to Capital Institute of Pediatrics, Beijing,100020, China.
Zhonghua Er Ke Za Zhi. 2003 Jun;41(6):441-4.
A new respiratory virus, human metapneumovirus (HMPV) was recently identified by scientists in the Netherlands first and then in a few other countries. To investigate if this newly discovered virus is associated with the acute respiratory infections in pediatric patients in Beijing, tests were developed to detect HPMV gene fragments from nasopharyngeal aspirates collected from infants and young children hospitalized for acute respiratory infections from November 2002 to March 2003.
The HMPV was screened by reverse transcription-polymerase chain reaction (RT-PCR). RNAs were extracted by Trizol from 247 specimens which had been determined as negative for conventional respiratory viruses including RSV, influenza A and B, parainfluenza I, II, III and adenovirus by indirect immunofluorescence test as well as virus isolation. The HMPV RNAs were detected by reverse transcription tests using random primer and M-MLV reverse transcriptase followed by PCR using the primers designed from the published sequence of the N protein-encoding gene from the first HMPV identified in the Netherlands. PCR products were visualized by 1.2% agarose gel electrophoresis. Selected positive PCR products were sequenced and the sequences of the nucleotides and deduced amino acids were compared with those in the GenBank.
Among those 247 specimens negative for common respiratory viruses, 74 (30.0%) showed the predicted 213 bp PCR products in agarose gel. Most of clinical diagnoses for these 58 patients were pneumonia (36, 48.6%), bronchiolitis (21, 28.4%), and bronchitis and asthma in some patients. Nearly 90 percent of positive specimens were from patients under 2 years of age. Ten out of 74 amplicons were randomly selected for sequence analysis. When compared with the sequences in the GenBank, the nucleotide sequences of these 10 amplicons shared high homology only with those of HMPVs. The nucleotide sequence identities of these 10 samples with those from the Netherlands and Canada were 87% - 99%. When compared with the nucleotide sequence from the first reported strain by Van den Hoogen (strain HMPV 00-1), the sequence identities of these 10 fragments ranged from 88.7% to 99.1%. Among the 10 amplicons from the specimens, the nucleotide identities were 87.3% - 100%. One of the 10 amplicons (No. 1816) shared lower identity with others (87.3% - 89.7%), whereas the other 9 shared higher identities (95.8% - 100%) with each other. The comparison of amino acids showed that these 10 amplicons showed high homology (95.8% - 100%). Again, amplicon No.1816 shared lower homology (95.8% - 97.2%) with others, whereas the other 9 shared higher homology (98.6% - 100%). The amino acid homology between No.1816 and HMPV 00-1 was 95.8%, whereas that of the other 9 with HMPV 00-1 was 98.6% - 100%.
These data suggested that some of acute respiratory infections in pediatric patients in Beijing area are related to the newly identified human metapneumovirus. The HMPV circulating in Beijing may have different genotypes.
一种新型呼吸道病毒——人偏肺病毒(HMPV)最近首先由荷兰科学家鉴定出来,随后在其他一些国家也有发现。为调查这种新发现的病毒是否与北京地区儿科患者的急性呼吸道感染有关,研究人员开发了检测方法,以检测2002年11月至2003年3月期间因急性呼吸道感染住院的婴幼儿鼻咽抽吸物中的HMPV基因片段。
采用逆转录-聚合酶链反应(RT-PCR)对HMPV进行筛查。通过Trizol从247份标本中提取RNA,这些标本经间接免疫荧光试验和病毒分离法检测,已确定对包括呼吸道合胞病毒(RSV)、甲型和乙型流感病毒、副流感病毒Ⅰ、Ⅱ、Ⅲ型以及腺病毒在内的常规呼吸道病毒呈阴性。使用随机引物和M-MLV逆转录酶通过逆转录试验检测HMPV RNA,随后使用根据在荷兰首次鉴定的HMPV的N蛋白编码基因的已发表序列设计的引物进行PCR。PCR产物通过1.2%琼脂糖凝胶电泳进行可视化分析。对选定的阳性PCR产物进行测序,并将核苷酸和推导氨基酸序列与GenBank中的序列进行比较。
在这247份对常见呼吸道病毒呈阴性的标本中,74份(30.0%)在琼脂糖凝胶中显示出预期的213 bp PCR产物。这58例患者的大多数临床诊断为肺炎(36例,48.6%)、细支气管炎(21例,28.4%),部分患者为支气管炎和哮喘。近90%的阳性标本来自2岁以下患者。从74个扩增子中随机选择10个进行序列分析。与GenBank中的序列相比,这10个扩增子的核苷酸序列仅与HMPV的序列具有高度同源性。这10个样本与来自荷兰和加拿大的样本的核苷酸序列同一性为87% - 99%。与Van den Hoogen首次报道的毒株(毒株HMPV 00-1)的核苷酸序列相比,这10个片段的序列同一性范围为88.7%至99.1%。在来自标本的10个扩增子中,核苷酸同一性为87.3% - 100%。10个扩增子中的一个(编号1816)与其他扩增子的同一性较低(87.3% - 89.7%),而其他9个彼此之间的同一性较高(95.8% - 100%)。氨基酸比较显示,这10个扩增子具有高度同源性(95.8% - 100%)。同样,扩增子1816与其他扩增子的同源性较低(95.8% - 97.2%),而其他9个与其他扩增子的同源性较高(98.6% - 100%)。1816与HMPV 00-1之间的氨基酸同源性为95.8%,而其他9个与HMPV 00-1的氨基酸同源性为98.6% - 100%。
这些数据表明,北京地区儿科患者的一些急性呼吸道感染与新鉴定的人偏肺病毒有关。在北京流行的HMPV可能具有不同的基因型。