Fjaerli Hans-Olav, Bukholm Geir, Krog Anne, Skjaeret Camilla, Holden Marit, Nakstad Britt
University of Oslo, Faculty Division Akershus University Hospital, Department of Paediatrics, Akershus University Hospital, Norway.
BMC Infect Dis. 2006 Dec 13;6:175. doi: 10.1186/1471-2334-6-175.
Respiratory syncytial virus (RSV) is a major cause of viral bronchiolitis in infants worldwide, and environmental, viral and host factors are all of importance for disease susceptibility and severity. To study the systemic host response to this disease we used the microarray technology to measure mRNA gene expression levels in whole blood of five male infants hospitalised with acute RSV, subtype B, bronchiolitis versus five one year old male controls exposed to RSV during infancy without bronchiolitis. The gene expression levels were further evaluated in a new experiment using quantitative real-time polymerase chain reaction (QRT-PCR) both in the five infants selected for microarray and in 13 other infants hospitalised with the same disease.
Among the 30 genes most differentially expressed by microarray nearly 50% were involved in immunological processes. We found the highly upregulated interferon, alpha-inducible protein 27 (IFI27) and the highly downregulated gene Charcot-Leyden crystal protein (CLC) to be the two most differentially expressed genes in the microarray study. When performing QRT-PCR on these genes IFI27 was upregulated in all but one infant, and CLC was downregulated in all 18 infants, and similar to that given by microarray.
The gene IFI27 is upregulated and the gene CLC is downregulated in whole blood of infants hospitalised with RSV, subtype B, bronchiolitis and is not reported before. More studies are needed to elucidate the specificity of these gene expressions in association with host response to this virus in bronchiolitis of moderate severity.
呼吸道合胞病毒(RSV)是全球范围内引起婴儿病毒性细支气管炎的主要原因,环境、病毒和宿主因素对疾病的易感性和严重程度均至关重要。为了研究宿主对该疾病的全身反应,我们使用微阵列技术测量了5名因急性B型RSV细支气管炎住院的男婴全血中的mRNA基因表达水平,并与5名在婴儿期接触过RSV但未患细支气管炎的1岁男童进行了对照。在一项新实验中,我们使用定量实时聚合酶链反应(QRT-PCR)对微阵列研究中选取的5名婴儿以及另外13名患有相同疾病的住院婴儿的基因表达水平进行了进一步评估。
在微阵列差异表达最明显的30个基因中,近50%参与免疫过程。我们发现,在微阵列研究中,干扰素α诱导蛋白27(IFI27)高度上调,而夏科-莱登结晶蛋白(CLC)基因高度下调,是差异表达最明显的两个基因。对这些基因进行QRT-PCR检测时,除一名婴儿外,IFI27在所有婴儿中均上调,CLC在所有18名婴儿中均下调,且与微阵列结果相似。
在因B型RSV细支气管炎住院的婴儿全血中,IFI27基因上调,CLC基因下调,此前未见相关报道描述。需要更多研究来阐明这些基因表达在中度严重程度细支气管炎中与宿主对该病毒反应的相关性。