Department of Developmental Medical Sciences, Institute of International Health, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
J Virol Methods. 2010 Oct;169(1):193-7. doi: 10.1016/j.jviromet.2010.07.038. Epub 2010 Aug 4.
A novel reverse transcription-multiplex polymerase chain reaction assay was developed to detect Aichi virus, human parechovirus, enteroviruses, and human bocavirus. A mixture of four pairs of published specific primers, 6261 and 6779, ev22(+) and ev22(-), F1 and R1, 188F and 542R, was used to amplify the viral genomes and specifically generate four different amplicon sizes of 519, 270, 440, and 354 bp for Aichi virus, human parechovirus, enteroviruses, and human bocavirus, respectively. A total of 247 fecal specimens previously screened for rotavirus, adenovirus, norovirus, sapovirus, and astrovirus-negative, collected from infants and children with acute gastroenteritis in Japan from July 2007 to June 2008, were tested further for the presence of the four viruses, Aichi virus, human parechovirus, enteroviruses, and human bocavirus, by RT-multiplex PCR. The total detection rate of these viruses was 26.7% (66 out of 247 samples). Of these, HPeV, EVs, and HBoV were identified in 20, 41, and 5 specimens. No Aichi virus was found among these subjects. The sensitivity and specificity of RT-multiplex PCR were assessed and demonstrated a strong validation against RT-monoplex PCR. This is the first report of detecting these types of viruses in fecal samples from infants and children with acute gastroenteritis by RT-multiplex PCR.
一种新型的逆转录-多重聚合酶链反应检测方法被开发出来,用于检测 Aichi 病毒、人副肠孤病毒、肠病毒和人博卡病毒。使用混合了四对已发表的特异性引物,即 6261 和 6779、ev22(+) 和 ev22(-)、F1 和 R1、188F 和 542R,来扩增病毒基因组,并特异性地产生 519、270、440 和 354 bp 的四种不同大小的扩增子,分别用于 Aichi 病毒、人副肠孤病毒、肠病毒和人博卡病毒。总共检测了 247 份来自日本 2007 年 7 月至 2008 年 6 月患有急性肠胃炎的婴儿和儿童的粪便样本,这些样本之前已经筛选过轮状病毒、腺病毒、诺如病毒、星状病毒和星状病毒,结果均为阴性。通过 RT-多重 PCR 进一步检测这些样本中是否存在 Aichi 病毒、人副肠孤病毒、肠病毒和人博卡病毒。这些病毒的总检出率为 26.7%(247 份样本中有 66 份)。其中,HPeV、EVs 和 HBoV 在 20、41 和 5 份样本中被发现。在这些样本中未发现 Aichi 病毒。RT-多重 PCR 的敏感性和特异性得到了评估,并与 RT-单重 PCR 进行了强有力的验证。这是首次报道通过 RT-多重 PCR 检测急性肠胃炎患儿粪便样本中的这些病毒。