The University of Queensland, Brisbane, Queensland, Australia.
Emerg Infect Dis. 2011 Feb;17(2):296-8. doi: 10.3201/eid1702.101123.
We conducted a preliminary comparison of the relative sensitivity of a cross-section of published human rhinovirus (HRV)-specific PCR primer pairs, varying the oligonucleotides and annealing temperature. None of the pairs could detect all HRVs in 2 panels of genotyped clinical specimens; >1 PCR is required for accurate description of HRV epidemiology.
我们对已发表的人鼻病毒(HRV)特异性 PCR 引物对的相对敏感性进行了初步比较,改变了寡核苷酸和退火温度。在 2 组基因分型临床标本中,没有一对引物能够检测到所有 HRV;为了准确描述 HRV 流行病学,需要进行多次 PCR。