Barlow K L, Tosswill J H, Clewley J P
Hepatitis and Retrovirus Laboratory, Central Public Health Laboratory, London, UK.
J Virol Methods. 1995 Mar;52(1-2):65-74. doi: 10.1016/0166-0934(94)00139-8.
The Roche Amplicor PCR kit was used to detect HIV-1 DNA in UK patients of known serostatus. Four false-negative and/or equivocal results were obtained from patients who were known to be anti HIV seropositive (Tosswill et al., 1994). Cells from the blood of these patients were shown to contain HIV DNA after extraction, concentration and amplification by nested PCR using primers flanking those in the kit. To determine whether DNA sequence divergence was the cause of these discrepancies, the gag region targeted by the primers in the kit was sequenced for specimens giving positive, equivocal and false-negative results. No greater degree of sequence divergence was found within the primer and probe target regions among the equivocals and false-negatives than among the positive control specimens. The few misleading results were probably attributable to low copy numbers of proviral DNA in these specimens. Sequences obtained from the target and flanking regions of the kit were sufficient to allow the genotype of the virus to be determined.
罗氏Amplicor PCR试剂盒用于检测已知血清学状态的英国患者体内的HIV-1 DNA。在已知抗HIV血清学阳性的患者中获得了4例假阴性和/或不确定结果(Tosswill等人,1994年)。通过使用试剂盒中引物侧翼的引物进行巢式PCR,对这些患者血液中的细胞进行提取、浓缩和扩增后,显示含有HIV DNA。为了确定DNA序列差异是否是这些差异的原因,对试剂盒中引物靶向的gag区域进行测序,检测结果为阳性、不确定和假阴性的标本。在不确定和假阴性标本的引物和探针靶区域内,未发现比阳性对照标本更大程度的序列差异。这些误导性结果可能归因于这些标本中前病毒DNA的拷贝数较低。从试剂盒的靶区域和侧翼区域获得的序列足以确定病毒的基因型。