Rish J A, Eisenach K D, Cave M D, Reddy M V, Gangadharam P R, Bates J H
Department of Medicine, University of Arkansas College of Medicine, Little Rock, USA.
Am J Respir Crit Care Med. 1996 Apr;153(4 Pt 1):1419-23. doi: 10.1164/ajrccm.153.4.8616575.
Use of the polymerase chain reaction (PCR) to detect Mycobacterium tuberculosis in formalin-fixed, paraffin-embedded tissue would be of great diagnostic value. However, formaldehyde has been reported to decrease the efficiency of amplification by structurally altering the polynucleotide chain. We sought to determine the ability of the PCR assay to detect M. tuberculosis in formalin-fixed, paraffin-embedded tissue in a mouse experimentally infected with the H37Rv strain of M. tuberculosis. Lung tissue from the infected mouse was cultured to determine the number of organisms per gram of tissue. The remaining lung tissue was divided into eight portions, seven of which were fixed in 10% neutral buffered formalin for 24-h intervals over periods lasting from 1 to 7 d, and a control portion was placed in isotonic saline. The tissue samples were then paraffin-embedded, and sections were obtained from each tissue block for PCR analysis. We show that the PCR assay can detect as few as nine organisms in a 5-micron section of tissue, and that up to 7 d of fixation in 10% neutral buffered formalin has a negligible effect on the assay. The PCR assay can detect low numbers of M. tuberculosis organisms in formalin-fixed, paraffin-embedded tissue.
使用聚合酶链反应(PCR)检测福尔马林固定、石蜡包埋组织中的结核分枝杆菌具有重要的诊断价值。然而,据报道甲醛会通过结构改变多核苷酸链而降低扩增效率。我们试图确定PCR检测法在实验性感染结核分枝杆菌H37Rv菌株的小鼠的福尔马林固定、石蜡包埋组织中检测结核分枝杆菌的能力。对感染小鼠的肺组织进行培养,以确定每克组织中的菌数。将剩余的肺组织分成八份,其中七份在10%中性缓冲福尔马林中固定,间隔24小时,持续1至7天,另一份对照组织置于等渗盐水中。然后将组织样本进行石蜡包埋,并从每个组织块中获取切片进行PCR分析。我们发现,PCR检测法在5微米厚的组织切片中能检测到低至9个菌,并且在10%中性缓冲福尔马林中固定长达7天对该检测法的影响可忽略不计。PCR检测法能够检测福尔马林固定、石蜡包埋组织中少量的结核分枝杆菌。