Tomaso Herbert, Scholz Holger C, Al Dahouk Sascha, Splettstoesser Wolf D, Neubauer Heinrich, Pfeffer Martin, Straube Eberhard
Militärspital Innsbruck, Innsbruck, Osterreich.
Wien Klin Wochenschr. 2007;119(19-20 Suppl 3):26-32. doi: 10.1007/s00508-007-0858-4.
In out of area military missions soldiers are potentially exposed to bacteria that are endemic in tropical areas and can be used as biological agents. It can be difficult to culture these bacteria due to sample contamination, low number of bacteria or pretreatment with antibiotics. Commercial biochemical identification systems are not optimized for these agents which can result in misidentification. Immunological assays are often not commercially available or not specific. Real-time PCR assays are very specific and sensitive and can shorten the time required to establish a diagnosis markedly. Therefore, real-time PCRs for the identification of Bacillus anthracis, Brucella spp., Burkholderia mallei und Burkholderia pseudomallei, Francisella tularensis und Yersinia pestis have been developed. PCR results can be false negative due to inadequate clinical samples, low number of bacteria in samples, DNA degradation, inhibitory substances and inappropriate DNA preparation. Hence, it is crucial to cultivate the organisms as a prerequisite for adequate antibiotic therapy and typing of the agent. In a bioterrorist scenario samples have to be treated according to rules applied in forensic medicine and documentation has to be flawless.
在境外军事任务中,士兵可能接触到热带地区特有的细菌,这些细菌可被用作生物制剂。由于样本污染、细菌数量少或使用抗生素进行预处理,培养这些细菌可能很困难。商业生化鉴定系统并未针对这些病原体进行优化,这可能导致错误鉴定。免疫测定通常没有商业产品或不具有特异性。实时PCR测定非常特异且灵敏,可显著缩短确诊所需时间。因此,已开发出用于鉴定炭疽芽孢杆菌、布鲁氏菌属、鼻疽伯克霍尔德菌、类鼻疽伯克霍尔德菌、土拉弗朗西斯菌和鼠疫耶尔森菌的实时PCR方法。由于临床样本不足、样本中细菌数量少、DNA降解、抑制性物质和不适当的DNA制备,PCR结果可能为假阴性。因此,培养病原体作为适当抗生素治疗和病原体分型的前提条件至关重要。在生物恐怖袭击的情况下,样本必须按照法医学适用的规则进行处理,文件记录必须完美无缺。