Division of Microbiology, Defence Research and Development Establishment, Jhansi Road, Gwalior, 474002 India.
Indian J Microbiol. 2013 Mar;53(1):41-7. doi: 10.1007/s12088-012-0330-7. Epub 2012 Nov 6.
The need for a rapid detection and characterization of biowarfare (BW) agents cannot be over emphasized. With diverse array of potential BW pathogen available presently, rapid identification of the pathogen is crucial, so that specific therapy and control measures can be initiated. We have developed a multiplex polymerase chain reaction based reverse line blot macroarray to simultaneously detect four pathogens of BW importance viz. Bacillus anthracis, Yersinia pestis, Brucella melitensis and Burkholderia pseudomallei. The multiplex PCR utilizes 14 pairs of primers targeting 18 specific markers. These markers include genes which are genus specific, species-specific chromosomal sequences and virulence markers of plasmid origin. The assay was evaluated on various human, environment and animal isolates. The assay w successful in simultaneous detection and characterization of isolates of the four pathogens on as a single platform with sensitivity ranging from 0.3 pg to 0.3 ng of genomic DNA. The assay was able to detect 5 × 10(2) cfu/ml for B. anthracis, 8 × 10(2) cfu/ml for Yersinia sp., 1.4 × 10(2) cfu/ml for B. melitensis and 4 × 10(2) cfu/ml for B. pseudomallei.
快速检测和鉴定生物战剂的需求怎么强调都不为过。目前存在着各种各样的潜在生物战病原体,快速鉴定病原体至关重要,以便能够立即采取特定的治疗和控制措施。我们开发了一种基于多重聚合酶链反应的反向线印迹宏阵列,可同时检测四种具有重要生物战意义的病原体,即炭疽芽孢杆菌、鼠疫耶尔森菌、布鲁氏菌和鼻疽伯克霍尔德菌。多重 PCR 利用了 14 对针对 18 个特定标记的引物。这些标记包括属特异性、种特异性染色体序列和质粒来源的毒力标记。该检测方法在各种人类、环境和动物分离株上进行了评估。该检测方法能够在单个平台上同时检测和鉴定这四种病原体的分离株,其灵敏度范围为 0.3 pg 至 0.3 ng 基因组 DNA。该检测方法能够检测到 5×10(2)cfu/ml 的炭疽芽孢杆菌、8×10(2)cfu/ml 的耶尔森菌、1.4×10(2)cfu/ml 的布鲁氏菌和 4×10(2)cfu/ml 的鼻疽伯克霍尔德菌。