Biotechnology Division, Defence Research and Development Establishment, Gwalior, India,
Curr Microbiol. 2011 Feb;62(2):547-56. doi: 10.1007/s00284-010-9743-x. Epub 2010 Aug 25.
Bacillus anthracis, the etiological agent of anthrax, is responsible for a serious and often fatal disease of mammalian livestock and humans and is an important biological warfare agent. Bacillus sp. AKG was isolated from a hot spring in western Himalayas and species-specific primers targeting gyrB gene identified the strain as B. anthracis within cereus-group. Cloning, sequencing, and phylogenetic analysis of the partial gyrB sequence from strain AKG indicated a close affiliation with B. anthracis and a few recently isolated strains of B. thuringiensis (e.g., strain Al Hakam and serovar konkukian). Phylogenetic analysis of two other housekeeping genes, clpC and gdpD yielded similar results. This observation is further substantiated by phylogenetic reconstruction using concatenated sequences (1680 bases) of the three genes (gyrB, clpC, and gdpD). Phenotypic features indicated a non-anthracis affiliation for the strain AKG. A novel strategy to distinguish among strains of B. anthracis, B. cereus, and B. thuringiensis based on whole proteome comparison was developed and tested for the identification of this environmental strain. Proteome comparison was used to establish the identity of this unknown environmental strain. Group of replicate 2DE gels for whole cell proteome were generated for each of the three species and strain AKG. Protein spots unique to each group and those showing match between the groups, in a pair-wise comparison, indicated strain AKG as a member of B. thuringiensis. This strategy can be used to assign strains of B. cereus group to their respective species.
炭疽芽孢杆菌是炭疽病的病原体,可导致哺乳动物家畜和人类发生严重且常常致命的疾病,同时也是一种重要的生物战剂。芽孢杆菌 AKG 是从西喜马拉雅山的温泉中分离出来的,针对 gyrB 基因的种特异性引物将该菌株鉴定为蜡样芽孢杆菌群中的炭疽芽孢杆菌。从 AKG 株的部分 gyrB 序列的克隆、测序和系统发育分析表明,它与炭疽芽孢杆菌和少数最近分离的苏云金芽孢杆菌(例如 Hakam 株和 konkukian 血清型)密切相关。来自另外两个管家基因 clpC 和 gdpD 的系统发育分析也得到了类似的结果。使用这三个基因(gyrB、clpC 和 gdpD)的串联序列(1680 个碱基)进行系统发育重建进一步证实了这一观察结果。基于全蛋白质组比较来区分炭疽芽孢杆菌、蜡样芽孢杆菌和苏云金芽孢杆菌菌株的新策略被开发出来,并用于鉴定这种环境菌株。蛋白质组比较用于确定这种未知环境菌株的身份。为三种生物和 AKG 株的全细胞蛋白质组生成了重复 2DE 凝胶组。每个组都有独特的蛋白质斑点,并且在两两比较中,显示出组间匹配的蛋白质斑点,表明 AKG 株是苏云金芽孢杆菌的成员。该策略可用于将蜡样芽孢杆菌群的菌株分配到各自的种。