Cuccui J, Easton A, Chu K K, Bancroft G J, Oyston P C F, Titball R W, Wren B W
Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, University of London, Keppel Street, London WC1E 7HT, United Kingdom.
Infect Immun. 2007 Mar;75(3):1186-95. doi: 10.1128/IAI.01240-06. Epub 2006 Dec 22.
Burkholderia pseudomallei, the causative agent of melioidosis, is an important human pathogen in Southeast Asia and northern Australia for which a vaccine is unavailable. A panel of 892 double signature-tagged mutants was screened for virulence using an intranasal BALB/c mouse model of infection. A novel DNA tag microarray identified 33 mutants as being attenuated in spleens, while 6 were attenuated in both lungs and spleens. The transposon insertion sites in spleen-attenuated mutants revealed genes involved in several stages of capsular polysaccharide biosynthesis and DNA replication and repair, a putative oxidoreductase, ABC transporters, and a lipoprotein that may be important in intercellular spreading. The six mutants identified as missing in both lungs and spleens were found to have insertions in recA involved in the SOS response and DNA repair; putative auxotrophs of leucine, threonine, p-aminobenzoic acid, and a mutant with an insertion in aroB causing auxotrophy for aromatic compounds were also found. Murine challenge studies revealed partial protection in BALB/c mice vaccinated with the aroB mutant. The refined signature-tagged mutagenesis approach developed in this study was used to efficiently identify attenuating mutants from this highly pathogenic species and could be applied to other organisms.
类鼻疽杆菌是类鼻疽病的病原体,是东南亚和澳大利亚北部一种重要的人类病原体,目前尚无针对它的疫苗。利用鼻内感染BALB/c小鼠模型,对一组892个双签名标签突变体进行了毒力筛选。一种新型DNA标签微阵列鉴定出33个突变体在脾脏中减毒,6个在肺和脾脏中均减毒。脾脏减毒突变体中的转座子插入位点揭示了参与荚膜多糖生物合成、DNA复制和修复多个阶段的基因、一种假定的氧化还原酶、ABC转运蛋白以及一种可能在细胞间传播中起重要作用的脂蛋白。在肺和脾脏中均缺失的6个突变体被发现其recA基因发生插入,recA参与SOS反应和DNA修复;还发现了亮氨酸、苏氨酸、对氨基苯甲酸的假定营养缺陷型,以及一个在aroB基因中发生插入导致芳香族化合物营养缺陷型的突变体。小鼠攻毒研究表明,用aroB突变体疫苗接种的BALB/c小鼠有部分保护作用。本研究中开发的改进型签名标签诱变方法用于从这种高致病性物种中有效鉴定减毒突变体,并可应用于其他生物体。