Puah Suat Moi, Puthucheary S D, Wang Jin Town, Pan Yi Jiun, Chua Kek Heng
Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.
Department of Medical Education, Research and Evaluation, Duke-NUS Graduate Medical School Singapore, 8 College Road, Singapore 169857.
ScientificWorldJournal. 2014;2014:590803. doi: 10.1155/2014/590803. Epub 2014 Aug 11.
The Gram-negative saprophyte Burkholderia pseudomallei is the causative agent of melioidosis, an infectious disease which is endemic in Southeast Asia and northern Australia. This bacterium possesses many virulence factors which are thought to contribute to its survival and pathogenicity. Using a virulent clinical isolate of B. pseudomallei and an attenuated strain of the same B. pseudomallei isolate, 6 genes BPSL2033, BP1026B_I2784, BP1026B_I2780, BURPS1106A_A0094, BURPS1106A_1131, and BURPS1710A_1419 were identified earlier by PCR-based subtractive hybridization. These genes were extensively characterized at the molecular level, together with an additional gene BPSL3147 that had been identified by other investigators. Through a reverse genetic approach, single-gene knockout mutants were successfully constructed by using site-specific insertion mutagenesis and were confirmed by PCR. BPSL2033::Km and BURPS1710A_1419::Km mutants showed reduced rates of survival inside macrophage RAW 264.7 cells and also low levels of virulence in the nematode infection model. BPSL2033::Km demonstrated weak statistical significance (P = 0.049) at 8 hours after infection in macrophage infection study but this was not seen in BURPS1710A_1419::Km. Nevertheless, complemented strains of both genes were able to partially restore the gene defects in both in vitro and in vivo studies, thus suggesting that they individually play a minor role in the virulence of B. pseudomallei.
革兰氏阴性腐生菌类鼻疽伯克霍尔德菌是类鼻疽的病原体,类鼻疽是一种在东南亚和澳大利亚北部流行的传染病。这种细菌拥有许多毒力因子,据认为这些毒力因子有助于其生存和致病性。使用类鼻疽伯克霍尔德菌的一个毒力临床分离株和同一类鼻疽伯克霍尔德菌分离株的一个减毒株,通过基于聚合酶链反应的消减杂交法早期鉴定出6个基因,即BPSL2033、BP1026B_I2784、BP1026B_I2780、BURPS1106A_A0094、BURPS1106A_1131和BURPS1710A_1419。这些基因在分子水平上得到了广泛表征,还有另一个由其他研究人员鉴定出的基因BPSL3147。通过反向遗传学方法,利用位点特异性插入诱变成功构建了单基因敲除突变体,并通过聚合酶链反应进行了确认。BPSL2033::Km和BURPS1710A_1419::Km突变体在巨噬细胞RAW 264.7细胞内的存活率降低,并且在秀丽隐杆线虫感染模型中的毒力水平也较低。在巨噬细胞感染研究中,BPSL2033::Km在感染后8小时显示出微弱的统计学意义(P = 0.049),但在BURPS1710A_1419::Km中未观察到这种情况。然而,这两个基因的互补菌株在体外和体内研究中都能够部分恢复基因缺陷,因此表明它们在类鼻疽伯克霍尔德菌的毒力中各自发挥较小的作用。