Ghazali Ahmad-Kamal, Firdaus-Raih Mohd, Uthaya Kumar Asqwin, Lee Wei-Kang, Hoh Chee-Choong, Nathan Sheila
Department of Biological Sciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia.
Department of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia.
Microbiol Spectr. 2023 Mar 1;11(2):e0383522. doi: 10.1128/spectrum.03835-22.
Burkholderia pseudomallei, a soil and water saprophyte, is responsible for the tropical human disease melioidosis. A hundred years since its discovery, there is still much to learn about B. pseudomallei proteins that are essential for the bacterium's survival in and interaction with the infected host, as well as their roles within the bacterium's natural soil habitat. To address this gap, bacteria grown under conditions mimicking the soil environment were subjected to transcriptome sequencing (RNA-seq) analysis. A dual RNA-seq approach was used on total RNA from spleens isolated from a B. pseudomallei mouse infection model at 5 days postinfection. Under these conditions, a total of 1,434 bacterial genes were induced, with 959 induced in the soil environment and 475 induced in bacteria residing within the host. Genes encoding metabolism and transporter proteins were induced when the bacteria were present in soil, while virulence factors, metabolism, and bacterial defense mechanisms were upregulated during active infection of mice. On the other hand, capsular polysaccharide and quorum-sensing pathways were inhibited during infection. In addition to virulence factors, reactive oxygen species, heat shock proteins, siderophores, and secondary metabolites were also induced to assist bacterial adaptation and survival in the host. Overall, this study provides crucial insights into the transcriptome-level adaptations which facilitate infection by soil-dwelling B. pseudomallei. Targeting novel therapeutics toward B. pseudomallei proteins required for adaptation provides an alternative treatment strategy given its intrinsic antimicrobial resistance and the absence of a vaccine. Burkholderia pseudomallei, a soil-dwelling bacterium, is the causative agent of melioidosis, a fatal infectious disease of humans and animals. The bacterium has a large genome consisting of two chromosomes carrying genes that encode proteins with important roles for survival in diverse environments as well as in the infected host. While a general mechanism of pathogenesis has been proposed, it is not clear which proteins have major roles when the bacteria are in the soil and whether the same proteins are key to successful infection and spread. To address this question, we grew the bacteria in soil medium and then in infected mice. At 5 days postinfection, bacteria were recovered from infected mouse organs and their gene expression was compared against that of bacteria grown in soil medium. The analysis revealed a list of genes expressed under soil growth conditions and a different set of genes encoding proteins which may be important for survival, replication, and dissemination in an infected host. These proteins are a potential resource for understanding the full adaptation mechanism of this pathogen. In the absence of a vaccine for melioidosis and with treatment being reliant on combinatorial antibiotic therapy, these proteins may be ideal targets for designing antimicrobials to treat melioidosis.
类鼻疽伯克霍尔德菌是一种存在于土壤和水中的腐生菌,可引发热带地区人类疾病类鼻疽。自其被发现至今已有百年,但对于该菌在受感染宿主体内存活及相互作用所必需的蛋白质,以及这些蛋白质在该菌自然土壤栖息地中的作用,仍有许多有待了解之处。为填补这一空白,对在模拟土壤环境条件下培养的细菌进行了转录组测序(RNA测序)分析。在感染后5天,对从类鼻疽伯克霍尔德菌小鼠感染模型分离的脾脏中的总RNA采用了双重RNA测序方法。在这些条件下,共诱导了1434个细菌基因,其中959个在土壤环境中被诱导,475个在宿主体内的细菌中被诱导。当细菌存在于土壤中时,编码代谢和转运蛋白的基因被诱导,而在小鼠的活跃感染期间,毒力因子、代谢和细菌防御机制被上调。另一方面,在感染期间,荚膜多糖和群体感应途径受到抑制。除毒力因子外,活性氧、热休克蛋白、铁载体和次生代谢产物也被诱导,以帮助细菌在宿主体内适应和存活。总体而言,本研究为促进土壤栖居的类鼻疽伯克霍尔德菌感染的转录组水平适应性提供了关键见解。鉴于其固有的抗菌耐药性且缺乏疫苗,针对类鼻疽伯克霍尔德菌适应所需的蛋白质开发新型疗法提供了一种替代治疗策略。类鼻疽伯克霍尔德菌是一种土壤栖居细菌,是类鼻疽的病原体,类鼻疽是一种人和动物的致命传染病。该菌拥有庞大的基因组,由两条染色体组成,携带的基因编码的蛋白质对其在不同环境以及受感染宿主体内存活具有重要作用。虽然已提出了一般的致病机制,但尚不清楚哪些蛋白质在细菌处于土壤中时起主要作用,以及这些蛋白质是否是成功感染和传播的关键。为解决这个问题,我们先在土壤培养基中培养细菌,然后将其接种到感染的小鼠体内。在感染后5天,从感染小鼠的器官中回收细菌,并将其基因表达与在土壤培养基中培养的细菌进行比较。分析揭示了在土壤生长条件下表达的一系列基因,以及另一组编码可能对在受感染宿主体内生存、复制和传播很重要的蛋白质的基因。这些蛋白质是了解这种病原体完整适应机制的潜在资源。鉴于类鼻疽缺乏疫苗且治疗依赖联合抗生素疗法,这些蛋白质可能是设计治疗类鼻疽的抗菌药物的理想靶点。