Gangaiah Dharanesh, Zhang Xinjun, Baker Beth, Fortney Kate R, Gao Hongyu, Holley Concerta L, Munson Robert S, Liu Yunlong, Spinola Stanley M
Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Infect Immun. 2016 Apr 22;84(5):1514-1525. doi: 10.1128/IAI.00048-16. Print 2016 May.
Haemophilus ducreyi causes the sexually transmitted disease chancroid in adults and cutaneous ulcers in children. In humans, H. ducreyi resides in an abscess and must adapt to a variety of stresses. Previous studies (D. Gangaiah, M. Labandeira-Rey, X. Zhang, K. R. Fortney, S. Ellinger, B. Zwickl, B. Baker, Y. Liu, D. M. Janowicz, B. P. Katz, C. A. Brautigam, R. S. MunsonJr, E. J. Hansen, and S. M. Spinola, mBio 5:e01081-13, 2014, http://dx.doi.org/10.1128/mBio.01081-13) suggested that H. ducreyi encounters growth conditions in human lesions resembling those found in stationary phase. However, how H. ducreyi transcriptionally responds to stress during human infection is unknown. Here, we determined the H. ducreyi transcriptome in biopsy specimens of human lesions and compared it to the transcriptomes of bacteria grown to mid-log, transition, and stationary phases. Multidimensional scaling showed that the in vivo transcriptome is distinct from those of in vitro growth. Compared to the inoculum (mid-log-phase bacteria), H. ducreyi harvested from pustules differentially expressed ∼93 genes, of which 62 were upregulated. The upregulated genes encode homologs of proteins involved in nutrient transport, alternative carbon pathways (l-ascorbate utilization and metabolism), growth arrest response, heat shock response, DNA recombination, and anaerobiosis. H. ducreyi upregulated few genes (hgbA, flp-tad, and lspB-lspA2) encoding virulence determinants required for human infection. Most genes regulated by CpxRA, RpoE, Hfq, (p)ppGpp, and DksA, which control the expression of virulence determinants and adaptation to a variety of stresses, were not differentially expressed in vivo, suggesting that these systems are cycling on and off during infection. Taken together, these data suggest that the in vivo transcriptome is distinct from those of in vitro growth and that adaptation to nutrient stress and anaerobiosis is crucial for H. ducreyi survival in humans.
杜克雷嗜血杆菌可导致成人患性传播疾病软下疳以及儿童出现皮肤溃疡。在人类体内,杜克雷嗜血杆菌寄居于脓肿中,必须适应多种应激条件。先前的研究(D. 甘加亚、M. 拉班德雷亚 - 雷伊、X. 张、K. R. 福特尼、S. 埃林格、B. 茨维克、B. 贝克、Y. 刘、D. M. 贾诺维茨、B. P. 卡茨、C. A. 布劳蒂甘、R. S. 芒森 Jr、E. J. 汉森和 S. M. 斯皮诺拉,《mBio》5:e01081 - 13,2014,http://dx.doi.org/10.1128/mBio.01081 - 13)表明,杜克雷嗜血杆菌在人类病变中遇到的生长条件类似于稳定期的条件。然而,杜克雷嗜血杆菌在人类感染期间如何通过转录来应对应激尚不清楚。在此,我们确定了人类病变活检标本中的杜克雷嗜血杆菌转录组,并将其与生长至对数中期、转换期和稳定期的细菌转录组进行比较。多维标度分析表明,体内转录组与体外生长的转录组不同。与接种物(对数中期细菌)相比,从脓疱中收获的杜克雷嗜血杆菌差异表达约93个基因,其中62个基因上调。上调的基因编码参与营养物质转运、替代碳途径(l - 抗坏血酸利用和代谢)、生长停滞反应、热休克反应、DNA重组和厌氧的蛋白质同源物。杜克雷嗜血杆菌上调了少数编码人类感染所需毒力决定因素的基因(hgbA、flp - tad和lspB - lspA2)。大多数受CpxRA、RpoE、Hfq、(p)ppGpp和DksA调控的基因,这些基因控制毒力决定因素的表达以及对多种应激的适应,在体内并未差异表达,这表明这些系统在感染过程中处于循环开启和关闭状态。综上所述,这些数据表明体内转录组与体外生长的转录组不同,并且对营养应激和厌氧的适应对于杜克雷嗜血杆菌在人类中的生存至关重要。