Do Jimmy, Zafar Hassan, Saier Milton H
Department of Molecular Biology, Division of Biological Sciences, University of California at San Diego, La Jolla, CA 92093-0116, USA.
Department of Molecular Biology, Division of Biological Sciences, University of California at San Diego, La Jolla, CA 92093-0116, USA.
Microb Pathog. 2017 Jun;107:106-115. doi: 10.1016/j.micpath.2017.03.022. Epub 2017 Mar 24.
Escherichia coli is a genetically diverse species that can be pathogenic, probiotic, commensal, or a harmless laboratory strain. Pathogenic strains of E. coli cause urinary tract infections, diarrhea, hemorrhagic colitis, and pyelonephritis, while the two known probiotic E. coli strains combat inflammatory bowel disease and play a role in immunomodulation. Salmonella enterica, a close relative of E. coli, includes two important pathogenic serovars, Typhi and Typhimurium, causing typhoid fever and enterocolitis in humans, respectively, with the latter strain also causing a lethal typhoid fever-like disease in mice. In this study, we identify the transport systems and their substrates within seven E. coli strains: two probiotic strains, two extracellular pathogens, two intracellular pathogens, and K-12, as well as the two intracellular pathogenic S. enterica strains noted above. Transport systems characteristic of each probiotic or pathogenic species were thus identified, and the tabulated results obtained with all of these strains were compared. We found that the probiotic and pathogenic strains generally contain more iron-siderophore and sugar transporters than E. coli K-12. Pathogens have increased numbers of pore-forming toxins, protein secretion systems, decarboxylation-driven Na exporters, electron flow-driven monovalent cation exporters, and putative transporters of unknown function compared to the probiotic strains. Both pathogens and probiotic strains encode metabolite transporters that reflect their intracellular versus extracellular environments. The results indicate that the probiotic strains live extracellularly. It seems that relatively few virulence factors can convert a beneficial or commensal microorganism into a pathogen. Taken together, the results reveal the distinguishing features of these strains and provide a starting point for future engineering of beneficial enteric bacteria.
大肠杆菌是一个基因多样化的物种,它可以是致病性的、益生菌性的、共生性的,或者是无害的实验室菌株。致病性大肠杆菌菌株会引起尿路感染、腹泻、出血性结肠炎和肾盂肾炎,而两种已知的益生菌性大肠杆菌菌株则可对抗炎症性肠病并在免疫调节中发挥作用。大肠杆菌的近亲肠炎沙门氏菌包括两个重要的致病性血清型,伤寒杆菌和鼠伤寒杆菌,分别导致人类患伤寒和小肠结肠炎,后者在小鼠中还会引发一种致命的伤寒样疾病。在本研究中,我们鉴定了七种大肠杆菌菌株中的转运系统及其底物:两种益生菌菌株、两种细胞外病原体、两种细胞内病原体以及K-12,还有上述两种细胞内致病性肠炎沙门氏菌菌株。由此确定了每种益生菌或病原体物种特有的转运系统,并比较了所有这些菌株的列表结果。我们发现,与大肠杆菌K-12相比,益生菌和致病性菌株通常含有更多的铁载体和糖转运蛋白。与益生菌菌株相比,病原体的成孔毒素、蛋白质分泌系统、脱羧驱动的钠转运蛋白、电子流驱动的单价阳离子转运蛋白以及功能未知的推定转运蛋白数量有所增加。病原体和益生菌菌株都编码反映其细胞内与细胞外环境的代谢物转运蛋白。结果表明,益生菌菌株在细胞外生存。似乎相对较少的毒力因子就能将有益或共生微生物转变为病原体。综上所述,这些结果揭示了这些菌株的显著特征,并为未来有益肠道细菌的工程改造提供了一个起点。