Department of Microbiology, Molecular Genetics, and Immunology, University of Kansas Medical Centre, Kansas City, Kansas 66160, USA.
Antimicrob Agents Chemother. 2011 Apr;55(4):1460-9. doi: 10.1128/AAC.01094-10. Epub 2011 Jan 31.
Streptococcus mutans, a Gram-positive organism, is the primary causative agent in the formation of dental caries in humans. To persist in the oral cavity, S. mutans must be able to tolerate rapid environmental fluctuations and exposure to various toxic chemicals. However, the mechanisms underlying the ability of this cariogenic pathogen to survive and proliferate under harsh environmental conditions remain largely unknown. Here, we wanted to understand the mechanisms by which S. mutans withstands exposure to methyl viologen (MV), a quaternary ammonium compound (QAC) that generates superoxide radicals in the cell. To elucidate the essential genes for MV tolerance, screening of ∼3,500 mutants generated by ISS1 mutagenesis, revealed 15 MV-sensitive mutants. Among them, five and four independent insertions had occurred in SMU.905 and SMU.906 genes, respectively. These two genes are appeared to be organized in an operon and encode a putative ABC transporter complex; we designated the genes as vltA and vltB, for viologen transporter. To verify our results, vltA was deleted by using an antibiotic resistance marker; the mutant was just as sensitive to MV as the ISS1 insertion mutants. Furthermore, vltA and vltB mutants were also sensitive to other viologen compounds such as benzyl and ethyl viologens. Complementation assays were also carried out to confirm the role of VltA and VltB in viologen tolerance. Sensitivity to various drugs, including a wide range of QACs, was evaluated. It appears that a functional VltA is also required for full resistance toward acriflavin, ethidium bromide, and safranin; all are well-known QACs. These results indicate that VltA/B constitute a heterodimeric multidrug efflux pump of the ABC family. BLAST-P analysis suggests that homologs of VltA/B are widely present in streptococci, enterococci, and other important Gram-positive pathogens.
变形链球菌,一种革兰氏阳性菌,是人类龋齿形成的主要致病因子。为了在口腔中持续存在,变形链球菌必须能够耐受快速的环境波动和暴露于各种有毒化学物质。然而,这种致龋病原体在恶劣环境条件下生存和增殖的能力的机制在很大程度上仍然未知。在这里,我们想要了解变形链球菌如何耐受甲基紫精(MV)的机制,MV 是一种季铵化合物(QAC),会在细胞内产生超氧自由基。为了阐明 MV 耐受所必需的基因,通过 ISS1 诱变筛选了约 3500 个突变体,发现了 15 个 MV 敏感突变体。其中,SMU.905 和 SMU.906 基因分别有 5 个和 4 个独立的插入。这两个基因似乎组织在一个操纵子中,并编码一个假定的 ABC 转运体复合物;我们将这些基因命名为 vltA 和 vltB,代表紫精转运体。为了验证我们的结果,使用抗生素抗性标记物删除了 vltA;该突变体对 MV 的敏感性与 ISS1 插入突变体一样。此外,vltA 和 vltB 突变体对其他紫精化合物如苄基和乙基紫精也敏感。还进行了互补测定以确认 VltA 和 VltB 在紫精耐受中的作用。评估了对各种药物的敏感性,包括广泛的 QAC。似乎功能正常的 VltA 对于吖啶黄素、溴化乙锭和番红的完全抗性也是必需的;所有这些都是众所周知的 QAC。这些结果表明,VltA/B 构成 ABC 家族的异二聚体多药外排泵。BLAST-P 分析表明,VltA/B 的同源物广泛存在于链球菌、肠球菌和其他重要的革兰氏阳性病原体中。