Australian Infectious Diseases Research Centre, School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia.
BMC Microbiol. 2012 Jan 15;12:8. doi: 10.1186/1471-2180-12-8.
The Gram-positive bacterium Staphylococcus saprophyticus is the second most frequent causative agent of community-acquired urinary tract infections (UTI), accounting for up to 20% of cases. A common feature of staphylococci is colonisation of the human skin. This involves survival against innate immune defenses including antibacterial unsaturated free fatty acids such as linoleic acid which act by disrupting bacterial cell membranes. Indeed, S. saprophyticus UTI is usually preceded by perineal skin colonisation.
In this study we identified a previously undescribed 73.5 kDa cell wall-anchored protein of S. saprophyticus, encoded on plasmid pSSAP2 of strain MS1146, which we termed S. saprophyticus surface protein F (SssF). The sssF gene is highly prevalent in S. saprophyticus clinical isolates and we demonstrate that the SssF protein is expressed at the cell surface. However, unlike all other characterised cell wall-anchored proteins of S. saprophyticus, we were unable to demonstrate a role for SssF in adhesion. SssF shares moderate sequence identity to a surface protein of Staphylococcus aureus (SasF) recently shown to be an important mediator of linoleic acid resistance. Using a heterologous complementation approach in a S. aureus sasF null genetic background, we demonstrate that SssF is associated with resistance to linoleic acid. We also show that S. saprophyticus strains lacking sssF are more sensitive to linoleic acid than those that possess it. Every staphylococcal genome sequenced to date encodes SssF and SasF homologues. Proteins in this family share similar predicted secondary structures consisting almost exclusively of α-helices in a probable coiled-coil formation.
Our data indicate that SssF is a newly described and highly prevalent surface-localised protein of S. saprophyticus that contributes to resistance against the antibacterial effects of linoleic acid. SssF is a member of a protein family widely disseminated throughout the staphylococci.
革兰氏阳性菌尿生殖支原体是社区获得性尿路感染(UTI)的第二大常见病原体,占病例的 20%。葡萄球菌的一个共同特征是定植在人体皮肤上。这涉及到对先天免疫防御的生存,包括抗菌不饱和游离脂肪酸,如亚油酸,它通过破坏细菌细胞膜起作用。事实上,尿生殖支原体 UTI 通常先于会阴皮肤定植。
在这项研究中,我们鉴定了尿生殖支原体中一种以前未描述的 73.5 kDa 细胞壁锚定蛋白,该蛋白由菌株 MS1146 的质粒 pSSAP2 编码,我们将其命名为尿生殖支原体表面蛋白 F(SssF)。sssF 基因在尿生殖支原体临床分离株中高度流行,我们证明 SssF 蛋白在细胞表面表达。然而,与尿生殖支原体所有其他已鉴定的细胞壁锚定蛋白不同,我们无法证明 SssF 在粘附中的作用。SssF 与金黄色葡萄球菌(SasF)的一种表面蛋白具有中等序列同一性,最近该蛋白被证明是抵抗亚油酸的重要介质。在金黄色葡萄球菌 sasF 缺失遗传背景下使用异源互补方法,我们证明 SssF 与抵抗亚油酸有关。我们还表明,缺乏 sssF 的尿生殖支原体菌株比具有 sssF 的菌株对亚油酸更敏感。迄今为止,所有测序的葡萄球菌基因组都编码 SssF 和 SasF 同源物。该家族的蛋白质具有相似的预测二级结构,几乎完全由可能形成卷曲螺旋的α-螺旋组成。
我们的数据表明,SssF 是尿生殖支原体中新描述的高度流行的表面定位蛋白,有助于抵抗亚油酸的抗菌作用。SssF 是一种广泛分布在葡萄球菌中的蛋白质家族的成员。