Department of Microbiology and Molecular Genetics, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.
Arch Oral Biol. 2013 Oct;58(10):1378-84. doi: 10.1016/j.archoralbio.2013.05.001. Epub 2013 Jun 2.
Mycoplasma salivarium is a human oral potential pathogen that preferentially resides in dental plaques and gingival sulci. It has been suggested that this organism may play an etiological role in inflammatory processes in the oral cavity. The aim of this work was to determine whether M. salivarium possesses a potent oxidant scavenging capacity (OSC).
The OSC of M. salivarium was quantified by a highly sensitive luminal-dependent chemiluminescence assay in the presence of cocktails that induced a constant flux of luminescence resulting from the generation of peroxide, hydroxyl radical (cocktail A) and NO, superoxide and peroxynitrites (cocktail B).
M. salivarium markedly reduced oxidative stress by scavenging both free reactive oxygen and nitrogen species. The OSC of M. salivarium was much higher than that of other Mycoplasma species. Most of M. salivarium OSC was confined to the cytosolic fraction and was markedly increased in the presence of tannic acid, red blood cells or mucin. The cytosolic OSC of M. salivarium was heat stable and not affected by sodium azide or prolonged proteolysis. However, it was markedly decreased upon dialysis, suggesting that the major reducing activity is not enzymatic but rather, a low molecular weight compound(s).
The ability of M. salivarium to scavenge oxidants may play a role in the survival and pathogenicity of this microorganism. The enhanced OSC of M. salivarium in the presence of tannic acid, red blood cells or mucin might have a significant importance to assess complex interactions with polyphenols from nutrients, salivary proteins and red blood cells extravasated from injured capillaries during infection and inflammation in oral tissues.
口腔唾液支原体是一种人类口腔潜在病原体,优先存在于牙菌斑和牙龈沟中。有人认为,这种生物可能在口腔炎症过程中发挥病因作用。本研究旨在确定口腔唾液支原体是否具有强大的氧化剂清除能力(OSC)。
采用高度敏感的腔依赖性化学发光测定法,在诱导过氧化氢、羟基自由基(鸡尾酒 A)和 NO、超氧化物和过氧亚硝酸盐(鸡尾酒 B)持续产生的发光的混合物存在的情况下,定量测定口腔唾液支原体的 OSC。
口腔唾液支原体通过清除游离活性氧和氮物种显著减轻氧化应激。口腔唾液支原体的 OSC 远高于其他支原体物种。口腔唾液支原体的 OSC 主要局限于胞质部分,并且在单宁酸、红细胞或粘蛋白存在下显著增加。口腔唾液支原体的胞质 OSC 热稳定,不受叠氮化钠或长时间蛋白水解的影响。然而,它在透析时明显减少,表明主要的还原活性不是酶,而是一种低分子量化合物(或多种化合物)。
口腔唾液支原体清除氧化剂的能力可能在这种微生物的生存和致病性中发挥作用。在单宁酸、红细胞或粘蛋白存在下,口腔唾液支原体的 OSC 增强,这对于评估与营养物质中的多酚、唾液蛋白和感染和炎症期间从毛细血管渗出的红细胞之间的复杂相互作用可能具有重要意义。