Matthijs Severine, Hernalsteens Jean-Pierre, Roelants Kim
Amphibian Evolution Lab, Biology Department, Vrije Universiteit Brussel, Pleinlaan 2, 1050, Brussels, Belgium.
Viral Genetics Research Group, Vrije Universiteit Brussel, Pleinlaan 2, 1050, Brussels, Belgium.
Dev Comp Immunol. 2017 Feb;67:395-403. doi: 10.1016/j.dci.2016.08.012. Epub 2016 Aug 25.
Host-defense peptides and proteins are vital for first line protection against bacteria. Most host-defense peptides and proteins common in vertebrates have been studied primarily in mammals, while their orthologues in non-mammalian vertebrates received less attention. We found that the European Common Frog Rana temporaria expresses a protein in its skin that is evolutionarily related to the host-defense protein S100A7. This prompted us to test if the encoded protein, which is an important microbicidal protein in human skin, shows similar activity in frogs. The R. temporaria protein lacks the zinc-binding sites that are key to the antimicrobial activity of human S100A7 at neutral pH. However, despite being less potent, the R. temporaria protein does compromise bacterial membranes at low pH, similar to its human counterpart. We postulate that, while amphibian S100A7 likely serves other functions, the capacity to compromise bacterial cell membranes evolved early in tetrapod evolution.
宿主防御肽和蛋白质对于抵御细菌的一线保护至关重要。脊椎动物中常见的大多数宿主防御肽和蛋白质主要在哺乳动物中进行了研究,而它们在非哺乳动物脊椎动物中的直系同源物受到的关注较少。我们发现欧洲普通青蛙(林蛙)的皮肤中表达一种与宿主防御蛋白S100A7在进化上相关的蛋白质。这促使我们测试这种编码蛋白(它是人类皮肤中一种重要的杀菌蛋白)在青蛙中是否表现出类似的活性。林蛙蛋白缺乏锌结合位点,而锌结合位点是人类S100A7在中性pH值下抗菌活性的关键。然而,尽管效力较低,但林蛙蛋白在低pH值下确实会破坏细菌膜,类似于其人类对应物。我们推测,虽然两栖动物的S100A7可能具有其他功能,但破坏细菌细胞膜的能力在四足动物进化早期就已出现。