Miller Samuel I
Departments of Microbiology, Medicine & Genome Sciences, University of Washington, Seattle, Washington, USA
mBio. 2016 Sep 27;7(5):e01541-16. doi: 10.1128/mBio.01541-16.
The Gram-negative outer membrane is an important barrier that provides protection against toxic compounds, which include antibiotics and host innate immune molecules such as cationic antimicrobial peptides. Recently, significant research progress has been made in understanding the biogenesis, regulation, and functioning of the outer membrane, including a recent paper from the laboratory of Dr. Brett Finlay at the University of British Columbia (J. van der Heijden et al., mBio 7:e01238-16, 2016, http://dx.doi.org/10.1128/mBio.01541-16). These investigators demonstrate that toxic oxygen radicals, such as those found in host tissues, regulate outer membrane permeability by altering the outer membrane porin protein channels to regulate the influx of oxygen radicals as well as β-lactam antibiotics. This commentary provides context about this interesting paper and discusses the prospects of utilizing increased knowledge of outer membrane biology to develop new antibiotics for antibiotic-resistant Gram-negative bacteria.
革兰氏阴性菌外膜是一道重要屏障,可抵御包括抗生素以及宿主天然免疫分子(如阳离子抗菌肽)在内的有毒化合物。最近,在理解外膜的生物合成、调控及功能方面取得了重大研究进展,其中包括不列颠哥伦比亚大学布雷特·芬利博士实验室发表的一篇近期论文(J. van der Heijden等人,《mBio》7:e01238 - 16,2016年,http://dx.doi.org/10.1128/mBio.01541 - 16)。这些研究人员证明,宿主组织中存在的有毒氧自由基通过改变外膜孔蛋白通道来调节外膜通透性,进而调控氧自由基以及β - 内酰胺抗生素的流入。本述评提供了关于这篇有趣论文的背景信息,并讨论了利用对外膜生物学的更多了解来开发针对耐抗生素革兰氏阴性菌的新型抗生素的前景。