a Department of Veterinary Diagnostic and Production Animal Medicine , College of Veterinary Medicine, Iowa State University , Ames , IA , USA.
b Department of Veterinary Preventive Medicine , College of Veterinary Medicine, Nanjing Agricultural University , Nanjing , China.
Virulence. 2018 Dec 31;9(1):666-680. doi: 10.1080/21505594.2018.1433979.
Extraintestinal pathogenic Escherichia coli (ExPEC) is the leading cause of bloodstream and other extraintestinal infections in human and animals. The greatest challenge encountered by ExPEC during an infection is posed by the host defense mechanisms, including lysozyme. ExPEC have developed diverse strategies to overcome this challenge. The aim of this study was to characterize the molecular mechanism of ExPEC resistance to lysozyme. For this, 15,000 transposon mutants of a lysozyme-resistant ExPEC strain NMEC38 were screened; 20 genes were identified as involved in ExPEC resistance to lysozyme-of which five were located in the gene cluster between galF and gnd, and were further confirmed to be involved in O-specific polysaccharide biosynthesis. The O-specific polysaccharide was able to inhibit the hydrolytic activity of lysozyme; it was also required by the complete lipopolysaccharide (LPS)-mediated protection of ExPEC against the bactericidal activity of lysozyme. The O-specific polysaccharide was further shown to be able to directly interact with lysozyme. Furthermore, LPS from ExPEC strains of different O serotypes was also able to inhibit the hydrolytic activity of lysozyme. Because of their cell surface localization and wide distribution in Gram-negative bacteria, O-specific polysaccharides appear to play a long-overlooked role in protecting bacteria against exogenous lysozyme.
肠外致病性大肠杆菌(ExPEC)是人类和动物血液感染和其他肠外感染的主要原因。ExPEC 在感染过程中遇到的最大挑战来自宿主防御机制,包括溶菌酶。ExPEC 已经开发出多种策略来克服这一挑战。本研究旨在描述 ExPEC 抵抗溶菌酶的分子机制。为此,筛选了对溶菌酶具有抗性的 ExPEC 菌株 NMEC38 的 15000 个转座子突变体;鉴定出 20 个与 ExPEC 抵抗溶菌酶相关的基因,其中 5 个位于 galF 和 gnd 之间的基因簇中,进一步证实它们参与 O 特异性多糖的生物合成。O 特异性多糖能够抑制溶菌酶的水解活性;它也是完整脂多糖(LPS)介导的 ExPEC 对溶菌酶杀菌活性的保护所必需的。O 特异性多糖还能够直接与溶菌酶相互作用。此外,不同 O 血清型的 ExPEC 菌株的 LPS 也能够抑制溶菌酶的水解活性。由于其在细胞表面的定位和在革兰氏阴性菌中的广泛分布,O 特异性多糖似乎在保护细菌免受外源溶菌酶的侵害方面发挥了长期被忽视的作用。