Research Centre for Infectious Disease, School of Molecular and Biomedical Science, The University of Adelaide, North Terrace Campus, Adelaide 5005, Australia.
BMC Microbiol. 2012 Jul 31;12:159. doi: 10.1186/1471-2180-12-159.
adhC from Haemophilus influenzae encodes a glutathione-dependent alcohol dehydrogenase that has previously been shown to be required for protection against killing by S-nitrosoglutathione (GSNO). This group of enzymes is known in other systems to be able to utilize substrates that form adducts with glutathione, such as aldehydes.
Here, we show that expression of adhC is maximally induced under conditions of high oxygen tension as well as specifically with glucose as a carbon source. adhC could also be induced in response to formaldehyde but not GSNO. An adhC mutant was more susceptible than wild-type Haemophilus influenzae Rd KW20 to killing by various short chain aliphatic aldehydes, all of which can be generated endogenously during cell metabolism but are also produced by the host as part of the innate immune response.
These results indicate that AdhC plays a role in defense against endogenously generated reactive carbonyl electrophiles in Haemophilus influenzae and may also play a role in defense against the host innate immune system.
流感嗜血杆菌的 adhC 基因编码一种谷胱甘肽依赖的醇脱氢酶,先前的研究表明该酶对于抵御 S-亚硝基谷胱甘肽(GSNO)的杀伤作用是必需的。在其他系统中,这类酶已知能够利用与谷胱甘肽形成加合物的底物,如醛类。
在这里,我们表明,adhC 的表达在高氧张力条件下以及特定的葡萄糖作为碳源时被最大程度地诱导。adhC 也可以响应甲醛而不是 GSNO 被诱导。adhC 突变体比野生型流感嗜血杆菌 Rd KW20 更容易被各种短链脂肪醛杀伤,所有这些醛都可以在细胞代谢过程中内源性产生,但也可以作为宿主固有免疫反应的一部分由宿主产生。
这些结果表明,AdhC 在抵御流感嗜血杆菌内源性产生的反应性羰基亲电子试剂中发挥作用,并且可能在抵御宿主固有免疫系统方面也发挥作用。