Khan Naveed Ahmed, Goldsworthy Graham John
Department of Biology, School of Biological and Chemical Sciences, Birkbeck, University of London, London WC1E 7HX, United Kingdom.
Infect Immun. 2007 Dec;75(12):5735-9. doi: 10.1128/IAI.00740-07. Epub 2007 Sep 17.
It is shown here for the first time that locusts can be used as a model to study Escherichia coli K1 pathogenesis. E. coli K-12 strain HB101 has very low pathogenicity to locusts and does not invade the locust brain, whereas the injection of 2 x 10(6) E. coli K1 strain RS218 (O18:K1:H7) kills almost 100% of locusts within 72 h and invades the brain within 24 h of injection. Both mortality and invasion of the brain in locusts after injection of E. coli K1 require at least two of the known virulence determinants shown for mammals. Thus, deletion mutants that lack outer membrane protein A or cytotoxic necrotizing factor 1 have reduced abilities to kill locusts and to invade the locust brain compared to the parent E. coli K1. Interestingly, deletion mutants lacking FimH or the NeuDB gene cluster are still able to cause high mortality. It is argued that the likely existence of additional virulence determinants can be investigated in vivo by using this insect system.
本文首次表明蝗虫可作为研究大肠杆菌K1致病机制的模型。大肠杆菌K - 12菌株HB101对蝗虫的致病性非常低,且不会侵入蝗虫大脑,而注射2×10⁶个大肠杆菌K1菌株RS218(O18:K1:H7)会在72小时内杀死几乎100%的蝗虫,并在注射后24小时内侵入大脑。注射大肠杆菌K1后蝗虫的死亡率和脑部入侵都至少需要两种已知的对哺乳动物起作用的毒力决定因素。因此,与亲本大肠杆菌K1相比,缺乏外膜蛋白A或细胞毒性坏死因子1的缺失突变体杀死蝗虫和侵入蝗虫大脑的能力有所降低。有趣的是,缺乏FimH或NeuDB基因簇的缺失突变体仍然能够导致高死亡率。有人认为,利用这种昆虫系统可以在体内研究可能存在的其他毒力决定因素。