Schwan William R
Department of Microbiology, University of Wisconsin-La Crosse, 1725 State Street, La Crosse, WI 54601, USA.
Int J Med Microbiol. 2008 Jul;298(5-6):441-7. doi: 10.1016/j.ijmm.2007.05.009. Epub 2007 Sep 20.
Uropathogenic Escherichia coli (UPEC) cause bladder and kidney infections in humans and mice. UPEC initiate many kidney infections by ascending out of infected bladders, but how this occurs is not well understood. To determine if the flagella were responsible for the ascension of UPEC to the kidneys, a fliC mutation in strain NU149 was created. The fliC mutant spread poorly on soft agar plates, and 12h post-inoculation of murine urinary tracts, ascension into the murine kidneys was compromised in this mutant strain compared with wild-type bacteria. Complementation of the mutation restored the ability to spread on soft agar plates and ascend into the murine kidneys. To confirm the fliC mutant results, an anti-flagella monoclonal antibody that has been previously described inhibited the spread of UPEC strain NU149 on soft agar plates. When the anti-flagella antibody was mixed with strain NU149 cells and the antibody-treated bacterial cells were used to infect mice, significantly fewer mice had kidney infections than mice that were injected with strain NU149 cells mixed with normal mouse serum or anti-type 1 pili antibody. These results suggest that E. coli flagella may be of importance in allowing the bacteria to ascend from the bladder and initiate kidney infections in humans, and the use of an antibody against the flagella could prevent the spread of UPEC into the kidneys.
尿路致病性大肠杆菌(UPEC)可导致人类和小鼠的膀胱及肾脏感染。UPEC通过从受感染的膀胱上行引发许多肾脏感染,但具体机制尚不清楚。为了确定鞭毛是否是UPEC上行至肾脏的原因,构建了菌株NU149的fliC突变体。fliC突变体在软琼脂平板上的扩散能力较差,在接种小鼠尿道12小时后,与野生型细菌相比,该突变菌株上行至小鼠肾脏的能力受损。突变体的互补恢复了其在软琼脂平板上扩散并上行至小鼠肾脏的能力。为了证实fliC突变体的结果,一种先前描述的抗鞭毛单克隆抗体抑制了UPEC菌株NU149在软琼脂平板上的扩散。当将抗鞭毛抗体与菌株NU149细胞混合,并使用经抗体处理的细菌细胞感染小鼠时,与注射了与正常小鼠血清或抗1型菌毛抗体混合的菌株NU149细胞的小鼠相比,发生肾脏感染的小鼠明显减少。这些结果表明,大肠杆菌鞭毛可能在使细菌从膀胱上行并引发人类肾脏感染中起重要作用,使用抗鞭毛抗体可防止UPEC扩散至肾脏。