Goh Shan, Chang Barbara J, Riley Thomas V
Microbiology, School of Biomedical & Chemical Sciences, The University of Western Australia, Queen Elizabeth II Medical Centre1, and Division of Microbiology and Infectious Diseases, The Western Australian Centre for Pathology and Medical Research2, Nedlands, Australia 6009.
J Med Microbiol. 2005 Feb;54(Pt 2):129-135. doi: 10.1099/jmm.0.45821-0.
Infection with Clostridium difficile and subsequent production of toxins A and B may result in C. difficile-associated diarrhoea and pseudomembranous colitis in hospital patients. The effect of four temperate phages, obtained by induction of clinical C. difficile isolates, on toxin production by C. difficile was determined. None of these phages converted a lysogenized non-toxigenic C. difficile strain to toxin production. One of the accessory toxin genes, tcdE, was detected in three phages, phiC2, phiC6 and phiC8; however, the non-repeating regions of tcdA and tcdB encoding the enzymic domains were not carried on phage DNA. Phage infection of toxigenic strains increased toxin B production in four of six lysogens, although the level of tcdB transcription as determined by real-time RT-PCR was not significantly altered. However, levels of toxin A transcription in two lysogens were significantly altered without any corresponding differences in toxin A production.
艰难梭菌感染及随后产生的毒素A和毒素B可能会导致医院患者出现艰难梭菌相关性腹泻和假膜性结肠炎。通过诱导临床艰难梭菌分离株获得了四种温和噬菌体,测定了它们对艰难梭菌毒素产生的影响。这些噬菌体均未使溶原化的非产毒艰难梭菌菌株转变为产毒菌株。在三种噬菌体phiC2、phiC6和phiC8中检测到一个辅助毒素基因tcdE;然而,编码酶结构域的tcdA和tcdB的非重复区域并未携带在噬菌体DNA上。产毒菌株的噬菌体感染使六个溶原菌中的四个增加了毒素B的产生,尽管通过实时逆转录聚合酶链反应测定的tcdB转录水平没有显著改变。然而,两个溶原菌中毒素A的转录水平发生了显著改变,而毒素A的产生却没有任何相应差异。