Oswald E, Pohl P, Jacquemin E, Lintermans P, Van Muylem K, O'Brien A D, Mainil J
Uniformed Services University of the Health Sciences, Department of Microbiology, Bethesda, MD 20814-4799.
J Med Microbiol. 1994 Jun;40(6):428-34. doi: 10.1099/00222615-40-6-428.
Cytotoxic necrotising factors type 1 (CNF1) and type 2 (CNF2) are produced by many Escherichia coli strains isolated from man and animals with intestinal or extra-intestinal colibacillosis. In most laboratories, CNF-producing strains are detected by a cell cytotoxicity assay and confirmed with a neutralisation assay or a mouse footpad assay. In this study, we sought to determine whether DNA probes could detect clinical isolates of E. coli producing CNF2 or CNF1, or both, without the need for cell cultures or animal assays. Two internal fragments of the gene encoding CNF2 were used as DNA probes: a 875-bp XhoI-PstI DNA fragment and an adjacent 335-bp PstI-ClaI fragment. A positive response with both DNA probes was associated with CNF2-producing strains, whereas a positive response with only the 335-bp probe was associated with CNF1-producing strains. Results of colony hybridisation experiments with 185 clinical isolates of E. coli demonstrated that these DNA probes detected CNF2-producing strains with a sensitivity and specificity of 100% and CNF1-producing strains with a sensitivity and specificity of 99%. These two DNA probes should greatly facilitate epidemiological studies to assess the importance of CNF-producing strains as agents of diarrhoea and septicaemia.
1型细胞毒性坏死因子(CNF1)和2型细胞毒性坏死因子(CNF2)由许多从患有肠道或肠道外大肠杆菌病的人和动物中分离出的大肠杆菌菌株产生。在大多数实验室中,通过细胞毒性试验检测产生CNF的菌株,并通过中和试验或小鼠足垫试验进行确认。在本研究中,我们试图确定DNA探针是否能够在无需细胞培养或动物试验的情况下,检测出产生CNF2或CNF1或两者的大肠杆菌临床分离株。编码CNF2的基因的两个内部片段被用作DNA探针:一个875 bp的XhoI - PstI DNA片段和一个相邻的335 bp的PstI - ClaI片段。对两种DNA探针均呈阳性反应与产生CNF2的菌株相关,而仅对335 bp探针呈阳性反应与产生CNF1的菌株相关。对185株大肠杆菌临床分离株进行菌落杂交实验的结果表明,这些DNA探针检测产生CNF2的菌株的灵敏度和特异性为100%,检测产生CNF1的菌株的灵敏度和特异性为99%。这两种DNA探针应能极大地促进流行病学研究,以评估产生CNF的菌株作为腹泻和败血症病原体的重要性。