Sokolowska-Köhler W, Schönian G, Bollmann R, Schubert A, Parschau J, Seeberg A, Presber W
Institut für Mikrobiologie und Hygiene, Universitätsklinikum Charite,Humboldt-Universität Berlin, Germany.
FEMS Immunol Med Microbiol. 1997 May;18(1):1-6. doi: 10.1111/j.1574-695X.1997.tb01021.x.
The presence of S and F1C/S-related fimbrial determinants was determined in 462 E. coli strains obtained from different extraintestinal infections and in 162 control isolates of E. coli by using two different DNA probes: an oligonucleotide probe consisting of three oligonucleotides that bind specifically to the S adhesin gene and a polynucleotide probe which is not able to distinguish between S, F1C, and S-related sequences. The expression of S and F1C phenotypes was tested by dot enzyme immunoassay with the corresponding monoclonal antibodies. S fimbriae genotypes were observed more frequently in septic (25%) and urinary (12%) isolates of E. coli than in faecal and water isolates (1%) and often occurred together with O2, O6, O18 and O83 antigens. F1C/S-related fimbrial DNA was detected with a higher frequency in UTI isolates (26%) than in septic (16%) and faecal (10%) isolates and was most frequently associated with O4, O6, and O75 serotypes. Since the production of S and F1C fimbriae was comparatively rare in all clinical and control isolates of E. coli, DNA hybridization assays which allow the sensitive and specific detection of fimbrial determinants even in the absence of their expression are preferable to phenotypic assays.
利用两种不同的DNA探针,对从不同的肠道外感染中分离得到的462株大肠杆菌菌株以及162株大肠杆菌对照菌株进行检测,以确定S和F1C/S相关菌毛决定簇的存在情况:一种由三条能特异性结合S黏附素基因的寡核苷酸组成的寡核苷酸探针,以及一种无法区分S、F1C和S相关序列的多核苷酸探针。通过用相应的单克隆抗体进行斑点酶免疫测定来检测S和F1C表型的表达。在大肠杆菌的败血症(25%)和泌尿道(12%)分离株中,观察到S菌毛基因型的频率高于粪便和水分离株(1%),并且常与O2、O6、O18和O83抗原同时出现。在泌尿道感染分离株(26%)中检测到F1C/S相关菌毛DNA的频率高于败血症(16%)和粪便(10%)分离株,并且最常与O4、O6和O75血清型相关。由于在所有临床和对照大肠杆菌分离株中,S和F1C菌毛的产生相对较少,因此即使在菌毛决定簇不表达的情况下,能进行灵敏且特异检测的DNA杂交试验比表型试验更可取。