AmbrožKičK Jerneja, OstroveršKnik Alenka, StarčKičK Marjanca, Kuhar Irena, Grabnar MiklavžK, Žgur-Bertok Darja
Department of Biology, Biotechnical Faculty, University of Ljubljana, VecKna pot 111, 1000 Ljubljana, Slovenia.
Microbiology (Reading). 1998 Feb;144 ( Pt 2):343-352. doi: 10.1099/00221287-144-2-343.
Uropathogenic Escherichia coli strains express chromosomal and plasmid-encoded virulence-associated factors such as specific adhesins, toxins and iron-uptake systems. A CoIV plasmid (pRK100) of a uropathogenic strain and its host KS533 were studied. The host strain encodes the K1 capsule, and P and S fimbriae, but neither haemolysin nor the cytotoxic-necrotic factor CNF1, indicating that this strain does not harbour a larger pathogenicity island. A restriction map of pRK100 was constructed on the basis of hybridization experiments and nucleotide sequencing. pRK100 harbours CoIV, the conserved replication region RepFIB, the aerobactin-uptake system, a RepFIC replicon and additionally Colla as well as transposon Tn5431. The location of the RepFIC replicon was similar to that in plasmid F. CoIV plasmids and F thus share a region spanning more than half the length of plasmid F. Even though their replication and transfer regions are homologous, CoIV plasmids are found only in E. coli strains. Among the four other species tested, conjugal transfer of pRK100 was demonstrated, with low frequency, only to Klebsiella pneumoniae, suggesting that a natural barrier effectively bars transfer. In vitro stability of the plasmid with integration into the chromosome to ensure maintenance in the presence of an incompatible plasmid was demonstrated.
尿路致病性大肠杆菌菌株表达染色体和质粒编码的毒力相关因子,如特定黏附素、毒素和铁摄取系统。对一株尿路致病性菌株的CoIV质粒(pRK100)及其宿主KS533进行了研究。宿主菌株编码K1荚膜、P菌毛和S菌毛,但不编码溶血素和细胞毒性坏死因子CNF1,这表明该菌株不含有更大的致病岛。基于杂交实验和核苷酸测序构建了pRK100的限制酶切图谱。pRK100含有CoIV、保守的复制区域RepFIB、气杆菌素摄取系统、一个RepFIC复制子,此外还含有Colla以及转座子Tn5431。RepFIC复制子的位置与质粒F中的相似。CoIV质粒和F因此共享一个跨越质粒F长度一半以上的区域。尽管它们的复制和转移区域是同源的,但CoIV质粒仅在大肠杆菌菌株中发现。在所测试的其他四个物种中,仅以低频率证明了pRK100向肺炎克雷伯菌的接合转移,这表明存在一种天然屏障有效地阻止了转移。证明了该质粒整合到染色体中的体外稳定性,以确保在存在不相容质粒的情况下得以维持。