Hornick D B, Thommandru J, Smits W, Clegg S
Department of Internal Medicine, University of Iowa College of Medicine, Iowa City 52242-1081, USA.
Infect Immun. 1995 May;63(5):2026-32. doi: 10.1128/iai.63.5.2026-2032.1995.
The role of the mrkD gene in attachment by a type 3 fimbriate Klebsiella pneumoniae strain was further characterized. A clinical isolate, K. pneumoniae IA565, was found to contain two copies of the gene encoding the fimbrial subunit, mrkA, and one copy of the gene encoding the adhesin subunit, mrkD. One copy of mrkA was located on the bacterial chromosome, and the other copy was associated with mrkD and located on a plasmid. The plasmid-borne mrk gene cluster was lost when K. pneumoniae IA565 was subcultured serially in broth at 44 degrees C. The resulting mrkD-negative strain, designated K. pneumoniae IApc35, did not exhibit the following adherence characteristics associated with K. pneumoniae possessing MrkD-positive fimbriae: agglutination of tannic acid-treated human erythrocytes and attachment to trypsinized human buccal cells. However, K. pneumoniae IApc35 produced type 3 fimbriae that were composed of the characteristic 21.5-kDa major fimbrial subunit, were reactive with specific serum, and were visualized specifically by immunoelectron microscopy. K. pneumoniae IApc35 retained a copy of the mrkA gene on its chromosome. This mrkA-containing gene cluster could be complemented by a recombinant plasmid carrying only the mrkD gene, resulting in restoration of the K. pneumoniae IA565-like adhesive phenotype and demonstration of type 3 filament-associated MrkD subunits by using colloidal gold labeling and immunoelectron microscopy. These data indicate that K. pneumoniae may contain multiple copies of the mrk genes which may be present simultaneously on both plasmid and chromosomal DNAs and which may encode fimbriae with different binding specificities.
对mrkD基因在3型菌毛肺炎克雷伯菌菌株黏附中的作用进行了进一步表征。发现一株临床分离株肺炎克雷伯菌IA565含有编码菌毛亚基mrkA的两个基因拷贝,以及编码黏附素亚基mrkD的一个基因拷贝。mrkA的一个拷贝位于细菌染色体上,另一个拷贝与mrkD相关并位于质粒上。当肺炎克雷伯菌IA565在44℃肉汤中连续传代培养时,质粒携带的mrk基因簇丢失。产生的mrkD阴性菌株,命名为肺炎克雷伯菌IApc35,不表现出与具有MrkD阳性菌毛的肺炎克雷伯菌相关的以下黏附特性:鞣酸处理的人红细胞凝集以及对胰蛋白酶处理的人颊细胞的黏附。然而,肺炎克雷伯菌IApc35产生了3型菌毛,其由特征性的21.5 kDa主要菌毛亚基组成,与特异性血清反应,并通过免疫电子显微镜特异性观察到。肺炎克雷伯菌IApc35在其染色体上保留了mrkA基因的一个拷贝。这个含mrkA的基因簇可以被仅携带mrkD基因的重组质粒互补,导致肺炎克雷伯菌IA565样黏附表型的恢复,并通过使用胶体金标记和免疫电子显微镜证明3型丝状相关的MrkD亚基。这些数据表明,肺炎克雷伯菌可能含有mrk基因的多个拷贝,这些拷贝可能同时存在于质粒和染色体DNA上,并且可能编码具有不同结合特异性的菌毛。