Monecke Stefan, Helbig Jürgen H, Jacobs Enno
Institute for Medical Microbiology and Hygiene, Medical Faculty, Technical University of Dresden, Germany.
Int J Med Microbiol. 2003 Jun;293(2-3):203-11. doi: 10.1078/1438-4221-00239.
Ureaplasma urealyticum and U. parvum are common commensals and, possibly, pathogens of the human urogenital tract. Like other Mycoplasmatales they possess variable surface proteins. The multiple banded (MB) protein shows a striking variability of its molecular weight. This is caused by changes of the number of C-terminal repeating units. In this study, selective pressure was imposed against cytadherence of U. urealyticum and U. parvum. Ureaplasmas were co-incubated with either erythrocytes or HeLa cells and the cell-bound fraction was removed. Additionally, U. urealyticum populations were transferred serially through broth containing specific polyclonal antibodies. Both approaches led to the emergence of escape variants in which no MB protein was detectable. PCR studies with several primers on different parts of the mba gene indicated major differences between wild-type strains and MB-negative escape variants. In experiments with clonal lineages, however, the loss of the MB protein was shown to be reversible. Therefore, it is proposed that the multiple banded proteins of U. urealyticum and U. parvum are subjected to a phase-switching mechanism as it has already been described for several other Mycoplasmatales.
解脲脲原体和微小脲原体是人类泌尿生殖道常见的共生菌,也可能是病原体。与其他支原体目细菌一样,它们拥有可变表面蛋白。多带(MB)蛋白的分子量呈现出显著的变异性。这是由C末端重复单元数量的变化引起的。在本研究中,对解脲脲原体和微小脲原体的细胞黏附施加了选择性压力。脲原体与红细胞或HeLa细胞共同孵育,然后去除细胞结合部分。此外,解脲脲原体群体在含有特定多克隆抗体的肉汤中连续传代。这两种方法都导致了逃逸变体的出现,在这些变体中检测不到MB蛋白。用几种针对mba基因不同部位的引物进行的PCR研究表明,野生型菌株与MB阴性逃逸变体之间存在重大差异。然而,在克隆谱系实验中,MB蛋白的缺失被证明是可逆的。因此,有人提出解脲脲原体和微小脲原体的多带蛋白受到一种相转换机制的影响,这一机制已在其他几种支原体目细菌中有所描述。