Institut de Biotecnologia i Biomedicina and Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, Barcelona, Spain.
PLoS One. 2009 Oct 14;4(10):e7452. doi: 10.1371/journal.pone.0007452.
The terminal organelle is a complex structure involved in many aspects of the biology of mycoplasmas such as cell adherence, motility or cell division. Mycoplasma genitalium cells display a single terminal organelle and duplicate this structure prior to cytokinesis in a coordinated manner with the cell division process. Despite the significance of the terminal organelle in mycoplasma virulence, little is known about the mechanisms governing its duplication.
METHODOLOGY/PRINCIPAL FINDINGS: In this study we describe the isolation of a mutant, named T192, with a transposon insertion close to the 3' end of the mg192 gene encoding for P110 adhesin. This mutant shows a truncated P110, low levels of P140 and P110 adhesins, a large number of non-motile cells and a high frequency of new terminal organelle formation. Further analyses revealed that the high rates of new terminal organelle formation in T192 cells are a direct consequence of the reduced levels of P110 and P140 rather than to the expression of a truncated P110. Consistently, the phenotype of the T192 mutant was successfully complemented by the reintroduction of the mg192 WT allele which restored the levels of P110 and P140 to those of the WT strain. Quantification of DAPI-stained DNA also showed that the increase in the number of terminal organelles in T192 cells is not accompanied by a higher DNA content, indicating that terminal organelle duplication does not trigger DNA replication in mycoplasmas.
CONCLUSIONS/SIGNIFICANCE: Our results demonstrate the existence of a mechanism regulating terminal organelle duplication in M. genitalium and strongly suggest the implication of P110 and P140 adhesins in this mechanism.
末端器是一个复杂的结构,参与支原体生物学的许多方面,如细胞黏附、运动或细胞分裂。生殖道支原体细胞显示出单个末端器,并在有丝分裂前以协调的方式与细胞分裂过程一起复制这个结构。尽管末端器在支原体毒力中具有重要意义,但对于控制其复制的机制知之甚少。
方法/主要发现:在这项研究中,我们描述了一个突变体 T192 的分离,该突变体带有一个转座子插入,靠近编码 P110 黏附素的 mg192 基因的 3'端。该突变体显示出截断的 P110、低水平的 P140 和 P110 黏附素、大量的非运动细胞和高频率的新末端器形成。进一步的分析表明,T192 细胞中新末端器形成的高频率是 P110 和 P140 水平降低的直接结果,而不是表达截断的 P110 的结果。一致地,T192 突变体的表型通过引入 mg192 WT 等位基因成功地得到了互补,该等位基因将 P110 和 P140 的水平恢复到 WT 株的水平。DAPI 染色 DNA 的定量也表明,T192 细胞中端末器数量的增加并不伴随着 DNA 含量的增加,这表明末端器复制不会在支原体中触发 DNA 复制。
结论/意义:我们的结果证明了生殖道支原体末端器复制的调节机制的存在,并强烈表明 P110 和 P140 黏附素在这个机制中具有重要作用。