Roth L E, Stacey G
Department of Zoology, University of Tennesse, Knoxville 37996-0810.
Eur J Cell Biol. 1989 Jun;49(1):24-32.
Two Bradyrhizobium japonicum, Tn5-induced, mutant strains, ML126 and ML150, were studied. Both induce host cell division to form normal-sized nodules that do not fix nitrogen and whose cells have very few bacteroids (Bar-). Early-infection (15 days post infection) cells have much endoplasmic reticulum (ER), numerous Golgi bodies, and large vacuoles that are probably secondary lysosomes. Later the cytoplasm of the host cells of both are dominated by hundreds of vesicles containing only finely fibrous material and that appear to originate by the degradation of the cell walls of the infection threads; they have been named "infection-thread wall degradation vesicles" (IWDV). Phosphotungstic acid-chromic acid (PACA) staining of thin sections shows that IWDV membranes and the plasma membranes of both the cells and infection threads usually stain quite intensely, while the membranes of other cell organelles do not. The membranes of the few symbiosomes present in the mutants also stain with PACA. This evidence suggests that largely the host-cell plasma membrane gives rise to both the vesicle and symbiosome membranes in these mutants. In cells induced by both mutants, ER appears to be deficient, a finding suggesting that an ER-synthesis signal is involved in the normal release process, that ER synthesis is prerequisite to a normal volume of release, and that insufficient ER can impair symbiosome formation. In the mutant-induced infections, normal lysosomes develop and engulf both symbiosomes and cytoplasmic vesicles, but the retardation of this activity is the probable cause of the cytoplasm becoming overloaded with vesicles.
对两株慢生根瘤菌日本种(Bradyrhizobium japonicum)的Tn5诱导突变株ML126和ML150进行了研究。这两株突变株均诱导宿主细胞分裂形成正常大小但不固氮的根瘤,其细胞中类菌体极少(Bar-)。感染早期(感染后15天)的细胞内质网(ER)丰富、高尔基体众多,还有大量可能是次级溶酶体的大液泡。后来,这两株突变株宿主细胞的细胞质中都充斥着数百个仅含有细微纤维状物质的小泡,这些小泡似乎起源于感染丝细胞壁的降解;它们被命名为“感染丝壁降解小泡”(IWDV)。对薄片进行磷钨酸-铬酸(PACA)染色显示,IWDV膜以及细胞和感染丝的质膜通常染色较深,而其他细胞器的膜则不然。突变株中存在的少数共生体的膜也能用PACA染色。这一证据表明,在这些突变株中,小泡膜和共生体膜很大程度上源自宿主细胞质膜。在这两株突变株诱导的细胞中,内质网似乎有缺陷,这一发现表明内质网合成信号参与正常释放过程,内质网合成是正常释放量的前提,内质网不足会损害共生体形成。在突变株诱导的感染中,正常的溶酶体形成并吞噬共生体和细胞质小泡,但这种活动的延迟可能是细胞质中充满小泡的原因。