Department of Bacteriology I, National Institute of Infectious Diseases, Toyama 1-23-1, Shinjuku-ku, Tokyo 162-8640, Japan.
Infect Immun. 2011 Jan;79(1):380-92. doi: 10.1128/IAI.00497-10. Epub 2010 Oct 18.
Meningococcal internalization into human cells is likely to be a consequence of meningococcal adhesion to human epithelial and endothelial cells. Here, we identified three transposon mutants of Neisseria meningitidis that were primarily defective in the internalization of human brain microvascular endothelial cells (HBMEC), with insertions occurring in the gltT (a sodium-independent L-glutamate transporter) gene or its neighboring gene, NMB1964 (unknown function). NMB1964 was tentatively named gltM in this study because of the presence of a mammalian cell entry (MCE)-related domain in the deduced amino acid sequences. The null ΔgltT-ΔgltM N. meningitidis mutant was also defective in the internalization into human umbilical vein endothelial cells and the human lung carcinoma epithelial cell line A549, and the defect was suppressed by transcomplementation of the mutants with gltT(+)-gltM(+) genes. The intracellular survival of the ΔgltT-ΔgltM mutant in HBMEC was not largely different from that of the wild-type strain under our experimental conditions. Introduction of a1-bp deletion and amber or ochre mutations in gltT-gltM genes resulted in the loss of efficient internalization into HBMEC. The defect in meningococcal internalization into HBMEC and L-glutamate uptake in the ΔgltT-ΔgltM mutant were suppressed only in strains expressing both GltT and GltM proteins. The efficiency of meningococcal invasion to HBMEC decreased under L-glutamate-depleted conditions. Furthermore, ezrin, a key membrane-cytoskeleton linker, accumulated beneath colonies of the gltT(+)-gltM(+) N. meningitidis strain but not of the ΔgltT-ΔgltM mutant. These findings suggest that l-glutamate influx via the GltT-GltM L-glutamate ABC transporter serves as a cue for N. meningitidis internalization into host cells.
脑膜炎奈瑟菌进入人体细胞可能是由于其与人体上皮细胞和内皮细胞黏附的结果。在此,我们鉴定了脑膜炎奈瑟菌的三个转座子突变体,这些突变体主要在人类脑微血管内皮细胞(HBMEC)内化中存在缺陷,插入发生在 gltT(一种非钠依赖性 L-谷氨酸转运蛋白)基因或其邻近基因 NMB1964(未知功能)中。在本研究中,由于推测的氨基酸序列中存在哺乳动物细胞进入(MCE)相关结构域,因此 NMB1964 被暂时命名为 gltM。ΔgltT-ΔgltM N. meningitidis 突变体也不能内化入人脐静脉内皮细胞和人肺癌细胞系 A549,并且突变体的缺失可以通过 gltT(+) - gltM(+) 基因的反式互补来抑制。在我们的实验条件下,ΔgltT-ΔgltM 突变体在 HBMEC 中的细胞内生存能力与野生型菌株没有太大差异。在 gltT-gltM 基因中引入 1-bp 缺失和琥珀或赭石突变导致 HBMEC 中有效内化的丧失。只有在表达 GltT 和 GltM 蛋白的菌株中,ΔgltT-ΔgltM 突变体的脑膜炎奈瑟菌内化和 L-谷氨酸摄取缺陷才能被抑制。在 L-谷氨酸耗尽的条件下,脑膜炎奈瑟菌侵袭 HBMEC 的效率降低。此外,ezrin,一种关键的膜-细胞骨架连接蛋白,在 gltT(+) - gltM(+) N. meningitidis 菌株的菌落下积累,但在ΔgltT-ΔgltM 突变体中则不然。这些发现表明,通过 GltT-GltM L-谷氨酸 ABC 转运蛋白的 L-谷氨酸流入为脑膜炎奈瑟菌进入宿主细胞提供了一个线索。