Nyholm Spencer V, Deplancke Bart, Gaskins H Rex, Apicella Michael A, McFall-Ngai Margaret J
Pacific Biomedical Research Center, Kewalo Marine Laboratory, University of Hawaii, Honolulu, Hawaii 96813, USA.
Appl Environ Microbiol. 2002 Oct;68(10):5113-22. doi: 10.1128/AEM.68.10.5113-5122.2002.
During light organ colonization of the squid Euprymna scolopes by Vibrio fischeri, host-derived mucus provides a surface upon which environmental V. fischeri forms a biofilm and aggregates prior to colonization. In this study we defined the temporal and spatial characteristics of this process. Although permanent colonization is specific to certain strains of V. fischeri, confocal microscopy analyses revealed that light organ crypt spaces took up nonspecific bacteria and particles that were less than 2 micro m in diameter during the first hour after hatching. However, within 2 h after inoculation, these cells or particles were not detectable, and further entry by nonspecific bacteria or particles appeared to be blocked. Exposure to environmental gram-negative or -positive bacteria or bacterial peptidoglycan caused the cells of the organ's superficial ciliated epithelium to release dense mucin stores at 1 to 2 h after hatching that were used to form the substrate upon which V. fischeri formed a biofilm and aggregated. Whereas the uncolonized organ surface continued to shed mucus, within 48 h of symbiont colonization mucus shedding ceased and the formation of bacterial aggregations was no longer observed. Eliminating the symbiont from the crypts with antibiotics restored the ability of the ciliated fields to secrete mucus and aggregate bacteria. While colonization by V. fischeri inhibited mucus secretion by the surface epithelium, secretion of host-derived mucus was induced in the crypt spaces. Together, these data indicate that although initiation of mucus secretion from the superficial epithelium is nonspecific, the inhibition of mucus secretion in these cells and the concomitant induction of secretion in the crypt cells are specific to natural colonization by V. fischeri.
在费氏弧菌定殖于夏威夷短尾鱿鱼的发光器官的过程中,宿主来源的黏液提供了一个表面,环境中的费氏弧菌在定殖之前会在该表面形成生物膜并聚集。在本研究中,我们定义了这一过程的时间和空间特征。虽然永久定殖特定于某些费氏弧菌菌株,但共聚焦显微镜分析显示,在孵化后的第一个小时内,发光器官隐窝空间摄取了直径小于2微米的非特异性细菌和颗粒。然而,在接种后2小时内,这些细胞或颗粒无法检测到,并且非特异性细菌或颗粒的进一步进入似乎被阻断。在孵化后1至2小时,暴露于环境中的革兰氏阴性或阳性细菌或细菌肽聚糖会导致器官表面纤毛上皮细胞释放密集的黏蛋白储存,这些黏蛋白用于形成费氏弧菌形成生物膜并聚集的底物。未定殖的器官表面持续分泌黏液,而在共生菌定殖48小时内,黏液分泌停止,并且不再观察到细菌聚集的形成。用抗生素从隐窝中清除共生菌可恢复纤毛区域分泌黏液和聚集细菌的能力。虽然费氏弧菌的定殖抑制了表面上皮细胞的黏液分泌,但在隐窝空间中诱导了宿主来源黏液的分泌。总之,这些数据表明,虽然表面上皮细胞黏液分泌的起始是非特异性的,但这些细胞中黏液分泌的抑制以及隐窝细胞中分泌的伴随诱导对于费氏弧菌的自然定殖是特异性的。