Banin E, Israely T, Kushmaro A, Loya Y, Orr E, Rosenberg E
Department of Molecular Microbiology and Biotechnology, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Ramat Aviv, Israel.
Appl Environ Microbiol. 2000 Jul;66(7):3031-6. doi: 10.1128/AEM.66.7.3031-3036.2000.
Inoculation of the coral-bleaching bacterium Vibrio shiloi into seawater containing its host Oculina patagonica led to adhesion of the bacteria to the coral surface via a beta-D-galactose receptor, followed by penetration of the bacteria into the coral tissue. The internalized V. shiloi cells were observed inside the exodermal layer of the coral by electron microscopy and fluorescence microscopy using specific anti-V. shiloi antibodies to stain the intracellular bacteria. At 29 degrees C, 80% of the bacteria bound to the coral within 8 h. Penetration, measured by the viable count (gentamicin invasion assay) inside the coral tissue, was 5.6, 20.9, and 21.7% of the initial inoculum at 8, 12, and 24 h, respectively. The viable count in the coral tissue decreased to 5.3% at 48 h, and none could be detected at 72 h. Determination of V. shiloi total counts (using the anti-V. shiloi antibodies) in the coral tissue showed results similar to viable counts for the first 12 h of infection. After 12 h, however, the total count more than doubled from 12 to 24 h and continued to rise, reaching a value 6 times that of the initial inoculum at 72 h. Thus, the intracellular V. shiloi organisms were transformed into a form that could multiply inside the coral tissue but did not form colonies on agar medium. Internalization of the bacteria was accompanied by the production of high concentrations of V. shiloi toxin P activity in the coral tissue. Internalization and multiplication of V. shiloi are discussed in terms of the mechanism of bacterial bleaching of corals.
将导致珊瑚白化的希氏弧菌接种到含有其宿主巴塔哥尼亚石珊瑚的海水中,细菌会通过β-D-半乳糖受体黏附到珊瑚表面,随后侵入珊瑚组织。利用电子显微镜和荧光显微镜,借助特异性抗希氏弧菌抗体对细胞内细菌进行染色,在珊瑚的外皮层内观察到了内化的希氏弧菌细胞。在29摄氏度下,80%的细菌在8小时内与珊瑚结合。通过珊瑚组织内的活菌计数(庆大霉素侵袭试验)测定,在8、12和24小时时,侵入珊瑚组织的细菌分别占初始接种量的5.6%、20.9%和21.7%。在48小时时,珊瑚组织中的活菌计数降至5.3%,在72小时时无法检测到活菌。对珊瑚组织中希氏弧菌总数(使用抗希氏弧菌抗体)的测定结果显示,在感染的前12小时内与活菌计数相似。然而,12小时后,总数在12至24小时内增加了一倍多,并持续上升,在72小时时达到初始接种量的6倍。因此,细胞内的希氏弧菌转变为一种能够在珊瑚组织内繁殖但在琼脂培养基上不形成菌落 的形式。细菌的内化伴随着珊瑚组织中高浓度希氏弧菌毒素P活性的产生。从珊瑚细菌白化机制的角度讨论了希氏弧菌的内化和繁殖。