Boleza K A, Burnett L E, Burnett K G
Department of Microbiology and Immunology, Medical University of South Carolina, Charleston 29412, USA.
Fish Shellfish Immunol. 2001 Oct;11(7):593-610. doi: 10.1006/fsim.2001.0339.
Acute hypoxia can cause massive fish and shellfish mortality. Less clear is the role that chronic sublethal hypoxia might play in aquatic animal health. This study tested whether production of reactive oxygen species (ROS) and bactericidal activity of fish phagocytic cells are suppressed under the conditions of decreased oxygen and pH and increased carbon dioxide which occur in the blood and tissue of animals exposed to sublethal hypoxia. Anterior head kidney (AHK) cells of the mummichog, Fundulus heteroclitus, were exposed in parallel to normoxic (pO2=45 torr, pCO2=3.8 torr, pH=7.6) or hypoxic (pO2=15 torr, pCO2=8.0 torr, pH=7.0) conditions and stimulated with a yeast cell wall extract, zymosan. or live Vibrio parahaemolyticus. Hypercapnic hypoxia suppressed zymosan-stimulated ROS production by 76.0% as measured in the chemiluminescence assay and by 58.5% in the nitroblue tetrazolium (NBT) assay. The low O2, high CO2 and low pH conditions also suppressed superoxide production by 75.0 and 47.3% as measured by the NBT assay at two different challenge ratios of cells:bacteria (1:1 and 1:10, respectively). In addition to its effects on ROS production, hypercapnic hypoxia also reduced bactericidal activity by 23.6 and 72.5% at the 1:1 and 1:10 challenge ratios, respectively. Low oxygen levels alone (pO2=15 torr, pCO2=0.76 torr, pH=7.6) did not significantly compromise the killing activity of cells challenged with equal numbers of V. parahaemolyticus. At the higher 1:10 AHK:bacteria challenge ratio, low oxygen caused a small (26.3%) but significant suppression of bactericidal activity as compared to aerial conditions (pO2=155 torr, pCO2=0.76 torr, pH=7.6). This study demonstrates that while hypoxia alone has detrimental effects on immune function, suppression of phagocytic cell activity is compounded by naturally occurring conditions of hypercapnia and low pH, creating conditions that might be exploited by opportunistic pathogens. These results indicate that the adverse health effects of chronic hypercapnic hypoxia might greatly exceed the effects of low oxygen alone.
急性缺氧可导致大量鱼类和贝类死亡。慢性亚致死性缺氧在水生动物健康中可能发挥的作用尚不清楚。本研究测试了在暴露于亚致死性缺氧的动物血液和组织中出现的氧气减少、pH值降低和二氧化碳增加的条件下,活性氧(ROS)的产生以及鱼类吞噬细胞的杀菌活性是否受到抑制。将底鳉(Fundulus heteroclitus)的前肾(AHK)细胞同时暴露于常氧(pO2 = 45托,pCO2 = 3.8托,pH = 7.6)或缺氧(pO2 = 15托,pCO2 = 8.0托,pH = 7.0)条件下,并用酵母细胞壁提取物、zymosan或活的副溶血性弧菌进行刺激。高碳酸血症性缺氧抑制了zymosan刺激的ROS产生,在化学发光测定中为76.0%,在硝基蓝四氮唑(NBT)测定中为58.5%。在细胞与细菌的两种不同挑战比例(分别为1:1和1:10)下,低氧、高二氧化碳和低pH条件也使超氧化物产生分别被抑制了75.0%和47.3%(通过NBT测定)。除了对ROS产生的影响外,高碳酸血症性缺氧在1:1和1:10挑战比例下还分别使杀菌活性降低了23.6%和72.5%。单独的低氧水平(pO2 = 15托,pCO2 = 0.76托,pH = 7.6)并未显著损害用等量副溶血性弧菌攻击的细胞的杀伤活性。在较高的1:10 AHK:细菌挑战比例下,与空气条件(pO2 = 155托,pCO2 = 0.76托,pH = 7.6)相比,低氧导致杀菌活性有小幅度(26.3%)但显著的抑制。本研究表明,虽然单独的缺氧对免疫功能有有害影响,但吞噬细胞活性的抑制因高碳酸血症和低pH的自然条件而加剧,从而创造了可能被机会性病原体利用的条件。这些结果表明,慢性高碳酸血症性缺氧对健康的不利影响可能大大超过单独低氧的影响。