Macey Brett M, Rathburn Charles K, Thibodeaux Lindy K, Burnett Louis E, Burnett Karen G
Grice Marine Laboratory, College of Charleston and Hollings Marine Laboratory, Charleston, SC 29412, USA.
Fish Shellfish Immunol. 2008 Dec;25(6):718-30. doi: 10.1016/j.fsi.2008.02.009. Epub 2008 Feb 19.
The Atlantic blue crab, Callinectes sapidus (Rathbun), lives in a bacteria-rich environment that experiences daily fluctuations in water quality. In the present study, we tested the hypothesis that crustaceans with prior or ongoing exposure to bacteria in their hemolymph have an increased susceptibility to subsequent infections, and that acute exposure to low dissolved oxygen (hypoxia) and elevated carbon dioxide levels (hypercapnia) may further confound the ability of blue crabs to counter a subsequent infection. Adult male blue crabs held in well-aerated (normoxic; P O2=20.7 kPA; CO(2)<0.06 kPa; pH 7.8-8.0) or hypercapnic hypoxic (HH; P O2=4 kPa; CO(2)=1.8 kPa; pH 6.9-7.2) seawater received an injection (pre-challenge dose) of 1 x 10(5)Vibrio campbellii g(-1) crab. Control animals were injected with an equivalent dose of HEPES-buffered saline (1 microl g(-1) crab). At 2h or 24h after the pre-challenge injection, both Vibrio and saline-pre-challenged animals were injected with a dose of live V. campbellii (1 x 10(5)g(-1) crab). This second injection will be referred to as a second injection or challenge injection. Degradation in or physical removal of intact bacteria from hemolymph was quantified using real-time PCR; bacteriostasis was quantified as the percentage of intact bacteria that could not be recovered by selective plating. We demonstrated that bacteriostasis occurs in the hemolymph of blue crabs. Furthermore, blue crabs that received a challenge injection 2h after a pre-challenge dose of V. campbellii cleared culturable bacteria from their hemolymph more rapidly when compared to animals that received a pre-challenge dose of saline. This enhanced clearance of culturable bacteria was associated with an increase in antibacterial activity in the cell-free hemolymph. However, the enhanced clearance of culturable bacteria disappeared when the time interval between the pre-challenge and challenge dose was extended to 24h and when crabs were held in HH seawater throughout the experiment. Neither the time interval between the pre-challenge and the challenge dose nor exposure to HH altered the pattern of intact bacterial clearance in blue crabs. These results demonstrate that prior exposure to bacteria does not increase the susceptibility of C. sapidus to a second, sublethal dose of V. campbellii. In fact, a recent exposure to V. campbellii enhances the ability of blue crabs to render bacteria non-culturable and the immune mechanisms/effectors responsible for this are short lived and appear to be sensitive to low dissolved oxygen and high carbon dioxide concentrations in the environment.
大西洋蓝蟹(Callinectes sapidus,拉特本)生活在富含细菌的环境中,水质每天都会发生波动。在本研究中,我们检验了以下假设:血淋巴中先前或持续接触细菌的甲壳类动物对后续感染的易感性增加,并且急性暴露于低溶解氧(缺氧)和高二氧化碳水平(高碳酸血症)可能会进一步混淆蓝蟹抵抗后续感染的能力。将成年雄性蓝蟹饲养在通气良好(常氧;PO2 = 20.7 kPA;CO2 < 0.06 kPa;pH 7.8 - 8.0)或高碳酸血症缺氧(HH;PO2 = 4 kPa;CO2 = 1.8 kPa;pH 6.9 - 7.2)的海水中,给它们注射(预激发剂量)每克蟹1×105坎氏弧菌。对照动物注射等量的HEPES缓冲盐水(每克蟹1微升)。在预激发注射后2小时或24小时,给弧菌预激发组和盐水预激发组动物都注射一剂活的坎氏弧菌(每克蟹1×105)。第二次注射将被称为第二次注射或激发注射。使用实时PCR对血淋巴中完整细菌的降解或物理清除进行定量;抑菌作用以通过选择性平板培养无法回收的完整细菌的百分比来定量。我们证明了蓝蟹的血淋巴中存在抑菌作用。此外,与接受盐水预激发剂量的动物相比,在接受坎氏弧菌预激发剂量2小时后接受激发注射的蓝蟹能更快地从其血淋巴中清除可培养细菌。可培养细菌的这种增强清除与无细胞血淋巴中抗菌活性的增加有关。然而,当预激发和激发剂量之间的时间间隔延长至24小时以及在整个实验过程中将蟹饲养在HH海水中时,可培养细菌的增强清除消失了。预激发和激发剂量之间的时间间隔以及暴露于HH均未改变蓝蟹中完整细菌清除的模式。这些结果表明,先前接触细菌不会增加锯缘青蟹对第二次亚致死剂量坎氏弧菌的易感性。事实上,最近接触坎氏弧菌增强了蓝蟹使细菌不可培养的能力,负责此作用的免疫机制/效应物寿命短暂,并且似乎对环境中的低溶解氧和高二氧化碳浓度敏感。