Piazza Veronica, Dragić Ivanka, Sepčić Kristina, Faimali Marco, Garaventa Francesca, Turk Tom, Berne Sabina
ISMAR-CNR Institute of Marine Science, U.O.S. Genova, Via De Marini 6, 16149 Genova, Italy.
Department of Biology, Biotechnical Faculty, University of Ljubljana, Večna pot 111, Ljubljana 1000, Slovenia.
Mar Drugs. 2014 Apr 2;12(4):1959-76. doi: 10.3390/md12041959.
Polymeric alkylpyridinium salts (poly-APS) isolated from the Mediterranean marine sponge, Haliclona (Rhizoniera) sarai, effectively inhibit barnacle larva settlement and natural marine biofilm formation through a non-toxic and reversible mechanism. Potential use of poly-APS-like compounds as antifouling agents led to the chemical synthesis of monomeric and oligomeric 3-alkylpyridinium analogues. However, these are less efficient in settlement assays and have greater toxicity than the natural polymers. Recently, a new chemical synthesis method enabled the production of poly-APS analogues with antibacterial, antifungal and anti-acetylcholinesterase activities. The present study examines the antifouling properties and toxicity of six of these synthetic poly-APS using the barnacle (Amphibalanus amphitrite) as a model (cyprids and II stage nauplii larvae) in settlement, acute and sub-acute toxicity assays. Two compounds, APS8 and APS12-3, show antifouling effects very similar to natural poly-APS, with an anti-settlement effective concentration that inhibits 50% of the cyprid population settlement (EC₅₀) after 24 h of 0.32 mg/L and 0.89 mg/L, respectively. The toxicity of APS8 is negligible, while APS12-3 is three-fold more toxic (24-h LC₅₀: nauplii, 11.60 mg/L; cyprids, 61.13 mg/L) than natural poly-APS. This toxicity of APS12-3 towards nauplii is, however, 60-fold and 1200-fold lower than that of the common co-biocides, Zn- and Cu-pyrithione, respectively. Additionally, exposure to APS12-3 for 24 and 48 h inhibits the naupliar swimming ability with respective IC₅₀ of 4.83 and 1.86 mg/L.
从地中海海洋海绵Haliclona (Rhizoniera) sarai中分离出的聚合烷基吡啶盐(poly-APS),通过无毒且可逆的机制有效抑制藤壶幼虫附着和天然海洋生物膜形成。聚-APS类化合物作为防污剂的潜在用途促使了单体和低聚3-烷基吡啶类似物的化学合成。然而,这些类似物在附着试验中效率较低,且比天然聚合物毒性更大。最近,一种新的化学合成方法能够生产具有抗菌、抗真菌和抗乙酰胆碱酯酶活性的聚-APS类似物。本研究以藤壶(Amphibalanus amphitrite)为模型(无节幼虫和Ⅱ期无节幼虫),在附着、急性和亚急性毒性试验中检测了六种此类合成聚-APS的防污性能和毒性。两种化合物APS8和APS12-3表现出与天然聚-APS非常相似的防污效果,其抗附着有效浓度分别为0.32 mg/L和0.89 mg/L,在24小时后可抑制50%的金星幼虫附着(EC₅₀)。APS8的毒性可忽略不计,而APS12-3的毒性比天然聚-APS高三倍(24小时LC₅₀:无节幼虫为11.60 mg/L;金星幼虫为61.13 mg/L)。然而,APS12-3对无节幼虫的这种毒性分别比常见的辅助杀生剂吡啶硫酮锌和吡啶硫酮铜低60倍和1200倍。此外,暴露于APS12-3 24小时和48小时会抑制无节幼虫的游泳能力,其IC₅₀分别为4.83 mg/L和1.86 mg/L。