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648                                  渔  业  研  究                                     第 47 卷

              灿烂弧菌、溶藻弧菌具有不同的关键结构域导致的。                               [J]. Aquaculture, 2020, 519: 734897.
                  抗生素曾经在弧菌病的防治中发挥重要作用,                        [  4  ]   Gómez-León J, Villamil L, Lemos M L, et al. Isolation
              但是抗生素在环境中的残留亦可导致病原菌抗性基                                of Vibrio alginolyticus and Vibrio splendidus from aqua-
              因的产生、传播及环境微生态的破坏                [34] 。与抗生素            cultured carpet shell clam (Ruditapes decussatus) larvae
              相比, “抗毒力”策略靶向病原菌的致病因子与致                               associated with mass mortalities[J]. Applied and Envir-
              病过程,在病害防控中发挥更为积极的作用                      [35] 。       onmental Microbiology, 2005, 71(1): 98 − 104.
              本研究在明确大牡蛎弧菌            S2  胶原酶作为致病因子            [  5  ]   Travers M A, Miller K B, Roque A, et al. Bacterial dis-
              及其对菲律宾蛤仔免疫调控基础上,以大牡蛎弧                                 eases in marine bivalves[J]. Journal of Invertebrate Patho-
              菌  S2  胶原酶活性为抑制靶标,从蛋白酶抑制剂中                            logy, 2015, 131: 11 − 31.
                                                              [  6  ]   Garnier M, Labreuche Y, Garcia C, et al. Evidence for
              筛选了有效药物,即苯扎氯氨、盐酸巴马汀、2’-
                                                                    the involvement of pathogenic bacteria in summer mor-
              羟基查尔酮、氯己定、核黄素和原花青素。这些药
                                                                    talities  of  the  Pacific  oyster  Crassostrea  gigas[J].  Mi-
              物均可与大牡蛎弧菌          S2  胶原酶结合,进而对胶原
                                                                    crobial Ecology, 2007, 53(2): 187 − 196.
              酶活性产生抑制作用。这是首次针对水产养殖动物
                                                              [  7  ]   Guillard R R L. Further evidence of the destruction of bi-
              胶原酶活性为指标的生物制剂筛选,为后续弧菌病
                                                                    valve larvae by bacteria[J]. The Biological Bulletin, 1959,
              的防控提供新思路。
                                                                    117(2): 258 − 266.
                  本研究克隆了大牡蛎弧菌            S2  胶原酶,并在大
                                                              [  8  ]   Kesarcodi-Watson  A,  Kaspar  H,  Lategan  M  J,  et  al.
              肠杆菌表达菌株中重组表达,获得了                rCol 。rCol Vc
                                                  Vc
                                                                    Challenge  of  New  Zealand  Greenshell™  mussel  Perna
              可降解菲律宾蛤仔的胶原蛋白,且注射                  rCol V c  可导
                                                                    canaliculus larvae using two Vibrio pathogens: a hatch-
              致菲律宾蛤仔个体存活率下降,因此胶原酶是大牡
                                                                    ery study[J]. Diseases of Aquatic Organisms, 2009, 86
              蛎弧菌    S2  的致病因子。注射胶原酶后,菲律宾蛤
                                                                    (1): 15 − 20.
              仔体内下调的差异表达基因显著富集于                     DNA  重
                                                              [  9  ]   Rahmani A, Delavat F, Lambert C, et al. Implication of
              组、DNA    整合、DNA     代谢等生物学过程,以及肌
                                                                    the type Ⅳ secretion system in the pathogenicity of Vi-
              动蛋白结合、细胞骨架蛋白结合等分子结合功能;
                                                                    brio tapetis, the etiological agent of brown ring disease
              下调的差异表达基因主要富集于肌动蛋白细胞骨架                                affecting  the  Manila  clam  Ruditapes  philippinarum[J].
              调控通路。这些发现为进一步理解弧菌的致病机制                                Frontiers in Cellular and Infection Microbiology, 2021,
              提供了重要的理论基础,同时也为菲律宾蛤仔弧菌
                                                                    11: 634427.
              病的防控提供了潜在的靶位点。                                  [10]   Liu Y, Liao K, Zhu Y, et al. Effects of dietary taurine on
                                                                    growth, taurine metabolism and Vibrio crassostreae res-
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