Lal Tamrin M, Sano Motohiko, Ransangan Julian
Microbiology and Fish Disease Laboratory, Borneo Marine Research Institute, Universiti Malaysia Sabah, Jalan UMS, Kota Kinabalu, Sabah, Malaysia.
Laboratory of Fish Pathology, Department of Marine Biosciences, Tokyo University of Marine Science and Technology, Minato-ku, Tokyo, Japan.
J Basic Microbiol. 2016 Aug;56(8):872-88. doi: 10.1002/jobm.201500611. Epub 2016 Mar 9.
Vibrio parahaemolyticus has long been known pathogenic to shrimp but only recently it is also reported pathogenic to tropical cultured marine finfish. Traditionally, bacterial diseases in aquaculture are often treated using synthetic antibiotics but concern due to side effects of these chemicals is elevating hence, new control strategies which are both environmental and consumer friendly, are urgently needed. One promising control strategy is the bacteriophage therapy. In this study, we report the isolation and characterization of a novel vibriophage (VpKK5), belonging to the family Siphoviridae that was specific and capable of complete lysing the fish pathogenic strain of V. parahaemolyticus. The VpKK5 exhibited short eclipse and latent periods of 24 and 36 min, respectively, but with a large burst size of 180 pfu/cell. The genome analysis revealed that the VpKK5 is a novel bacteriophage with the estimated genome size of 56,637 bp and has 53.1% G + C content. The vibriophage has about 80 predicted open reading frames consisted of 37 complete coding sequences which did not match to any protein databases. The analysis also found no lysogeny and virulence genes in the genome of VpKK5. With such genome features, we suspected the vibriophage is novel and could be explored for phage therapy against fish pathogenic strains of V. parahaemolyticus in the near future.
副溶血性弧菌长期以来被认为对虾具有致病性,但直到最近才报道其对热带养殖海水鱼类也具有致病性。传统上,水产养殖中的细菌性疾病通常使用合成抗生素进行治疗,但由于这些化学物质的副作用,人们的担忧日益增加,因此迫切需要既环保又对消费者友好的新控制策略。一种有前景的控制策略是噬菌体疗法。在本研究中,我们报告了一种新型噬菌体(VpKK5)的分离和特性,它属于长尾噬菌体科,具有特异性,能够完全裂解副溶血性弧菌的鱼类致病菌株。VpKK5的潜伏期和隐蔽期较短,分别为24分钟和36分钟,但裂解量较大,为180个噬菌斑形成单位/细胞。基因组分析表明,VpKK5是一种新型噬菌体,估计基因组大小为56,637 bp,G + C含量为53.1%。该噬菌体约有80个预测的开放阅读框,由37个完整的编码序列组成,与任何蛋白质数据库均不匹配。分析还发现VpKK5的基因组中没有溶原性和毒力基因。基于这些基因组特征,我们怀疑该噬菌体是新型的,在不久的将来可用于探索针对副溶血性弧菌鱼类致病菌株的噬菌体疗法。