Juíz-Río Sandra, Osorio Carlos R, de Lorenzo Víctor, Lemos Manuel L
Departamento de Biotecnología Microbiana, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas, Campus de Cantoblanco, 28049 Madrid, Spain.
Departamento de Microbiología y Parasitología, Instituto de Acuicultura, Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain.
Microbiology (Reading). 2005 Aug;151(Pt 8):2659-2669. doi: 10.1099/mic.0.27891-0.
Photobacterium damselae subsp. piscicida is the causative agent of fish pasteurellosis, a severe disease affecting cultured marine fish worldwide. In this study, suppression subtractive hybridization was used to identify DNA fragments present in the virulent strain PC554.2, but absent in the avirulent strain EPOY 8803-II. Twenty-one genomic regions of this type (that included twenty-six distinct putative ORFs) were analysed by DNA sequencing. Twenty ORFs encoded proteins with homology to proteins in other bacteria, including four homologues involved in siderophore biosynthesis, and four homologues related to mobile elements; three of these were putative transposases and one was a putative conjugative transposon related to the Vibrio cholerae SXT element. This sequence was shown to be integrated into a prfC gene homologue. Six ORFs showed no significant homology to known bacterial proteins. Among the 21 DNA fragments specific to strain PC554.2, 5 DNA fragments (representing 7 ORFs) were also absent in the avirulent strain ATCC 29690. The analysis of these differential regions, as well as the screening of their presence in a collection of strains, demonstrated the high genetic heterogeneity of this pathogen.
美人鱼发光杆菌杀鱼亚种是鱼类巴氏杆菌病的病原体,这是一种严重影响全球养殖海鱼的疾病。在本研究中,抑制性消减杂交技术被用于鉴定在强毒株PC554.2中存在但无毒株EPOY 8803-II中不存在的DNA片段。通过DNA测序分析了21个这种类型的基因组区域(其中包括26个不同的假定开放阅读框)。20个开放阅读框编码的蛋白质与其他细菌中的蛋白质具有同源性,其中包括4个与铁载体生物合成相关的同源物,以及4个与可移动元件相关的同源物;其中3个是假定的转座酶,1个是与霍乱弧菌SXT元件相关的假定接合转座子。该序列被证明整合到一个prfC基因同源物中。6个开放阅读框与已知细菌蛋白质没有显著同源性。在PC554.2菌株特有的21个DNA片段中,无毒株ATCC 29690中也不存在5个DNA片段(代表7个开放阅读框)。对这些差异区域的分析以及它们在一系列菌株中的存在情况筛选,证明了这种病原体具有高度的遗传异质性。