Saldarriaga-Córdoba Mónica, Avendaño-Herrera Ruben
Centro de Investigación en Recursos Naturales y Sustentabilidad, Universidad Bernardo O'Higgins, Santiago, Chile.
Centro FONDAP, Interdisciplinary Center for Aquaculture Research (INCAR), Universidad Andrés Bello, Viña del Mar, Chile.
J Fish Dis. 2022 Aug;45(8):1173-1188. doi: 10.1111/jfd.13653. Epub 2022 May 23.
Renibacterium salmoninarum, a Gram-positive intracellular pathogen, is the causative agent of bacterial kidney disease (BKD), the impacts of which are high mortalities and economic losses for the salmon industry. This study provides novel analyses for the whole-genome sequences of 50 R. salmoninarum isolates and the reference strain ATCC 33209 using a pan-genomic approach to elucidate phylogenomic relationships and identify unique and shared genes associated with pathogenicity and infection mechanisms. Genome size varied from 3,061,638 to 3,155,332 bp; gene count from 3452 to 3580; and predicted coding sequences from 3402 to 3527. Comparative analyses revealed an open, but approaching closed, pan-genome. The pan-genome analysis recovered 4064 genes, with a core genome containing 3306 genes. Phylogenetic analysis of R. salmoninarum showed high genomic homogeneity, apart from one isolate obtained from Salmo trutta in Norway. All genomes presented the 57-kDa protein (p57). Strain ATCC 33209 and the Chilean isolates H-2 and DJ2R presented two copies of the msa gene, while the remaining isolates had one copy. The pan-genome analysis further identified differences in the number of copies and length of the signalling peptide for p57, the principal virulence factor reported for this bacterium. This heterogeneity could be associated with the secretion levels of p57, potentially influencing virulence. Additionally identified were numerous common genes related to iron uptake, the stress response and regulation, and cell signalling-all of which constitute the pathogenic repertoire of R. salmoninarum. This investigation provides information that is applicable in future studies for identifying therapeutic targets and/or for designing new strategies (e.g., vaccines) to prevent BKD infections in salmon farming.
鲑肾杆菌是一种革兰氏阳性细胞内病原体,是细菌性肾病(BKD)的病原体,该病会导致高死亡率并给鲑鱼产业造成经济损失。本研究采用泛基因组方法,对50株鲑肾杆菌分离株和参考菌株ATCC 33209的全基因组序列进行了新的分析,以阐明系统发育关系,并识别与致病性和感染机制相关的独特基因和共享基因。基因组大小从3,061,638到3,155,332 bp不等;基因数量从3452到3580个;预测的编码序列从3402到3527个。比较分析揭示了一个开放但接近封闭的泛基因组。泛基因组分析共获得4064个基因,核心基因组包含3306个基因。除了从挪威褐鳟分离得到的一个菌株外,鲑肾杆菌的系统发育分析显示出高度的基因组同质性。所有基因组都呈现出57 kDa蛋白(p57)。菌株ATCC 33209以及智利分离株H-2和DJ2R呈现出两个拷贝的msa基因,而其余分离株有一个拷贝。泛基因组分析进一步确定了p57信号肽的拷贝数和长度的差异,p57是该细菌报道的主要毒力因子。这种异质性可能与p57的分泌水平有关,可能影响毒力。此外,还鉴定出许多与铁摄取、应激反应和调节以及细胞信号传导相关的共同基因,所有这些都构成了鲑肾杆菌的致病库。这项研究提供的信息可应用于未来的研究,以识别治疗靶点和/或设计预防鲑鱼养殖中BKD感染的新策略(如疫苗)。