Department of Pathology, Bacteriology and Avian Diseases, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820, Merelbeke, Belgium.
Flanders Marine Institute, Wandelaarkaai 7, 8400, Ostend, Belgium.
Vet Res. 2021 Feb 12;52(1):18. doi: 10.1186/s13567-021-00899-w.
This study reports the comparative analyses of four Flavobacterium columnare isolates that have different virulence and antimicrobial resistance patterns. The main research goal was to reveal new insights into possible virulence genes by comparing the genomes of bacterial isolates that could induce tissue damage and mortality versus the genome of a non-virulent isolate. The results indicated that only the genomes of the virulent isolates possessed unique genes encoding amongst others a methyl-accepting chemotaxis protein possibly involved in the initial colonization of tissue, and several VgrG proteins engaged in interbacterial competition. Furthermore, comparisons of genes unique for the genomes of the highly virulent (HV) carp and trout isolates versus the, respectively, low and non-virulent carp and trout isolates were performed. An important part of the identified unique virulence genes of the HV-trout isolate was located in one particular gene region identified as a genomic island. This region contained araC and nodT genes, both linked to pathogenic and multidrug-resistance, and a luxR-gene, functional in bacterial cell-to-cell communication. Furthermore, the genome of the HV-trout isolate possessed unique sugar-transferases possibly important in bacterial adhesion. The second research goal was to obtain insights into the genetic basis of acquired antimicrobial resistance. Several point-mutations were discovered in gyrase-genes of an isolate showing phenotypic resistance towards first and second-generation quinolones, which were absent in isolates susceptible to quinolones. Tetracycline-resistance gene tetA was found in an isolate displaying acquired phenotypic resistance towards oxytetracycline. Although not localized on a prophage, several flanking genes were indicative of the gene's mobile character.
本研究报告了四种不同毒力和抗菌药物耐药模式的柱状黄杆菌分离株的比较分析。主要研究目标是通过比较能够引起组织损伤和死亡率的细菌分离株与非毒性分离株的基因组,揭示可能的毒力基因的新见解。结果表明,只有毒性分离株的基因组具有独特的基因,这些基因编码的甲基接受趋化蛋白可能参与组织的初始定植,以及几种参与细菌间竞争的 VgrG 蛋白。此外,还比较了高毒力(HV)鲤鱼和鳜鱼分离株的基因组中特有的基因与相应的低毒力和非毒力鲤鱼和鳜鱼分离株的基因组中特有的基因。鉴定出的 HV-鳜鱼分离株的独特毒力基因的一个重要部分位于一个特定的基因区域,该区域被确定为一个基因组岛。该区域包含 araC 和 nodT 基因,两者都与致病性和多药耐药性有关,以及一个 luxR 基因,该基因在细菌细胞间通讯中起作用。此外,HV-鳜鱼分离株的基因组具有独特的糖转移酶,可能在细菌黏附中起重要作用。第二个研究目标是了解获得性抗菌药物耐药的遗传基础。在对第一代和第二代喹诺酮类药物表现出表型耐药的分离株中发现了拓扑异构酶基因中的几个点突变,而对喹诺酮类药物敏感的分离株中不存在这些突变。在对土霉素表现出获得性表型耐药的分离株中发现了四环素耐药基因 tetA。虽然该基因不在噬菌体上,但几个侧翼基因表明该基因具有移动性。