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迟钝爱德华氏菌的大型抗生素抗性质粒有助于其在鱼类中的毒力。

Large antibiotic-resistance plasmid of Edwardsiella tarda contributes to virulence in fish.

机构信息

Department of Microbiology, Pusan National University, Busan 609-735, South Korea.

出版信息

Microb Pathog. 2012 May;52(5):259-66. doi: 10.1016/j.micpath.2012.01.006. Epub 2012 Feb 7.

Abstract

Edwardsiella tarda, an enteric gram negative bacterium, infects a wide range of fish and causes a systemic fish disease called edwardsiellosis. E. tarda CK41, isolated from Japanese flounder diagnosed with edwardsiellosis, has exhibited a high degree of resistance to multiple antibiotics, including kanamycin, tetracycline, streptomycin, among others. As the bacterial antibiotic-resistance genes are usually contained in plasmids, we hypothesized that E. tarda CK41 may harbor one or more plasmids for antibiotic resistance. We showed the existence of plasmids in E. tarda CK41, and the size of the plasmid, designated as pCK41, was estimated to be approximately 70 kb. Escherichia coli DH5α transformed by the pCK41 plasmid exhibited an antibiotic-resistance phenotype against kanamycin (30 μg/mL), tetracycline (30 μg/mL), and streptomycin (10 μg/mL), indicating the existence of at least 3 antibiotic-resistance genes in pCK41. Through a procedure for pCK41 plasmid curing, a plasmid-cured strain, designated as E. tarda CK108, was identified, which was unable to grow in the presence of either kanamycin or tetracycline. As virulence-associated genes are occasionally encoded in bacterial plasmids, we examined the virulence of E. tarda CK108 in Japanese flounder. The virulence of plasmid-cured E. tarda CK108 was lower (survival rate 80%) than that of CK41 (20%), indicating the existence of virulence-associated genes in pCK41. The strain also appeared to be attenuated in both goldfish and zebrafish pathogenesis models. To analyze genes for antibiotic resistance and virulence in pCK41, the entire nucleotide sequences of pCK41 were determined (GenBank accession number: HQ332785). A total of 84 open reading frames (ORFs) were annotated. The pCK41 plasmid consists of potential virulence genes, transposases, plasmid maintenance genes, antibiotic-resistance genes (including kanamycin, tetracycline, and streptomycin), conjugal transfer genes, and unknown ORFs. These results suggest that pCK41 is a virulence plasmid of substantial importance in the E. tarda pathogenesis to fish.

摘要

迟缓爱德华氏菌是一种肠道革兰氏阴性菌,可感染多种鱼类并引起全身性鱼类疾病,称为爱德华氏菌病。从被诊断患有爱德华氏菌病的日本牙鲆中分离出的迟缓爱德华氏菌 CK41 对多种抗生素(包括卡那霉素、四环素、链霉素等)表现出高度耐药性。由于细菌抗生素耐药基因通常包含在质粒中,我们假设迟缓爱德华氏菌 CK41 可能携带一个或多个抗生素耐药质粒。我们证明了迟缓爱德华氏菌 CK41 中存在质粒,并且质粒的大小,命名为 pCK41,估计约为 70kb。用 pCK41 质粒转化的大肠杆菌 DH5α 对卡那霉素(30μg/mL)、四环素(30μg/mL)和链霉素(10μg/mL)表现出抗生素耐药表型,表明 pCK41 中至少存在 3 个抗生素耐药基因。通过 pCK41 质粒消除程序,鉴定出一种不能在卡那霉素或四环素存在的情况下生长的质粒消除株,命名为迟缓爱德华氏菌 CK108。由于毒力相关基因偶尔编码在细菌质粒中,我们检查了迟缓爱德华氏菌 CK108 在日本牙鲆中的毒力。质粒消除的迟缓爱德华氏菌 CK108 的毒力较低(存活率 80%),低于 CK41(20%),表明 pCK41 中存在毒力相关基因。该菌株在金鱼和斑马鱼发病模型中也表现出减毒。为了分析 pCK41 中的抗生素耐药和毒力基因,我们确定了 pCK41 的整个核苷酸序列(GenBank 登录号:HQ332785)。共注释了 84 个开放阅读框(ORFs)。pCK41 质粒由潜在的毒力基因、转座酶、质粒维持基因、抗生素耐药基因(包括卡那霉素、四环素和链霉素)、共轭转移基因和未知 ORFs 组成。这些结果表明,pCK41 是迟缓爱德华氏菌对鱼类发病机制中重要的毒力质粒。

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