Mobilizable multidrug resistance plasmid identified in Staphylococcus xylosus isolated from fermented soybean food.

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Sumin Seo, Do-Won Jeong, Sooyoung Sul, Jong-Hoon Lee
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引用次数: 0

Abstract

We identified two Staphylococcus xylosus strains that were isolated from the same Korean fermented soybean food with different antibiotic resistance (AR) profiles. Strain 14BME10 showed multidrug resistance to erythromycin and tetracycline, whereas strain 14BME18 was resistant to tetracycline only. We sought to elucidate the genetic background of the AR in these strains. A comparative genomic analysis with three other antibiotic-sensitive S. xylosus strains revealed AR determinants located on two mobilizable plasmids in the isolates. The 73.7-kb plasmid p14BME10-1, encoding the ABC-F-type ribosomal protection protein gene msr(A) and the Mph(C) family macrolide 2'-phosphotransferase gene mph(C), might have contributed to erythromycin resistance. The 4.4-kb plasmid harboring the tetracycline efflux major facilitator superfamily (MFS) transporter gene tet(K) conferred tetracycline resistance and showed 100% DNA sequence identity with the prototype tetracycline resistance plasmid pT181, widely identified in staphylococci. We discovered that the MOBP relaxase gene cluster in p14BME10-1 consists of four genes and an oriT, which might be involved in plasmid mobilization and was also found in many staphylococcal plasmids. The plasmid p14BME10-1 harbors multiple genes for replication, mobilization, transposition, recombination, and resistance to erythromycin, streptomycin, and bacitracin, indicating several occurrences of recombination and integration events but lacks the genes necessary for conjugal transfer.

发酵大豆食品中木糖葡萄球菌可动员多药耐药质粒的鉴定。
我们从同一种韩国发酵大豆食品中分离出两株木糖葡萄球菌,它们具有不同的抗生素耐药性。菌株14BME10对红霉素和四环素多重耐药,而菌株14BME18仅对四环素耐药。我们试图阐明这些菌株抗生素耐药性的遗传背景。与其他三种抗生素敏感的木糖葡萄球菌菌株的比较基因组分析显示,菌株的抗生素抗性决定因素位于两个可移动的质粒上。73.7 kb的质粒p14BME10-1编码ABC-F型核糖体保护蛋白基因msr(A)和Mph(C)家族大环内酯2'-磷酸转移酶基因Mph(C),可能与红霉素耐药有关。含有四环素外排MFS转运基因tet(K)的4.4 kb质粒具有四环素抗性,并与在葡萄球菌中广泛鉴定的原型四环素抗性质粒pT181的DNA序列100%一致。我们发现p14BME10-1中的MOBP松弛基因簇由四个基因和一个oriT组成,该基因簇可能参与质粒动员,并且在许多葡萄球菌质粒中也发现。质粒p14BME10-1含有多个复制、动员、转位、重组和对红霉素、链霉素和杆菌素耐药的基因,表明发生过多次重组和整合事件,但缺乏偶联转移所需的基因。
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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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