首页> 外文期刊>International Journal of Genomics >Florfenicol Resistance in Enterobacteriaceae and Whole-Genome Sequence Analysis of Florfenicol-Resistant Leclercia adecarboxylata Strain R25
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Florfenicol Resistance in Enterobacteriaceae and Whole-Genome Sequence Analysis of Florfenicol-Resistant Leclercia adecarboxylata Strain R25

机译:氟苯纤维植物植物植物抗性叶绿素抗性叶片菌菌和全基因组序列分析R25

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Due to inappropriate use, florfenicol resistance is becoming increasingly serious among animal respiratory tract and gut bacteria. To detect the florfenicol resistance mechanism among Enterobacteriaceae bacteria, 292 isolates from animal feces were examined. The agar dilution method was conducted to determine the minimum inhibitory concentration (MIC) for florfenicol, and polymerase chain reaction (PCR) was performed to detect florfenicol resistance genes. To further explore the molecular mechanism of florfenicol resistance, the whole-genome Leclercia adecarboxylata R25 was sequenced. Of the strains tested, 61.6% (180/292) were resistant to florfenicol, 64.4% (188/292) were positive for floR, and 1.0% (3/292) for cfr. The whole-genome sequence analysis of L. adecarboxylata R25 revealed that the floR gene is carried by a transposon and located on a plasmid (pLA-64). Seven other resistance genes are also encoded on pLA-64, all of which were found to be related to mobile genetic elements. The sequences sharing the greatest similarities to pLA-64 are the plasmids p02085-tetA of Citrobacter freundii and p234 and p388, both from Enterobacter cloacae. The resistance gene-related mobile genetic elements also share homologous sequences from different species or genera of bacteria. These findings indicate that floR mainly contributes to the high rate of florfenicol resistance among Enterobacteriaceae. The resistance gene-related mobile genetic elements encoded by pLA-64 may be transferred among bacteria of different species or genera, resulting in resistance dissemination.
机译:由于使用不当,弗洛林比洛酚抗性在动物呼吸道和肠道细菌中越来越严重。为了检测肠杆菌的细菌之间的氟苯硅胶质机制,检查了动物粪便的292分离物。进行琼脂稀释方法以确定氟苯氰基酚的最小抑制浓度(MIC),并进行聚合酶链式反应(PCR)以检测氟苯酯抗性基因。为了进一步探讨氟苯硅醇抗性的分子机制,对整个基因组leclerciaAdecarboxylata R25测序。在测试的菌株中,61.6%(180/292)对弗洛林尼耐药,64.4%(188/292)均为Flor,1.0%(3/292)CFR。 L.AdecarBoxylata R25的全基因组序列分析显示Flor基因由转座子携带并位于质粒(PLA-64)上。七种其他抗性基因也在PLA-64上编码,所有这些抗性基因都被发现与移动遗传元件有关。共享与PLA-64最大相似性的序列是含有肠杆菌Cloacaa的酸杆菌FreundII和P234和P388的质粒p02085-TETA。抗性基因相关的流动遗传元素也分享来自不同物种或细菌的同源序列。这些发现表明,Flor主要有助于肠杆菌痤疮植物之间的氟苯纤维抗性的高速率。通过PLA-64编码的抗性基因相关的移动遗传元素可以在不同物种或属的细菌之间转移,导致抗性传播。

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