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Florfenicol Resistance in Enterobacteriaceae and Whole-Genome Sequence Analysis of Florfenicol-Resistant Leclercia adecarboxylata Strain R25

机译:肠杆菌科细菌对氟苯尼考的​​耐药性和耐氟苯尼考的​​莱德卡莱德氏菌R25菌株全基因组序列分析

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摘要

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,在动物呼吸道和肠道细菌中对氟苯尼考的​​耐药性变得越来越严重。为了检测肠杆菌科细菌对氟苯尼考的​​耐药机制,对动物粪便中的292株细菌进行了检测。进行琼脂稀释法以确定氟苯尼考的​​最低抑制浓度(MIC),并进行聚合酶链反应(PCR)检测氟苯尼考耐药基因。为了进一步研究氟苯尼考抗性的分子机制,对全基因组阿德莱特氏菌R25进行了测序。在测试的菌株中,氟苯尼考耐药率为61.6%(180/292),floR阳性率为64.4%(188/292),而cfr阳性率为1.0%(3/292)。阿德莫氏乳杆菌R25的全基因组序列分析表明,floR基因由转座子携带并位于质粒(pLA-64)上。 pLA-64上还编码了其他七个抗性基因,所有这些基因均与移动遗传元件有关。与pLA-64具有最大相似性的序列是弗氏柠檬酸杆菌的质粒p02085-tetA和阴沟肠杆菌的p234和p388。抗性基因相关的移动遗传元件也共享来自不同物种或细菌属的同源序列。这些发现表明,floR主要是导致肠杆菌科细菌对氟苯尼考的​​高耐药率。由pLA-64编码的与抗性基因相关的移动遗传元件可能会在不同物种或属的细菌之间转移,从而导致抗性传播。

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