环丙沙星治疗后肠道中耐氟喹诺酮类大肠杆菌的演变

IF 4.5 3区 医学 Q1 MICROBIOLOGY
V. de Lastours , I. El Meouche , F. Chau , J. Beghain , D. Chevret , A. Aubert-Frambourg , O. Clermont , G. Royer , O. Bouvet , E. Denamur , B. Fantin , for the CIPHARES Group
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引用次数: 1

摘要

背景:三名健康志愿者在环丙沙星治疗前后14天的肠道中携带相似的喹诺酮耐药大肠杆菌(QREC)(脉冲场凝胶电泳图谱)。考虑到选择压力的强度和喹诺酮类药物的致突变性,我们确定这些菌株是否在表型和/或基因组水平上进化。材料与方法比较3名志愿者服用环丙沙星第0天(D0)和服用环丙沙星第14天(D42)后1个月的QREC。进行生长实验;在D0和D42时测定乙酸水平、突变频率、喹诺酮类药物mic和抗生素耐受性。采用dissnp和breseq方法对D0和D42的单核苷酸多态性(snp)进行分析。提取细胞质蛋白,采用高效液相色谱法,用X!串联软件;丰度通过质谱法测定,采用光谱计数(SC)和萃取离子色谱(XIC)积分法。结果D0和D42在mic、生长特性、醋酸盐浓度、突变频率、耐受性谱、系统群、o型和h型、fimH等位基因和序列类型等方面均无差异。2/3受试者的D0和D42分离株间未发现SNP变异;其中1例出现2个SNP变异。在蛋白质水平上,D0和D42之间的蛋白质丰度差异不显著。结论尽管在肠道中大量暴露于环丙沙星,但未观察到共生QREC的适应性、耐受性、代谢或基因组进化。这三种菌株的表现似乎没有受到环丙沙星的影响,这表明肠道可能是一个避难所,在那里细菌可以免受抗生素的影响,并在没有任何有害影响的情况下生存。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evolution of fluoroquinolone-resistant Escherichia coli in the gut after ciprofloxacin treatment

Background

Three healthy volunteers carried similar quinolone-resistant E. coli (QREC) (pulsed field gel electrophoresis profiles) in their gut before and after 14 days ciprofloxacin treatment. Given the intensity of the selective pressure and the mutagenic properties of quinolones, we determined whether these strains had evolved at the phenotypic and/or genomic levels.

Material and methods

Commensal QREC from before day-0 (D0), and a month after 14 days of ciprofloxacin (D42) were compared in 3 volunteers. Growth experiments were performed; acetate levels, mutation frequencies, quinolone MICs and antibiotic tolerance were measured at D0 and D42. Genomes were sequenced and single nucleotide polymorphisms (SNPs) between D0 and D42 were analyzed using DiscoSNP and breseq methods. Cytoplasmic proteins were extracted, HPLC performed and proteins identified using X!tandem software; abundances were measured by mass spectrometry using the Spectral Counting (SC) and eXtraction Ion Chromatograms (XIC) integration methods.

Results

No difference was found in MICs, growth characteristics, acetate concentrations, mutation frequencies, tolerance profiles, phylogroups, O-and H-types, fimH alleles and sequence types between D0 and D42. No SNP variation was evidenced between D0 and D42 isolates for 2/3 subjects; 2 SNP variations were evidenced in one. At the protein level, very few significant protein abundance differences were identified between D0 and D42.

Conclusion

No fitness, tolerance, metabolic or genomic evolution of commensal QREC was observed overtime, despite massive exposure to ciprofloxacin in the gut. The three strains behaved as if they had been unaffected by ciprofloxacin, suggesting that gut may act as a sanctuary where bacteria would be protected from the effect of antibiotics and survive without any detrimental effect of stress.

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来源期刊
CiteScore
9.70
自引率
0.00%
发文量
18
审稿时长
45 days
期刊介绍: Pathogen genome sequencing projects have provided a wealth of data that need to be set in context to pathogenicity and the outcome of infections. In addition, the interplay between a pathogen and its host cell has become increasingly important to understand and interfere with diseases caused by microbial pathogens. IJMM meets these needs by focussing on genome and proteome analyses, studies dealing with the molecular mechanisms of pathogenicity and the evolution of pathogenic agents, the interactions between pathogens and host cells ("cellular microbiology"), and molecular epidemiology. To help the reader keeping up with the rapidly evolving new findings in the field of medical microbiology, IJMM publishes original articles, case studies and topical, state-of-the-art mini-reviews in a well balanced fashion. All articles are strictly peer-reviewed. Important topics are reinforced by 2 special issues per year dedicated to a particular theme. Finally, at irregular intervals, current opinions on recent or future developments in medical microbiology are presented in an editorial section.
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