Indole May Help the Horizontal Transmission of Antibiotic Resistance Genes in E. coli Under Subinhibitory Concentrations of Cefotaxime Stress

被引:0
作者
Dong, Weiqi [1 ]
Du, Panpan [1 ]
Huang, Ruisen [1 ]
Lv, Shuoyan [1 ]
Chen, Hong [1 ]
Guan, Songlei [1 ]
机构
[1] Jilin Agr Univ, Coll Life Sci, Changchun, Peoples R China
关键词
antibiotic resistance genes; conjugation; indole; SOS response; subinhibitory concentrations of antibiotics; SOS RESPONSE; ESCHERICHIA-COLI; SIGNALING MOLECULE; EXPRESSION;
D O I
10.1155/2024/9018205
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objectives: Subinhibitory concentration of antibiotics in the environment is an important risk factor for the horizontal transmission of antibiotic resistance genes (ARGs). The signaling mechanism of resistance gene transmission remains unknown. The aim of this study was to investigate whether indole could be used as a molecular signal to help the spread of ARGs under the stress of subinhibitory concentrations of antibiotics. Methods: The effect of indole on conjugation frequency was investigated through a conjugation test, and its effect on the Type IV secretion system and pili gene expression of E. coli was observed. Meanwhile, we were investigating the trend of changes in indole regulatory factors ibpA, tnaA, and concentration pumps. Subsequently, we predicted the receptors that specifically bind to indole. Finally, our study focused on elucidating the regulatory mechanism of indole synthesis. Results: Conjugate frequency was significantly increased under 1/5MIC concentration cefotaxime stress. The transferred ARGs were bla(CTX-M) and foxA. The mobile plasmid was IncY or IncI2. Meanwhile, the concentration of endogenous indole was also significantly increased. And, surprisingly, inhibition of endogenous indole production resulted in a significant decrease in conjugate frequency. However, the conjugate frequency increased once again when the strains reacquired the exogenous indole. Furthermore, the fluctuation trends of indole-regulated factor (ibpA, tnaA) mRNA and concentration pumps (acrEF, mtr) mRNA consistently with that of indole. Then, we found that the receptors of indole may be four targets of TCSs: CreC, PhoB, AtoC, and UhpA. More than that, when strains retrieved the exogenous indole again, the mRNA levels of T4SS (virB2, virB6, and virD4) and pppA (coding Pili precursor) genes significantly increased. This indicates that there is a close relationship between indole and conjugated channels, which are necessary for horizontal transfer of genetic material. And then, the trends of indole and tnaA mRNA were consistent with that of ibpA (one of SOS response). So, this result confirmed that indole was regulated by SOS response under subinhibitory concentrations of antibiotics. Conclusions: It is always known that subinhibitory concentrations of antibiotics stimulate an SOS response in E. coli, which helps in the horizontal spread of ARGs by modulating indole.
引用
收藏
页数:13
相关论文
共 40 条
[1]   SOS response promotes horizontal dissemination of antibiotic resistance genes [J].
Beaber, JW ;
Hochhut, B ;
Waldor, MK .
NATURE, 2004, 427 (6969) :72-74
[2]   In Vivo Structures of the Helicobacter pylori cag Type IV Secretion System [J].
Chang, Yi-Wei ;
Shaffer, Carrie L. ;
Rettberg, Lee A. ;
Ghosal, Debnath ;
Jensen, Grant J. .
CELL REPORTS, 2018, 23 (03) :673-681
[3]   The SOS response promotes qnrB quinolone-resistance determinant expression [J].
Da Re, Sandra ;
Garnier, Fabien ;
Guerin, Emilie ;
Campoy, Susana ;
Denis, Francois ;
Ploy, Marie-Cecile .
EMBO REPORTS, 2009, 10 (08) :929-933
[4]   Sub-inhibitory concentrations of fluoroquinolones increase conjugation frequency [J].
E, Shun-Mei ;
Zeng, Jian-Ming ;
Yuan, Hui ;
Lu, Yang ;
Cai, Ren-Xin ;
Chen, Cha .
MICROBIAL PATHOGENESIS, 2018, 114 :57-62
[5]   A second prepilin peptidase gene in Escherichia coli K-12 [J].
Francetic, O ;
Lory, S ;
Pugsley, AP .
MOLECULAR MICROBIOLOGY, 1998, 27 (04) :763-775
[6]   The Indole Pulse: A New Perspective on Indole Signalling in Escherichia coli [J].
Gaimster, Hannah ;
Cama, Jehangir ;
Hernandez-Ainsa, Silvia ;
Keyser, Ulrich F. ;
Summers, David K. .
PLOS ONE, 2014, 9 (04)
[7]   Comparison of Nine Phenotypic Methods for Detection of Extended-Spectrum β-Lactamase Production by Enterobacteriaceae [J].
Garrec, Helene ;
Drieux-Rouzet, Laurence ;
Golmard, Jean-Louis ;
Jarlier, Vincent ;
Robert, Jerome .
JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (03) :1048-1057
[8]   β-lactam antibiotics promote bacterial mutagenesis via an RpoS-mediated reduction in replication fidelity [J].
Gutierrez, A. ;
Laureti, L. ;
Crussard, S. ;
Abida, H. ;
Rodriguez-Rojas, A. ;
Blazquez, J. ;
Baharoglu, Z. ;
Mazel, D. ;
Darfeuille, F. ;
Vogel, J. ;
Matic, I. .
NATURE COMMUNICATIONS, 2013, 4
[9]   Mutation of tryptophanase gene tnaA in Edwardsiella tarda reduces lipopolysaccharide production, antibiotic resistance and virulence [J].
Han, Yin ;
Yang, Chun-Li ;
Yang, Qian ;
Qi, Zizhong ;
Liu, Wenzheng ;
Xu, Zhi-Hong ;
Zhu, Wei-Ming ;
Bossier, Peter ;
Zhang, Xiao-Hua .
ENVIRONMENTAL MICROBIOLOGY REPORTS, 2011, 3 (05) :603-612
[10]   The impact and mechanism of quaternary ammonium compounds on the transmission of antibiotic resistance genes [J].
Han, Yue ;
Zhou, Zhen-Chao ;
Zhu, Lin ;
Wei, Yuan-Yuan ;
Feng, Wan-Qiu ;
Xu, Lan ;
Liu, Yang ;
Lin, Ze-Jun ;
Shuai, Xin-Yi ;
Zhang, Zhi-Jian ;
Chen, Hong .
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2019, 26 (27) :28352-28360