Antibiotic Resistance: In the Perspective of Causes, Current Status, Mechanism and Reverting

A special issue of Antibiotics (ISSN 2079-6382). This special issue belongs to the section "Mechanism and Evolution of Antibiotic Resistance".

Deadline for manuscript submissions: closed (31 December 2021) | Viewed by 8054

Special Issue Editor


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Guest Editor
Center for Proteomics and Metabolomics, State Key Laboratory of Bio-Control, School of Life Sciences, Sun Yat-sen University, University City, Guangzhou 510006, China
Interests: functional metabolomics for antibiotic resistance

Special Issue Information

Dear Collogues,

The surge of antibiotic-resistant bacteria brings huge challenges to modern medicine, threatening human health and causing huge economic loss. Understanding the mechanism conferring antibiotic resistance is essential for developing strategies to overcome resistance. Tremendous progress has been made over past decades in deciphering the key determinants of antibiotic resistance. A comprehensive understanding of the action of antibiotics also sheds light on the traits of antibiotic-resistant bacteria. However, preventive and control measures are still lacking. It is noteworthy that many studies have focused on how, for example, certain genes, efflux pumps, and antibiotic modification enzymes contribute to the antibiotic response and how the inhibitors to counteract such effects have been designed. However, an important aspect that is always being ignored is how we can reverse antibiotic resistance or re-sensitize antibiotic-resistant bacteria to current available antibiotics based on the identified mechanism. With this consideration in mind, we have proposed a Special Issue that will specifically address the mechanism that can be harnessed to reverse antibiotic resistance. Besides classical studies on genes, efflux pumps, and antibiotic modification enzymes, we therefore encourage submissions from a broad perspective that enhance our understanding of the resistant mechanism and its use for reversing antibiotic resistance.

Prof. Xuanxian Peng
Guest Editor

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Keywords

  • Antibiotic resistance
  • Antibiotic resistance reverting
  • Antibiotic resistance mechanisms
  • Metabolomics
  • Proteomics
  • Metabolome-reprogramming

Published Papers (3 papers)

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Research

11 pages, 1768 KiB  
Article
Exogenous Alanine Reverses the Bacterial Resistance to Zhongshengmycin with the Promotion of the P Cycle in Xanthomonas oryzae
by Yi Guan, Peihua Shen, Meiyun Lin and Xiuyun Ye
Antibiotics 2022, 11(2), 245; https://doi.org/10.3390/antibiotics11020245 - 14 Feb 2022
Cited by 12 | Viewed by 1989
Abstract
Microbial antibiotic resistance has become a worldwide concern, as it weakens the efficiency of the control of pathogenic microbes in both the fields of medicine and plant protection. A better understanding of antibiotic resistance mechanisms is helpful for the development of efficient approaches [...] Read more.
Microbial antibiotic resistance has become a worldwide concern, as it weakens the efficiency of the control of pathogenic microbes in both the fields of medicine and plant protection. A better understanding of antibiotic resistance mechanisms is helpful for the development of efficient approaches to settle this issue. In the present study, GC-MS-based metabolomic analysis was applied to explore the mechanisms of Zhongshengmycin (ZSM) resistance in Xanthomonas oryzae (Xoo), a bacterium that causes serious disease in rice. Our results show that the decline in the pyruvate cycle (the P cycle) was a feature for ZSM resistance in the metabolome of ZSM-resistant strain (Xoo-ZSM), which was further demonstrated as the expression level of genes involved in the P cycle and two enzyme activities were reduced. On the other hand, alanine was considered a crucial metabolite as it was significantly decreased in Xoo-ZSM. Exogenous alanine promoted the P cycle and enhanced the ZSM-mediated killing efficiency in Xoo-ZSM. Our study highlights that the depressed P cycle is a feature in Xoo-ZSM for the first time. Additionally, exogenous alanine is a candidate enhancer and can be applied with ZSM to improve the antibiotic-mediated killing efficiency in the control of infection caused by Xoo. Full article
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13 pages, 3009 KiB  
Article
Elevation of Fatty Acid Biosynthesis Metabolism Contributes to Zhongshengmycin Resistance in Xanthomonas oryzae
by Qiaoxing Wang, Meiyun Lin, Peihua Shen and Yi Guan
Antibiotics 2021, 10(10), 1166; https://doi.org/10.3390/antibiotics10101166 - 25 Sep 2021
Cited by 19 | Viewed by 2434
Abstract
Xanthomonas oryzae severely impacts the yield and quality of rice. Antibiotics are the most common control measure for this pathogen; however, the overuse of antibiotics in past decades has caused bacterial resistance to these antibiotics. The agricultural context is of particular importance as [...] Read more.
Xanthomonas oryzae severely impacts the yield and quality of rice. Antibiotics are the most common control measure for this pathogen; however, the overuse of antibiotics in past decades has caused bacterial resistance to these antibiotics. The agricultural context is of particular importance as antibiotic-resistant bacteria are prevalent, but the resistance mechanism largely remains unexplored. Herein, using gas chromatography–mass spectrometry (GC–MS), we demonstrated that zhongshengmycin-resistant X. oryzae (Xoo-Rzs) and zhongshengmycin-sensitive X. oryzae (Xoo-S) have distinct metabolic profiles. We found that the resistance to zhongshengmycin (ZS) in X. oryzae is related to increased fatty acid biosynthesis. This was demonstrated by measuring the Acetyl-CoA carboxylase (ACC) activity, the expression levels of enzyme genes involved in the fatty acid biosynthesis and degradation pathways, and adding exogenous materials, i.e., triclosan and fatty acids. Our work provides a basis for the subsequent control of the production of antibiotic-resistant strains of X. oryzae and the development of coping strategies. Full article
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10 pages, 775 KiB  
Article
Molecular Characterization of Cephalosporin and Fluoroquinolone Resistant Salmonella Choleraesuis Isolated from Patients with Systemic Salmonellosis in Thailand
by Pichapak Sriyapai, Chaiwat Pulsrikarn, Kosum Chansiri, Arin Nyamniyom and Thayat Sriyapai
Antibiotics 2021, 10(7), 844; https://doi.org/10.3390/antibiotics10070844 - 12 Jul 2021
Cited by 10 | Viewed by 2513
Abstract
The antimicrobial resistance of nontyphoidal Salmonella has become a major clinical and public health problem. Southeast Asia has a high level of multidrug-resistant Salmonella and isolates resistant to both fluoroquinolone and third-generation cephalosporins. The incidence of co-resistance to both drug classes is a [...] Read more.
The antimicrobial resistance of nontyphoidal Salmonella has become a major clinical and public health problem. Southeast Asia has a high level of multidrug-resistant Salmonella and isolates resistant to both fluoroquinolone and third-generation cephalosporins. The incidence of co-resistance to both drug classes is a serious therapeutic problem in Thailand. The aim of this study was to determine the antimicrobial resistance patterns, antimicrobial resistance genes and genotypic relatedness of third-generation cephalosporins and/or fluoroquinolone-resistant Salmonella Choleraesuis isolated from patients with systemic salmonellosis in Thailand. Antimicrobial susceptibility testing was performed using the agar disk diffusion method, and ESBL production was detected by the combination disc method. A molecular evaluation of S. Choleraesuis isolates was performed using PCR and DNA sequencing. Then, a genotypic relatedness study of S. Choleraesuis was performed by pulse field gel electrophoresis. All 62 cefotaxime-resistant S. Choleraesuis isolates obtained from 61 clinical specimens were multidrug resistant. Forty-four isolates (44/62, 71.0%) were positive for ESBL phenotypes. Based on the PCR sequencing, 21, 1, 13, 23, 20 and 6 ESBL-producing isolates harboured the ESBL genes blaCTX-M-14, blaCTX-M-15, blaCTX-M-55, blaCMY-2, blaACC-1 and blaTEM-1, respectively. This study also found that nine (9/62, 14.5%) isolates exhibited co-resistance to ciprofloxacin and cefotaxime. All of the co-resistant isolates harboured at least one PMQR gene. The qnr genes and the aac(6′)-Ib-cr gene were the most prevalent genes detected. The QRDR mutation, including the gyrA (D87Y and D87G) and parC (T57S) genes, was also detected. PFGE patterns revealed a high degree of clonal diversity among the ESBL-producing isolates. Full article
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