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Integrons, a diverse group of genetic elements, have emerged as key players in bacterial adaptation and evolution. These elements, commonly found in both environmental as well as clinical settings, facilitate the acquisition, exchange, and expression of integron cassettes, allowing bacteria to rapidly adapt to changing environments and acquire antibiotic resistance. This review provides an in-depth exploration of the various classes of clinical integrons, including class 1, 2, and 3, highlighting their origins, distribution, and associated mobile elements. We delve into the astonishing success of "class 1 integrons", emphasizing their ability to recognize diverse attachment sites known as "attC sites" and getting integrated within many different integron cassettes from diverse sources. Class 1 integrons are able to propagate widely among bacterial hosts due to their lack of host specificity, interaction with transposons, and broad host range plasmids. Moreover, we discuss the substantial impact of class 1 integrons in antimicrobial resistance, as they accumulate an array of resistance genes through strong positive selection. Additionally, we address the challenging issue regarding the evolution and function of integrons and integron cassettes, including the role of promoters, origins of integron cassettes, and the abundance of unknown proteins encoded within them. The future prospects of integron research are also explored, highlighting the need to understand cassette expression patterns, assess the contribution of chromosomal/superintegron arrays to host fitness, unravel the mechanisms of cassette generation, and investigate the connection between the SOS induction and horizontal gene transfer. Overall, this review underlines the significance of integrons as hidden architects driving bacterial adaptation and evolution, providing valuable insights into their ecological and evolutionary dynamics, and shaping the future direction of research in this field.
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http://dx.doi.org/10.1007/s10482-025-02103-x | DOI Listing |
J Antimicrob Chemother
September 2025
US Food and Drug Administration, Center for Veterinary Medicine, Office of Applied Science, Laurel, MD, USA.
Objectives: Integrons facilitate the capture and expression of exogenous genes, including antimicrobial resistance (AMR) genes. This study aimed to detect the presence of integrons, examine their genomic structure and location, and analyse integron-associated AMR, virulence and stress response genes in Salmonella using WGS.
Methods: WGS data from 193 Salmonella strains, representing 38 serotypes isolated from food animals and related meat products (2001-2019), were analysed using bioinformatic tools to assess integron presence and characterize their genomic architectures.
Pol J Microbiol
September 2025
1School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, China.
Carbapenems, as the preferred treatment for multidrug-resistant , are increasingly facing issues of insufficient therapeutic efficacy. This study aims to investigate the antimicrobial resistance mechanisms of clinical isolates to carbapenems. The whole genome sequencing revealed various β-lactamase genes, including the intrinsic genes and , as well as the acquired (n = 6), and (n = 10) in 40 carbapenem-resistant (CRPA) isolates.
View Article and Find Full Text PDFJ Environ Manage
August 2025
Office of Research and Development, US Environmental Protection Agency, Cincinnati, OH, 45268, USA. Electronic address:
Improperly treated wastewater and surface runoff can degrade water quality by introducing microbial contaminants, including antibiotic-resistant bacteria (ARB) and their genes (ARGs). Constructed treatment wetlands (CTWs) offer a low-resource solution for managing impaired watersheds. However, their ability to mitigate microbial contaminants, particularly ARGs, requires further study.
View Article and Find Full Text PDFPLoS One
July 2025
Department of Veterinary Preventive Medicine, The Ohio State University, Coumbus, Ohio, United States of America.
The blaIMP resistance gene encodes a metallo-beta-lactamase in bacteria, which confers reduced susceptibility or resistance to all the beta-lactams, including carbapenems which are critical for treating life-threatening infections. The dissemination of blaIMP among various taxonomic families shows the diversity and range of horizontal gene transfer. Using short-read whole genome sequencing and bioinformatic tools, we determined the genetic motifs surrounding blaIMP present in 32 bacterial isolates recovered from environmental sources and agriculture facilities.
View Article and Find Full Text PDFZhonghua Yu Fang Yi Xue Za Zhi
July 2025
Affiliated Hospital of North China University of Science and Technology, Tangshan 063000, China.
To analyze the carriage status, subtype distribution and flanking gene sequence characteristics of oxacillinases (OXA enzyme) in 241 clinical strains of Pseudomonas aeruginosa, and assess their roles in the drug resistance of and ability to horizontally transfer across species. Clinical isolates were collected from four hospitals in Sanya, Tangshan, Zhangjiakou, and Beijing. The prevalence of oxacillinases and their flanking gene sequences was analyzed by whole-genome sequencing (NGS) and bioinformatic approaches.
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