Plasmid Sequence Data Analysis to Investigate Antibiotic Resistance Gene Transfer among Swine, Swine Farm and Their Owners
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Antibiotics either kill or inhibit the growth of bacteria. However, antibiotic-resistant bacteria are difficult to treat with antibiotics. Infections caused by such bacteria often lead to severe diseases. Antibiotic resistance genes (ARG) can be horizontally transmitted across different bacterial species, necessitating a comprehensive understanding of how ARGs spread across various environments. In this study, we analyzed the plasmid sequences of 33 extended-spectrum beta-lactamases (ESBL) producing Escherichia coli isolated from pigs, farms, and their owners. We conducted an antibiotic susceptibility test (AST) with aztreonam and seven other antibiotics, as well as whole genome sequencing (WGS) of the strains using MinION. Our results demonstrated that the plasmids that did not harbor ARGs were mostly nonconjugative, whereas the plasmids that harbored ARGs were conjugative. The arrangement of these ARGs exhibited a pattern of organization featuring a series of ARG cassettes, some of which were identical across the isolates collected from different sources. Therefore, this study suggests that the sets of ARG cassettes on plasmids were mostly shared between pigs and their owners. Hence, enhanced surveillance of ARG should be implemented in farm environments to proactively mitigate the risk of antibiotic-resistant bacterial infections.
Abstract
Antibiotics either kill or inhibit the growth of bacteria. However, antibiotic-resistant bacteria are difficult to treat with antibiotics. Infections caused by such bacteria often lead to severe diseases. Antibiotic resistance genes (ARG) can be horizontally transmitted across different bacterial species, necessitating a comprehensive understanding of how ARGs spread across various environments. In this study, we analyzed the plasmid sequences of 33 extended-spectrum beta-lactamases (ESBL) producing Escherichia coli isolated from pigs, farms, and their owners. We conducted an antibiotic susceptibility test (AST) with aztreonam and seven other antibiotics, as well as whole genome sequencing (WGS) of the strains using MinION. Our results demonstrated that the plasmids that did not harbor ARGs were mostly nonconjugative, whereas the plasmids that harbored ARGs were conjugative. The arrangement of these ARGs exhibited a pattern of organization featuring a series of ARG cassettes, some of which were identical across the isolates collected from different sources. Therefore, this study suggests that the sets of ARG cassettes on plasmids were mostly shared between pigs and their owners. Hence, enhanced surveillance of ARG should be implemented in farm environments to proactively mitigate the risk of antibiotic-resistant bacterial infections.
참고문헌 (42)
- Malik B, "Antibiotic drug-resistance as a complex system driven by socio-economic growth and antibiotic misuse", Scientific Reports, 9(1), pp.9788~ (2019)[DOI]
- Gould I, "A review of the role of antibiotic policies in the control of antibiotic resistance", Journal of Antimicrobial Chemotherapy, 43(4), pp.459~465 (1999)[DOI]
- Baquero F, "Antibiotics and antibiotic resistance in water environments", Current Opinion in Biotechnology, 19(3), pp.260~265 (2008)[DOI]
- Aslam B, "Antibiotic resistance : a rundown of a global crisis", Infection and Drug Resistance, pp.1645~1658 (2018)[DOI]
- Larsson DJ, "Antibiotic resistance in the environment", Nature Reviews Microbiology, 20(5), pp.257~269 (2022)[DOI]
- Dibner J, "Antibiotic growth promoters in agriculture : history and mode of action", Poultry Science, 84(4), pp.634~643 (2005)[DOI]
- 임숙경, "국내 가축 및 수산에서 항생제 판매 추이(2003-2012)", 대한수의학회지, 54(2), pp.81~86 (2014), 대한수의학회[DOI]
- Kunhikannan S, "Environmental hotspots for antibiotic resistance genes", Microbiologyopen, 10(3), pp.e1197~ (2021)[DOI]
- Yang F, "Swine liquid manure : A hotspot of mobile genetic elements and antibiotic resistance genes", Scientific Reports, 10(1), pp.15037~ (2020)[DOI]
- Massé DI, "Potential of biological processes to eliminate antibiotics in livestock manure : An overview", Animals, 4(2), pp.146~163 (2014)[DOI]
- He Y, "Antibiotic resistance genes from livestock waste : Occurrence, dissemination, and treatment", NPJ Clean Water, 3(1), pp.4~ (2020)[DOI]
- Zhao X, "Field-based evidence for enrichment of antibiotic resistance genes and mobile genetic elements in manure-amended vegetable soils", Science of the Total Environment, 654, pp.906~913 (2019)[DOI]
- Jechalke S, "Fate and effects of veterinary antibiotics in soil", Trends in Microbiology, 22(9), pp.536~545 (2014)[DOI]
- Ghimpeţeanu OM, "Antibiotic use in livestock and residues in food—A public health threat : A review", Foods, 11(10), pp.1430~ (2022)[DOI]
- Chen J, "Antibiotic residues in food : Extraction, analysis, and human health concerns", Journal of Agricultural and Food Chemistry, 67(27), pp.7569~7586 (2019)[DOI]
- Jiang Q, "Effects and relevant mechanisms of non-antibiotic factors on the horizontal transfer of antibiotic resistance genes in water environments : A review", Science of The Total Environment, 806, pp.150568~ (2022)[DOI]
- Von Wintersdorff CJ, "Dissemination of antimicrobial resistance in microbial ecosystems through horizontal gene transfer", Frontiers in Microbiology, 7, pp.173~ (2016)[DOI]
- Christie PJ, "Bacterial type IV secretion : Conjugation systems adapted to deliver effector molecules to host cells", Trends in Microbiology, 8(8), pp.354~360 (2000)[DOI]
- Cochrane RR, "Superior conjugative plasmids delivered by bacteria to diverse fungi", BioDesign Research, 2022, pp.9802168~ (2022)[DOI]
- Xiao X, "Subinhibitory concentration of colistin promotes the conjugation frequencies of mcr-1-and bla NDM-5-positive plasmids", Microbiology Spectrum, 10(2), pp.e02160~21 (2022)[DOI]
- Lekagul A, "Patterns of antibiotic use in global pig production : A systematic review", Veterinary and Animal Science, 7, pp.100058~ (2019)[DOI]
- Clinical & Institute LS, "Performance standards for antimicrobial susceptibility testing", Clinical and Laboratory Standards Institute Wayne, 106~112 (2017)
- Ward Jr JH, "Hierarchical grouping to optimize an objective function", Journal of the American Statistical Association, 58(301), pp.236~244 (1963)[DOI]
- Shen W, "SeqKit : A cross-platform and ultrafast toolkit for FASTA", Q file manipulation, 2016, pp.11(10), e0163962~
- Kolmogorov M, "Assembly of long, error-prone reads using repeat graphs", Nature Biotechnology, 37(5), pp.540~546 (2019)[DOI]
- Pellow D, "PlasClass improves plasmid sequence classification", PLoS Computational Biology, 16(4), pp.e1007781~ (2020)[DOI]
- Robertson J, "suite: Software tools for clustering, reconstruction and typing of plasmids from draft assemblies", Microbial Genomics, 4(8), pp.e000206~ (2018)[DOI]
- Hyatt D, "Prodigal : prokaryotic gene recognition and translation initiation site identification", BMC Bioinformatics, 11(1), pp.1~11 (2010)[DOI]
- Buchfink B, "Sensitive protein alignments at tree-of-life scale using DIAMOND", Nature Methods, 18(4), pp.366~368 (2021)[DOI]
- Alcock BP, "CARD 2020 : Antibiotic resistome surveillance with the comprehensive antibiotic resistance database", Nucleic Acids Research, 48(D1), pp.D517~D525 (2020)[DOI]
- Seemann T, "Prokka : Rapid prokaryotic genome annotation", Bioinformatics, 30(14), pp.2068~2069 (2014)[DOI]
- Sullivan MJ, "Easyfig : A genome comparison visualizer", Bioinformatics, 27(7), pp.1009~1010 (2011)[DOI]
- San Millan A, "Multicopy plasmids potentiate the evolution of antibiotic resistance in bacteria", Nature Ecology & Evolution, 1(1), pp.0010~ (2016)[DOI]
- Van Gompel L, "Description and determinants of the faecal resistome and microbiome of farmers and slaughterhouse workers : A metagenome-wide cross-sectional study", Environment International, 143, pp.105939~ (2020)[DOI]
- Chang Q, "Antibiotics in agriculture and the risk to human health : how worried should we be?", Evolutionary Applications, 8(3), pp.240~247 (2015)[DOI]
- Gao FZ, "Untreated swine wastes changed antibiotic resistance and microbial community in the soils and impacted abundances of antibiotic resistance genes in the vegetables", Science of the Total Environment, 741, pp.140482~ (2020)[DOI]
- Monger XC, "Antibiotic resistance : From pig to meat", Antibiotics, 10(10), pp.1209~ (2021)[DOI]
- Blanc DS, "Comparison of whole genome(wg-)and core genome(cg-)MLST(BioNumericsTM)versus SNP variant calling for epidemiological investigation of Pseudomonas aeruginosa", Frontiers in Microbiology, 11, pp.1729~ (2020)[DOI]
- Smillie C, "Mobility of plasmids", Microbiology and Molecular Biology Reviews, 74(3), pp.434~452 (2010)[DOI]
- Ruppé E, "Establishing genotype-to-phenotype relationships in bacteria causing hospital-acquired pneumonia : A prelude to the application of clinical metagenomics", Antibiotics, 6(4), pp.30~ (2017)[DOI]
- González-Santamarina B, "Genomic characterization of multidrug-resistant salmonella serovars derby and rissen from the pig value chain in Vietnam", Frontiers in Veterinary Science, 8, pp.705044~ (2021)[DOI]
- Moran RA, "Prediction of antibiotic resistance from antibiotic resistance genes detected in antibiotic-resistant commensal Escherichia coli using PCR or WGS", Journal of Antimicrobial Chemotherapy, 72(3), pp.700~704 (2017)[DOI]
