Ryan T. Botts , Dawne M. Page , Joseph A. Bravo , Madelaine L. Brown , Claudia C. Castilleja , Victoria L. Guzman , Samantha Hall , Jacob D. Henderson , Shelby M. Kenney , Mariele E. Lensink , Megan V. Paternoster , Sarah L. Pyle , Lucas Ustick , Chara J. Walters-Laird , Eva M. Top , David E. Cummings
{"title":"受污染湿地含有编码ctx - m型广谱β-内酰胺酶的多药耐药质粒","authors":"Ryan T. Botts , Dawne M. Page , Joseph A. Bravo , Madelaine L. Brown , Claudia C. Castilleja , Victoria L. Guzman , Samantha Hall , Jacob D. Henderson , Shelby M. Kenney , Mariele E. Lensink , Megan V. Paternoster , Sarah L. Pyle , Lucas Ustick , Chara J. Walters-Laird , Eva M. Top , David E. Cummings","doi":"10.1016/j.plasmid.2023.102682","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>While most detailed analyses of antibiotic resistance plasmids focus on those found in clinical isolates, less is known about the vast environmental reservoir of </span>mobile genetic elements<span> and the resistance and virulence factors they encode. We selectively isolated three strains of cefotaxime-resistant </span></span><em>Escherichia coli</em> from a wastewater-impacted coastal wetland. The cefotaxime-resistant phenotype was transmissible to a lab strain of <em>E. coli</em> after one hour, with frequencies as high as 10<sup>−3</sup><span> transconjugants per recipient. Two of the plasmids also transferred cefotaxime resistance to </span><span><em>Pseudomonas putida</em></span>, but these were unable to back-transfer this resistance from <em>P. putida</em> to <em>E. coli</em>. In addition to the cephalosporins, <em>E. coli</em><span> transconjugants inherited resistance to at least seven distinct classes of antibiotics. Complete nucleotide sequences<span> revealed large IncF-type plasmids with globally distributed replicon sequence types F31:A4:B1 and F18:B1:C4 carrying diverse antibiotic resistance and virulence genes. The plasmids encoded extended-spectrum β-lactamases </span></span><em>bla</em><sub><em>CTX-M-15</em></sub> or <em>bla</em><sub><em>CTX-M-55</em></sub>, each associated with the insertion sequence IS<em>Ec9</em><span>, although in different local arrangements. Despite similar resistance profiles, the plasmids shared only one resistance gene in common, the aminoglycoside<span> acetyltransferase </span></span><em>aac(3)-IIe</em><span>. Plasmid accessory cargo also included virulence factors involved in iron acquisition and defense against host immunity. Despite their sequence similarities, several large-scale recombination events were detected, including rearrangements and inversions. In conclusion, selection with a single antibiotic, cefotaxime, yielded conjugative plasmids conferring multiple resistance and virulence factors. Clearly, efforts to limit the spread of antibiotic resistance and virulence among bacteria must include a greater understanding of mobile elements in the natural and human-impacted environments.</span></p></div>","PeriodicalId":49689,"journal":{"name":"Plasmid","volume":"126 ","pages":"Article 102682"},"PeriodicalIF":1.8000,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213127/pdf/","citationCount":"0","resultStr":"{\"title\":\"Polluted wetlands contain multidrug-resistance plasmids encoding CTX-M-type extended-spectrum β-lactamases\",\"authors\":\"Ryan T. Botts , Dawne M. Page , Joseph A. Bravo , Madelaine L. Brown , Claudia C. Castilleja , Victoria L. Guzman , Samantha Hall , Jacob D. Henderson , Shelby M. Kenney , Mariele E. Lensink , Megan V. Paternoster , Sarah L. Pyle , Lucas Ustick , Chara J. Walters-Laird , Eva M. Top , David E. Cummings\",\"doi\":\"10.1016/j.plasmid.2023.102682\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>While most detailed analyses of antibiotic resistance plasmids focus on those found in clinical isolates, less is known about the vast environmental reservoir of </span>mobile genetic elements<span> and the resistance and virulence factors they encode. We selectively isolated three strains of cefotaxime-resistant </span></span><em>Escherichia coli</em> from a wastewater-impacted coastal wetland. The cefotaxime-resistant phenotype was transmissible to a lab strain of <em>E. coli</em> after one hour, with frequencies as high as 10<sup>−3</sup><span> transconjugants per recipient. Two of the plasmids also transferred cefotaxime resistance to </span><span><em>Pseudomonas putida</em></span>, but these were unable to back-transfer this resistance from <em>P. putida</em> to <em>E. coli</em>. In addition to the cephalosporins, <em>E. coli</em><span> transconjugants inherited resistance to at least seven distinct classes of antibiotics. Complete nucleotide sequences<span> revealed large IncF-type plasmids with globally distributed replicon sequence types F31:A4:B1 and F18:B1:C4 carrying diverse antibiotic resistance and virulence genes. The plasmids encoded extended-spectrum β-lactamases </span></span><em>bla</em><sub><em>CTX-M-15</em></sub> or <em>bla</em><sub><em>CTX-M-55</em></sub>, each associated with the insertion sequence IS<em>Ec9</em><span>, although in different local arrangements. Despite similar resistance profiles, the plasmids shared only one resistance gene in common, the aminoglycoside<span> acetyltransferase </span></span><em>aac(3)-IIe</em><span>. Plasmid accessory cargo also included virulence factors involved in iron acquisition and defense against host immunity. Despite their sequence similarities, several large-scale recombination events were detected, including rearrangements and inversions. In conclusion, selection with a single antibiotic, cefotaxime, yielded conjugative plasmids conferring multiple resistance and virulence factors. Clearly, efforts to limit the spread of antibiotic resistance and virulence among bacteria must include a greater understanding of mobile elements in the natural and human-impacted environments.</span></p></div>\",\"PeriodicalId\":49689,\"journal\":{\"name\":\"Plasmid\",\"volume\":\"126 \",\"pages\":\"Article 102682\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2023-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213127/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plasmid\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0147619X23000136\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plasmid","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0147619X23000136","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
While most detailed analyses of antibiotic resistance plasmids focus on those found in clinical isolates, less is known about the vast environmental reservoir of mobile genetic elements and the resistance and virulence factors they encode. We selectively isolated three strains of cefotaxime-resistant Escherichia coli from a wastewater-impacted coastal wetland. The cefotaxime-resistant phenotype was transmissible to a lab strain of E. coli after one hour, with frequencies as high as 10−3 transconjugants per recipient. Two of the plasmids also transferred cefotaxime resistance to Pseudomonas putida, but these were unable to back-transfer this resistance from P. putida to E. coli. In addition to the cephalosporins, E. coli transconjugants inherited resistance to at least seven distinct classes of antibiotics. Complete nucleotide sequences revealed large IncF-type plasmids with globally distributed replicon sequence types F31:A4:B1 and F18:B1:C4 carrying diverse antibiotic resistance and virulence genes. The plasmids encoded extended-spectrum β-lactamases blaCTX-M-15 or blaCTX-M-55, each associated with the insertion sequence ISEc9, although in different local arrangements. Despite similar resistance profiles, the plasmids shared only one resistance gene in common, the aminoglycoside acetyltransferase aac(3)-IIe. Plasmid accessory cargo also included virulence factors involved in iron acquisition and defense against host immunity. Despite their sequence similarities, several large-scale recombination events were detected, including rearrangements and inversions. In conclusion, selection with a single antibiotic, cefotaxime, yielded conjugative plasmids conferring multiple resistance and virulence factors. Clearly, efforts to limit the spread of antibiotic resistance and virulence among bacteria must include a greater understanding of mobile elements in the natural and human-impacted environments.
期刊介绍:
Plasmid publishes original research on genetic elements in all kingdoms of life with emphasis on maintenance, transmission and evolution of extrachromosomal elements. Objects of interest include plasmids, bacteriophages, mobile genetic elements, organelle DNA, and genomic and pathogenicity islands.