{"title":"携带tet(C)四环素抗性决定因子的is26结合伪复合转座子的进化","authors":"Carol H. Pong, Robert A. Moran , Ruth M. Hall","doi":"10.1016/j.plasmid.2020.102541","DOIUrl":null,"url":null,"abstract":"<div><p>A large plasmid, pCERC14, found in an antibiotic resistant commensal <em>Escherichia coli</em><span> isolate recovered from a healthy adult was sequenced. pCERC14 was 162,926 bp and carried FII-18 and FIB-1 replicons and an F-like transfer region as well as several virulence determinants, some of which are involved in the uptake of iron which would be advantageous for the commensal lifestyle. The plasmid backbone is interrupted in 11 places by complete IS (IS</span><em>1</em> (4 copies), IS<em>2</em> (2), IS<em>629</em> (2) and single IS<em>100</em>, IS<em>186</em><span>, ISEc33) and in three places by partial IS copies. The antibiotic resistance genes were found in two IS</span><em>26</em><span><span>-bounded pseudo-compound transposons (PCT). One contained a remnant of a class 1 </span>integron that includes a </span><em>dfrA5</em><span> gene cassette and the </span><em>sul1</em><span><span> gene conferring resistance to trimethoprim and </span>sulphonamides, respectively. The second, named PTn</span><em>tet</em><span>(C)-var, contained a 4828 bp DNA segment that includes the </span><em>tet</em><span>(C) tetracycline resistance determinant. As </span><em>tet</em>(C) is relatively rare in <em>E. coli</em> and other Gram-negative bacterial isolates, the structure and evolution of <em>tet</em>(C)-containing PCT in available sequences was examined. The largest identified was PTn<em>tet</em>(C), a close relative of PTn<em>tet</em>(C)-var, and a potential progenitor for these PCT. Most PCT shared one internal boundary with PTn<em>tet</em>(C) but the length of the central <em>tet</em>(C)-containing segment was shorter due to IS<em>26</em>-mediated deletions. The most abundant variant form, previously named Tn<em>6309</em>, was widely distributed and, in a derivative of it, most of the <em>tetA</em>(C) gene has been replaced by the <em>tetA</em><span>(A) gene presumably by homologous recombination.</span></p></div>","PeriodicalId":49689,"journal":{"name":"Plasmid","volume":"112 ","pages":"Article 102541"},"PeriodicalIF":1.8000,"publicationDate":"2020-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.plasmid.2020.102541","citationCount":"2","resultStr":"{\"title\":\"Evolution of IS26-bounded pseudo-compound transposons carrying the tet(C) tetracycline resistance determinant\",\"authors\":\"Carol H. Pong, Robert A. Moran , Ruth M. Hall\",\"doi\":\"10.1016/j.plasmid.2020.102541\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A large plasmid, pCERC14, found in an antibiotic resistant commensal <em>Escherichia coli</em><span> isolate recovered from a healthy adult was sequenced. pCERC14 was 162,926 bp and carried FII-18 and FIB-1 replicons and an F-like transfer region as well as several virulence determinants, some of which are involved in the uptake of iron which would be advantageous for the commensal lifestyle. The plasmid backbone is interrupted in 11 places by complete IS (IS</span><em>1</em> (4 copies), IS<em>2</em> (2), IS<em>629</em> (2) and single IS<em>100</em>, IS<em>186</em><span>, ISEc33) and in three places by partial IS copies. The antibiotic resistance genes were found in two IS</span><em>26</em><span><span>-bounded pseudo-compound transposons (PCT). One contained a remnant of a class 1 </span>integron that includes a </span><em>dfrA5</em><span> gene cassette and the </span><em>sul1</em><span><span> gene conferring resistance to trimethoprim and </span>sulphonamides, respectively. The second, named PTn</span><em>tet</em><span>(C)-var, contained a 4828 bp DNA segment that includes the </span><em>tet</em><span>(C) tetracycline resistance determinant. As </span><em>tet</em>(C) is relatively rare in <em>E. coli</em> and other Gram-negative bacterial isolates, the structure and evolution of <em>tet</em>(C)-containing PCT in available sequences was examined. The largest identified was PTn<em>tet</em>(C), a close relative of PTn<em>tet</em>(C)-var, and a potential progenitor for these PCT. Most PCT shared one internal boundary with PTn<em>tet</em>(C) but the length of the central <em>tet</em>(C)-containing segment was shorter due to IS<em>26</em>-mediated deletions. The most abundant variant form, previously named Tn<em>6309</em>, was widely distributed and, in a derivative of it, most of the <em>tetA</em>(C) gene has been replaced by the <em>tetA</em><span>(A) gene presumably by homologous recombination.</span></p></div>\",\"PeriodicalId\":49689,\"journal\":{\"name\":\"Plasmid\",\"volume\":\"112 \",\"pages\":\"Article 102541\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2020-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.plasmid.2020.102541\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plasmid\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0147619X20300536\",\"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/S0147619X20300536","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Evolution of IS26-bounded pseudo-compound transposons carrying the tet(C) tetracycline resistance determinant
A large plasmid, pCERC14, found in an antibiotic resistant commensal Escherichia coli isolate recovered from a healthy adult was sequenced. pCERC14 was 162,926 bp and carried FII-18 and FIB-1 replicons and an F-like transfer region as well as several virulence determinants, some of which are involved in the uptake of iron which would be advantageous for the commensal lifestyle. The plasmid backbone is interrupted in 11 places by complete IS (IS1 (4 copies), IS2 (2), IS629 (2) and single IS100, IS186, ISEc33) and in three places by partial IS copies. The antibiotic resistance genes were found in two IS26-bounded pseudo-compound transposons (PCT). One contained a remnant of a class 1 integron that includes a dfrA5 gene cassette and the sul1 gene conferring resistance to trimethoprim and sulphonamides, respectively. The second, named PTntet(C)-var, contained a 4828 bp DNA segment that includes the tet(C) tetracycline resistance determinant. As tet(C) is relatively rare in E. coli and other Gram-negative bacterial isolates, the structure and evolution of tet(C)-containing PCT in available sequences was examined. The largest identified was PTntet(C), a close relative of PTntet(C)-var, and a potential progenitor for these PCT. Most PCT shared one internal boundary with PTntet(C) but the length of the central tet(C)-containing segment was shorter due to IS26-mediated deletions. The most abundant variant form, previously named Tn6309, was widely distributed and, in a derivative of it, most of the tetA(C) gene has been replaced by the tetA(A) gene presumably by homologous recombination.
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.