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Capture of armA by a novel ISCR element, ISCR28.
Yuan, Min; Nie, Lu; Huang, Zhenzhou; Xu, Shuai; Qiu, Xiaotong; Han, Lichao; Kang, Yutong; Li, Fang; Yao, Jiang; Li, Qixin; Li, Huan; Li, Dan; Zhu, Xiong; Li, Zhenjun.
Affiliation
  • Yuan M; National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
  • Nie L; Department of Laboratory Medicine, The First People's Hospital of Foshan, Foshan, Guangdong, China.
  • Huang Z; National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
  • Xu S; National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
  • Qiu X; National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
  • Han L; National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
  • Kang Y; National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
  • Li F; National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
  • Yao J; School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, China.
  • Li Q; Department of Laboratory Medicine, The First People's Hospital of Foshan, Foshan, Guangdong, China.
  • Li H; Central and Clinical Laboratory of Sanya People's Hospital, Sanya, Hainan, China.
  • Li D; National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
  • Zhu X; Central and Clinical Laboratory of Sanya People's Hospital, Sanya, Hainan, China. Electronic address: zhuxiong6@163.com.
  • Li Z; National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China. Electronic address: lizhenjun@icdc.cn.
Int J Antimicrob Agents ; 64(3): 107250, 2024 Sep.
Article in En | MEDLINE | ID: mdl-38908532
ABSTRACT
ISCR28 is a fully functional and active member of the IS91-like family of insertion sequences. ISCR28 is 1,708-bp long and contains a 1,293-bp long putative open reading frame that codes a transposase. Sixty ISCR28-containing sequences from GenBank generated 27 non-repeat genetic contexts, all of which represented naturally occurring biological events that had occurred in a wide range of gram-negative organisms. Insertion of ISCR28 into target DNA preferred the presence of a 5'-GXXT-3' sequence at its terIS (replication terminator) end. Loss of the first 4 bp of its oriIS (origin of replication) likely caused ISCR28 to be trapped in ISApl1-based transposons or similar structures. Loss of terIS and fusion with a mobile element upstream likely promoted co-transfer of ISCR28 and the downstream resistance genes. ArmA and its downstream intact ISCR28 can be excised from recombinant pKD46 plasmids forming circular intermediates, further elucidating its activity as a transposase.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Transposable Elements / Transposases Language: En Journal: Int J Antimicrob Agents / Int. j. antimicrob. agents / International journal of antimicrobial agents Year: 2024 Document type: Article Affiliation country: China Country of publication: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Transposable Elements / Transposases Language: En Journal: Int J Antimicrob Agents / Int. j. antimicrob. agents / International journal of antimicrobial agents Year: 2024 Document type: Article Affiliation country: China Country of publication: Países Bajos