Literature DB >> 32395746

Plasmids of novel incompatibility group IncpRBL16 from Pseudomonas species.

Xiaoyuan Jiang1, Zhe Yin1, Min Yuan2, Qiaoxiang Cheng3, Lingfei Hu1, Yanan Xu3, Wenhui Yang1, Huiying Yang1, Yuee Zhao1, Xiaodong Zhao1, Bo Gao1, Erhei Dai3, Yajun Song1, Dongsheng Zhou1.   

Abstract

OBJECTIVES: To dissect genomic features of IncpRBL16 plasmids from Pseudomonas.
METHODS: An extensive genomic comparison was applied to all 17 available sequenced IncpRBL16 plasmids, including 8 sequenced in this study and another 2 sequenced in two of our previous studies.
RESULTS: Conserved IncpRBL16 backbone markers repAIncpRBL16 together with its iterons, parB2-parA, che, pil and ter were present in all 17 plasmids. At least 18 regions or sites across IncpRBL16 genomes exhibited major modular differences, including insertion of accessory modules, deletion of backbone regions surrounding insertion sites and substitution of multiple-gene backbone regions. Ten plasmids carried a sole IncpRBL16 replicon, while exogenous acquisition of an auxiliary replicon (located in an accessory module) besides the primary IncpRBL16 replicon was observed in each of the remaining seven plasmids. The 17 IncpRBL16 plasmids carried at least 71 different accessory modules, notably including Tn1403-related regions, Tn7-family transposons, Tn6571-family transposons, integrative and conjugative elements, and integrative and mobilizable elements. There were a total of 40 known resistance genes, which were involved in resistance to 15 categories of antibiotics and heavy metals, notably including blaIMP-9, blaIMP-45, blaVIM-2, blaDIM-2, blaOXA-246, blaPER-1, aphA and armA.
CONCLUSIONS: Different IncpRBL16 plasmids contain different profiles of accessory modules and thus diverse collections of resistance genes. To the best of our knowledge, this is the first report of fully sequenced blaOXA-246-carrying (p12939-PER) and blaPER-1-carrying (p12939-PER and pA681-IMP) IncpRBL16 plasmids and also that of 14 novel (first identified in this study) and additionally 31 newly named (first designated in this study, but with previously determined sequences) mobile elements.
© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

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Year:  2020        PMID: 32395746     DOI: 10.1093/jac/dkaa143

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  7 in total

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2.  Diversification and prevalence of the quinolone resistance crpP genes and the crpP-carrying Tn6786-related integrative and conjugative elements in Pseudomonas aeruginosa.

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5.  Precise classification of antimicrobial resistance-associated IncP-2 megaplasmids for molecular epidemiological studies on Pseudomonas species.

Authors:  Masaki Shintani; Haruo Suzuki; Hideaki Nojiri; Masato Suzuki
Journal:  J Antimicrob Chemother       Date:  2022-03-31       Impact factor: 5.790

6.  Comparative analysis reveals the modular functional structure of conjugative megaplasmid pTTS12 of Pseudomonas putida S12: A paradigm for transferable traits, plasmid stability, and inheritance?

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7.  An IncP-2 plasmid sublineage associated with dissemination of blaIMP-45 among carbapenem-resistant Pseudomonas aeruginosa.

Authors:  Xuefei Zhang; Leilei Wang; Dan Li; Pei Li; Lili Yuan; Fan Yang; Qinglan Guo; Minggui Wang
Journal:  Emerg Microbes Infect       Date:  2021-12       Impact factor: 7.163

  7 in total

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