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Genetic diversity and characteristics of high-level tigecycline resistance Tet(X) in Acinetobacter species

BACKGROUND: The recent emergence and dissemination of high-level mobile tigecycline resistance Tet(X) challenge the clinical effectiveness of tigecycline, one of the last-resort therapeutic options for complicated infections caused by multidrug-resistant Gram-negative and Gram-positive pathogens. Al...

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Autores principales: Chen, Chong, Cui, Chao-Yue, Yu, Jun-Jun, He, Qian, Wu, Xiao-Ting, He, Yu-Zhang, Cui, Ze-Hua, Li, Cang, Jia, Qiu-Lin, Shen, Xiang-Guang, Sun, Ruan-Yang, Wang, Xi-Ran, Wang, Min-Ge, Tang, Tian, Zhang, Yan, Liao, Xiao-Ping, Kreiswirth, Barry N., Zhou, Shi-Dan, Huang, Bin, Du, Hong, Sun, Jian, Chen, Liang, Liu, Ya-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722449/
https://www.ncbi.nlm.nih.gov/pubmed/33287863
http://dx.doi.org/10.1186/s13073-020-00807-5
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author Chen, Chong
Cui, Chao-Yue
Yu, Jun-Jun
He, Qian
Wu, Xiao-Ting
He, Yu-Zhang
Cui, Ze-Hua
Li, Cang
Jia, Qiu-Lin
Shen, Xiang-Guang
Sun, Ruan-Yang
Wang, Xi-Ran
Wang, Min-Ge
Tang, Tian
Zhang, Yan
Liao, Xiao-Ping
Kreiswirth, Barry N.
Zhou, Shi-Dan
Huang, Bin
Du, Hong
Sun, Jian
Chen, Liang
Liu, Ya-Hong
author_facet Chen, Chong
Cui, Chao-Yue
Yu, Jun-Jun
He, Qian
Wu, Xiao-Ting
He, Yu-Zhang
Cui, Ze-Hua
Li, Cang
Jia, Qiu-Lin
Shen, Xiang-Guang
Sun, Ruan-Yang
Wang, Xi-Ran
Wang, Min-Ge
Tang, Tian
Zhang, Yan
Liao, Xiao-Ping
Kreiswirth, Barry N.
Zhou, Shi-Dan
Huang, Bin
Du, Hong
Sun, Jian
Chen, Liang
Liu, Ya-Hong
author_sort Chen, Chong
collection PubMed
description BACKGROUND: The recent emergence and dissemination of high-level mobile tigecycline resistance Tet(X) challenge the clinical effectiveness of tigecycline, one of the last-resort therapeutic options for complicated infections caused by multidrug-resistant Gram-negative and Gram-positive pathogens. Although tet(X) has been found in various bacterial species, less is known about phylogeographic distribution and phenotypic variance of different genetic variants. METHODS: Herein, we conducted a multiregional whole-genome sequencing study of tet(X)-positive Acinetobacter isolates from human, animal, and their surrounding environmental sources in China. The molecular and enzymatic features of tet(X) variants were characterized by clonal expression, microbial degradation, reverse transcription, and gene transfer experiments, while the tet(X) genetic diversity and molecular evolution were explored by comparative genomic and Bayesian evolutionary analyses. RESULTS: We identified 193 tet(X)-positive isolates from 3846 samples, with the prevalence ranging from 2.3 to 25.3% in nine provinces in China. The tet(X) was broadly distributed in 12 Acinetobacter species, including six novel species firstly described here. Besides tet(X3) (n = 188) and tet(X4) (n = 5), two tet(X5) variants, tet(X5.2) (n = 36) and tet(X5.3) (n = 4), were also found together with tet(X3) or tet(X4) but without additive effects on tetracyclines. These tet(X)-positive Acinetobacter spp. isolates exhibited 100% resistance rates to tigecycline and tetracycline, as well as high minimum inhibitory concentrations to eravacycline (2–8 μg/mL) and omadacycline (8–16 μg/mL). Genetic analysis revealed that different tet(X) variants shared an analogous ISCR2-mediated transposon structure. The molecular evolutionary analysis indicated that Tet(X) variants likely shared the same common ancestor with the chromosomal monooxygenases that are found in environmental Flavobacteriaceae bacteria, but sequence divergence suggested separation ~ 9900 years ago (7887 BC), presumably associated with the mobilization of tet(X)-like genes through horizontal transfer. CONCLUSIONS: Four tet(X) variants were identified in this study, and they were widely distributed in multiple Acinetobacter spp. strains from various ecological niches across China. Our research also highlighted the crucial role of ISCR2 in mobilizing tet(X)-like genes between different Acinetobacter species and explored the evolutionary history of Tet(X)-like monooxygenases. Further studies are needed to evaluate the clinical impact of these mobile tigecycline resistance genes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-020-00807-5.
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spelling pubmed-77224492020-12-08 Genetic diversity and characteristics of high-level tigecycline resistance Tet(X) in Acinetobacter species Chen, Chong Cui, Chao-Yue Yu, Jun-Jun He, Qian Wu, Xiao-Ting He, Yu-Zhang Cui, Ze-Hua Li, Cang Jia, Qiu-Lin Shen, Xiang-Guang Sun, Ruan-Yang Wang, Xi-Ran Wang, Min-Ge Tang, Tian Zhang, Yan Liao, Xiao-Ping Kreiswirth, Barry N. Zhou, Shi-Dan Huang, Bin Du, Hong Sun, Jian Chen, Liang Liu, Ya-Hong Genome Med Research BACKGROUND: The recent emergence and dissemination of high-level mobile tigecycline resistance Tet(X) challenge the clinical effectiveness of tigecycline, one of the last-resort therapeutic options for complicated infections caused by multidrug-resistant Gram-negative and Gram-positive pathogens. Although tet(X) has been found in various bacterial species, less is known about phylogeographic distribution and phenotypic variance of different genetic variants. METHODS: Herein, we conducted a multiregional whole-genome sequencing study of tet(X)-positive Acinetobacter isolates from human, animal, and their surrounding environmental sources in China. The molecular and enzymatic features of tet(X) variants were characterized by clonal expression, microbial degradation, reverse transcription, and gene transfer experiments, while the tet(X) genetic diversity and molecular evolution were explored by comparative genomic and Bayesian evolutionary analyses. RESULTS: We identified 193 tet(X)-positive isolates from 3846 samples, with the prevalence ranging from 2.3 to 25.3% in nine provinces in China. The tet(X) was broadly distributed in 12 Acinetobacter species, including six novel species firstly described here. Besides tet(X3) (n = 188) and tet(X4) (n = 5), two tet(X5) variants, tet(X5.2) (n = 36) and tet(X5.3) (n = 4), were also found together with tet(X3) or tet(X4) but without additive effects on tetracyclines. These tet(X)-positive Acinetobacter spp. isolates exhibited 100% resistance rates to tigecycline and tetracycline, as well as high minimum inhibitory concentrations to eravacycline (2–8 μg/mL) and omadacycline (8–16 μg/mL). Genetic analysis revealed that different tet(X) variants shared an analogous ISCR2-mediated transposon structure. The molecular evolutionary analysis indicated that Tet(X) variants likely shared the same common ancestor with the chromosomal monooxygenases that are found in environmental Flavobacteriaceae bacteria, but sequence divergence suggested separation ~ 9900 years ago (7887 BC), presumably associated with the mobilization of tet(X)-like genes through horizontal transfer. CONCLUSIONS: Four tet(X) variants were identified in this study, and they were widely distributed in multiple Acinetobacter spp. strains from various ecological niches across China. Our research also highlighted the crucial role of ISCR2 in mobilizing tet(X)-like genes between different Acinetobacter species and explored the evolutionary history of Tet(X)-like monooxygenases. Further studies are needed to evaluate the clinical impact of these mobile tigecycline resistance genes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-020-00807-5. BioMed Central 2020-12-07 /pmc/articles/PMC7722449/ /pubmed/33287863 http://dx.doi.org/10.1186/s13073-020-00807-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Chong
Cui, Chao-Yue
Yu, Jun-Jun
He, Qian
Wu, Xiao-Ting
He, Yu-Zhang
Cui, Ze-Hua
Li, Cang
Jia, Qiu-Lin
Shen, Xiang-Guang
Sun, Ruan-Yang
Wang, Xi-Ran
Wang, Min-Ge
Tang, Tian
Zhang, Yan
Liao, Xiao-Ping
Kreiswirth, Barry N.
Zhou, Shi-Dan
Huang, Bin
Du, Hong
Sun, Jian
Chen, Liang
Liu, Ya-Hong
Genetic diversity and characteristics of high-level tigecycline resistance Tet(X) in Acinetobacter species
title Genetic diversity and characteristics of high-level tigecycline resistance Tet(X) in Acinetobacter species
title_full Genetic diversity and characteristics of high-level tigecycline resistance Tet(X) in Acinetobacter species
title_fullStr Genetic diversity and characteristics of high-level tigecycline resistance Tet(X) in Acinetobacter species
title_full_unstemmed Genetic diversity and characteristics of high-level tigecycline resistance Tet(X) in Acinetobacter species
title_short Genetic diversity and characteristics of high-level tigecycline resistance Tet(X) in Acinetobacter species
title_sort genetic diversity and characteristics of high-level tigecycline resistance tet(x) in acinetobacter species
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722449/
https://www.ncbi.nlm.nih.gov/pubmed/33287863
http://dx.doi.org/10.1186/s13073-020-00807-5
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