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Phenotypic and genotypic characterization of multi-drug-resistant Escherichia coli isolates harboring bla(CTX-M) group extended-spectrum β-lactamases recovered from pediatric patients in Shenzhen, southern China

Aims and Objectives: The emergence and spread of extended-spectrum β-lactamases (ESBLs) particularly CTX-M producing multi-drug-resistant (MDR) Escherichia coli (E. coli) is one of the greatest challenges for community health globally. The study investigated the phenotypic and genotypic characterist...

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Autores principales: Patil, Sandip, Chen, Xiaowen, Lian, Ma, Wen, Feiqiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529603/
https://www.ncbi.nlm.nih.gov/pubmed/31190921
http://dx.doi.org/10.2147/IDR.S199861
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author Patil, Sandip
Chen, Xiaowen
Lian, Ma
Wen, Feiqiu
author_facet Patil, Sandip
Chen, Xiaowen
Lian, Ma
Wen, Feiqiu
author_sort Patil, Sandip
collection PubMed
description Aims and Objectives: The emergence and spread of extended-spectrum β-lactamases (ESBLs) particularly CTX-M producing multi-drug-resistant (MDR) Escherichia coli (E. coli) is one of the greatest challenges for community health globally. The study investigated the phenotypic and genotypic characteristics of ESBLs-producing E. coli recovered from pediatric patients from Shenzhen Children’s Hospital, China. Materials and methods: Present study, a total of 2,670 isolates of E. coli were collected from Shenzhen Children’s Hospital, China of which 950 were ESBLs producer. ESBLs production was confirmed by using the combination disc diffusion method, and antimicrobial susceptibility test was detected. In addition, β-lactamase-producing genes and co-existence of carbapenem/colistin resistance genes were determined by PCR assay and sequencing. The diversity and phylogenetic relationship were determined by multi-locus sequence typing method. Results: Thirty-five percent (n=950) prevalence of ESBLs-producing E. coli we reported in Shenzhen, China of which 50 ESBLs producing E. coli were randomly selected for a further characterization. All 50 ESBLs- producing E. coli isolates revealed MDR phenotype and 100% were resistant to Ampicillin/sulbactam, Ampicillin, Cefazolin, and Ceftriaxone. All 50 ESBLs producers harbored at least one type of β-lactamase gene particular bla(CTX-M). The PCR and sequencing revealed the most common CTX-M subtype was bla(CTX-M-15) (n=18), followed by bla(CTX-M-14) (n=16), bla(CTX-M-90) (n=9), bla(CTX-M-55) (n=3), bla(CTX-M-27), bla(CTX-M-101), and bla(CTX-M-211) each (n=1). Co-existence of bla(CTX-M) with bla(TEM), bla(SHV), bla(GES), and bla(VEB) was detected in few isolates. Among identified sequence types, ST131 (12%) was more dominant in ESBLs-producing E. coli. Phylogenetic group A was the most prominent group among the ESBLs-producing E. coli based on multiplex PCR. Conclusion: Our study shows the prevalence of bla(CTX-M) gene in ESBLs-producing E. coli in pediatric patients in Shenzhen, China. We highlight the importance to monitor the emergence and trends of ESBLs-producing isolates in a pediatric healthcare setting.
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spelling pubmed-65296032019-06-12 Phenotypic and genotypic characterization of multi-drug-resistant Escherichia coli isolates harboring bla(CTX-M) group extended-spectrum β-lactamases recovered from pediatric patients in Shenzhen, southern China Patil, Sandip Chen, Xiaowen Lian, Ma Wen, Feiqiu Infect Drug Resist Original Research Aims and Objectives: The emergence and spread of extended-spectrum β-lactamases (ESBLs) particularly CTX-M producing multi-drug-resistant (MDR) Escherichia coli (E. coli) is one of the greatest challenges for community health globally. The study investigated the phenotypic and genotypic characteristics of ESBLs-producing E. coli recovered from pediatric patients from Shenzhen Children’s Hospital, China. Materials and methods: Present study, a total of 2,670 isolates of E. coli were collected from Shenzhen Children’s Hospital, China of which 950 were ESBLs producer. ESBLs production was confirmed by using the combination disc diffusion method, and antimicrobial susceptibility test was detected. In addition, β-lactamase-producing genes and co-existence of carbapenem/colistin resistance genes were determined by PCR assay and sequencing. The diversity and phylogenetic relationship were determined by multi-locus sequence typing method. Results: Thirty-five percent (n=950) prevalence of ESBLs-producing E. coli we reported in Shenzhen, China of which 50 ESBLs producing E. coli were randomly selected for a further characterization. All 50 ESBLs- producing E. coli isolates revealed MDR phenotype and 100% were resistant to Ampicillin/sulbactam, Ampicillin, Cefazolin, and Ceftriaxone. All 50 ESBLs producers harbored at least one type of β-lactamase gene particular bla(CTX-M). The PCR and sequencing revealed the most common CTX-M subtype was bla(CTX-M-15) (n=18), followed by bla(CTX-M-14) (n=16), bla(CTX-M-90) (n=9), bla(CTX-M-55) (n=3), bla(CTX-M-27), bla(CTX-M-101), and bla(CTX-M-211) each (n=1). Co-existence of bla(CTX-M) with bla(TEM), bla(SHV), bla(GES), and bla(VEB) was detected in few isolates. Among identified sequence types, ST131 (12%) was more dominant in ESBLs-producing E. coli. Phylogenetic group A was the most prominent group among the ESBLs-producing E. coli based on multiplex PCR. Conclusion: Our study shows the prevalence of bla(CTX-M) gene in ESBLs-producing E. coli in pediatric patients in Shenzhen, China. We highlight the importance to monitor the emergence and trends of ESBLs-producing isolates in a pediatric healthcare setting. Dove 2019-05-16 /pmc/articles/PMC6529603/ /pubmed/31190921 http://dx.doi.org/10.2147/IDR.S199861 Text en © 2019 Patil et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Patil, Sandip
Chen, Xiaowen
Lian, Ma
Wen, Feiqiu
Phenotypic and genotypic characterization of multi-drug-resistant Escherichia coli isolates harboring bla(CTX-M) group extended-spectrum β-lactamases recovered from pediatric patients in Shenzhen, southern China
title Phenotypic and genotypic characterization of multi-drug-resistant Escherichia coli isolates harboring bla(CTX-M) group extended-spectrum β-lactamases recovered from pediatric patients in Shenzhen, southern China
title_full Phenotypic and genotypic characterization of multi-drug-resistant Escherichia coli isolates harboring bla(CTX-M) group extended-spectrum β-lactamases recovered from pediatric patients in Shenzhen, southern China
title_fullStr Phenotypic and genotypic characterization of multi-drug-resistant Escherichia coli isolates harboring bla(CTX-M) group extended-spectrum β-lactamases recovered from pediatric patients in Shenzhen, southern China
title_full_unstemmed Phenotypic and genotypic characterization of multi-drug-resistant Escherichia coli isolates harboring bla(CTX-M) group extended-spectrum β-lactamases recovered from pediatric patients in Shenzhen, southern China
title_short Phenotypic and genotypic characterization of multi-drug-resistant Escherichia coli isolates harboring bla(CTX-M) group extended-spectrum β-lactamases recovered from pediatric patients in Shenzhen, southern China
title_sort phenotypic and genotypic characterization of multi-drug-resistant escherichia coli isolates harboring bla(ctx-m) group extended-spectrum β-lactamases recovered from pediatric patients in shenzhen, southern china
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529603/
https://www.ncbi.nlm.nih.gov/pubmed/31190921
http://dx.doi.org/10.2147/IDR.S199861
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