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Virulence and Genomic Feature of Multidrug Resistant Campylobacter jejuni Isolated from Broiler Chicken

The aim of this study was to reveal the molecular mechanism involved in multidrug resistance and virulence of Campylobacter jejuni isolated from broiler chickens. The virulence of six multidrug resistant C. jejuni was determined by in vitro and in vivo methods. The de novo whole genome sequencing te...

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Autores principales: Hao, Haihong, Ren, Ni, Han, Jing, Foley, Steven L., Iqbal, Zahid, Cheng, Guyue, Kuang, Xiuhua, Liu, Jie, Liu, Zhenli, Dai, Menghong, Wang, Yulian, Yuan, Zonghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064177/
https://www.ncbi.nlm.nih.gov/pubmed/27790202
http://dx.doi.org/10.3389/fmicb.2016.01605
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author Hao, Haihong
Ren, Ni
Han, Jing
Foley, Steven L.
Iqbal, Zahid
Cheng, Guyue
Kuang, Xiuhua
Liu, Jie
Liu, Zhenli
Dai, Menghong
Wang, Yulian
Yuan, Zonghui
author_facet Hao, Haihong
Ren, Ni
Han, Jing
Foley, Steven L.
Iqbal, Zahid
Cheng, Guyue
Kuang, Xiuhua
Liu, Jie
Liu, Zhenli
Dai, Menghong
Wang, Yulian
Yuan, Zonghui
author_sort Hao, Haihong
collection PubMed
description The aim of this study was to reveal the molecular mechanism involved in multidrug resistance and virulence of Campylobacter jejuni isolated from broiler chickens. The virulence of six multidrug resistant C. jejuni was determined by in vitro and in vivo methods. The de novo whole genome sequencing technology and molecular biology methods were used to analyze the genomic features associated with the multidrug resistance and virulence of a selected isolate (C. jejuni 1655). The comparative genomic analyses revealed a large number of single nucleotide polymorphisms, deletions, rearrangements, and inversions in C. jejuni 1655 compared to reference C. jejuni genomes. The co-emergence of Thr-86-Ile mutation in gyrA gene, A2075G mutation in 23S rRNA gene, tetO, aphA and aadE genes and pTet plasmid in C. jejuni 1655 contributed its multidrug resistance to fluoroquinolones, macrolides, tetracycline, and aminoglycosides. The combination of multiple virulence genes may work together to confer the relative higher virulence in C. jejuni 1655. The co-existence of mobile gene elements (e.g., pTet) and CRISPR-Cas system in C. jejuni 1655 may play an important role in the gene transfer and immune defense. The present study provides basic information of phenotypic and genomic features of C. jejuni 1655, a strain recently isolated from a chicken displaying multidrug resistance and relatively high level of virulence.
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spelling pubmed-50641772016-10-27 Virulence and Genomic Feature of Multidrug Resistant Campylobacter jejuni Isolated from Broiler Chicken Hao, Haihong Ren, Ni Han, Jing Foley, Steven L. Iqbal, Zahid Cheng, Guyue Kuang, Xiuhua Liu, Jie Liu, Zhenli Dai, Menghong Wang, Yulian Yuan, Zonghui Front Microbiol Microbiology The aim of this study was to reveal the molecular mechanism involved in multidrug resistance and virulence of Campylobacter jejuni isolated from broiler chickens. The virulence of six multidrug resistant C. jejuni was determined by in vitro and in vivo methods. The de novo whole genome sequencing technology and molecular biology methods were used to analyze the genomic features associated with the multidrug resistance and virulence of a selected isolate (C. jejuni 1655). The comparative genomic analyses revealed a large number of single nucleotide polymorphisms, deletions, rearrangements, and inversions in C. jejuni 1655 compared to reference C. jejuni genomes. The co-emergence of Thr-86-Ile mutation in gyrA gene, A2075G mutation in 23S rRNA gene, tetO, aphA and aadE genes and pTet plasmid in C. jejuni 1655 contributed its multidrug resistance to fluoroquinolones, macrolides, tetracycline, and aminoglycosides. The combination of multiple virulence genes may work together to confer the relative higher virulence in C. jejuni 1655. The co-existence of mobile gene elements (e.g., pTet) and CRISPR-Cas system in C. jejuni 1655 may play an important role in the gene transfer and immune defense. The present study provides basic information of phenotypic and genomic features of C. jejuni 1655, a strain recently isolated from a chicken displaying multidrug resistance and relatively high level of virulence. Frontiers Media S.A. 2016-10-14 /pmc/articles/PMC5064177/ /pubmed/27790202 http://dx.doi.org/10.3389/fmicb.2016.01605 Text en Copyright © 2016 Hao, Ren, Han, Foley, Iqbal, Cheng, Kuang, Liu, Liu, Dai, Wang and Yuan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Hao, Haihong
Ren, Ni
Han, Jing
Foley, Steven L.
Iqbal, Zahid
Cheng, Guyue
Kuang, Xiuhua
Liu, Jie
Liu, Zhenli
Dai, Menghong
Wang, Yulian
Yuan, Zonghui
Virulence and Genomic Feature of Multidrug Resistant Campylobacter jejuni Isolated from Broiler Chicken
title Virulence and Genomic Feature of Multidrug Resistant Campylobacter jejuni Isolated from Broiler Chicken
title_full Virulence and Genomic Feature of Multidrug Resistant Campylobacter jejuni Isolated from Broiler Chicken
title_fullStr Virulence and Genomic Feature of Multidrug Resistant Campylobacter jejuni Isolated from Broiler Chicken
title_full_unstemmed Virulence and Genomic Feature of Multidrug Resistant Campylobacter jejuni Isolated from Broiler Chicken
title_short Virulence and Genomic Feature of Multidrug Resistant Campylobacter jejuni Isolated from Broiler Chicken
title_sort virulence and genomic feature of multidrug resistant campylobacter jejuni isolated from broiler chicken
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064177/
https://www.ncbi.nlm.nih.gov/pubmed/27790202
http://dx.doi.org/10.3389/fmicb.2016.01605
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