Next-Generation Sequencing for Typing and Detection of ESBL and MBL E. coli causing UTI

Next-generation sequencing (NGS) has the potential to provide typing results and detect resistance genes in a single assay, thus guiding timely treatment decisions and allowing rapid tracking of transmission of resistant clones. We can be evaluated the performance of a new NGS assay during an outbre...

Full description

Bibliographic Details
Main Authors: Nabakishore Nayak, Mahesh Chanda Sahu
Format: Article
Language:English
Published: Science Planet Inc. 2017-10-01
Series:Canadian Journal of Biotechnology
Online Access:https://www.canadianjbiotech.com/CAN_J_BIOTECH/Archives/v1/Special Issue/cjb.2017-a118.pdf
id doaj-582069506bd448ecafa69dd53fe52f56
record_format Article
spelling doaj-582069506bd448ecafa69dd53fe52f562020-11-24T22:48:53ZengScience Planet Inc.Canadian Journal of Biotechnology2560-83042017-10-011Special Issue13213210.24870/cjb.2017-a118Next-Generation Sequencing for Typing and Detection of ESBL and MBL E. coli causing UTINabakishore Nayak0Mahesh Chanda Sahu1Directorate of Medical Research, IMS & Sum Hospital, Siksha ‘O’ Anusandhan University, K-8, Kalinga Nagar, Bhubaneswar 751003, Odisha, INDIADirectorate of Medical Research, IMS & Sum Hospital, Siksha ‘O’ Anusandhan University, K-8, Kalinga Nagar, Bhubaneswar 751003, Odisha, INDIANext-generation sequencing (NGS) has the potential to provide typing results and detect resistance genes in a single assay, thus guiding timely treatment decisions and allowing rapid tracking of transmission of resistant clones. We can be evaluated the performance of a new NGS assay during an outbreak of sequence type 131 (ST131) Escherichia coli infections in a teaching hospital. The assay will be performed on 100 extended-spectrum- beta-lactamase (ESBL) E. coli isolates collected from UTI during last 5 years. Typing results will be compared to those of amplified fragment length polymorphism (AFLP), whereby we will be visually assessed the agreement of the Bio-Detection phylogenetic tree with clusters defined by AFLP. A microarray will be considered the gold standard for detection of resistance genes. AFLP will be identified a large cluster of different indistinguishable isolates on adjacent departments, indicating clonal spread. The BioDetection phylogenetic tree will be showed that all isolates of this outbreak cluster will be strongly related, while the further arrangement of the tree also largely agreed with other clusters defined by AFLP. With these experiments we will detect the ESBL and MBL strains and the patient can be prescribed the antibiotics accordingly.https://www.canadianjbiotech.com/CAN_J_BIOTECH/Archives/v1/Special Issue/cjb.2017-a118.pdf
collection DOAJ
language English
format Article
sources DOAJ
author Nabakishore Nayak
Mahesh Chanda Sahu
spellingShingle Nabakishore Nayak
Mahesh Chanda Sahu
Next-Generation Sequencing for Typing and Detection of ESBL and MBL E. coli causing UTI
Canadian Journal of Biotechnology
author_facet Nabakishore Nayak
Mahesh Chanda Sahu
author_sort Nabakishore Nayak
title Next-Generation Sequencing for Typing and Detection of ESBL and MBL E. coli causing UTI
title_short Next-Generation Sequencing for Typing and Detection of ESBL and MBL E. coli causing UTI
title_full Next-Generation Sequencing for Typing and Detection of ESBL and MBL E. coli causing UTI
title_fullStr Next-Generation Sequencing for Typing and Detection of ESBL and MBL E. coli causing UTI
title_full_unstemmed Next-Generation Sequencing for Typing and Detection of ESBL and MBL E. coli causing UTI
title_sort next-generation sequencing for typing and detection of esbl and mbl e. coli causing uti
publisher Science Planet Inc.
series Canadian Journal of Biotechnology
issn 2560-8304
publishDate 2017-10-01
description Next-generation sequencing (NGS) has the potential to provide typing results and detect resistance genes in a single assay, thus guiding timely treatment decisions and allowing rapid tracking of transmission of resistant clones. We can be evaluated the performance of a new NGS assay during an outbreak of sequence type 131 (ST131) Escherichia coli infections in a teaching hospital. The assay will be performed on 100 extended-spectrum- beta-lactamase (ESBL) E. coli isolates collected from UTI during last 5 years. Typing results will be compared to those of amplified fragment length polymorphism (AFLP), whereby we will be visually assessed the agreement of the Bio-Detection phylogenetic tree with clusters defined by AFLP. A microarray will be considered the gold standard for detection of resistance genes. AFLP will be identified a large cluster of different indistinguishable isolates on adjacent departments, indicating clonal spread. The BioDetection phylogenetic tree will be showed that all isolates of this outbreak cluster will be strongly related, while the further arrangement of the tree also largely agreed with other clusters defined by AFLP. With these experiments we will detect the ESBL and MBL strains and the patient can be prescribed the antibiotics accordingly.
url https://www.canadianjbiotech.com/CAN_J_BIOTECH/Archives/v1/Special Issue/cjb.2017-a118.pdf
work_keys_str_mv AT nabakishorenayak nextgenerationsequencingfortypinganddetectionofesblandmblecolicausinguti
AT maheshchandasahu nextgenerationsequencingfortypinganddetectionofesblandmblecolicausinguti
_version_ 1725678314836721664