Cargando…
Non-lactose fermenting Escherichia coli: Following in the footsteps of lactose fermenting E. coli high-risk clones
Multi-resistant pathogenic strains of non-lactose fermenting Escherichia coli (NLF E. coli) are responsible for various intestinal and extraintestinal infections. Although several studies have characterised such strains using conventional methods, they have not been comprehensively studied at the ge...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669651/ https://www.ncbi.nlm.nih.gov/pubmed/36406419 http://dx.doi.org/10.3389/fmicb.2022.1027494 |
_version_ | 1784832151120773120 |
---|---|
author | Mazumder, Razib Hussain, Arif Phelan, Jody E. Campino, Susana Haider, S. M. Arefeen Mahmud, Araf Ahmed, Dilruba Asadulghani, Md Clark, Taane G. Mondal, Dinesh |
author_facet | Mazumder, Razib Hussain, Arif Phelan, Jody E. Campino, Susana Haider, S. M. Arefeen Mahmud, Araf Ahmed, Dilruba Asadulghani, Md Clark, Taane G. Mondal, Dinesh |
author_sort | Mazumder, Razib |
collection | PubMed |
description | Multi-resistant pathogenic strains of non-lactose fermenting Escherichia coli (NLF E. coli) are responsible for various intestinal and extraintestinal infections. Although several studies have characterised such strains using conventional methods, they have not been comprehensively studied at the genomic level. To address this gap, we used whole-genome sequencing (WGS) coupled with detailed microbiological and biochemical testing to investigate 17 NLF E. coli from a diagnostic centre (icddr,b) in Dhaka, Bangladesh. The prevalence of NLF E. coli was 10%, of which 47% (8/17) exhibited multi-drug resistant (MDR) phenotypes. All isolates (17/17) were confirmed as E. coli and could not ferment lactose sugar. WGS data analysis revealed international high-risk clonal lineages. The most prevalent sequence types (STs) were ST131 (23%), ST1193 (18%), ST12 (18%), ST501 (12%), ST167 (6%), ST73 (6%) and ST12 (6%). Phylogenetic analysis corroborated a striking clonal population amongst the studied NLF E. coli isolates. The predominant phylogroup detected was B2 (65%). The bla(CTX-M-15) extended-spectrum beta-lactamase gene was present in 53% of isolates (9/17), whilst 64.7% (11/17) isolates were affiliated with pathogenic pathotypes. All extraintestinal pathogenic E. coli pathotypes demonstrated β-hemolysis. Our study underscores the presence of critical pathogens and MDR clones amongst non-lactose fermenting E. coli. We suggest that non-lactose fermenting E. coli be considered equally capable as lactose fermenting forms in causing intestinal and extraintestinal infections. Further, there is a need to undertake systematic, unbiased monitoring of predominant lineages amongst non-lactose fermenting E. coli that would help in better treatment and prevention strategies. |
format | Online Article Text |
id | pubmed-9669651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96696512022-11-18 Non-lactose fermenting Escherichia coli: Following in the footsteps of lactose fermenting E. coli high-risk clones Mazumder, Razib Hussain, Arif Phelan, Jody E. Campino, Susana Haider, S. M. Arefeen Mahmud, Araf Ahmed, Dilruba Asadulghani, Md Clark, Taane G. Mondal, Dinesh Front Microbiol Microbiology Multi-resistant pathogenic strains of non-lactose fermenting Escherichia coli (NLF E. coli) are responsible for various intestinal and extraintestinal infections. Although several studies have characterised such strains using conventional methods, they have not been comprehensively studied at the genomic level. To address this gap, we used whole-genome sequencing (WGS) coupled with detailed microbiological and biochemical testing to investigate 17 NLF E. coli from a diagnostic centre (icddr,b) in Dhaka, Bangladesh. The prevalence of NLF E. coli was 10%, of which 47% (8/17) exhibited multi-drug resistant (MDR) phenotypes. All isolates (17/17) were confirmed as E. coli and could not ferment lactose sugar. WGS data analysis revealed international high-risk clonal lineages. The most prevalent sequence types (STs) were ST131 (23%), ST1193 (18%), ST12 (18%), ST501 (12%), ST167 (6%), ST73 (6%) and ST12 (6%). Phylogenetic analysis corroborated a striking clonal population amongst the studied NLF E. coli isolates. The predominant phylogroup detected was B2 (65%). The bla(CTX-M-15) extended-spectrum beta-lactamase gene was present in 53% of isolates (9/17), whilst 64.7% (11/17) isolates were affiliated with pathogenic pathotypes. All extraintestinal pathogenic E. coli pathotypes demonstrated β-hemolysis. Our study underscores the presence of critical pathogens and MDR clones amongst non-lactose fermenting E. coli. We suggest that non-lactose fermenting E. coli be considered equally capable as lactose fermenting forms in causing intestinal and extraintestinal infections. Further, there is a need to undertake systematic, unbiased monitoring of predominant lineages amongst non-lactose fermenting E. coli that would help in better treatment and prevention strategies. Frontiers Media S.A. 2022-11-03 /pmc/articles/PMC9669651/ /pubmed/36406419 http://dx.doi.org/10.3389/fmicb.2022.1027494 Text en Copyright © 2022 Mazumder, Hussain, Phelan, Campino, Haider, Mahmud, Ahmed, Asadulghani, Clark and Mondal. https://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) and the copyright owner(s) 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 Mazumder, Razib Hussain, Arif Phelan, Jody E. Campino, Susana Haider, S. M. Arefeen Mahmud, Araf Ahmed, Dilruba Asadulghani, Md Clark, Taane G. Mondal, Dinesh Non-lactose fermenting Escherichia coli: Following in the footsteps of lactose fermenting E. coli high-risk clones |
title | Non-lactose fermenting Escherichia coli: Following in the footsteps of lactose fermenting E. coli high-risk clones |
title_full | Non-lactose fermenting Escherichia coli: Following in the footsteps of lactose fermenting E. coli high-risk clones |
title_fullStr | Non-lactose fermenting Escherichia coli: Following in the footsteps of lactose fermenting E. coli high-risk clones |
title_full_unstemmed | Non-lactose fermenting Escherichia coli: Following in the footsteps of lactose fermenting E. coli high-risk clones |
title_short | Non-lactose fermenting Escherichia coli: Following in the footsteps of lactose fermenting E. coli high-risk clones |
title_sort | non-lactose fermenting escherichia coli: following in the footsteps of lactose fermenting e. coli high-risk clones |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669651/ https://www.ncbi.nlm.nih.gov/pubmed/36406419 http://dx.doi.org/10.3389/fmicb.2022.1027494 |
work_keys_str_mv | AT mazumderrazib nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones AT hussainarif nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones AT phelanjodye nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones AT campinosusana nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones AT haidersmarefeen nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones AT mahmudaraf nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones AT ahmeddilruba nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones AT asadulghanimd nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones AT clarktaaneg nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones AT mondaldinesh nonlactosefermentingescherichiacolifollowinginthefootstepsoflactosefermentingecolihighriskclones |