Cargando…

P26 Evaluating the antibacterial activity of recombinant phage-encoded lysin against drug-resistant uropathogenic Escherichia coli

BACKGROUND: Atrocious use of antibiotics has led to the emergence of MDR in uropathogenic Escherichia coli (UPEC) that poses a serious challenge in the management of urinary tract infections (UTIs). The WHO has described antibiotic resistance in uropathogens as a key pressure point in the burgeoning...

Descripción completa

Detalles Bibliográficos
Autores principales: Dhar, Sakshi, Nain, Sonia, Gupta, Vaishali, Gaharwar, Utkarsh, Chavan, Bhakti, Das, Ritam, Hanif, Sarmad, Bajpai, Urmi, Sikriwal, Deepa, Choudhary, Aasiya, Syeda, Safia, Shah, Sanket, Ahmed, Syed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395439/
http://dx.doi.org/10.1093/jacamr/dlad077.030
_version_ 1785083576808636416
author Dhar, Sakshi
Nain, Sonia
Gupta, Vaishali
Gaharwar, Utkarsh
Chavan, Bhakti
Das, Ritam
Hanif, Sarmad
Bajpai, Urmi
Sikriwal, Deepa
Choudhary, Aasiya
Syeda, Safia
Shah, Sanket
Ahmed, Syed
author_facet Dhar, Sakshi
Nain, Sonia
Gupta, Vaishali
Gaharwar, Utkarsh
Chavan, Bhakti
Das, Ritam
Hanif, Sarmad
Bajpai, Urmi
Sikriwal, Deepa
Choudhary, Aasiya
Syeda, Safia
Shah, Sanket
Ahmed, Syed
author_sort Dhar, Sakshi
collection PubMed
description BACKGROUND: Atrocious use of antibiotics has led to the emergence of MDR in uropathogenic Escherichia coli (UPEC) that poses a serious challenge in the management of urinary tract infections (UTIs). The WHO has described antibiotic resistance in uropathogens as a key pressure point in the burgeoning global antimicrobial resistance crisis. Given this grim situation, we are exploring phage-encoded lysins as plausible alternatives. OBJECTIVES: Our study involved an in silico strategy for the discovery and characterization of lysin sequences (seq) targeting E. coli cell wall and evaluating the bactericidal activity of these recombinant lysins using in-vitro assays. METHODS: Novel lysin sequences were searched by BLAST homology and by screening E. coli prophages in the database (using PHASTER). Lysozyme-like domain was observed in 9 out of 16 lysins. Their characterization depicted modular or globular structure. Based on the physicochemical properties, 7 out of 16 lysins were selected for cloning, expression, and purification as recombinant proteins for evaluating the bactericidal activity. RESULTS: Among the several lysins screened, lysin seq 5 demonstrated the highest activity using in vitro assays. Using static biofilm assay, lysin seq 5 (180 μg) showed efficient reduction (>50%) in the biofilm formed by ATCC UPEC 700928 strain. As per turbidity reduction method, lysin seq 5 (50 μg) showed 37% drop in OD(600nm) on UPEC 700928 strain after 3 h of incubation at 37°C. Using spot on lawn assay, lysin seq 5 (20 μg) exhibited lytic activity (zone of inhibition) on five drug-resistant clinical UTI isolates, which were pretreated with an outer membrane permeabilizer (OMP), viz., EDTA (0.3 mM). CONCLUSIONS: Lysin seq 5 exhibited antibiofilm activity against UPEC 700928 strain as well as lytic activity against drug-resistant clinical UTI isolates. Screening of additional drug-resistant clinical isolates from UTI patients is underway.
format Online
Article
Text
id pubmed-10395439
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-103954392023-08-03 P26 Evaluating the antibacterial activity of recombinant phage-encoded lysin against drug-resistant uropathogenic Escherichia coli Dhar, Sakshi Nain, Sonia Gupta, Vaishali Gaharwar, Utkarsh Chavan, Bhakti Das, Ritam Hanif, Sarmad Bajpai, Urmi Sikriwal, Deepa Choudhary, Aasiya Syeda, Safia Shah, Sanket Ahmed, Syed JAC Antimicrob Resist Abstracts BACKGROUND: Atrocious use of antibiotics has led to the emergence of MDR in uropathogenic Escherichia coli (UPEC) that poses a serious challenge in the management of urinary tract infections (UTIs). The WHO has described antibiotic resistance in uropathogens as a key pressure point in the burgeoning global antimicrobial resistance crisis. Given this grim situation, we are exploring phage-encoded lysins as plausible alternatives. OBJECTIVES: Our study involved an in silico strategy for the discovery and characterization of lysin sequences (seq) targeting E. coli cell wall and evaluating the bactericidal activity of these recombinant lysins using in-vitro assays. METHODS: Novel lysin sequences were searched by BLAST homology and by screening E. coli prophages in the database (using PHASTER). Lysozyme-like domain was observed in 9 out of 16 lysins. Their characterization depicted modular or globular structure. Based on the physicochemical properties, 7 out of 16 lysins were selected for cloning, expression, and purification as recombinant proteins for evaluating the bactericidal activity. RESULTS: Among the several lysins screened, lysin seq 5 demonstrated the highest activity using in vitro assays. Using static biofilm assay, lysin seq 5 (180 μg) showed efficient reduction (>50%) in the biofilm formed by ATCC UPEC 700928 strain. As per turbidity reduction method, lysin seq 5 (50 μg) showed 37% drop in OD(600nm) on UPEC 700928 strain after 3 h of incubation at 37°C. Using spot on lawn assay, lysin seq 5 (20 μg) exhibited lytic activity (zone of inhibition) on five drug-resistant clinical UTI isolates, which were pretreated with an outer membrane permeabilizer (OMP), viz., EDTA (0.3 mM). CONCLUSIONS: Lysin seq 5 exhibited antibiofilm activity against UPEC 700928 strain as well as lytic activity against drug-resistant clinical UTI isolates. Screening of additional drug-resistant clinical isolates from UTI patients is underway. Oxford University Press 2023-08-02 /pmc/articles/PMC10395439/ http://dx.doi.org/10.1093/jacamr/dlad077.030 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Dhar, Sakshi
Nain, Sonia
Gupta, Vaishali
Gaharwar, Utkarsh
Chavan, Bhakti
Das, Ritam
Hanif, Sarmad
Bajpai, Urmi
Sikriwal, Deepa
Choudhary, Aasiya
Syeda, Safia
Shah, Sanket
Ahmed, Syed
P26 Evaluating the antibacterial activity of recombinant phage-encoded lysin against drug-resistant uropathogenic Escherichia coli
title P26 Evaluating the antibacterial activity of recombinant phage-encoded lysin against drug-resistant uropathogenic Escherichia coli
title_full P26 Evaluating the antibacterial activity of recombinant phage-encoded lysin against drug-resistant uropathogenic Escherichia coli
title_fullStr P26 Evaluating the antibacterial activity of recombinant phage-encoded lysin against drug-resistant uropathogenic Escherichia coli
title_full_unstemmed P26 Evaluating the antibacterial activity of recombinant phage-encoded lysin against drug-resistant uropathogenic Escherichia coli
title_short P26 Evaluating the antibacterial activity of recombinant phage-encoded lysin against drug-resistant uropathogenic Escherichia coli
title_sort p26 evaluating the antibacterial activity of recombinant phage-encoded lysin against drug-resistant uropathogenic escherichia coli
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395439/
http://dx.doi.org/10.1093/jacamr/dlad077.030
work_keys_str_mv AT dharsakshi p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT nainsonia p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT guptavaishali p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT gaharwarutkarsh p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT chavanbhakti p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT dasritam p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT hanifsarmad p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT bajpaiurmi p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT sikriwaldeepa p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT choudharyaasiya p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT syedasafia p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT shahsanket p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli
AT ahmedsyed p26evaluatingtheantibacterialactivityofrecombinantphageencodedlysinagainstdrugresistanturopathogenicescherichiacoli