Loading…

Efficacy of Fosfomycin against planktonic and biofilm-associated MDR Uropathogenic 'Escherichia Coli' clinical isolates

Urinary tract infections (UTI) are a severe public health problem and are caused mainly by the uropathogenic 'Escherichia coli' (UPEC). Antimicrobial resistance and limited development of new antimicrobials have led to the reuse of old antibiotics such as fosfomycin. The aim of this study...

Full description

Saved in:
Bibliographic Details
Published in:Tropical medicine and infectious disease 2022-09, Vol.7 (9), p.1-11
Main Authors: Haziel Eleazar Dzib-Baak, Andres Humberto Uc-Cachon, Angel de Jesus Dzul-Beh, Rey Fernando Rosado-Manzano, Carlos Gracida-Osorno, Gloria Maria Molina-Salinas
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c503t-fff4e8308bcbda29469d90b0a217fffeba249020b33ea706e7db3e687282b7523
cites cdi_FETCH-LOGICAL-c503t-fff4e8308bcbda29469d90b0a217fffeba249020b33ea706e7db3e687282b7523
container_end_page 11
container_issue 9
container_start_page 1
container_title Tropical medicine and infectious disease
container_volume 7
creator Haziel Eleazar Dzib-Baak
Andres Humberto Uc-Cachon
Angel de Jesus Dzul-Beh
Rey Fernando Rosado-Manzano
Carlos Gracida-Osorno
Gloria Maria Molina-Salinas
description Urinary tract infections (UTI) are a severe public health problem and are caused mainly by the uropathogenic 'Escherichia coli' (UPEC). Antimicrobial resistance and limited development of new antimicrobials have led to the reuse of old antibiotics such as fosfomycin. The aim of this study was to evaluate the in vitro efficacy of fosfomycin on a collection of multidrug-resistant (MDR) UPEC and the degradative activity on biofilm producers. A total of 100 MDR UPEC clinical isolates were collected from patients at Mexican second- and third-level hospitals. Microorganism identification was performed using an automated system, the evaluation of the susceptibility of clinical isolates to fosfomycin was performed using the resazurin microtiter assay, and the identification of biofilm producers and the effect of fosfomycin in biofilms were evaluated using the crystal violet method. Among planktonic MDR UPEC, 93% were susceptible to fosfomycin. Eighty-three MDR UPEC were categorized as weak (39.8%), moderate (45.2%), and strong (14.5%) biofilm producers. Fosfomycin exhibited degradative activity ranging from 164.4 g/mL to 1045 g/mL. Weak producers required statistically lower concentrations of fosfomycin to destroy the biofilm, contrary to moderate and strong producers. In conclusion, fosfomycin could be an option for the treatment of infections caused by MDR UPEC, for which the antimicrobial treatment is more often becoming limited.
doi_str_mv 10.3390/tropicalmed7090235
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_ef8e218b597440889073372066e6cf01</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><informt_id>10.3316/informit.050763492924778</informt_id><doaj_id>oai_doaj_org_article_ef8e218b597440889073372066e6cf01</doaj_id><sourcerecordid>2716943093</sourcerecordid><originalsourceid>FETCH-LOGICAL-c503t-fff4e8308bcbda29469d90b0a217fffeba249020b33ea706e7db3e687282b7523</originalsourceid><addsrcrecordid>eNplkk9vEzEQxVcIRKvSL8ABrcShXAKzttd_LkgopFCpCAm1Z8vrtRMHrx1sB5Rvj5OU0sLJlt9vnt-MpmledvAWYwHvSoobp5WfzMhAAML9k-YUkY7MKKb06YP7SXOe8xoAOt4DJfC8OcG0qwKhp82vhbXVRu_aaNvLmG2cdtqFVi2VC7m0G6_C9xKD060KYzu4aJ2fZirnqJ0qZmy_fPzW3tYwqqzi0uzBi0XWK5OcXjnVzqN3F632LuzTti5HX8vyi-aZVT6b87vzrLm9XNzMP8-uv366mn-4nukecJlZa4nhGPigh1EhQagYBQygUMeqZgaFSG0eBoyNYkANGwdsKGeIo4H1CJ81V0ffMaq13CQ3qbSTUTl5eIhpKVUqTnsjjeUGdXzoBSMEOBfAMGYIKDVUW-iq1_uj12Y71LFrE0pS_pHpYyW4lVzGn1L00Ncs1eDNnUGKP7YmFzm5rI2vMzZxmyViHRUEg9ijr_9B13GbQh3VgaJAkeCVQkdKp5hzMvY-TAdyvyby_zWpRa8etnFf8mcpKnBzBNLkitTRe6OLiyGvVckyG5X0Srpg40Hfj3CM7vhjR_8K0AOjmAgkEGGM499AzNo0</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2716606298</pqid></control><display><type>article</type><title>Efficacy of Fosfomycin against planktonic and biofilm-associated MDR Uropathogenic 'Escherichia Coli' clinical isolates</title><source>Open Access: PubMed Central</source><source>Publicly Available Content Database</source><creator>Haziel Eleazar Dzib-Baak ; Andres Humberto Uc-Cachon ; Angel de Jesus Dzul-Beh ; Rey Fernando Rosado-Manzano ; Carlos Gracida-Osorno ; Gloria Maria Molina-Salinas</creator><creatorcontrib>Haziel Eleazar Dzib-Baak ; Andres Humberto Uc-Cachon ; Angel de Jesus Dzul-Beh ; Rey Fernando Rosado-Manzano ; Carlos Gracida-Osorno ; Gloria Maria Molina-Salinas</creatorcontrib><description>Urinary tract infections (UTI) are a severe public health problem and are caused mainly by the uropathogenic 'Escherichia coli' (UPEC). Antimicrobial resistance and limited development of new antimicrobials have led to the reuse of old antibiotics such as fosfomycin. The aim of this study was to evaluate the in vitro efficacy of fosfomycin on a collection of multidrug-resistant (MDR) UPEC and the degradative activity on biofilm producers. A total of 100 MDR UPEC clinical isolates were collected from patients at Mexican second- and third-level hospitals. Microorganism identification was performed using an automated system, the evaluation of the susceptibility of clinical isolates to fosfomycin was performed using the resazurin microtiter assay, and the identification of biofilm producers and the effect of fosfomycin in biofilms were evaluated using the crystal violet method. Among planktonic MDR UPEC, 93% were susceptible to fosfomycin. Eighty-three MDR UPEC were categorized as weak (39.8%), moderate (45.2%), and strong (14.5%) biofilm producers. Fosfomycin exhibited degradative activity ranging from 164.4 g/mL to 1045 g/mL. Weak producers required statistically lower concentrations of fosfomycin to destroy the biofilm, contrary to moderate and strong producers. In conclusion, fosfomycin could be an option for the treatment of infections caused by MDR UPEC, for which the antimicrobial treatment is more often becoming limited.</description><identifier>ISSN: 2414-6366</identifier><identifier>EISSN: 2414-6366</identifier><identifier>DOI: 10.3390/tropicalmed7090235</identifier><identifier>PMID: 36136646</identifier><language>eng</language><publisher>Basel, Switzerland: MDPI</publisher><subject>Antibiotics ; Antimicrobial agents ; Bacteria ; biofilm ; Biofilms ; Care ; Control ; Diagnosis ; Drug resistance ; E coli ; Escherichia coli ; Fosfomycin ; Multidrug resistant organisms ; multidrug-resistant ; Patients ; Treatment ; Urinary tract infections ; uropathogenic Escherichia coli</subject><ispartof>Tropical medicine and infectious disease, 2022-09, Vol.7 (9), p.1-11</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-fff4e8308bcbda29469d90b0a217fffeba249020b33ea706e7db3e687282b7523</citedby><cites>FETCH-LOGICAL-c503t-fff4e8308bcbda29469d90b0a217fffeba249020b33ea706e7db3e687282b7523</cites><orcidid>0000-0003-3845-7930 ; 0000-0002-4971-7833 ; 0000-0002-3961-6449 ; 0000-0002-4697-9707</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2716606298/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2716606298?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36136646$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Haziel Eleazar Dzib-Baak</creatorcontrib><creatorcontrib>Andres Humberto Uc-Cachon</creatorcontrib><creatorcontrib>Angel de Jesus Dzul-Beh</creatorcontrib><creatorcontrib>Rey Fernando Rosado-Manzano</creatorcontrib><creatorcontrib>Carlos Gracida-Osorno</creatorcontrib><creatorcontrib>Gloria Maria Molina-Salinas</creatorcontrib><title>Efficacy of Fosfomycin against planktonic and biofilm-associated MDR Uropathogenic 'Escherichia Coli' clinical isolates</title><title>Tropical medicine and infectious disease</title><addtitle>Trop Med Infect Dis</addtitle><description>Urinary tract infections (UTI) are a severe public health problem and are caused mainly by the uropathogenic 'Escherichia coli' (UPEC). Antimicrobial resistance and limited development of new antimicrobials have led to the reuse of old antibiotics such as fosfomycin. The aim of this study was to evaluate the in vitro efficacy of fosfomycin on a collection of multidrug-resistant (MDR) UPEC and the degradative activity on biofilm producers. A total of 100 MDR UPEC clinical isolates were collected from patients at Mexican second- and third-level hospitals. Microorganism identification was performed using an automated system, the evaluation of the susceptibility of clinical isolates to fosfomycin was performed using the resazurin microtiter assay, and the identification of biofilm producers and the effect of fosfomycin in biofilms were evaluated using the crystal violet method. Among planktonic MDR UPEC, 93% were susceptible to fosfomycin. Eighty-three MDR UPEC were categorized as weak (39.8%), moderate (45.2%), and strong (14.5%) biofilm producers. Fosfomycin exhibited degradative activity ranging from 164.4 g/mL to 1045 g/mL. Weak producers required statistically lower concentrations of fosfomycin to destroy the biofilm, contrary to moderate and strong producers. In conclusion, fosfomycin could be an option for the treatment of infections caused by MDR UPEC, for which the antimicrobial treatment is more often becoming limited.</description><subject>Antibiotics</subject><subject>Antimicrobial agents</subject><subject>Bacteria</subject><subject>biofilm</subject><subject>Biofilms</subject><subject>Care</subject><subject>Control</subject><subject>Diagnosis</subject><subject>Drug resistance</subject><subject>E coli</subject><subject>Escherichia coli</subject><subject>Fosfomycin</subject><subject>Multidrug resistant organisms</subject><subject>multidrug-resistant</subject><subject>Patients</subject><subject>Treatment</subject><subject>Urinary tract infections</subject><subject>uropathogenic Escherichia coli</subject><issn>2414-6366</issn><issn>2414-6366</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkk9vEzEQxVcIRKvSL8ABrcShXAKzttd_LkgopFCpCAm1Z8vrtRMHrx1sB5Rvj5OU0sLJlt9vnt-MpmledvAWYwHvSoobp5WfzMhAAML9k-YUkY7MKKb06YP7SXOe8xoAOt4DJfC8OcG0qwKhp82vhbXVRu_aaNvLmG2cdtqFVi2VC7m0G6_C9xKD060KYzu4aJ2fZirnqJ0qZmy_fPzW3tYwqqzi0uzBi0XWK5OcXjnVzqN3F632LuzTti5HX8vyi-aZVT6b87vzrLm9XNzMP8-uv366mn-4nukecJlZa4nhGPigh1EhQagYBQygUMeqZgaFSG0eBoyNYkANGwdsKGeIo4H1CJ81V0ffMaq13CQ3qbSTUTl5eIhpKVUqTnsjjeUGdXzoBSMEOBfAMGYIKDVUW-iq1_uj12Y71LFrE0pS_pHpYyW4lVzGn1L00Ncs1eDNnUGKP7YmFzm5rI2vMzZxmyViHRUEg9ijr_9B13GbQh3VgaJAkeCVQkdKp5hzMvY-TAdyvyby_zWpRa8etnFf8mcpKnBzBNLkitTRe6OLiyGvVckyG5X0Srpg40Hfj3CM7vhjR_8K0AOjmAgkEGGM499AzNo0</recordid><startdate>20220908</startdate><enddate>20220908</enddate><creator>Haziel Eleazar Dzib-Baak</creator><creator>Andres Humberto Uc-Cachon</creator><creator>Angel de Jesus Dzul-Beh</creator><creator>Rey Fernando Rosado-Manzano</creator><creator>Carlos Gracida-Osorno</creator><creator>Gloria Maria Molina-Salinas</creator><general>MDPI</general><general>MDPI AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-3845-7930</orcidid><orcidid>https://orcid.org/0000-0002-4971-7833</orcidid><orcidid>https://orcid.org/0000-0002-3961-6449</orcidid><orcidid>https://orcid.org/0000-0002-4697-9707</orcidid></search><sort><creationdate>20220908</creationdate><title>Efficacy of Fosfomycin against planktonic and biofilm-associated MDR Uropathogenic 'Escherichia Coli' clinical isolates</title><author>Haziel Eleazar Dzib-Baak ; Andres Humberto Uc-Cachon ; Angel de Jesus Dzul-Beh ; Rey Fernando Rosado-Manzano ; Carlos Gracida-Osorno ; Gloria Maria Molina-Salinas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-fff4e8308bcbda29469d90b0a217fffeba249020b33ea706e7db3e687282b7523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibiotics</topic><topic>Antimicrobial agents</topic><topic>Bacteria</topic><topic>biofilm</topic><topic>Biofilms</topic><topic>Care</topic><topic>Control</topic><topic>Diagnosis</topic><topic>Drug resistance</topic><topic>E coli</topic><topic>Escherichia coli</topic><topic>Fosfomycin</topic><topic>Multidrug resistant organisms</topic><topic>multidrug-resistant</topic><topic>Patients</topic><topic>Treatment</topic><topic>Urinary tract infections</topic><topic>uropathogenic Escherichia coli</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haziel Eleazar Dzib-Baak</creatorcontrib><creatorcontrib>Andres Humberto Uc-Cachon</creatorcontrib><creatorcontrib>Angel de Jesus Dzul-Beh</creatorcontrib><creatorcontrib>Rey Fernando Rosado-Manzano</creatorcontrib><creatorcontrib>Carlos Gracida-Osorno</creatorcontrib><creatorcontrib>Gloria Maria Molina-Salinas</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Tropical medicine and infectious disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haziel Eleazar Dzib-Baak</au><au>Andres Humberto Uc-Cachon</au><au>Angel de Jesus Dzul-Beh</au><au>Rey Fernando Rosado-Manzano</au><au>Carlos Gracida-Osorno</au><au>Gloria Maria Molina-Salinas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of Fosfomycin against planktonic and biofilm-associated MDR Uropathogenic 'Escherichia Coli' clinical isolates</atitle><jtitle>Tropical medicine and infectious disease</jtitle><addtitle>Trop Med Infect Dis</addtitle><date>2022-09-08</date><risdate>2022</risdate><volume>7</volume><issue>9</issue><spage>1</spage><epage>11</epage><pages>1-11</pages><issn>2414-6366</issn><eissn>2414-6366</eissn><abstract>Urinary tract infections (UTI) are a severe public health problem and are caused mainly by the uropathogenic 'Escherichia coli' (UPEC). Antimicrobial resistance and limited development of new antimicrobials have led to the reuse of old antibiotics such as fosfomycin. The aim of this study was to evaluate the in vitro efficacy of fosfomycin on a collection of multidrug-resistant (MDR) UPEC and the degradative activity on biofilm producers. A total of 100 MDR UPEC clinical isolates were collected from patients at Mexican second- and third-level hospitals. Microorganism identification was performed using an automated system, the evaluation of the susceptibility of clinical isolates to fosfomycin was performed using the resazurin microtiter assay, and the identification of biofilm producers and the effect of fosfomycin in biofilms were evaluated using the crystal violet method. Among planktonic MDR UPEC, 93% were susceptible to fosfomycin. Eighty-three MDR UPEC were categorized as weak (39.8%), moderate (45.2%), and strong (14.5%) biofilm producers. Fosfomycin exhibited degradative activity ranging from 164.4 g/mL to 1045 g/mL. Weak producers required statistically lower concentrations of fosfomycin to destroy the biofilm, contrary to moderate and strong producers. In conclusion, fosfomycin could be an option for the treatment of infections caused by MDR UPEC, for which the antimicrobial treatment is more often becoming limited.</abstract><cop>Basel, Switzerland</cop><pub>MDPI</pub><pmid>36136646</pmid><doi>10.3390/tropicalmed7090235</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-3845-7930</orcidid><orcidid>https://orcid.org/0000-0002-4971-7833</orcidid><orcidid>https://orcid.org/0000-0002-3961-6449</orcidid><orcidid>https://orcid.org/0000-0002-4697-9707</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2414-6366
ispartof Tropical medicine and infectious disease, 2022-09, Vol.7 (9), p.1-11
issn 2414-6366
2414-6366
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_ef8e218b597440889073372066e6cf01
source Open Access: PubMed Central; Publicly Available Content Database
subjects Antibiotics
Antimicrobial agents
Bacteria
biofilm
Biofilms
Care
Control
Diagnosis
Drug resistance
E coli
Escherichia coli
Fosfomycin
Multidrug resistant organisms
multidrug-resistant
Patients
Treatment
Urinary tract infections
uropathogenic Escherichia coli
title Efficacy of Fosfomycin against planktonic and biofilm-associated MDR Uropathogenic 'Escherichia Coli' clinical isolates
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T23%3A34%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Efficacy%20of%20Fosfomycin%20against%20planktonic%20and%20biofilm-associated%20MDR%20Uropathogenic%20'Escherichia%20Coli'%20clinical%20isolates&rft.jtitle=Tropical%20medicine%20and%20infectious%20disease&rft.au=Haziel%20Eleazar%20Dzib-Baak&rft.date=2022-09-08&rft.volume=7&rft.issue=9&rft.spage=1&rft.epage=11&rft.pages=1-11&rft.issn=2414-6366&rft.eissn=2414-6366&rft_id=info:doi/10.3390/tropicalmed7090235&rft_dat=%3Cproquest_doaj_%3E2716943093%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c503t-fff4e8308bcbda29469d90b0a217fffeba249020b33ea706e7db3e687282b7523%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2716606298&rft_id=info:pmid/36136646&rft_informt_id=10.3316/informit.050763492924778&rfr_iscdi=true