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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...
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Published in: | Tropical medicine and infectious disease 2022-09, Vol.7 (9), p.1-11 |
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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 |
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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. 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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> |
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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 |
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