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In vitro Synergistic Activities of Fosfomycin in Combination with Other Antimicrobial Agents Against Carbapenem -Resistant Escherichia coli Harboring [bla.sub.NDM-1] on the IncN2 Plasmid and a Study of the Genomic Characteristics of These Pathogens

Purpose: The spread of New Delhi metallo-[beta]-lactamase (NDM) encoded by the [bla.sub.NDM] gene has been a global health crisis for many years. Most of [bla.sub.NDM]-harboring bacteria commonly carry various antimicrobial resistance (AMR) genes on their chromosomes or plasmids, leading to limited...

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Published in:Infection and drug resistance 2022-04, Vol.15, p.1777
Main Authors: Phaothong, Chanitnart, Jeenkeawpiam, Kongpop, Sakunrang, Chanida, Charernmak, Boonsri, Pomwised, Rattanaruji, Chusri, Sarunyou, Kaewnirat, Kalyarat, Hortiwakul, Thanaporn, Phoo, May Thet Paing, Surachat, Komwit, Chukamnerd, Arnon, Chuaychob, Surachat
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container_title Infection and drug resistance
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creator Phaothong, Chanitnart
Jeenkeawpiam, Kongpop
Sakunrang, Chanida
Charernmak, Boonsri
Pomwised, Rattanaruji
Chusri, Sarunyou
Kaewnirat, Kalyarat
Hortiwakul, Thanaporn
Phoo, May Thet Paing
Surachat, Komwit
Chukamnerd, Arnon
Chuaychob, Surachat
description Purpose: The spread of New Delhi metallo-[beta]-lactamase (NDM) encoded by the [bla.sub.NDM] gene has been a global health crisis for many years. Most of [bla.sub.NDM]-harboring bacteria commonly carry various antimicrobial resistance (AMR) genes on their chromosomes or plasmids, leading to limited treatment options. Thus, we aimed to evaluate the synergistic effects of fosfomycin in combination with other antimicrobial agents against [bla.sub.NDM]-harboring carbapenem-resistant Escherichia coli (CREC) and to characterize the wholegenome and plasmid sequences of these pathogens. Methods: Thirty-eight CREC isolates were collected from patients in the Medicine Ward, Songklanagarind Hospital, Thailand. The activity of fosfomycin in combination with other antimicrobial agents against CREC isolates harboring [bla.sub.NDM] on the plasmid was evaluated using the checkerboard method. In this method, the serial dilutions of two antibiotics were mixed with the cultured CREC, the mixtures were incubated, and FICI was calculated to interpret the synergistic activity of the combination. The whole-genome and particular plasmids of these pathogens were sequenced using next-generation sequencing. Sequence analysis, especially on antimicrobial resistance (AMR) genes, mobile-genetic elements (MGEs), and virulence genes was performed using many bioinformatics tools. Results: Of the E. coli 38 isolates, only 3 isolates contained the [bla.sub.NDM-1] gene, which is located on the IncN2 plasmid. The combinations of fosfomycin with aminoglycosides, colistin, tigecycline, sitafloxacin, and ciprofloxacin were synergies against [bla.sub.NDM-1]-harboring CREC isolates. Genomic analysis revealed that these isolates harbored many [beta] -lactam resistance genes and other AMR genes that may confer resistance to aminoglycoside, fluoroquinolone, rifampicin, trimethoprim, sulfonamide, tetracycline, and macrolide. Also, various MGEs, especially the [bla.sub.NDM-1]-bearing IncN2 plasmid, were present in these isolates. Conclusion: Our study demonstrated some synergistic effects of antimicrobial combination against CREC isolates harboring [bla.sub.NDM-1] on the IncN2 plasmid. Also, our data on the whole-genome and plasmid sequences might be beneficial in the control of the spread of [bla.sub.NDM-1]-harboring CREC isolates. The linkages between [bla.sub.NDM-1]-carrying plasmid, patient information, and time of collection will be elucidated to track the horizontal gene transfer in the future. K
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Most of [bla.sub.NDM]-harboring bacteria commonly carry various antimicrobial resistance (AMR) genes on their chromosomes or plasmids, leading to limited treatment options. Thus, we aimed to evaluate the synergistic effects of fosfomycin in combination with other antimicrobial agents against [bla.sub.NDM]-harboring carbapenem-resistant Escherichia coli (CREC) and to characterize the wholegenome and plasmid sequences of these pathogens. Methods: Thirty-eight CREC isolates were collected from patients in the Medicine Ward, Songklanagarind Hospital, Thailand. The activity of fosfomycin in combination with other antimicrobial agents against CREC isolates harboring [bla.sub.NDM] on the plasmid was evaluated using the checkerboard method. In this method, the serial dilutions of two antibiotics were mixed with the cultured CREC, the mixtures were incubated, and FICI was calculated to interpret the synergistic activity of the combination. The whole-genome and particular plasmids of these pathogens were sequenced using next-generation sequencing. Sequence analysis, especially on antimicrobial resistance (AMR) genes, mobile-genetic elements (MGEs), and virulence genes was performed using many bioinformatics tools. Results: Of the E. coli 38 isolates, only 3 isolates contained the [bla.sub.NDM-1] gene, which is located on the IncN2 plasmid. The combinations of fosfomycin with aminoglycosides, colistin, tigecycline, sitafloxacin, and ciprofloxacin were synergies against [bla.sub.NDM-1]-harboring CREC isolates. Genomic analysis revealed that these isolates harbored many [beta] -lactam resistance genes and other AMR genes that may confer resistance to aminoglycoside, fluoroquinolone, rifampicin, trimethoprim, sulfonamide, tetracycline, and macrolide. Also, various MGEs, especially the [bla.sub.NDM-1]-bearing IncN2 plasmid, were present in these isolates. Conclusion: Our study demonstrated some synergistic effects of antimicrobial combination against CREC isolates harboring [bla.sub.NDM-1] on the IncN2 plasmid. Also, our data on the whole-genome and plasmid sequences might be beneficial in the control of the spread of [bla.sub.NDM-1]-harboring CREC isolates. The linkages between [bla.sub.NDM-1]-carrying plasmid, patient information, and time of collection will be elucidated to track the horizontal gene transfer in the future. Keywords: antimicrobial resistance gene, checkerboard method, next-generation sequencing, bioinformatics tool, mobile genetic element</description><identifier>ISSN: 1178-6973</identifier><identifier>EISSN: 1178-6973</identifier><identifier>DOI: 10.2147/IDR.S357965</identifier><language>eng</language><publisher>Dove Medical Press Limited</publisher><subject>Analysis ; Antibacterial agents ; Antibiotics ; Beta lactamases ; Care and treatment ; Ciprofloxacin ; Drug resistance in microorganisms ; Genes ; Genetic research ; Genomics ; Pathogenic microorganisms ; Patient education ; Sulbactam ; Sulfonamides ; Transposons ; Virulence (Microbiology)</subject><ispartof>Infection and drug resistance, 2022-04, Vol.15, p.1777</ispartof><rights>COPYRIGHT 2022 Dove Medical Press Limited</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Phaothong, Chanitnart</creatorcontrib><creatorcontrib>Jeenkeawpiam, Kongpop</creatorcontrib><creatorcontrib>Sakunrang, Chanida</creatorcontrib><creatorcontrib>Charernmak, Boonsri</creatorcontrib><creatorcontrib>Pomwised, Rattanaruji</creatorcontrib><creatorcontrib>Chusri, Sarunyou</creatorcontrib><creatorcontrib>Kaewnirat, Kalyarat</creatorcontrib><creatorcontrib>Hortiwakul, Thanaporn</creatorcontrib><creatorcontrib>Phoo, May Thet Paing</creatorcontrib><creatorcontrib>Surachat, Komwit</creatorcontrib><creatorcontrib>Chukamnerd, Arnon</creatorcontrib><creatorcontrib>Chuaychob, Surachat</creatorcontrib><title>In vitro Synergistic Activities of Fosfomycin in Combination with Other Antimicrobial Agents Against Carbapenem -Resistant Escherichia coli Harboring [bla.sub.NDM-1] on the IncN2 Plasmid and a Study of the Genomic Characteristics of These Pathogens</title><title>Infection and drug resistance</title><description>Purpose: The spread of New Delhi metallo-[beta]-lactamase (NDM) encoded by the [bla.sub.NDM] gene has been a global health crisis for many years. Most of [bla.sub.NDM]-harboring bacteria commonly carry various antimicrobial resistance (AMR) genes on their chromosomes or plasmids, leading to limited treatment options. Thus, we aimed to evaluate the synergistic effects of fosfomycin in combination with other antimicrobial agents against [bla.sub.NDM]-harboring carbapenem-resistant Escherichia coli (CREC) and to characterize the wholegenome and plasmid sequences of these pathogens. Methods: Thirty-eight CREC isolates were collected from patients in the Medicine Ward, Songklanagarind Hospital, Thailand. The activity of fosfomycin in combination with other antimicrobial agents against CREC isolates harboring [bla.sub.NDM] on the plasmid was evaluated using the checkerboard method. In this method, the serial dilutions of two antibiotics were mixed with the cultured CREC, the mixtures were incubated, and FICI was calculated to interpret the synergistic activity of the combination. The whole-genome and particular plasmids of these pathogens were sequenced using next-generation sequencing. Sequence analysis, especially on antimicrobial resistance (AMR) genes, mobile-genetic elements (MGEs), and virulence genes was performed using many bioinformatics tools. Results: Of the E. coli 38 isolates, only 3 isolates contained the [bla.sub.NDM-1] gene, which is located on the IncN2 plasmid. The combinations of fosfomycin with aminoglycosides, colistin, tigecycline, sitafloxacin, and ciprofloxacin were synergies against [bla.sub.NDM-1]-harboring CREC isolates. Genomic analysis revealed that these isolates harbored many [beta] -lactam resistance genes and other AMR genes that may confer resistance to aminoglycoside, fluoroquinolone, rifampicin, trimethoprim, sulfonamide, tetracycline, and macrolide. Also, various MGEs, especially the [bla.sub.NDM-1]-bearing IncN2 plasmid, were present in these isolates. Conclusion: Our study demonstrated some synergistic effects of antimicrobial combination against CREC isolates harboring [bla.sub.NDM-1] on the IncN2 plasmid. Also, our data on the whole-genome and plasmid sequences might be beneficial in the control of the spread of [bla.sub.NDM-1]-harboring CREC isolates. The linkages between [bla.sub.NDM-1]-carrying plasmid, patient information, and time of collection will be elucidated to track the horizontal gene transfer in the future. Keywords: antimicrobial resistance gene, checkerboard method, next-generation sequencing, bioinformatics tool, mobile genetic element</description><subject>Analysis</subject><subject>Antibacterial agents</subject><subject>Antibiotics</subject><subject>Beta lactamases</subject><subject>Care and treatment</subject><subject>Ciprofloxacin</subject><subject>Drug resistance in microorganisms</subject><subject>Genes</subject><subject>Genetic research</subject><subject>Genomics</subject><subject>Pathogenic microorganisms</subject><subject>Patient education</subject><subject>Sulbactam</subject><subject>Sulfonamides</subject><subject>Transposons</subject><subject>Virulence (Microbiology)</subject><issn>1178-6973</issn><issn>1178-6973</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptUU1r3DAQNaWFhjSn_oGBQm92_SlZR-N8LaRJyO6tlDCSJXuKLRVLm7L_vMdq2x62UEnDiOHNvPekJHlf5FlZ1PzT5vIp21YNF6x5lZwVBW9TJnj1-uT-Nrnw_lseVyVYzcuz5OfGwguF1cH2YPU6kg-koFOBYpW0B2fg2nnjloMiC_H0bpFkMZCz8IPCBA9h0it0NtBCanWScIZu1Db4mJCsD9DjKvG7tnqB9En7SII2wJVXsZPURAjKzQS3EeZWsiN8kTNmfi-z-8vPafEVIldkgY1V9yU8zugXGgBtDNiG_XA4yjwCbrR1UQX0E66oQpx-9PPbxW7SXsMjhslFcf5d8sbg7PXF33ye7K6vdv1tevdws-m7u3QUbZUOTEjJTCFLzhjnIr6cNlLmrKkbIbQWiLwpVG7q3OQDk3XTDo3mQyvQDMhZdZ58-DN2xFk_kzUuRGELefXc8bzO25I1VURl_0HFPejoxlltKNb_afh40jBpnMPk3bw__oo_Bf4CLXepxg</recordid><startdate>20220430</startdate><enddate>20220430</enddate><creator>Phaothong, Chanitnart</creator><creator>Jeenkeawpiam, Kongpop</creator><creator>Sakunrang, Chanida</creator><creator>Charernmak, Boonsri</creator><creator>Pomwised, Rattanaruji</creator><creator>Chusri, Sarunyou</creator><creator>Kaewnirat, Kalyarat</creator><creator>Hortiwakul, Thanaporn</creator><creator>Phoo, May Thet Paing</creator><creator>Surachat, Komwit</creator><creator>Chukamnerd, Arnon</creator><creator>Chuaychob, Surachat</creator><general>Dove Medical Press Limited</general><scope/></search><sort><creationdate>20220430</creationdate><title>In vitro Synergistic Activities of Fosfomycin in Combination with Other Antimicrobial Agents Against Carbapenem -Resistant Escherichia coli Harboring [bla.sub.NDM-1] on the IncN2 Plasmid and a Study of the Genomic Characteristics of These Pathogens</title><author>Phaothong, Chanitnart ; 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Most of [bla.sub.NDM]-harboring bacteria commonly carry various antimicrobial resistance (AMR) genes on their chromosomes or plasmids, leading to limited treatment options. Thus, we aimed to evaluate the synergistic effects of fosfomycin in combination with other antimicrobial agents against [bla.sub.NDM]-harboring carbapenem-resistant Escherichia coli (CREC) and to characterize the wholegenome and plasmid sequences of these pathogens. Methods: Thirty-eight CREC isolates were collected from patients in the Medicine Ward, Songklanagarind Hospital, Thailand. The activity of fosfomycin in combination with other antimicrobial agents against CREC isolates harboring [bla.sub.NDM] on the plasmid was evaluated using the checkerboard method. In this method, the serial dilutions of two antibiotics were mixed with the cultured CREC, the mixtures were incubated, and FICI was calculated to interpret the synergistic activity of the combination. The whole-genome and particular plasmids of these pathogens were sequenced using next-generation sequencing. Sequence analysis, especially on antimicrobial resistance (AMR) genes, mobile-genetic elements (MGEs), and virulence genes was performed using many bioinformatics tools. Results: Of the E. coli 38 isolates, only 3 isolates contained the [bla.sub.NDM-1] gene, which is located on the IncN2 plasmid. The combinations of fosfomycin with aminoglycosides, colistin, tigecycline, sitafloxacin, and ciprofloxacin were synergies against [bla.sub.NDM-1]-harboring CREC isolates. Genomic analysis revealed that these isolates harbored many [beta] -lactam resistance genes and other AMR genes that may confer resistance to aminoglycoside, fluoroquinolone, rifampicin, trimethoprim, sulfonamide, tetracycline, and macrolide. Also, various MGEs, especially the [bla.sub.NDM-1]-bearing IncN2 plasmid, were present in these isolates. Conclusion: Our study demonstrated some synergistic effects of antimicrobial combination against CREC isolates harboring [bla.sub.NDM-1] on the IncN2 plasmid. Also, our data on the whole-genome and plasmid sequences might be beneficial in the control of the spread of [bla.sub.NDM-1]-harboring CREC isolates. The linkages between [bla.sub.NDM-1]-carrying plasmid, patient information, and time of collection will be elucidated to track the horizontal gene transfer in the future. Keywords: antimicrobial resistance gene, checkerboard method, next-generation sequencing, bioinformatics tool, mobile genetic element</abstract><pub>Dove Medical Press Limited</pub><doi>10.2147/IDR.S357965</doi></addata></record>
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subjects Analysis
Antibacterial agents
Antibiotics
Beta lactamases
Care and treatment
Ciprofloxacin
Drug resistance in microorganisms
Genes
Genetic research
Genomics
Pathogenic microorganisms
Patient education
Sulbactam
Sulfonamides
Transposons
Virulence (Microbiology)
title In vitro Synergistic Activities of Fosfomycin in Combination with Other Antimicrobial Agents Against Carbapenem -Resistant Escherichia coli Harboring [bla.sub.NDM-1] on the IncN2 Plasmid and a Study of the Genomic Characteristics of These Pathogens
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