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Nanoformulation target virulence genes to break antibiotic resistance in MDR E. coli
Bacterial infection causes a large impact on the health of humans, animals, plants, and marine organisms. The infection caused by bacteria can be cured with the usage of prescribed antibiotics. However, inappropriate consumption of antibiotics leads to the raise of more antibiotic-resistant strains....
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Published in: | Applied nanoscience 2023-08, Vol.13 (8), p.5615-5626 |
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description | Bacterial infection causes a large impact on the health of humans, animals, plants, and marine organisms. The infection caused by bacteria can be cured with the usage of prescribed antibiotics. However, inappropriate consumption of antibiotics leads to the raise of more antibiotic-resistant strains. For the past few decades, antimicrobial resistance has been considered a global health problem. One of the most common Gram-negative species is
Escherichia coli
, causing several infections in all living forms. During the last few decades, extended-spectrum beta-lactamases (ESBL) producers involved in the spread of drug resistance genes and cause several diseases. Therefore, it is important to choose an ecofriendly alternative to control infections caused by multidrug-resistant, biofilm-forming
E. coli
. Green silver nanoparticles with unique properties are reported to show superior antimicrobial and antibiofilm activity. Hence, this paper focuses on evaluating the antibacterial potential of polyherbal nanoformulation (PHNF) against
Escherichia coli
strains isolated from human samples through various antimicrobial assays and Cefotaximase-Munich (CTX-M-15) gene expression studies. The results of agar well-diffusion method suggest enhanced antibacterial activity even at a very low concentration of PHNF. MIC concentration was found as 0.78 μg/ml in EC ATCC (25,922), 1.56 μg/ml for EC 13, and EC 36, 0.78 μg/ml for in EC 36, and EC 3 T. MBC was found as 0.78 μg /ml in EC ATCC (25,922), 3.125 μg/ml for EC 13, 6.25 μg/ml for EC 16, 0.78 μg /ml for EC 36, and 1.56 μg/ml for EC 3 T. Upon treatment with PHNF at their MIC concentration, the formation of biofilm in
E. coli
strains was reduced in all the EC strains. PHNF treatment in EC strains suppressed CTX-M-15 gene at minimum bacteriostatic concentration, but not in the ampicillin treatment. The results upon PHNF treatment were very promising by showing bacteriostatic, bactericidal, and antibiofilm property. Moreover, the CTX-M-15 gene was also abolished completely upon treatment with PHNF. This confirms the potential of PHNF as potent antibacterial agent. To the best of our knowledge, this is the first report on novel polyherbal nanoformulation known to inhibit the growth, biofilm formation, and interference with the CTX-M-15 gene in tested strains of
Escherichia coli.
The principle of synergism works very well, both in the preparation of the PHNF and also exhibiting its potent function without harming the living being |
doi_str_mv | 10.1007/s13204-023-02782-w |
format | article |
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Escherichia coli
, causing several infections in all living forms. During the last few decades, extended-spectrum beta-lactamases (ESBL) producers involved in the spread of drug resistance genes and cause several diseases. Therefore, it is important to choose an ecofriendly alternative to control infections caused by multidrug-resistant, biofilm-forming
E. coli
. Green silver nanoparticles with unique properties are reported to show superior antimicrobial and antibiofilm activity. Hence, this paper focuses on evaluating the antibacterial potential of polyherbal nanoformulation (PHNF) against
Escherichia coli
strains isolated from human samples through various antimicrobial assays and Cefotaximase-Munich (CTX-M-15) gene expression studies. The results of agar well-diffusion method suggest enhanced antibacterial activity even at a very low concentration of PHNF. MIC concentration was found as 0.78 μg/ml in EC ATCC (25,922), 1.56 μg/ml for EC 13, and EC 36, 0.78 μg/ml for in EC 36, and EC 3 T. MBC was found as 0.78 μg /ml in EC ATCC (25,922), 3.125 μg/ml for EC 13, 6.25 μg/ml for EC 16, 0.78 μg /ml for EC 36, and 1.56 μg/ml for EC 3 T. Upon treatment with PHNF at their MIC concentration, the formation of biofilm in
E. coli
strains was reduced in all the EC strains. PHNF treatment in EC strains suppressed CTX-M-15 gene at minimum bacteriostatic concentration, but not in the ampicillin treatment. The results upon PHNF treatment were very promising by showing bacteriostatic, bactericidal, and antibiofilm property. Moreover, the CTX-M-15 gene was also abolished completely upon treatment with PHNF. This confirms the potential of PHNF as potent antibacterial agent. To the best of our knowledge, this is the first report on novel polyherbal nanoformulation known to inhibit the growth, biofilm formation, and interference with the CTX-M-15 gene in tested strains of
Escherichia coli.
The principle of synergism works very well, both in the preparation of the PHNF and also exhibiting its potent function without harming the living beings in the environment.</description><identifier>ISSN: 2190-5509</identifier><identifier>EISSN: 2190-5517</identifier><identifier>DOI: 10.1007/s13204-023-02782-w</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Ampicillin ; Antibiotics ; Antimicrobial agents ; Bacteria ; Bacterial infections ; Biofilms ; Chemistry and Materials Science ; Drug resistance ; E coli ; Gene expression ; Genes ; Marine animals ; Marine plants ; Materials Science ; Membrane Biology ; Nanochemistry ; Nanoparticles ; Nanotechnology ; Nanotechnology and Microengineering ; Original Article ; Public health ; Silver</subject><ispartof>Applied nanoscience, 2023-08, Vol.13 (8), p.5615-5626</ispartof><rights>King Abdulaziz City for Science and Technology 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c234w-ab38cb179a03a9689d0803b4f889f2727d597c79052b6a1ddf3810554a3fa05d3</citedby><cites>FETCH-LOGICAL-c234w-ab38cb179a03a9689d0803b4f889f2727d597c79052b6a1ddf3810554a3fa05d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Ranjani, S.</creatorcontrib><creatorcontrib>Hemalatha, S.</creatorcontrib><title>Nanoformulation target virulence genes to break antibiotic resistance in MDR E. coli</title><title>Applied nanoscience</title><addtitle>Appl Nanosci</addtitle><description>Bacterial infection causes a large impact on the health of humans, animals, plants, and marine organisms. The infection caused by bacteria can be cured with the usage of prescribed antibiotics. However, inappropriate consumption of antibiotics leads to the raise of more antibiotic-resistant strains. For the past few decades, antimicrobial resistance has been considered a global health problem. One of the most common Gram-negative species is
Escherichia coli
, causing several infections in all living forms. During the last few decades, extended-spectrum beta-lactamases (ESBL) producers involved in the spread of drug resistance genes and cause several diseases. Therefore, it is important to choose an ecofriendly alternative to control infections caused by multidrug-resistant, biofilm-forming
E. coli
. Green silver nanoparticles with unique properties are reported to show superior antimicrobial and antibiofilm activity. Hence, this paper focuses on evaluating the antibacterial potential of polyherbal nanoformulation (PHNF) against
Escherichia coli
strains isolated from human samples through various antimicrobial assays and Cefotaximase-Munich (CTX-M-15) gene expression studies. The results of agar well-diffusion method suggest enhanced antibacterial activity even at a very low concentration of PHNF. MIC concentration was found as 0.78 μg/ml in EC ATCC (25,922), 1.56 μg/ml for EC 13, and EC 36, 0.78 μg/ml for in EC 36, and EC 3 T. MBC was found as 0.78 μg /ml in EC ATCC (25,922), 3.125 μg/ml for EC 13, 6.25 μg/ml for EC 16, 0.78 μg /ml for EC 36, and 1.56 μg/ml for EC 3 T. Upon treatment with PHNF at their MIC concentration, the formation of biofilm in
E. coli
strains was reduced in all the EC strains. PHNF treatment in EC strains suppressed CTX-M-15 gene at minimum bacteriostatic concentration, but not in the ampicillin treatment. The results upon PHNF treatment were very promising by showing bacteriostatic, bactericidal, and antibiofilm property. Moreover, the CTX-M-15 gene was also abolished completely upon treatment with PHNF. This confirms the potential of PHNF as potent antibacterial agent. To the best of our knowledge, this is the first report on novel polyherbal nanoformulation known to inhibit the growth, biofilm formation, and interference with the CTX-M-15 gene in tested strains of
Escherichia coli.
The principle of synergism works very well, both in the preparation of the PHNF and also exhibiting its potent function without harming the living beings in the environment.</description><subject>Ampicillin</subject><subject>Antibiotics</subject><subject>Antimicrobial agents</subject><subject>Bacteria</subject><subject>Bacterial infections</subject><subject>Biofilms</subject><subject>Chemistry and Materials Science</subject><subject>Drug resistance</subject><subject>E coli</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Marine animals</subject><subject>Marine plants</subject><subject>Materials Science</subject><subject>Membrane Biology</subject><subject>Nanochemistry</subject><subject>Nanoparticles</subject><subject>Nanotechnology</subject><subject>Nanotechnology and Microengineering</subject><subject>Original Article</subject><subject>Public health</subject><subject>Silver</subject><issn>2190-5509</issn><issn>2190-5517</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMoWLR_wFPA89ZJstlkj1LrB1QFqeeQ3c2W1G1Sk6zFf-_WFb05MMwcnncGHoQuCMwIgLiKhFHIM6BsaCFptj9CE0pKyDgn4vh3h_IUTWPcwFA8FwXjE7R60s63Pmz7TifrHU46rE3CHzb0nXG1wWvjTMTJ4yoY_Ya1S7ayPtkaBxNtTPoAWYcfb17wYoZr39lzdNLqLprpzzxDr7eL1fw-Wz7fPcyvl1lNWb7PdMVkXRFRamC6LGTZgARW5a2UZUsFFQ0vRS1K4LQqNGmalkkCnOeatRp4w87Q5Xh3F_x7b2JSG98HN7xUVDJgUBAhB4qOVB18jMG0ahfsVodPRUAdBKpRoBoEqm-Baj-E2BiKA-zWJvyd_if1Be5Tcsw</recordid><startdate>20230801</startdate><enddate>20230801</enddate><creator>Ranjani, S.</creator><creator>Hemalatha, S.</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20230801</creationdate><title>Nanoformulation target virulence genes to break antibiotic resistance in MDR E. coli</title><author>Ranjani, S. ; Hemalatha, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c234w-ab38cb179a03a9689d0803b4f889f2727d597c79052b6a1ddf3810554a3fa05d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Ampicillin</topic><topic>Antibiotics</topic><topic>Antimicrobial agents</topic><topic>Bacteria</topic><topic>Bacterial infections</topic><topic>Biofilms</topic><topic>Chemistry and Materials Science</topic><topic>Drug resistance</topic><topic>E coli</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Marine animals</topic><topic>Marine plants</topic><topic>Materials Science</topic><topic>Membrane Biology</topic><topic>Nanochemistry</topic><topic>Nanoparticles</topic><topic>Nanotechnology</topic><topic>Nanotechnology and Microengineering</topic><topic>Original Article</topic><topic>Public health</topic><topic>Silver</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ranjani, S.</creatorcontrib><creatorcontrib>Hemalatha, S.</creatorcontrib><collection>CrossRef</collection><jtitle>Applied nanoscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ranjani, S.</au><au>Hemalatha, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nanoformulation target virulence genes to break antibiotic resistance in MDR E. coli</atitle><jtitle>Applied nanoscience</jtitle><stitle>Appl Nanosci</stitle><date>2023-08-01</date><risdate>2023</risdate><volume>13</volume><issue>8</issue><spage>5615</spage><epage>5626</epage><pages>5615-5626</pages><issn>2190-5509</issn><eissn>2190-5517</eissn><abstract>Bacterial infection causes a large impact on the health of humans, animals, plants, and marine organisms. The infection caused by bacteria can be cured with the usage of prescribed antibiotics. However, inappropriate consumption of antibiotics leads to the raise of more antibiotic-resistant strains. For the past few decades, antimicrobial resistance has been considered a global health problem. One of the most common Gram-negative species is
Escherichia coli
, causing several infections in all living forms. During the last few decades, extended-spectrum beta-lactamases (ESBL) producers involved in the spread of drug resistance genes and cause several diseases. Therefore, it is important to choose an ecofriendly alternative to control infections caused by multidrug-resistant, biofilm-forming
E. coli
. Green silver nanoparticles with unique properties are reported to show superior antimicrobial and antibiofilm activity. Hence, this paper focuses on evaluating the antibacterial potential of polyherbal nanoformulation (PHNF) against
Escherichia coli
strains isolated from human samples through various antimicrobial assays and Cefotaximase-Munich (CTX-M-15) gene expression studies. The results of agar well-diffusion method suggest enhanced antibacterial activity even at a very low concentration of PHNF. MIC concentration was found as 0.78 μg/ml in EC ATCC (25,922), 1.56 μg/ml for EC 13, and EC 36, 0.78 μg/ml for in EC 36, and EC 3 T. MBC was found as 0.78 μg /ml in EC ATCC (25,922), 3.125 μg/ml for EC 13, 6.25 μg/ml for EC 16, 0.78 μg /ml for EC 36, and 1.56 μg/ml for EC 3 T. Upon treatment with PHNF at their MIC concentration, the formation of biofilm in
E. coli
strains was reduced in all the EC strains. PHNF treatment in EC strains suppressed CTX-M-15 gene at minimum bacteriostatic concentration, but not in the ampicillin treatment. The results upon PHNF treatment were very promising by showing bacteriostatic, bactericidal, and antibiofilm property. Moreover, the CTX-M-15 gene was also abolished completely upon treatment with PHNF. This confirms the potential of PHNF as potent antibacterial agent. To the best of our knowledge, this is the first report on novel polyherbal nanoformulation known to inhibit the growth, biofilm formation, and interference with the CTX-M-15 gene in tested strains of
Escherichia coli.
The principle of synergism works very well, both in the preparation of the PHNF and also exhibiting its potent function without harming the living beings in the environment.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1007/s13204-023-02782-w</doi><tpages>12</tpages></addata></record> |
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subjects | Ampicillin Antibiotics Antimicrobial agents Bacteria Bacterial infections Biofilms Chemistry and Materials Science Drug resistance E coli Gene expression Genes Marine animals Marine plants Materials Science Membrane Biology Nanochemistry Nanoparticles Nanotechnology Nanotechnology and Microengineering Original Article Public health Silver |
title | Nanoformulation target virulence genes to break antibiotic resistance in MDR E. coli |
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