Exploring the Therapeutic Efficacy of Zingerone Nanoparticles in Treating Biofilm-Associated Pyelonephritis Caused by Pseudomonas aeruginosa in the Murine Model
Biofilms of Pseudomonas aeruginosa can cause complicated urinary tract infections especially in people with indwelling catheters which may result in pyelonephritis. Microorganisms in biofilm demonstrate high resistance to both antibiotics and host protection mechanisms, often resulting in chronic an...
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creator | Sharma, Karuna Bose, Sunil Kumar Chhibber, Sanjay Harjai, Kusum |
description | Biofilms of
Pseudomonas aeruginosa
can cause complicated urinary tract infections especially in people with indwelling catheters which may result in pyelonephritis. Microorganisms in biofilm demonstrate high resistance to both antibiotics and host protection mechanisms, often resulting in chronic and difficult-to-treat infections. This study is aimed to assess
in vivo
and
ex vivo
efficacy of Zingerone nanoparticles (Z-NPs) against
P. aeruginosa
biofilm-associated murine acute pyelonephritis. In the present study, Zingerone and chitosan acted synergistically in the form of Z-NPs and found to be nontoxic to the kidney cell lines as depicted in MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide] assay demonstrating their cytocompatibility.
In vivo
experiments indicated that Z-NPs (100 mg/kg) treatment reduced
P. aeruginosa
pathogenicity and enhanced the clearance of bacterial count from the renal and bladder tissue. Z-NPs improved the disease outcome by lowering the levels of various inflammatory markers, and histopathological examination revealed better recovery in renal and bladder tissue. Besides,
ex vivo
efficacy also confirmed that Z-NPs enhanced serum bactericidal effect along with increased phagocytic uptake and intracellular killing of
P. aeruginosa
as confirmed by fluorescent microscopy. To the best of our knowledge, this is the first study to provide evidence that Z-NPs are effective therapeutic agents for combating
P. aeruginosa
associated pyelonephritis. |
doi_str_mv | 10.1007/s10753-020-01304-y |
format | Article |
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Pseudomonas aeruginosa
can cause complicated urinary tract infections especially in people with indwelling catheters which may result in pyelonephritis. Microorganisms in biofilm demonstrate high resistance to both antibiotics and host protection mechanisms, often resulting in chronic and difficult-to-treat infections. This study is aimed to assess
in vivo
and
ex vivo
efficacy of Zingerone nanoparticles (Z-NPs) against
P. aeruginosa
biofilm-associated murine acute pyelonephritis. In the present study, Zingerone and chitosan acted synergistically in the form of Z-NPs and found to be nontoxic to the kidney cell lines as depicted in MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide] assay demonstrating their cytocompatibility.
In vivo
experiments indicated that Z-NPs (100 mg/kg) treatment reduced
P. aeruginosa
pathogenicity and enhanced the clearance of bacterial count from the renal and bladder tissue. Z-NPs improved the disease outcome by lowering the levels of various inflammatory markers, and histopathological examination revealed better recovery in renal and bladder tissue. Besides,
ex vivo
efficacy also confirmed that Z-NPs enhanced serum bactericidal effect along with increased phagocytic uptake and intracellular killing of
P. aeruginosa
as confirmed by fluorescent microscopy. To the best of our knowledge, this is the first study to provide evidence that Z-NPs are effective therapeutic agents for combating
P. aeruginosa
associated pyelonephritis.</description><identifier>ISSN: 0360-3997</identifier><identifier>EISSN: 1573-2576</identifier><identifier>DOI: 10.1007/s10753-020-01304-y</identifier><identifier>PMID: 32948964</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Animal models ; Animals ; Antibiotics ; Biofilms ; Biomedical and Life Sciences ; Biomedicine ; Catheters ; Cell lines ; Chitosan ; Disease Models, Animal ; Guaiacol - analogs & derivatives ; Guaiacol - pharmacology ; HEK293 Cells ; Humans ; Immunology ; Inflammation ; Internal Medicine ; Intracellular killing ; Kidneys ; Malondialdehyde ; Mice ; Microscopy, Electron, Scanning ; Nanoparticles ; Nanoparticles - chemistry ; Original Article ; Pathogenicity ; Pathology ; Peroxidase ; Phagocytes ; Phagocytosis ; Pharmacology/Toxicology ; Pseudomonas aeruginosa ; Pseudomonas aeruginosa - metabolism ; Pseudomonas Infections - drug therapy ; Pyelonephritis ; Pyelonephritis - drug therapy ; Pyelonephritis - metabolism ; Rheumatology ; Stem Cells ; Tetrazolium Salts - chemistry ; Thiazoles - chemistry ; Urinary tract ; Zingerone</subject><ispartof>Inflammation, 2020-12, Vol.43 (6), p.2344-2356</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-62c27bb2bebcd31d584382676e3a4de8cbeda96911d94a13dd148f6999d2e3de3</citedby><cites>FETCH-LOGICAL-c375t-62c27bb2bebcd31d584382676e3a4de8cbeda96911d94a13dd148f6999d2e3de3</cites><orcidid>0000-0002-5431-8183</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10753-020-01304-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10753-020-01304-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32948964$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sharma, Karuna</creatorcontrib><creatorcontrib>Bose, Sunil Kumar</creatorcontrib><creatorcontrib>Chhibber, Sanjay</creatorcontrib><creatorcontrib>Harjai, Kusum</creatorcontrib><title>Exploring the Therapeutic Efficacy of Zingerone Nanoparticles in Treating Biofilm-Associated Pyelonephritis Caused by Pseudomonas aeruginosa in the Murine Model</title><title>Inflammation</title><addtitle>Inflammation</addtitle><addtitle>Inflammation</addtitle><description>Biofilms of
Pseudomonas aeruginosa
can cause complicated urinary tract infections especially in people with indwelling catheters which may result in pyelonephritis. Microorganisms in biofilm demonstrate high resistance to both antibiotics and host protection mechanisms, often resulting in chronic and difficult-to-treat infections. This study is aimed to assess
in vivo
and
ex vivo
efficacy of Zingerone nanoparticles (Z-NPs) against
P. aeruginosa
biofilm-associated murine acute pyelonephritis. In the present study, Zingerone and chitosan acted synergistically in the form of Z-NPs and found to be nontoxic to the kidney cell lines as depicted in MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide] assay demonstrating their cytocompatibility.
In vivo
experiments indicated that Z-NPs (100 mg/kg) treatment reduced
P. aeruginosa
pathogenicity and enhanced the clearance of bacterial count from the renal and bladder tissue. Z-NPs improved the disease outcome by lowering the levels of various inflammatory markers, and histopathological examination revealed better recovery in renal and bladder tissue. Besides,
ex vivo
efficacy also confirmed that Z-NPs enhanced serum bactericidal effect along with increased phagocytic uptake and intracellular killing of
P. aeruginosa
as confirmed by fluorescent microscopy. To the best of our knowledge, this is the first study to provide evidence that Z-NPs are effective therapeutic agents for combating
P. aeruginosa
associated pyelonephritis.</description><subject>Animal models</subject><subject>Animals</subject><subject>Antibiotics</subject><subject>Biofilms</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Catheters</subject><subject>Cell lines</subject><subject>Chitosan</subject><subject>Disease Models, Animal</subject><subject>Guaiacol - analogs & derivatives</subject><subject>Guaiacol - pharmacology</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Immunology</subject><subject>Inflammation</subject><subject>Internal Medicine</subject><subject>Intracellular killing</subject><subject>Kidneys</subject><subject>Malondialdehyde</subject><subject>Mice</subject><subject>Microscopy, Electron, Scanning</subject><subject>Nanoparticles</subject><subject>Nanoparticles - chemistry</subject><subject>Original Article</subject><subject>Pathogenicity</subject><subject>Pathology</subject><subject>Peroxidase</subject><subject>Phagocytes</subject><subject>Phagocytosis</subject><subject>Pharmacology/Toxicology</subject><subject>Pseudomonas aeruginosa</subject><subject>Pseudomonas aeruginosa - metabolism</subject><subject>Pseudomonas Infections - drug therapy</subject><subject>Pyelonephritis</subject><subject>Pyelonephritis - drug therapy</subject><subject>Pyelonephritis - metabolism</subject><subject>Rheumatology</subject><subject>Stem Cells</subject><subject>Tetrazolium Salts - chemistry</subject><subject>Thiazoles - chemistry</subject><subject>Urinary tract</subject><subject>Zingerone</subject><issn>0360-3997</issn><issn>1573-2576</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc1u1DAUhS0EotPCC7BAltiwMfgvcbwso6EgFehi2LCxHPum4yqJg51I5G14VDydAhILVleyvnN8pA-hF4y-YZSqt5lRVQlCOSWUCSrJ-ghtWKUE4ZWqH6MNFTUlQmt1hs5zvqOUNroRT9GZ4Fo2upYb9HP3Y-pjCuMtng-A9wdIdoJlDg7vui4461YcO_ytAJDiCPizHeNkUwF6yDiMeJ_Azsf8uxC70A_kMufogp3B45sV-hKaDinMIeOtXXJ5bVd8k2HxcYijzdhCWm7DGLM91h1XfFrKoHKih_4ZetLZPsPzh3uBvr7f7bcfyPWXq4_by2vihKpmUnPHVdvyFlrnBfNVI0XDa1WDsNJD41rwVteaMa-lZcJ7Jpuu1lp7DsKDuECvT71Tit8XyLMZQnbQ93aEuGTDpZRCNULLgr76B72LSxrLukIpVlWVqHmh-IlyKeacoDNTCoNNq2HUHP2Zkz9T_Jl7f2YtoZcP1Us7gP8T-S2sAOIE5CndO_n7939qfwGMEKnh</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>Sharma, Karuna</creator><creator>Bose, Sunil Kumar</creator><creator>Chhibber, Sanjay</creator><creator>Harjai, Kusum</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5431-8183</orcidid></search><sort><creationdate>20201201</creationdate><title>Exploring the Therapeutic Efficacy of Zingerone Nanoparticles in Treating Biofilm-Associated Pyelonephritis Caused by Pseudomonas aeruginosa in the Murine Model</title><author>Sharma, Karuna ; Bose, Sunil Kumar ; Chhibber, Sanjay ; Harjai, Kusum</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-62c27bb2bebcd31d584382676e3a4de8cbeda96911d94a13dd148f6999d2e3de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Antibiotics</topic><topic>Biofilms</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Catheters</topic><topic>Cell lines</topic><topic>Chitosan</topic><topic>Disease Models, Animal</topic><topic>Guaiacol - analogs & derivatives</topic><topic>Guaiacol - pharmacology</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Immunology</topic><topic>Inflammation</topic><topic>Internal Medicine</topic><topic>Intracellular killing</topic><topic>Kidneys</topic><topic>Malondialdehyde</topic><topic>Mice</topic><topic>Microscopy, Electron, Scanning</topic><topic>Nanoparticles</topic><topic>Nanoparticles - chemistry</topic><topic>Original Article</topic><topic>Pathogenicity</topic><topic>Pathology</topic><topic>Peroxidase</topic><topic>Phagocytes</topic><topic>Phagocytosis</topic><topic>Pharmacology/Toxicology</topic><topic>Pseudomonas aeruginosa</topic><topic>Pseudomonas aeruginosa - metabolism</topic><topic>Pseudomonas Infections - drug therapy</topic><topic>Pyelonephritis</topic><topic>Pyelonephritis - drug therapy</topic><topic>Pyelonephritis - metabolism</topic><topic>Rheumatology</topic><topic>Stem Cells</topic><topic>Tetrazolium Salts - chemistry</topic><topic>Thiazoles - chemistry</topic><topic>Urinary tract</topic><topic>Zingerone</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sharma, Karuna</creatorcontrib><creatorcontrib>Bose, Sunil Kumar</creatorcontrib><creatorcontrib>Chhibber, Sanjay</creatorcontrib><creatorcontrib>Harjai, Kusum</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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><jtitle>Inflammation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sharma, Karuna</au><au>Bose, Sunil Kumar</au><au>Chhibber, Sanjay</au><au>Harjai, Kusum</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exploring the Therapeutic Efficacy of Zingerone Nanoparticles in Treating Biofilm-Associated Pyelonephritis Caused by Pseudomonas aeruginosa in the Murine Model</atitle><jtitle>Inflammation</jtitle><stitle>Inflammation</stitle><addtitle>Inflammation</addtitle><date>2020-12-01</date><risdate>2020</risdate><volume>43</volume><issue>6</issue><spage>2344</spage><epage>2356</epage><pages>2344-2356</pages><issn>0360-3997</issn><eissn>1573-2576</eissn><abstract>Biofilms of
Pseudomonas aeruginosa
can cause complicated urinary tract infections especially in people with indwelling catheters which may result in pyelonephritis. Microorganisms in biofilm demonstrate high resistance to both antibiotics and host protection mechanisms, often resulting in chronic and difficult-to-treat infections. This study is aimed to assess
in vivo
and
ex vivo
efficacy of Zingerone nanoparticles (Z-NPs) against
P. aeruginosa
biofilm-associated murine acute pyelonephritis. In the present study, Zingerone and chitosan acted synergistically in the form of Z-NPs and found to be nontoxic to the kidney cell lines as depicted in MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide] assay demonstrating their cytocompatibility.
In vivo
experiments indicated that Z-NPs (100 mg/kg) treatment reduced
P. aeruginosa
pathogenicity and enhanced the clearance of bacterial count from the renal and bladder tissue. Z-NPs improved the disease outcome by lowering the levels of various inflammatory markers, and histopathological examination revealed better recovery in renal and bladder tissue. Besides,
ex vivo
efficacy also confirmed that Z-NPs enhanced serum bactericidal effect along with increased phagocytic uptake and intracellular killing of
P. aeruginosa
as confirmed by fluorescent microscopy. To the best of our knowledge, this is the first study to provide evidence that Z-NPs are effective therapeutic agents for combating
P. aeruginosa
associated pyelonephritis.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>32948964</pmid><doi>10.1007/s10753-020-01304-y</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-5431-8183</orcidid></addata></record> |
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source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Animal models Animals Antibiotics Biofilms Biomedical and Life Sciences Biomedicine Catheters Cell lines Chitosan Disease Models, Animal Guaiacol - analogs & derivatives Guaiacol - pharmacology HEK293 Cells Humans Immunology Inflammation Internal Medicine Intracellular killing Kidneys Malondialdehyde Mice Microscopy, Electron, Scanning Nanoparticles Nanoparticles - chemistry Original Article Pathogenicity Pathology Peroxidase Phagocytes Phagocytosis Pharmacology/Toxicology Pseudomonas aeruginosa Pseudomonas aeruginosa - metabolism Pseudomonas Infections - drug therapy Pyelonephritis Pyelonephritis - drug therapy Pyelonephritis - metabolism Rheumatology Stem Cells Tetrazolium Salts - chemistry Thiazoles - chemistry Urinary tract Zingerone |
title | Exploring the Therapeutic Efficacy of Zingerone Nanoparticles in Treating Biofilm-Associated Pyelonephritis Caused by Pseudomonas aeruginosa in the Murine Model |
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