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Global gene expression in Escherichia coli , isolated from the diseased ocular surface of the human eye with a potential to form biofilm
the gastrointestinal commensal, is also known to cause ocular infections such as conjunctivitis, keratitis and endophthalmitis. These infections are normally resolved by topical application of an appropriate antibiotic. But, at times these are resistant to the antibiotic and this could be due to for...
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Published in: | Gut pathogens 2017-04, Vol.9 (1), p.15-15, Article 15 |
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description | the gastrointestinal commensal, is also known to cause ocular infections such as conjunctivitis, keratitis and endophthalmitis. These infections are normally resolved by topical application of an appropriate antibiotic. But, at times these
are resistant to the antibiotic and this could be due to formation of a biofilm. In this study ocular
from patients with conjunctivitis, keratitis or endophthalmitis were screened for their antibiotic susceptibility and biofilm formation potential. In addition DNA-microarray analysis was done to identify genes that are involved in biofilm formation and antibiotic resistance.
Out of 12 ocular
isolated from patients ten isolates were resistant to one or more of the nine antibiotics tested and majority of the isolates were positive for biofilm formation. In
L-1216/2010, the best biofilm forming isolate, biofilm formation was confirmed by scanning electron microscopy. Confocal laser scanning microscopic studies indicated that the thickness of the biofilm increased up to 72 h of growth. Further, in the biofilm phase,
L-1216/2010 was 100 times more resistant to the eight antibiotics tested compared to planktonic phase. DNA microarray analysis indicated that in biofilm forming
L-1216/2010 genes encoding biofilm formation such as cell adhesion genes, LPS production genes, genes required for biofilm architecture and extracellular matrix remodeling and genes encoding for proteins that are integral to the cell membrane and those that influence antigen presentation are up regulated during biofilm formation. In addition genes that confer antimicrobial resistance such as genes encoding antimicrobial efflux (
M and
A), virulence (
Q,
K), toxin production (
K,
S,
B and
N), transport of amino-acids and other metabolites (
B,
C,
I and
B) are also up regulated. These genes could serve as potential targets for developing strategies for hacking biofilms and overcoming antibiotic resistance.
This is the first study on global gene expression in antibiotic resistant ocular
with a potential to form biofilm. Using native ocular isolates for antibiotic susceptibility testing, for biofilm formation and global gene expression is relevant and more acceptable than using type strains or non clinical strains which do not necessarily mimic the native isolate. |
doi_str_mv | 10.1186/s13099-017-0164-2 |
format | article |
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are resistant to the antibiotic and this could be due to formation of a biofilm. In this study ocular
from patients with conjunctivitis, keratitis or endophthalmitis were screened for their antibiotic susceptibility and biofilm formation potential. In addition DNA-microarray analysis was done to identify genes that are involved in biofilm formation and antibiotic resistance.
Out of 12 ocular
isolated from patients ten isolates were resistant to one or more of the nine antibiotics tested and majority of the isolates were positive for biofilm formation. In
L-1216/2010, the best biofilm forming isolate, biofilm formation was confirmed by scanning electron microscopy. Confocal laser scanning microscopic studies indicated that the thickness of the biofilm increased up to 72 h of growth. Further, in the biofilm phase,
L-1216/2010 was 100 times more resistant to the eight antibiotics tested compared to planktonic phase. DNA microarray analysis indicated that in biofilm forming
L-1216/2010 genes encoding biofilm formation such as cell adhesion genes, LPS production genes, genes required for biofilm architecture and extracellular matrix remodeling and genes encoding for proteins that are integral to the cell membrane and those that influence antigen presentation are up regulated during biofilm formation. In addition genes that confer antimicrobial resistance such as genes encoding antimicrobial efflux (
M and
A), virulence (
Q,
K), toxin production (
K,
S,
B and
N), transport of amino-acids and other metabolites (
B,
C,
I and
B) are also up regulated. These genes could serve as potential targets for developing strategies for hacking biofilms and overcoming antibiotic resistance.
This is the first study on global gene expression in antibiotic resistant ocular
with a potential to form biofilm. Using native ocular isolates for antibiotic susceptibility testing, for biofilm formation and global gene expression is relevant and more acceptable than using type strains or non clinical strains which do not necessarily mimic the native isolate.</description><identifier>ISSN: 1757-4749</identifier><identifier>EISSN: 1757-4749</identifier><identifier>DOI: 10.1186/s13099-017-0164-2</identifier><identifier>PMID: 28392838</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Antibiotic resistance ; Antibiotic susceptibility ; Antibiotics ; Antimicrobial activity ; Bacteria ; Bacteriology ; Biofilm ; Biofilms ; Differential expression of genes ; DNA microarray ; Drug resistance ; E coli ; Gene expression ; Gram-negative bacteria ; Infections ; Ocular E. coli ; Studies</subject><ispartof>Gut pathogens, 2017-04, Vol.9 (1), p.15-15, Article 15</ispartof><rights>Copyright BioMed Central 2017</rights><rights>The Author(s) 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-59d1f78e70952cc9ea0b76c9fe23cebdb05a8d8015845e5f5daaab21ba9073f73</citedby><cites>FETCH-LOGICAL-c493t-59d1f78e70952cc9ea0b76c9fe23cebdb05a8d8015845e5f5daaab21ba9073f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379667/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1883864306?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28392838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ranjith, Konduri</creatorcontrib><creatorcontrib>Arunasri, Kotakonda</creatorcontrib><creatorcontrib>Reddy, Gundlapally Sathyanarayana</creatorcontrib><creatorcontrib>Adicherla, HariKrishna</creatorcontrib><creatorcontrib>Sharma, Savitri</creatorcontrib><creatorcontrib>Shivaji, Sisinthy</creatorcontrib><title>Global gene expression in Escherichia coli , isolated from the diseased ocular surface of the human eye with a potential to form biofilm</title><title>Gut pathogens</title><addtitle>Gut Pathog</addtitle><description>the gastrointestinal commensal, is also known to cause ocular infections such as conjunctivitis, keratitis and endophthalmitis. These infections are normally resolved by topical application of an appropriate antibiotic. But, at times these
are resistant to the antibiotic and this could be due to formation of a biofilm. In this study ocular
from patients with conjunctivitis, keratitis or endophthalmitis were screened for their antibiotic susceptibility and biofilm formation potential. In addition DNA-microarray analysis was done to identify genes that are involved in biofilm formation and antibiotic resistance.
Out of 12 ocular
isolated from patients ten isolates were resistant to one or more of the nine antibiotics tested and majority of the isolates were positive for biofilm formation. In
L-1216/2010, the best biofilm forming isolate, biofilm formation was confirmed by scanning electron microscopy. Confocal laser scanning microscopic studies indicated that the thickness of the biofilm increased up to 72 h of growth. Further, in the biofilm phase,
L-1216/2010 was 100 times more resistant to the eight antibiotics tested compared to planktonic phase. DNA microarray analysis indicated that in biofilm forming
L-1216/2010 genes encoding biofilm formation such as cell adhesion genes, LPS production genes, genes required for biofilm architecture and extracellular matrix remodeling and genes encoding for proteins that are integral to the cell membrane and those that influence antigen presentation are up regulated during biofilm formation. In addition genes that confer antimicrobial resistance such as genes encoding antimicrobial efflux (
M and
A), virulence (
Q,
K), toxin production (
K,
S,
B and
N), transport of amino-acids and other metabolites (
B,
C,
I and
B) are also up regulated. These genes could serve as potential targets for developing strategies for hacking biofilms and overcoming antibiotic resistance.
This is the first study on global gene expression in antibiotic resistant ocular
with a potential to form biofilm. Using native ocular isolates for antibiotic susceptibility testing, for biofilm formation and global gene expression is relevant and more acceptable than using type strains or non clinical strains which do not necessarily mimic the native isolate.</description><subject>Antibiotic resistance</subject><subject>Antibiotic susceptibility</subject><subject>Antibiotics</subject><subject>Antimicrobial activity</subject><subject>Bacteria</subject><subject>Bacteriology</subject><subject>Biofilm</subject><subject>Biofilms</subject><subject>Differential expression of genes</subject><subject>DNA microarray</subject><subject>Drug resistance</subject><subject>E coli</subject><subject>Gene expression</subject><subject>Gram-negative bacteria</subject><subject>Infections</subject><subject>Ocular E. coli</subject><subject>Studies</subject><issn>1757-4749</issn><issn>1757-4749</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdUk1v1DAQjRCIlsIP4IIsceFAwI7jxL4goaqUSpW4wNkaO-ONV0682Emh_6A_u95uqVoOoxnNvHnzoVdVbxn9xJjsPmfGqVI1ZX2xrq2bZ9Ux60Vft32rnj-Kj6pXOW8p7dpWipfVUSO5KiaPq5vzEA0EssEZCf7dJczZx5n4mZxlO2LydvRAbAyefCQ-xwALDsSlOJFlRDL4jJBLJto1QCJ5TQ4skujuyuM6wUzwGskfv4wEyC4uOC--TFwicTFNxPjofJheVy8chIxv7v1J9evb2c_T7_Xlj_OL06-XtW0VX2qhBuZ6iT1VorFWIVDTd1Y5bLhFMxgqQA6SMiFbgcKJAQBMwwwo2nPX85Pq4sA7RNjqXfITpGsdweu7REwbDWnxNqCm3ABzRpjy7FaANapnVgiDwrLWIhSuLweu3WomHGy5LEF4Qvq0MvtRb-KVFrxXXbdf5sM9QYq_V8yLnny2GALMGNesmZQdF52QqkDf_wfdxjXN5VV7FJddy2lXUOyAsinmnNA9LMOo3mtGHzSji2b0XjO6KT3vHl_x0PFPJPwWLKm_qA</recordid><startdate>20170403</startdate><enddate>20170403</enddate><creator>Ranjith, Konduri</creator><creator>Arunasri, Kotakonda</creator><creator>Reddy, Gundlapally Sathyanarayana</creator><creator>Adicherla, HariKrishna</creator><creator>Sharma, Savitri</creator><creator>Shivaji, Sisinthy</creator><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</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>H94</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></search><sort><creationdate>20170403</creationdate><title>Global gene expression in Escherichia coli , isolated from the diseased ocular surface of the human eye with a potential to form biofilm</title><author>Ranjith, Konduri ; Arunasri, Kotakonda ; Reddy, Gundlapally Sathyanarayana ; Adicherla, HariKrishna ; Sharma, Savitri ; Shivaji, Sisinthy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-59d1f78e70952cc9ea0b76c9fe23cebdb05a8d8015845e5f5daaab21ba9073f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antibiotic resistance</topic><topic>Antibiotic susceptibility</topic><topic>Antibiotics</topic><topic>Antimicrobial activity</topic><topic>Bacteria</topic><topic>Bacteriology</topic><topic>Biofilm</topic><topic>Biofilms</topic><topic>Differential expression of genes</topic><topic>DNA microarray</topic><topic>Drug resistance</topic><topic>E coli</topic><topic>Gene expression</topic><topic>Gram-negative bacteria</topic><topic>Infections</topic><topic>Ocular E. coli</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ranjith, Konduri</creatorcontrib><creatorcontrib>Arunasri, Kotakonda</creatorcontrib><creatorcontrib>Reddy, Gundlapally Sathyanarayana</creatorcontrib><creatorcontrib>Adicherla, HariKrishna</creatorcontrib><creatorcontrib>Sharma, Savitri</creatorcontrib><creatorcontrib>Shivaji, Sisinthy</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & 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>DOAJ Directory of Open Access Journals</collection><jtitle>Gut pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ranjith, Konduri</au><au>Arunasri, Kotakonda</au><au>Reddy, Gundlapally Sathyanarayana</au><au>Adicherla, HariKrishna</au><au>Sharma, Savitri</au><au>Shivaji, Sisinthy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Global gene expression in Escherichia coli , isolated from the diseased ocular surface of the human eye with a potential to form biofilm</atitle><jtitle>Gut pathogens</jtitle><addtitle>Gut Pathog</addtitle><date>2017-04-03</date><risdate>2017</risdate><volume>9</volume><issue>1</issue><spage>15</spage><epage>15</epage><pages>15-15</pages><artnum>15</artnum><issn>1757-4749</issn><eissn>1757-4749</eissn><abstract>the gastrointestinal commensal, is also known to cause ocular infections such as conjunctivitis, keratitis and endophthalmitis. These infections are normally resolved by topical application of an appropriate antibiotic. But, at times these
are resistant to the antibiotic and this could be due to formation of a biofilm. In this study ocular
from patients with conjunctivitis, keratitis or endophthalmitis were screened for their antibiotic susceptibility and biofilm formation potential. In addition DNA-microarray analysis was done to identify genes that are involved in biofilm formation and antibiotic resistance.
Out of 12 ocular
isolated from patients ten isolates were resistant to one or more of the nine antibiotics tested and majority of the isolates were positive for biofilm formation. In
L-1216/2010, the best biofilm forming isolate, biofilm formation was confirmed by scanning electron microscopy. Confocal laser scanning microscopic studies indicated that the thickness of the biofilm increased up to 72 h of growth. Further, in the biofilm phase,
L-1216/2010 was 100 times more resistant to the eight antibiotics tested compared to planktonic phase. DNA microarray analysis indicated that in biofilm forming
L-1216/2010 genes encoding biofilm formation such as cell adhesion genes, LPS production genes, genes required for biofilm architecture and extracellular matrix remodeling and genes encoding for proteins that are integral to the cell membrane and those that influence antigen presentation are up regulated during biofilm formation. In addition genes that confer antimicrobial resistance such as genes encoding antimicrobial efflux (
M and
A), virulence (
Q,
K), toxin production (
K,
S,
B and
N), transport of amino-acids and other metabolites (
B,
C,
I and
B) are also up regulated. These genes could serve as potential targets for developing strategies for hacking biofilms and overcoming antibiotic resistance.
This is the first study on global gene expression in antibiotic resistant ocular
with a potential to form biofilm. Using native ocular isolates for antibiotic susceptibility testing, for biofilm formation and global gene expression is relevant and more acceptable than using type strains or non clinical strains which do not necessarily mimic the native isolate.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>28392838</pmid><doi>10.1186/s13099-017-0164-2</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibiotic resistance Antibiotic susceptibility Antibiotics Antimicrobial activity Bacteria Bacteriology Biofilm Biofilms Differential expression of genes DNA microarray Drug resistance E coli Gene expression Gram-negative bacteria Infections Ocular E. coli Studies |
title | Global gene expression in Escherichia coli , isolated from the diseased ocular surface of the human eye with a potential to form biofilm |
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