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- Publisher Website: 10.1002/pmic.201100356
- Scopus: eid_2-s2.0-84859240206
- PMID: 22246638
- WOS: WOS:000302151800013
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Article: Unraveling the resistance of microbial biofilms: Has proteomics been helpful?
Title | Unraveling the resistance of microbial biofilms: Has proteomics been helpful? | ||||
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Authors | |||||
Keywords | Biofilm Microbiology Resistance | ||||
Issue Date | 2012 | ||||
Publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/proteomics | ||||
Citation | Proteomics, 2012, v. 12 n. 4-5, p. 651-665 How to Cite? | ||||
Abstract | Biofilms are surface-attached, matrix-encased, structured microbial communities which display phenotypic features that are dramatically different from those of their free-floating, or planktonic, counterparts. Biofilms seem to be the preferred mode of growth of microorganisms in nature, and at least 65% of all human infections are associated with biofilms. The most notable and clinically relevant property of biofilms is their greater resistance to antimicrobials compared with their planktonic counterparts. Although both bacterial and fungal biofilms display this phenotypic feature, the exact mechanisms underlying their increased drug resistance are yet to be determined. Advances in proteomics techniques during the past decade have facilitated in-depth analysis of the possible mechanisms underpinning increased drug resistance in biofilms. These studies have demonstrated the ability of proteomics techniques to unravel new targets for combating microbial biofilms. In this review, we discuss the putative drug resistance mechanisms of microbial biofilms that have been uncovered by proteomics and critically evaluate the possible contribution of the new knowledge to future development in the field. We also summarize strategic uses of novel proteomics technologies in studies related to drug resistance mechanisms of microbial biofilms. | ||||
Persistent Identifier | http://hdl.handle.net/10722/169163 | ||||
ISSN | 2023 Impact Factor: 3.4 2023 SCImago Journal Rankings: 1.011 | ||||
ISI Accession Number ID |
Funding Information: The authors thank Dr. Trevor Lane for editorial assistance. Mixed species biofilm image was obtained by courtesy of Dr. C. H. Chu and Dr. M. Lei. This work was supported by HKU funding 200907176121 for C. J. S. and 20080717617 for L. P. S. | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Seneviratne, CJ | en_US |
dc.contributor.author | Wang, Y | en_US |
dc.contributor.author | Jin, L | en_US |
dc.contributor.author | Wong, SSW | en_US |
dc.contributor.author | Herath, MTDKH | en_US |
dc.contributor.author | Samaranayake, LP | en_US |
dc.date.accessioned | 2012-10-18T08:44:53Z | - |
dc.date.available | 2012-10-18T08:44:53Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Proteomics, 2012, v. 12 n. 4-5, p. 651-665 | en_US |
dc.identifier.issn | 1615-9853 | - |
dc.identifier.uri | http://hdl.handle.net/10722/169163 | - |
dc.description.abstract | Biofilms are surface-attached, matrix-encased, structured microbial communities which display phenotypic features that are dramatically different from those of their free-floating, or planktonic, counterparts. Biofilms seem to be the preferred mode of growth of microorganisms in nature, and at least 65% of all human infections are associated with biofilms. The most notable and clinically relevant property of biofilms is their greater resistance to antimicrobials compared with their planktonic counterparts. Although both bacterial and fungal biofilms display this phenotypic feature, the exact mechanisms underlying their increased drug resistance are yet to be determined. Advances in proteomics techniques during the past decade have facilitated in-depth analysis of the possible mechanisms underpinning increased drug resistance in biofilms. These studies have demonstrated the ability of proteomics techniques to unravel new targets for combating microbial biofilms. In this review, we discuss the putative drug resistance mechanisms of microbial biofilms that have been uncovered by proteomics and critically evaluate the possible contribution of the new knowledge to future development in the field. We also summarize strategic uses of novel proteomics technologies in studies related to drug resistance mechanisms of microbial biofilms. | - |
dc.language | eng | en_US |
dc.publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/proteomics | - |
dc.relation.ispartof | Proteomics | en_US |
dc.rights | Preprint This is the pre-peer reviewed version of the following article: Proteomics, 2012, v. 12 n. 4-5, p. 651-665, which has been published in final form at http://dx.doi.org/10.1002/pmic.201100356 | - |
dc.subject | Biofilm | - |
dc.subject | Microbiology | - |
dc.subject | Resistance | - |
dc.subject.mesh | Bacteria - drug effects | - |
dc.subject.mesh | Biofilms - drug effects - growth and development | - |
dc.subject.mesh | Drug Resistance, Fungal | - |
dc.subject.mesh | Drug Resistance, Multiple, Bacterial | - |
dc.subject.mesh | Fungi - drug effects - physiology | - |
dc.title | Unraveling the resistance of microbial biofilms: Has proteomics been helpful? | en_US |
dc.type | Article | en_US |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1615-9853&volume=12&issue=4-5&spage=651&epage=665&date=2012&atitle=Unraveling+the+resistance+of+microbial+biofilms:+Has+proteomics+been+helpful? | - |
dc.identifier.email | Seneviratne, CJ: jaya@hku.hk | en_US |
dc.identifier.email | Wang, Y: yuwanghk@hku.hk | en_US |
dc.identifier.email | Jin, L: ljjin@hkucc.hku.hk | en_US |
dc.identifier.email | Wong, SSW: h0616549@hku.hk | en_US |
dc.identifier.email | Samaranayake, LP: lakshman@hku.hk | en_US |
dc.identifier.authority | Seneviratne, CJ=rp01372 | en_US |
dc.identifier.authority | Wang, Y=rp00239 | en_US |
dc.identifier.authority | Jin, L=rp00028 | en_US |
dc.identifier.authority | Samaranayake, LP=rp00023 | en_US |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/pmic.201100356 | - |
dc.identifier.pmid | 22246638 | - |
dc.identifier.scopus | eid_2-s2.0-84859240206 | - |
dc.identifier.hkuros | 211984 | en_US |
dc.identifier.hkuros | 204602 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-84859240206&selection=ref&src=s&origin=recordpage | - |
dc.identifier.volume | 12 | en_US |
dc.identifier.issue | 4-5 | - |
dc.identifier.spage | 651 | en_US |
dc.identifier.epage | 665 | en_US |
dc.identifier.eissn | 1615-9861 | - |
dc.identifier.isi | WOS:000302151800013 | - |
dc.identifier.scopusauthorid | Seneviratne, CJ=55161876500 | - |
dc.identifier.scopusauthorid | Wang, Y=55164276500 | - |
dc.identifier.scopusauthorid | Jin, L=7403328850 | - |
dc.identifier.scopusauthorid | Wong, SSW=55162862100 | - |
dc.identifier.scopusauthorid | Herath, TDK=40561255100 | - |
dc.identifier.scopusauthorid | Samaranayake, LP=55164536100 | - |
dc.identifier.issnl | 1615-9853 | - |