File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1183/09031936.03.00097302
- Scopus: eid_2-s2.0-0038652119
- PMID: 12797484
- WOS: WOS:000183242900005
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Pseudomonas aeruginosa adherence to human basement membrane collagen in vitro
Title | Pseudomonas aeruginosa adherence to human basement membrane collagen in vitro |
---|---|
Authors | |
Keywords | Bacterial adherence Basement membrane Collagen Pseudomonas aeruginosa |
Issue Date | 2003 |
Publisher | European Respiratory Society. The Journal's web site is located at http://erj.ersjournals.com |
Citation | European Respiratory Journal, 2003, v. 21 n. 6, p. 932-938 How to Cite? |
Abstract | The mechanisms for Pseudomonas aeruginosa colonisation in the airways of patients with bronchiectasis and cystic fibrosis are poorly understood. P. aeruginosa could evade mucociliary clearance by adhering to the basement membrane at areas denuded of,intact respiratory epithelium. The authors have developed an in vitro model to study P. aeruginosa adherence to human basement membrane type-IV collagen by using scanning electron microscopy. P. aeruginosa adherence density was determined as the number of P. aeruginosa per 20 microscope fields (2,000x) to log inocular size after incubation at 37°C for 45 min. The presence of phytohaemagglutinin (PHA)-E, which binds specifically to D-galactose-β1-4-D-N-acetylglucosamine, significantly reduced P. aeruginosa adherence density compared with control. The presence of heparin and calcium also significantly reduced P. aeruginosa adherence density. P. aeruginosa adherence was not affected by the presence of proline, trans-hydroxyproline, glycine, galactose, N-acetylneuraminic acid, N-acetylglucosamine or Arachis hypogea. Pseudomonas aeruginosa adherence probably acts via recognition of the D-galactose-β1-4-D-N-acetylglucosamine sequence on type-IV collagen and this process could be inhibited by heparin and calcium. As persistent Pseudomonas aeruginosa colonisation is detrimental to patients with cystic fibrosis and bronchiectasis and there is currently no effective treatment for its eradication, these results could lead to novel therapy for persistent Pseudomonas aeruginosa infection. |
Persistent Identifier | http://hdl.handle.net/10722/147485 |
ISSN | 2023 Impact Factor: 16.6 2023 SCImago Journal Rankings: 3.810 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tsang, KW | en_HK |
dc.contributor.author | Shum, DK | en_HK |
dc.contributor.author | Chan, S | en_HK |
dc.contributor.author | Ng, P | en_HK |
dc.contributor.author | Mak, J | en_HK |
dc.contributor.author | Leung, R | en_HK |
dc.contributor.author | Shum, IH | en_HK |
dc.contributor.author | Ooi, GC | en_HK |
dc.contributor.author | Tipoe, GL | en_HK |
dc.contributor.author | Lam, WK | en_HK |
dc.date.accessioned | 2012-05-29T06:04:03Z | - |
dc.date.available | 2012-05-29T06:04:03Z | - |
dc.date.issued | 2003 | en_HK |
dc.identifier.citation | European Respiratory Journal, 2003, v. 21 n. 6, p. 932-938 | en_HK |
dc.identifier.issn | 0903-1936 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/147485 | - |
dc.description.abstract | The mechanisms for Pseudomonas aeruginosa colonisation in the airways of patients with bronchiectasis and cystic fibrosis are poorly understood. P. aeruginosa could evade mucociliary clearance by adhering to the basement membrane at areas denuded of,intact respiratory epithelium. The authors have developed an in vitro model to study P. aeruginosa adherence to human basement membrane type-IV collagen by using scanning electron microscopy. P. aeruginosa adherence density was determined as the number of P. aeruginosa per 20 microscope fields (2,000x) to log inocular size after incubation at 37°C for 45 min. The presence of phytohaemagglutinin (PHA)-E, which binds specifically to D-galactose-β1-4-D-N-acetylglucosamine, significantly reduced P. aeruginosa adherence density compared with control. The presence of heparin and calcium also significantly reduced P. aeruginosa adherence density. P. aeruginosa adherence was not affected by the presence of proline, trans-hydroxyproline, glycine, galactose, N-acetylneuraminic acid, N-acetylglucosamine or Arachis hypogea. Pseudomonas aeruginosa adherence probably acts via recognition of the D-galactose-β1-4-D-N-acetylglucosamine sequence on type-IV collagen and this process could be inhibited by heparin and calcium. As persistent Pseudomonas aeruginosa colonisation is detrimental to patients with cystic fibrosis and bronchiectasis and there is currently no effective treatment for its eradication, these results could lead to novel therapy for persistent Pseudomonas aeruginosa infection. | en_HK |
dc.language | eng | en_US |
dc.publisher | European Respiratory Society. The Journal's web site is located at http://erj.ersjournals.com | en_HK |
dc.relation.ispartof | European Respiratory Journal | en_HK |
dc.subject | Bacterial adherence | en_HK |
dc.subject | Basement membrane | en_HK |
dc.subject | Collagen | en_HK |
dc.subject | Pseudomonas aeruginosa | en_HK |
dc.subject.mesh | Amino Acids - Pharmacology | en_US |
dc.subject.mesh | Bacterial Adhesion - Drug Effects - Physiology | en_US |
dc.subject.mesh | Basement Membrane - Drug Effects - Physiopathology - Ultrastructure | en_US |
dc.subject.mesh | Bronchiectasis - Physiopathology | en_US |
dc.subject.mesh | Carbohydrates - Pharmacology | en_US |
dc.subject.mesh | Collagen Type Iv - Drug Effects - Physiology - Ultrastructure | en_US |
dc.subject.mesh | Colony Count, Microbial | en_US |
dc.subject.mesh | Cystic Fibrosis - Physiopathology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Ions - Pharmacology | en_US |
dc.subject.mesh | Lectins - Pharmacology | en_US |
dc.subject.mesh | Microscopy, Electron, Scanning | en_US |
dc.subject.mesh | Pseudomonas Aeruginosa - Drug Effects - Physiology - Ultrastructure | en_US |
dc.title | Pseudomonas aeruginosa adherence to human basement membrane collagen in vitro | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Shum, DK:shumdkhk@hkucc.hku.hk | en_HK |
dc.identifier.email | Mak, J:judymak@hku.hk | en_HK |
dc.identifier.email | Tipoe, GL:tgeorge@hkucc.hku.hk | en_HK |
dc.identifier.authority | Shum, DK=rp00321 | en_HK |
dc.identifier.authority | Mak, J=rp00352 | en_HK |
dc.identifier.authority | Tipoe, GL=rp00371 | en_HK |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1183/09031936.03.00097302 | - |
dc.identifier.pmid | 12797484 | - |
dc.identifier.scopus | eid_2-s2.0-0038652119 | en_HK |
dc.identifier.hkuros | 79041 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0038652119&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 21 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 932 | en_HK |
dc.identifier.epage | 938 | en_HK |
dc.identifier.isi | WOS:000183242900005 | - |
dc.publisher.place | Switzerland | en_HK |
dc.identifier.scopusauthorid | Tsang, KW=7201555024 | en_HK |
dc.identifier.scopusauthorid | Shum, DK=7004824447 | en_HK |
dc.identifier.scopusauthorid | Chan, S=14055434000 | en_HK |
dc.identifier.scopusauthorid | Ng, P=55107639000 | en_HK |
dc.identifier.scopusauthorid | Mak, J=7103323094 | en_HK |
dc.identifier.scopusauthorid | Leung, R=7101876102 | en_HK |
dc.identifier.scopusauthorid | Shum, IH=6602960338 | en_HK |
dc.identifier.scopusauthorid | Ooi, GC=7006176119 | en_HK |
dc.identifier.scopusauthorid | Tipoe, GL=7003550610 | en_HK |
dc.identifier.scopusauthorid | Lam, WK=7203021937 | en_HK |
dc.identifier.issnl | 0903-1936 | - |