Dynamics of Flagellum- and Pilus-Mediated Association of Pseudomonas aeruginosa with Contact Lens Surfaces

Author:

Tran Victoria B.1,Fleiszig Suzanne M. J.234,Evans David J.25,Radke Clayton J.13

Affiliation:

1. Chemical and Biomolecular Engineering Department, University of California, Berkeley, California 94720

2. School of Optometry, University of California, Berkeley, California 94720

3. Graduate Group in Vision Science, University of California, Berkeley, California 94720

4. Graduate Groups in Plant and Microbial Biology and Infectious Disease and Immunity, University of California, Berkeley, California 94720

5. College of Pharmacy, Touro University—California, Vallejo, California 94592

Abstract

ABSTRACT Flagella and pili are appendages that modulate attachment of Pseudomonas aeruginosa to solid surfaces. However, previous studies have mostly reported absolute attachment. Neither the dynamic roles of these appendages in surface association nor those of attachment phenotypes have been quantified. We used video microscopy to address this issue. Unworn, sterile, soft contact lenses were placed in a laminar-flow optical chamber. Initial lens association kinetics for P. aeruginosa strain PAK were assessed in addition to lens-surface association phenotypes. Comparisons were made to strains with mutations in flagellin ( fliC ) or pilin ( pilA ) or those in flagellum ( motAB ) or pilus ( pilU ) function. PAK and its mutants associated with the contact lens surface at a constant rate according to first-order kinetics. Nonswimming mutants associated ∼30 to 40 times slower than the wild type. PAK and its pilA mutant associated at similar rates, but each ∼4 times faster than the pilU mutant. Lens attachment by wild-type PAK induced multiple phenotypes (static, lateral, and rotational surface movement), each showing only minor detachment. Flagellin ( fliC ) and flagellar-motility ( motAB ) mutants did not exhibit surface rotation. Conversely, strains with mutations in pilin ( pilA ) and pilus retraction ( pilU ) lacked lateral-surface movement but displayed enhanced surface rotation. Slower surface association of swimming-incapable P. aeruginosa mutants was ascribed to lower convective-diffusion-arrival rates, not to an inability to adhere. Flagellum function (swimming) enhanced lens association, attachment, and rotation; hyperpiliation hindered lens association. P. aeruginosa bound through three different adhesion sites: flagellum, pili, and body. Reduction of bacterial attachment to contact lenses thus requires blockage of multiple adhesion phenotypes.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference62 articles.

1. The Pseudomonas aeruginosa Flagellar Cap Protein, FliD, Is Responsible for Mucin Adhesion

2. Determination of effective transport coefficients for bacterial migration in sand columns

3. BergH. C. 1993. Random walks in biology, expanded edition. Princeton University Press, Princeton, NJ.

4. Inhibition of bacterial adherence to contact lens cases and soft contact lenses, including high dk continuous wear silicone hydrogels: a new and unique attribute of ReNu with MoistureLoc solution;Borazjani N.;Invest. Ophthalmol. Vis. Sci,2005

5. Bacterial adhesion to surface hydrophilic and hydrophobic contact lenses;Bruinsma G. M.;Biomaterials,2001

Cited by 37 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3