首页> 外文学位 >The effect of environmental stress on cell surface properties and their relation to microbial adhesion in feedlot Escherichia coli isolates.
【24h】

The effect of environmental stress on cell surface properties and their relation to microbial adhesion in feedlot Escherichia coli isolates.

机译:饲养场大肠杆菌分离物中环境胁迫对细胞表面特性的影响及其与微生物粘附的关系。

获取原文
获取原文并翻译 | 示例

摘要

We built an exhaustive inventory of extant Escherichia coli population from a bovine feedlot at the University of Connecticut. Approximately 280 E. coli isolates were isolated, and a total of 89 distinct operational taxonomic units (OTUs) were identified by whole-cell BOX-PCR genomic fingerprints. Significant subspecies heterogeneity in interfacial behavior was revealed. Motility, measured by a soft agar assay, had a very broad range among the E. coli population and was positively correlated with biofilm-forming in minimal medium (MM, r = 0.619, P 10-4) but not in Luria broth (LB). More biofilm was formed by agn43+ strains in both MM and LB, with a larger effect in MM.; We developed two environmentally relevant growth conditions mimicking intestinal versus external conditions to investigate the phenotypic diversity across a subset of E. coli feedlot isolates in terms of surface characteristics and adhesion behavior. Although no significant difference was observed in zeta potentials, most strains become significantly more hydrophobic and form thicker biofilm on polystyrene microwells under external growth conditions. Furthermore, this enhanced biofilm formation was positive correlated with bacterial surface hydrophobicity (r2 = 0.66), and isolates that exhibited the highest surface hydrophobicity also formed visible clumps. Other than hydrophobicity, motility was determinant in affecting E. coli biofilm formation, with all four non-motile isolates characterized as thin-biofilm formers. The majority (88%) of Ag43+ isolates formed thick biofilms, whereas the majority (75%) of Ag43- isolates formed thin biofilms.; Eight isolates were selected for bacterial transport study by conducting operational retention tests (ORT) under conditions that simulate pulse application of a bacterial load followed by rainfall infiltration and then natural drainage. Flagella-mediated motility was an important variant in cell retardation for all tested materials; bacterial hydrophobicity was important on Pyrax RTM and dolomite; Ag43 expression was important on glass and dolomite. A significant variability in bacterial transport was observed across the E. coli isolates collection. The foodborne pathogen E. coli O157:H7 retained the least with all examined matrices; E. coli K-12 displayed moderate adhesion and may not be a proper model strain to predict E. coli transport. Overall, external growth conditions enhanced bacterial adhesion to all materials, and PyraxRTM might serve as a good candidate biobarrier material given its superior removal ability.
机译:我们从康涅狄格大学的牛饲养场建立了详尽的现存大肠杆菌种群清单。分离出大约280个大肠杆菌分离物,并通过全细胞BOX-PCR基因组指纹识别了总共89个不同的操作分类单位(OTU)。显着亚种界面行为的异质性。通过软琼脂分析测定的运动性在大肠杆菌群体中具有很宽的范围,并且与基本培养基中的生物膜形成呈正相关(MM,r = 0.619,P <10-4),而在Luria肉汤中则没有(磅)。在MM和LB中,由agn43 +菌株形成的生物膜更多,对MM的影响更大。我们开发了两种环境相关的生长条件,模拟了肠道条件和外部条件,以研究大肠杆菌饲养场分离物的一个子集在表面特性和粘附行为方面的表型多样性。尽管在ζ电势上未观察到显着差异,但是大多数菌株在外部生长条件下变得明显更疏水并且在聚苯乙烯微孔上形成更厚的生物膜。此外,这种增强的生物膜形成与细菌表面疏水性呈正相关(r2 = 0.66),表现出最高表面疏水性的分离物也形成可见的团块。除疏水性外,运动性是影响大肠杆菌生物膜形成的决定性因素,所有四个非运动性分离物均以生物膜形成剂为特征。大部分(88%)的Ag43 +分离物形成厚的生物膜,而大部分(75%)的Ag43-分离物形成薄的生物膜。通过在模拟细菌载荷脉冲施加,随后降雨入渗,然后自然排水的条件下进行操作保留测试(ORT),选择了八个分离物用于细菌迁移研究。鞭毛介导的运动力是所有测试材料的细胞发育迟缓的重要变体。细菌疏水性对Pyrax RTM和白云石很重要。 Ag43在玻璃和白云石上的表达很重要。在整个大肠杆菌分离株中观察到细菌运输的显着变化。食源性病原大肠杆菌O157:H7在所有检查的基质中保留最少。大肠杆菌K-12表现出中等的粘附力,可能不是预测大肠杆菌转运的合适模型菌株。总体而言,外部生长条件增强了细菌对所有材料的附着力,并且PyraxRTM鉴于其卓越的去除能力,可能成为良好的生物屏障材料。

著录项

  • 作者

    Yang, Hsiao-Hui.;

  • 作者单位

    The University of Connecticut.;

  • 授予单位 The University of Connecticut.;
  • 学科 Biology Microbiology.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 123 p.
  • 总页数 123
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 微生物学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号