Izano Era A, Shah Suhagi M, Kaplan Jeffrey B
Department of Oral Biology, New Jersey Dental School, Newark, NJ 07103, USA.
Microb Pathog. 2009 Apr;46(4):207-13. doi: 10.1016/j.micpath.2009.01.004. Epub 2009 Feb 4.
Respiratory infections caused by nontypeable Haemophilus influenzae (NTHi) are a major medical problem. Evidence suggests that the ability to form biofilms on mucosal surfaces may play a role in NTHi pathogenesis. However, the factors that contribute to NTHi biofilm cohesion remain largely unknown. In this study we investigated the biofilm growth and detachment phenotypes of eight NTHi clinical strains in vitro. We found that the majority of strains produced biofilms within 6h when cultured statically in tubes. Biofilm formation was inhibited when culture medium was supplemented with proteinase K or DNase I. Both enzymes also caused significant detachment of pre-formed NTHi biofilms. These findings indicate that both proteinaceous adhesins and extracellular DNA contribute to NTHi biofilm cohesion. Treatment of NTHi biofilms cultured in centrifugal filter devices with DNase I, but not with proteinase K, caused a significant decrease in fluid convection through the biofilms. These results suggest that extracellular DNA is the major volumetric component of the NTHi biofilm matrix. Mechanical or enzymatic disruption of NTHi biofilms cultured in microtiter plates significantly increased their sensitivity to killing by SDS, cetylpyridinium chloride, chlorhexidine gluconate, povidone iodine and sodium hypochlorite. These findings indicate that biocide resistance in NTHi biofilms is mediated to a large part by the cohesive and protective properties of the biofilm matrix. Understanding the mechanisms of biofilm cohesion and biocide resistance in NTHi biofilms may lead to new methods for treating NTHi-associated infections.
由不可分型流感嗜血杆菌(NTHi)引起的呼吸道感染是一个主要的医学问题。有证据表明,在粘膜表面形成生物膜的能力可能在NTHi发病机制中起作用。然而,导致NTHi生物膜凝聚的因素在很大程度上仍然未知。在本研究中,我们调查了8株NTHi临床分离株在体外的生物膜生长和脱落表型。我们发现,大多数菌株在试管中静态培养6小时内就能产生生物膜。当培养基中添加蛋白酶K或DNase I时,生物膜形成受到抑制。这两种酶也会导致预先形成的NTHi生物膜显著脱落。这些发现表明,蛋白质粘附素和细胞外DNA都有助于NTHi生物膜的凝聚。用DNase I而不是蛋白酶K处理在离心过滤装置中培养的NTHi生物膜,会导致通过生物膜的流体对流显著减少。这些结果表明,细胞外DNA是NTHi生物膜基质的主要体积成分。在微量滴定板中培养的NTHi生物膜的机械或酶促破坏显著增加了它们对十二烷基硫酸钠、十六烷基氯化吡啶、葡萄糖酸氯己定、聚维酮碘和次氯酸钠杀伤的敏感性。这些发现表明,NTHi生物膜中的抗微生物剂抗性在很大程度上是由生物膜基质的凝聚和保护特性介导的。了解NTHi生物膜中生物膜凝聚和抗微生物剂抗性的机制可能会导致治疗NTHi相关感染的新方法。