Adelaide Dental School, University of Adelaide, Adelaide, South Australia, Australia.
Adelaide Dental School, University of Adelaide, Adelaide, South Australia, Australia.
J Endod. 2018 Feb;44(2):269-273. doi: 10.1016/j.joen.2017.08.025. Epub 2017 Dec 6.
Extracellular material (ECM) surrounding Enterococcus faecalis may play a role in increasing resistance to environmental stresses. Our aim was to determine ECM levels in response to subminimal inhibitory concentrations of sodium hypochlorite (sub-MIC/NaOCl) or anaerobic growth and determine the impact on biofilm development.
From 37 E. faecalis clinical strains, 19 were selected according to their biofilm-producing ability by using a crystal violet biofilm assay: 10 strong, 4 intermediate, and 5 non-biofilm producers. Biofilm assays were subsequently performed on all strains when subjected to sub-MIC/NaOCl. All strains were evaluated for ECM production under aerobic and anaerobic conditions and with sub-MIC/NaOCl. ECM production was assessed by using scanning electron microscopy. Double-blinded independent assessors were used to score levels of ECM production. The esp gene was detected by using polymerase chain reaction. Gelatinase activity was determined by using Todd-Hewitt and gelatin agar.
In aerobic conditions, ECM was expressed in all strains. In the presence of sub-MIC/NaOCl, of the 10 strong biofilm producers, 5 increased their ECM production, and 4 showed increased biofilm growth. Two strains had less ECM production and showed decreased biofilm growth. One isolate demonstrated no observable changes. Most non-biofilm producers demonstrated no observable differences in ECM production, although 1 strain increased biofilm growth. ECM production in anaerobic conditions was highly variable. The esp gene (n = 15) and gelatinase activity (n = 7) were evident among the isolates.
Clonal diversity among strains of E. faecalis suggests that some strong biofilm producers can upregulate ECM production and increase biofilm growth in response to sub-MIC/NaOCl.
环绕粪肠球菌的细胞外基质(ECM)可能在增加其对环境应激的抵抗力方面发挥作用。我们的目的是确定 ECM 水平对亚最小抑菌浓度次氯酸钠(sub-MIC/NaOCl)或厌氧生长的反应,并确定其对生物膜形成的影响。
从 37 株粪肠球菌临床株中,根据结晶紫生物膜测定法选择了 19 株具有生物膜形成能力的菌株:10 株强、4 株中、5 株非生物膜形成株。随后对所有菌株进行亚 MIC/NaOCl 处理时进行生物膜测定。在有氧和厌氧条件下以及亚 MIC/NaOCl 条件下评估所有菌株的 ECM 产生情况。通过扫描电子显微镜评估 ECM 产生情况。使用双盲独立评估者对 ECM 产生水平进行评分。使用聚合酶链反应检测 esp 基因。通过 Todd-Hewitt 和明胶琼脂测定明胶酶活性。
在有氧条件下,所有菌株均表达 ECM。在存在亚 MIC/NaOCl 的情况下,10 株强生物膜形成株中,有 5 株增加了 ECM 产生,有 4 株显示出增加的生物膜生长。有 2 株的 ECM 产生减少,生物膜生长减少。有 1 株分离株没有观察到明显的变化。大多数非生物膜形成株的 ECM 产生没有观察到明显的差异,尽管有 1 株增加了生物膜生长。厌氧条件下的 ECM 产生高度可变。在分离株中检测到 esp 基因(n=15)和明胶酶活性(n=7)。
粪肠球菌株之间的克隆多样性表明,一些强生物膜形成株可以上调 ECM 产生,并在亚 MIC/NaOCl 作用下增加生物膜生长。