Lee Keehoon, Lee Kang-Mu, Kim Donggeun, Yoon Sang Sun
Department of Microbiology and Immunology, Yonsei University College of Medicine, Seoul, South Korea.
Brain Korea 21 PLUS Project for Medical Sciences, Yonsei University College of Medicine, Seoul, South Korea.
Appl Environ Microbiol. 2017 Oct 17;83(21). doi: 10.1128/AEM.01182-17. Print 2017 Nov 1.
Biofilms are microbial communities that inhabit various surfaces and are surrounded by extracellular matrices (ECMs). Clinical microbiologists have shown that the majority of chronic infections are caused by biofilms, following the introduction of the first biofilm infection model by J. W. Costerton and colleagues (J. Lam, R. Chan, K. Lam, and J. W. Costerton, Infect Immun 28:546-556, 1980). However, treatments for chronic biofilm infections are still limited to surgical removal of the infected sites. and are two frequently identified bacterial species in biofilm infections; nevertheless, the interactions between these two species, especially during biofilm growth, are not clearly understood. In this study, we observed phenotypic changes in a dual-species biofilm of and , including a dramatic increase in biofilm matrix thickness. For clear elucidation of the spatial distribution of the dual-species biofilm, and were labeled with red and green fluorescence, respectively. was located at the lower part of the dual-species biofilm, while developed a structured biofilm on the upper part. Mutants with altered exopolysaccharide (EPS) productions were constructed in order to determine the molecular basis for the synergistic effect of the dual-species biofilm. Increased biofilm matrix thickness was associated with EPSs, not extracellular DNA. In particular, Pel and Psl contributed to interspecies and intraspecies interactions, respectively, in the dual-species and biofilm. Accordingly, targeting Pel and Psl might be an effective part of eradicating polymicrobial biofilms. Chronic infection is a serious problem in the medical field. Scientists have observed that chronic infections are closely associated with biofilms, and the vast majority of infection-causing biofilms are polymicrobial. Many studies have reported that microbes in polymicrobial biofilms interact with each other and that the bacterial interactions result in elevated virulence, in terms of factors, such as infectivity and antibiotic resistance. and are frequently isolated pathogens in chronic biofilm infections. Nevertheless, while both bacteria are known to be agents of numerous nosocomial infections and can cause serious diseases, interactions between the bacteria in biofilms have rarely been examined. In this investigation, we aimed to characterize and dual-species biofilms and to determine the molecular factors that cause synergistic effects, especially on the matrix thickening of the biofilm. We suspect that our findings will contribute to the development of more efficient methods for eradicating polymicrobial biofilm infections.
生物膜是栖息于各种表面并被细胞外基质(ECM)包围的微生物群落。临床微生物学家已表明,自J. W. 科斯特顿及其同事引入首个生物膜感染模型以来(J. 林、R. 陈、K. 林和J. W. 科斯特顿,《感染与免疫》28:546 - 556,1980年),大多数慢性感染是由生物膜引起的。然而,慢性生物膜感染的治疗方法仍然局限于手术切除感染部位。[具体细菌名称1]和[具体细菌名称2]是生物膜感染中两种常见的细菌种类;然而,这两种细菌之间的相互作用,尤其是在生物膜生长过程中的相互作用,目前尚不清楚。在本研究中,我们观察了[具体细菌名称1]和[具体细菌名称2]双物种生物膜的表型变化,包括生物膜基质厚度显著增加。为了清晰阐明双物种生物膜的空间分布,[具体细菌名称1]和[具体细菌名称2]分别用红色和绿色荧光标记。[具体细菌名称1]位于双物种生物膜的下部,而[具体细菌名称2]在上部形成了结构有序的生物膜。构建了胞外多糖(EPS)产生改变的突变体,以确定双物种生物膜协同效应的分子基础。生物膜基质厚度增加与EPS有关,而非细胞外DNA。特别是,Pel和Psl分别在[具体细菌名称1]和[具体细菌名称2]双物种生物膜中促成了种间和种内相互作用。因此,针对Pel和Psl可能是根除[具体细菌名称1]多微生物生物膜的有效方法。慢性感染是医学领域的一个严重问题。科学家们观察到慢性感染与生物膜密切相关,并且绝大多数引起感染的生物膜是多微生物的。许多研究报告称,多微生物生物膜中的微生物相互作用,并且这种细菌间相互作用在诸如传染性和抗生素抗性等因素方面导致毒力增强。[具体细菌名称1]和[具体细菌名称2]是慢性生物膜感染中经常分离出的病原体。然而,虽然已知这两种细菌都是许多医院感染的病原体并且可导致严重疾病,但生物膜中细菌之间的相互作用很少被研究。在本研究中,我们旨在表征[具体细菌名称1]和[具体细菌名称2]双物种生物膜,并确定导致协同效应的分子因素,特别是对生物膜基质增厚的影响。我们怀疑我们的发现将有助于开发更有效的方法来根除多微生物生物膜感染。