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不可分型流感嗜血杆菌核酸酶在生物膜中微生物扩散中的作用。

Role of the nuclease of nontypeable Haemophilus influenzae in dispersal of organisms from biofilms.

作者信息

Cho Christine, Chande Aroon, Gakhar Lokesh, Bakaletz Lauren O, Jurcisek Joseph A, Ketterer Margaret, Shao Jian, Gotoh Kenji, Foster Eric, Hunt Jason, O'Brien Erin, Apicella Michael A

机构信息

Department of Microbiology and Internal Medicine, The University of Iowa, Iowa City, Iowa, USA.

Department of Biochemistry, The University of Iowa, Iowa City, Iowa, USA Protein Crystallography Facility, The University of Iowa, Iowa City, Iowa, USA.

出版信息

Infect Immun. 2015 Mar;83(3):950-7. doi: 10.1128/IAI.02601-14. Epub 2014 Dec 29.

Abstract

Nontypeable Haemophilus influenzae (NTHI) forms biofilms in the middle ear during human infection. The biofilm matrix of NTHI contains extracellular DNA. We show that NTHI possesses a potent nuclease, which is a homolog of the thermonuclease of Staphylococcus aureus. Using a biofilm dispersal assay, studies showed a biofilm dispersal pattern in the parent strain, no evidence of dispersal in the nuclease mutant, and a partial return of dispersion in the complemented mutant. Quantitative PCR of mRNA from biofilms from a 24-h continuous flow system demonstrated a significantly increased expression of the nuclease from planktonic organisms compared to those in the biofilm phase of growth (P < 0.042). Microscopic analysis of biofilms grown in vitro showed that in the nuclease mutant the nucleic acid matrix was increased compared to the wild-type and complemented strains. Organisms were typically found in large aggregates, unlike the wild-type and complement biofilms in which the organisms were evenly dispersed throughout the biofilm. At 48 h, the majority of the organisms in the mutant biofilm were dead. The nuclease mutant formed a biofilm in the chinchilla model of otitis media and demonstrated a propensity to also form similar large aggregates of organisms. These studies indicate that NTHI nuclease is involved in biofilm remodeling and organism dispersal.

摘要

不可分型流感嗜血杆菌(NTHI)在人类感染期间于中耳形成生物膜。NTHI的生物膜基质含有细胞外DNA。我们发现NTHI拥有一种强效核酸酶,它是金黄色葡萄球菌热核酸酶的同源物。通过生物膜分散试验,研究显示亲本菌株存在生物膜分散模式,核酸酶突变体中无分散迹象,而互补突变体中分散部分恢复。对来自24小时连续流动系统的生物膜的mRNA进行定量PCR分析表明,与处于生物膜生长阶段的生物相比,浮游生物中核酸酶的表达显著增加(P < 0.042)。对体外培养的生物膜进行显微镜分析显示,与野生型和互补菌株相比,核酸酶突变体中的核酸基质增加。与野生型和互补生物膜中生物均匀分散在整个生物膜中不同,突变体生物膜中的生物通常以大聚集体形式存在。在48小时时,突变体生物膜中的大多数生物死亡。核酸酶突变体在中耳炎的栗鼠模型中形成生物膜,并显示出形成类似生物大聚集体的倾向。这些研究表明,NTHI核酸酶参与生物膜重塑和生物分散。

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