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拉丁美洲分离株与流行 NAP1/027 株的生物膜形成能力比较。

Comparative biofilm-forming ability between strains isolated in Latin America and the epidemic NAP1/027 strain.

机构信息

Department of Morphology, Faculty of Medicine, Federal University of Ceará, Fortaleza, CE, Brazil.

Laboratory of Bacteriology, Department of Pathology, Faculty of Medicine, Federal University of Ceará, Fortaleza, CE, Brazil.

出版信息

Front Cell Infect Microbiol. 2022 Dec 1;12:1033698. doi: 10.3389/fcimb.2022.1033698. eCollection 2022.

Abstract

INTRODUCTION

One of the challenges in treating infection (CDI) is that the bacterium forms biofilms, a critical virulence mechanism known to promote antibiotic resistance and, as a result, consequently, a higher recurrence of the disease. The goal of this study was to compare the ability of three MLST Clade 2 strains to form a biofilm in vitro: ICC-45 (ribotype SLO231/UK[CE]821), a ST41 toxinotype IXb isolated in Brazil; and two epidemic NAP1/027/ST01 strains: NAP1/027/ST01 (LIBA5756), isolated during a 2010 outbreak in Costa Rica and the reference epidemic strain NAP1/027/ST01 (R20291); and ATCC700057, a non-toxigenic strain.

METHODS

The ability of strains to form biofilm was evaluated using crystal violet staining. In addition, samples were stained with the Film Tracer biofilm matrix (Invitrogen®) and the biofilm matrix thickness was measured using confocal microscopy. The matrix architecture was determined using Scanning electron microscop. Confocal microscopy was used to detect the presence of toxin A (tcdA) using an anti- TcdA antibody. The expression of virulence genes (, , , , , , and ) was examined, as well as the effect of antibiotics metronidazole (MTZ) and vancomycin (VAN) on biofilm growth.

RESULTS

All of the strains tested formed a moderate biofilm with 1.1 3.5. After 72h, biofilm biomass of the NAP1/027/ST01 epidemic strains (LIBA5756 and R20291) was significantly higher than ICC-45 and ATCC 700057 biofilms, as confirmed by electron and confocal microscopy. At 120h, the LIBA5756 biofilm biomass decreased compared to other strains. The toxigenic strains R20291 or LIBA 5756 had higher expression of genes , , , , and than ICC-45, but there were no significant differences in the expression levels of , and . In epidemic strains, VAN and MTZ inhibited biofilm formation; however, in the ICC-45 strain, MIC concentrations of VAN and MIC and 4MIC of MTZ did not inhibit biofilm formation.

CONCLUSION

The three MLST Clade 2 isolated from different rybotipes, two of which were isolated from Latin America, are competent biofilm-forming bacteria, indicating their ability to induce infection recurrence, making treatment difficult.

摘要

简介

治疗 感染 (CDI) 的挑战之一是细菌会形成生物膜,这是一种已知的关键毒力机制,可促进抗生素耐药性,因此导致疾病更高的复发率。本研究的目的是比较三种 MLST 克隆群 2 菌株在体外形成生物膜的能力:ICC-45(SLO231/UK[CE]821 型),一种在巴西分离的 ST41 毒素型 IXb 菌株;和两种流行的 NAP1/027/ST01 菌株:NAP1/027/ST01(LIBA5756),在 2010 年哥斯达黎加爆发期间分离得到;以及参考流行株 NAP1/027/ST01(R20291);和 ATCC700057,一种非产毒菌株。

方法

使用结晶紫染色评估菌株形成生物膜的能力。此外,还使用 Film Tracer 生物膜基质(Invitrogen®)对样品进行染色,并使用共聚焦显微镜测量生物膜基质的厚度。使用扫描电子显微镜确定基质结构。使用抗 TcdA 抗体通过共聚焦显微镜检测毒素 A (tcdA) 的存在。还检测了毒力基因(、、、、、、和)的表达,以及甲硝唑 (MTZ) 和万古霉素 (VAN) 对生物膜生长的影响。

结果

所有测试的菌株都形成了中等强度的生物膜,DO 值在 1.1 到 3.5 之间。72 小时后,NAP1/027/ST01 流行株(LIBA5756 和 R20291)的生物膜生物量明显高于 ICC-45 和 ATCC 700057 生物膜,这通过电子显微镜和共聚焦显微镜得到证实。在 120 小时时,LIBA5756 生物膜生物量与其他菌株相比有所下降。产毒株 R20291 或 LIBA 5756 中基因、、、、和 的表达水平高于 ICC-45,但基因、和 的表达水平没有显著差异。在流行株中,VAN 和 MTZ 抑制生物膜形成;然而,在 ICC-45 菌株中,VAN 和 MTZ 的 MIC 浓度以及 4MIC 的 MTZ 均不能抑制生物膜形成。

结论

从不同表型分离的三种 MLST 克隆群 2 分离株,其中两种来自拉丁美洲,都是有能力形成生物膜的细菌,表明它们有能力引起 感染的复发,使治疗变得困难。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a8/9815708/76dce72c6644/fcimb-12-1033698-g001.jpg

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