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抗PIA/PNAG抗体对生物膜形成影响的研究。 (原文中“in.”后面内容缺失,翻译只能到此为止)

Investigation of the effect of anti-PIA/PNAG antibodies on biofilm formation in .

作者信息

Shirmohammadpour Mina, Mehrasbi Mohammad Reza, Noshiranzadeh Nader, Afshar Davoud, Mansori Kamyar, Mirzaei Bahman

机构信息

Department of Microbiology and Virology, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.

Student Research Committee, Department of Medical Microbiology and Virology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.

出版信息

Front Microbiol. 2025 Mar 6;16:1552670. doi: 10.3389/fmicb.2025.1552670. eCollection 2025.

Abstract

Polysaccharide Intercellular Adhesin (PIA), a surface polysaccharide produced by and , is a compelling target for opsonic and protective antibodies against these bacteria. has recently made an exopolysaccharide called poly-(1,6)--acetylglucosamine (PNAG), biochemically indistinguishable from PIA. This study investigated the effect of antibodies generated against PNAG on biofilm formation and the opsonization activity of secreted antibodies in . Following purification and structural confirmation of PIA polysaccharide from producing , the ability to inhibit biofilm and the function of secreted antibodies for the mentioned polysaccharide were evaluated using semi-quantitative methods in a mouse model. Subsequently, the opsonic activity of antibodies targeting strain ATCC 25922 was evaluated. The extracted polysaccharide was confirmed using FTIR, NMR, and colorimetric methods, and the results showed that the purified PIA induced protective antibodies with 40.48% opsonization properties in . The sera of the PIA-immunized groups showed a significant increase in antibody production and protective IgG titer levels compared to the control group. Also, the antibodies produced showed a substantial difference in inhibiting biofilm production compared to non-immunized serum. Antibodies directed against PIA with a lethality of 40.48% showed a significant effect on the absence of biofilm formation in . Despite the opsonic properties of the antibodies for , the simultaneous impact of these antibodies on infections caused by and may have a role that requires further investigation and studies in animal models.

摘要

多糖细胞间黏附素(PIA)是由[具体细菌名称1]和[具体细菌名称2]产生的一种表面多糖,是针对这些细菌的调理和保护性抗体的一个极具吸引力的靶点。[具体细菌名称3]最近产生了一种胞外多糖,称为聚(1,6)-α-乙酰葡糖胺(PNAG),其生化性质与PIA无法区分。本研究调查了针对PNAG产生的抗体对生物膜形成的影响以及[具体细菌名称4]中分泌抗体的调理活性。从产生PIA多糖的[具体细菌名称5]中纯化并进行结构确认后,在小鼠模型中使用半定量方法评估了抑制生物膜的能力以及针对上述多糖的分泌抗体的功能。随后,评估了靶向[具体细菌名称6]菌株ATCC 25922的抗体的调理活性。使用傅里叶变换红外光谱(FTIR)、核磁共振(NMR)和比色法对提取的多糖进行了确认,结果表明纯化的PIA在[具体细菌名称7]中诱导出具有40.48%调理特性的保护性抗体。与对照组相比,PIA免疫组的血清中抗体产生和保护性IgG滴度水平显著增加。此外,与未免疫血清相比,产生的抗体在抑制生物膜产生方面表现出显著差异。对PIA的致死率为40.48%的抗体对[具体细菌名称8]中生物膜形成的缺失有显著影响。尽管这些抗体对[具体细菌名称9]具有调理特性,但这些抗体对由[具体细菌名称10]和[具体细菌名称11]引起的感染的同时影响可能具有需要在动物模型中进一步研究和探讨的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e606/11922938/924c9a6ded50/fmicb-16-1552670-g001.jpg

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