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饥饿和生物膜形成对变形链球菌耐酸性的影响。

Influence of starvation and biofilm formation on acid resistance of Streptococcus mutans.

作者信息

Zhu M, Takenaka S, Sato M, Hoshino E

机构信息

Cariology Research Unit, Department of Oral Microbiology, Niigata University School of Dentistry, Niigata, Japan.

出版信息

Oral Microbiol Immunol. 2001 Feb;16(1):24-7. doi: 10.1034/j.1399-302x.2001.160104.x.

Abstract

The aim of this study was to investigate acid resistance induced by starvation or biofilm formation in Streptococcus mutans ATCC 25175. The artificial biofilms were made on cover glasses, starved for 24 h and immersed in 0.1 M lactate buffer at pH 3.8 for 10 min. The biofilms were also exposed to 5% sucrose solution for 20 min to simulate acid shock produced by sucrose metabolism. Confocal laser scanning microscopy with fluorescein isothiocyanate staining measured the resultant minimum pH in biofilms. Live and dead organisms in biofilms were differentiated by confocal laser scanning microscopy with proidium iodide and SYTO9 staining. The same processes were used to treat planktonic organisms. The results showed that starved biofilms or planktonic cells showed significantly more viable bacteria after acid shock induced either by lactic acid or during sucrose consumption than non-starved biofilms or planktonic cells. In addition, biofilms showed greater resistance to acid shock induced by lactic acid than planktonic cells, whereas similar results were obtained where sucrose was used as a carbon source to reduce pH in biofilms and planktonic cells. Thus, it is suggested that starvation protects both biofilm and planktonic S. mutans from acid shock induced either by lactic acid or during sucrose consumption, while biofilm formation seemed to protect bacteria only from acid shock induced by pH 3.8 lactate buffer but not the acid shock of a slightly higher pH produced during sucrose consumption.

摘要

本研究的目的是调查变形链球菌ATCC 25175中饥饿或生物膜形成所诱导的耐酸性。人工生物膜在盖玻片上制成,饥饿24小时,然后浸入pH值为3.8的0.1 M乳酸缓冲液中10分钟。生物膜还暴露于5%蔗糖溶液中20分钟,以模拟蔗糖代谢产生的酸冲击。采用异硫氰酸荧光素染色的共聚焦激光扫描显微镜测量生物膜中产生的最低pH值。通过碘化丙啶和SYTO9染色的共聚焦激光扫描显微镜区分生物膜中的活细菌和死细菌。对浮游生物采用相同的处理方法。结果表明,与未饥饿的生物膜或浮游细胞相比,饥饿的生物膜或浮游细胞在乳酸诱导的酸冲击或蔗糖消耗过程中表现出明显更多的存活细菌。此外,生物膜对乳酸诱导的酸冲击的耐受性高于浮游细胞,而当使用蔗糖作为碳源降低生物膜和浮游细胞的pH值时,得到了类似的结果。因此,有人认为饥饿可保护生物膜和浮游变形链球菌免受乳酸诱导的酸冲击或蔗糖消耗过程中的酸冲击,而生物膜的形成似乎仅能保护细菌免受pH值为3.8的乳酸缓冲液诱导的酸冲击,而不能保护其免受蔗糖消耗过程中产生的略高pH值的酸冲击。

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