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用变形链球菌葡糖基转移酶的葡聚糖结合区或催化区的合成肽构建体对大鼠进行免疫可预防龋齿。

Immunization of rats with synthetic peptide constructs from the glucan-binding or catalytic region of mutans streptococcal glucosyltransferase protects against dental caries.

作者信息

Taubman M A, Holmberg C J, Smith D J

机构信息

Department of Immunology, Forsyth Dental Center, Boston, Massachusetts 02115, USA.

出版信息

Infect Immun. 1995 Aug;63(8):3088-93. doi: 10.1128/iai.63.8.3088-3093.1995.

Abstract

Previously, we have described peptide constructs from two regions of glucosyltransferase (GTF) of mutans streptococci. A putative catalytic site in the amino-terminal half of the molecule and a repeated glucan-binding site in the carboxyl-terminal half of GTF were the regions upon which sequences were based. The present study explored the effects of immunization with these peptide constructs (called CAT or GLU) and with streptococcal GTFs from Streptococcus sobrinus and S. mutans on immunological, microbiological, and disease parameters. Groups of immunized Sprague-Dawley rats were infected with either 10(8) S. sobrinus 6715 or 10(8) S. mutans SJ32 organisms. Serum immunoglobulin G antibody levels, determined by enzyme-linked immunosorbent assay, to the respective peptide constructs and to the appropriate streptococcal GTF were significantly increased (after immunization) prior to infection and at the end of the experiment. Also, serum antibody from CAT-, GLU-, and S. sobrinus GTF-immunized rats inhibited S. sobrinus GTF-mediated insoluble glucan synthesis (all) and S. mutans GTF-mediated soluble glucan synthesis (all except anti-GLU) from sucrose. Immunization with the CAT or GLU peptide construct resulted in significantly reduced smooth surface and sulcal caries after infection with S. sobrinus. Sulcal dental caries after infection with S. mutans SJ32 were also significantly reduced in CAT- and GLU-immunized rats. Thus, immunization with peptides whose sequences are based on putative functional domains of mutans streptococcal GTF are protective toward a cariogenic S. sobrinus or S. mutans infection.

摘要

此前,我们已经描述了变形链球菌葡糖基转移酶(GTF)两个区域的肽构建体。分子氨基末端一半中的一个假定催化位点以及GTF羧基末端一半中的一个重复葡聚糖结合位点是序列所基于的区域。本研究探讨了用这些肽构建体(称为CAT或GLU)以及来自远缘链球菌和变形链球菌的链球菌GTF进行免疫对免疫、微生物学和疾病参数的影响。将免疫的Sprague-Dawley大鼠组用10⁸个远缘链球菌6715或10⁸个变形链球菌SJ32菌株感染。通过酶联免疫吸附测定法测定的针对各自肽构建体和相应链球菌GTF的血清免疫球蛋白G抗体水平在感染前和实验结束时(免疫后)显著升高。此外,来自CAT、GLU和远缘链球菌GTF免疫大鼠的血清抗体抑制了远缘链球菌GTF介导的不溶性葡聚糖合成(全部)以及变形链球菌GTF介导的由蔗糖合成的可溶性葡聚糖合成(除抗GLU外全部)。用CAT或GLU肽构建体免疫导致感染远缘链球菌后光滑表面龋和龈沟龋显著减少。在感染变形链球菌SJ32后,CAT和GLU免疫的大鼠龈沟龋也显著减少。因此,用其序列基于变形链球菌GTF假定功能域的肽进行免疫对致龋性远缘链球菌或变形链球菌感染具有保护作用。

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Decreased cariogenicity of a mutant of Streptococcus mutans.变形链球菌突变体的致龋性降低。
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